Compartir
array:24 [
"pii" => "S1699258X18301682"
"issn" => "1699258X"
"doi" => "10.1016/j.reuma.2018.07.009"
"estado" => "S300"
"fechaPublicacion" => "2020-09-01"
"aid" => "1255"
"copyright" => "The Authors"
"copyrightAnyo" => "2018"
"documento" => "article"
"crossmark" => 1
"licencia" => "http://creativecommons.org/licenses/by-nc-nd/4.0/"
"subdocumento" => "fla"
"cita" => "Reumatol Clin. 2020;16:345-52"
"abierto" => array:3 [
"ES" => true
"ES2" => true
"LATM" => true
]
"gratuito" => true
"lecturas" => array:2 [
"total" => 1669
"formatos" => array:3 [
"EPUB" => 123
"HTML" => 1078
"PDF" => 468
]
]
"itemSiguiente" => array:19 [
"pii" => "S1699258X18302377"
"issn" => "1699258X"
"doi" => "10.1016/j.reuma.2018.10.008"
"estado" => "S300"
"fechaPublicacion" => "2020-09-01"
"aid" => "1293"
"copyright" => "Elsevier España, S.L.U. and Sociedad Española de Reumatología y Colegio Mexicano de Reumatología"
"documento" => "simple-article"
"crossmark" => 1
"subdocumento" => "crp"
"cita" => "Reumatol Clin. 2020;16:353-5"
"abierto" => array:3 [
"ES" => true
"ES2" => true
"LATM" => true
]
"gratuito" => true
"lecturas" => array:2 [
"total" => 13
"formatos" => array:2 [
"HTML" => 7
"PDF" => 6
]
]
"es" => array:12 [
"idiomaDefecto" => true
"cabecera" => "<span class="elsevierStyleTextfn">Original breve</span>"
"titulo" => "Tendencias en el abordaje posquirúrgico del síndrome del túnel del carpo. Práctica clínica actual"
"tienePdf" => "es"
"tieneTextoCompleto" => "es"
"tieneResumen" => array:2 [
0 => "es"
1 => "en"
]
"paginas" => array:1 [
0 => array:2 [
"paginaInicial" => "353"
"paginaFinal" => "355"
]
]
"titulosAlternativos" => array:1 [
"en" => array:1 [
"titulo" => "Tendencies in the Post-surgical Approach for Carpal Tunnel Syndrome. Current Clinical Practice"
]
]
"contieneResumen" => array:2 [
"es" => true
"en" => true
]
"contieneTextoCompleto" => array:1 [
"es" => true
]
"contienePdf" => array:1 [
"es" => true
]
"autores" => array:1 [
0 => array:2 [
"autoresLista" => "Raquel Cantero-Téllez, Santiago García Orza, Jorge Hugo Villafane, Iván Medina-Porqueres"
"autores" => array:4 [
0 => array:2 [
"nombre" => "Raquel"
"apellidos" => "Cantero-Téllez"
]
1 => array:2 [
"nombre" => "Santiago"
"apellidos" => "García Orza"
]
2 => array:2 [
"nombre" => "Jorge Hugo"
"apellidos" => "Villafane"
]
3 => array:2 [
"nombre" => "Iván"
"apellidos" => "Medina-Porqueres"
]
]
]
]
]
"idiomaDefecto" => "es"
"Traduccion" => array:1 [
"en" => array:9 [
"pii" => "S2173574319301728"
"doi" => "10.1016/j.reumae.2018.10.018"
"estado" => "S300"
"subdocumento" => ""
"abierto" => array:3 [
"ES" => false
"ES2" => false
"LATM" => false
]
"gratuito" => false
"lecturas" => array:1 [
"total" => 0
]
"idiomaDefecto" => "en"
"EPUB" => "https://multimedia.elsevier.es/PublicationsMultimediaV1/item/epub/S2173574319301728?idApp=UINPBA00004M"
]
]
"EPUB" => "https://multimedia.elsevier.es/PublicationsMultimediaV1/item/epub/S1699258X18302377?idApp=UINPBA00004M"
"url" => "/1699258X/00000016000005P1/v1_202008070719/S1699258X18302377/v1_202008070719/es/main.assets"
]
"itemAnterior" => array:18 [
"pii" => "S1699258X18301694"
"issn" => "1699258X"
"doi" => "10.1016/j.reuma.2018.07.010"
"estado" => "S300"
"fechaPublicacion" => "2020-09-01"
"aid" => "1256"
"copyright" => "Elsevier España, S.L.U. and Sociedad Española de Reumatología y Colegio Mexicano de Reumatología"
"documento" => "article"
"crossmark" => 1
"subdocumento" => "fla"
"cita" => "Reumatol Clin. 2020;16:339-44"
"abierto" => array:3 [
"ES" => true
"ES2" => true
"LATM" => true
]
"gratuito" => true
"lecturas" => array:2 [
"total" => 358
"formatos" => array:3 [
"EPUB" => 36
"HTML" => 199
"PDF" => 123
]
]
"en" => array:13 [
"idiomaDefecto" => true
"cabecera" => "<span class="elsevierStyleTextfn">Original Article</span>"
"titulo" => "Fatigue in Rheumatoid Arthritis Patients: Association With Sleep Quality, Mood Status, and Disease Activity"
"tienePdf" => "en"
"tieneTextoCompleto" => "en"
"tieneResumen" => array:2 [
0 => "en"
1 => "es"
]
"paginas" => array:1 [
0 => array:2 [
"paginaInicial" => "339"
"paginaFinal" => "344"
]
]
"titulosAlternativos" => array:1 [
"es" => array:1 [
"titulo" => "Fatiga en pacientes con artritis reumatoide: asociación con la calidad del sueño, el estado de ánimo y la actividad de la enfermedad"
]
]
"contieneResumen" => array:2 [
"en" => true
"es" => true
]
"contieneTextoCompleto" => array:1 [
"en" => true
]
"contienePdf" => array:1 [
"en" => true
]
"resumenGrafico" => array:2 [
"original" => 0
"multimedia" => array:7 [
"identificador" => "fig0005"
"etiqueta" => "Fig. 1"
"tipo" => "MULTIMEDIAFIGURA"
"mostrarFloat" => true
"mostrarDisplay" => false
"figura" => array:1 [
0 => array:4 [
"imagen" => "gr1.jpeg"
"Alto" => 1311
"Ancho" => 2175
"Tamanyo" => 108932
]
]
"descripcion" => array:1 [
"en" => "<p id="spar0045" class="elsevierStyleSimplePara elsevierViewall">Differences in MAF-GFI between RA patients who use and those not use specific drug therapy. <span class="elsevierStyleItalic">Abbreviations</span>: MAF-GFI: multidimensional assessment of fatigue-global fatigue index; MTX: methotrexate; HCQ: hydroxychloroquine; LFN: leflunomide; SZS: sulfasalazine; AZA: azathioprine; NSAIDs: nonsteroidal anti-inflammatory drugs. <span class="elsevierStyleItalic">Legend</span>: The differences in multidimensional assessment of fatigue-global fatigue index (MAF-GFI) between RA patients who use specific drug therapy and who do not show no significant difference in fatigue score were found.</p>"
]
]
]
"autores" => array:1 [
0 => array:2 [
"autoresLista" => "Nevin Hammam, Rania M. Gamal, Ahmed Mohammed Rashed, Noha Abo Elfetoh, Eman Mosad, Eman M. Khedr"
"autores" => array:6 [
0 => array:2 [
"nombre" => "Nevin"
"apellidos" => "Hammam"
]
1 => array:2 [
"nombre" => "Rania M."
"apellidos" => "Gamal"
]
2 => array:2 [
"nombre" => "Ahmed Mohammed"
"apellidos" => "Rashed"
]
3 => array:2 [
"nombre" => "Noha Abo"
"apellidos" => "Elfetoh"
]
4 => array:2 [
"nombre" => "Eman"
"apellidos" => "Mosad"
]
5 => array:2 [
"nombre" => "Eman M."
"apellidos" => "Khedr"
]
]
]
]
]
"idiomaDefecto" => "en"
"EPUB" => "https://multimedia.elsevier.es/PublicationsMultimediaV1/item/epub/S1699258X18301694?idApp=UINPBA00004M"
"url" => "/1699258X/00000016000005P1/v1_202008070719/S1699258X18301694/v1_202008070719/en/main.assets"
]
"en" => array:20 [
"idiomaDefecto" => true
"cabecera" => "<span class="elsevierStyleTextfn">Original Article</span>"
"titulo" => "Clinical, Patient-Reported, and Ultrasound Outcomes from an Open-Label, 12-week Observational Study of Certolizumab Pegol in Spanish Patients with Rheumatoid Arthritis with or without Prior Anti-TNF Exposure"
"tieneTextoCompleto" => true
"paginas" => array:1 [
0 => array:2 [
"paginaInicial" => "345"
"paginaFinal" => "352"
]
]
"autores" => array:1 [
0 => array:4 [
"autoresLista" => "Francisco J. Blanco, Esteban Rubio-Romero, Raimon Sanmartí, César Díaz-Torné, Pablo Talavera, Jochen Dunkel, Esperanza Naredo"
"autores" => array:8 [
0 => array:4 [
"nombre" => "Francisco J."
"apellidos" => "Blanco"
"email" => array:1 [
0 => "fj.blanco@usc.es"
]
"referencia" => array:2 [
0 => array:2 [
"etiqueta" => "<span class="elsevierStyleSup">a</span>"
"identificador" => "aff0005"
]
1 => array:2 [
"etiqueta" => "<span class="elsevierStyleSup">*</span>"
"identificador" => "cor0005"
]
]
]
1 => array:3 [
"nombre" => "Esteban"
"apellidos" => "Rubio-Romero"
"referencia" => array:1 [
0 => array:2 [
"etiqueta" => "<span class="elsevierStyleSup">b</span>"
"identificador" => "aff0010"
]
]
]
2 => array:3 [
"nombre" => "Raimon"
"apellidos" => "Sanmartí"
"referencia" => array:1 [
0 => array:2 [
"etiqueta" => "<span class="elsevierStyleSup">c</span>"
"identificador" => "aff0015"
]
]
]
3 => array:3 [
"nombre" => "César"
"apellidos" => "Díaz-Torné"
"referencia" => array:1 [
0 => array:2 [
"etiqueta" => "<span class="elsevierStyleSup">d</span>"
"identificador" => "aff0020"
]
]
]
4 => array:3 [
"nombre" => "Pablo"
"apellidos" => "Talavera"
"referencia" => array:1 [
0 => array:2 [
"etiqueta" => "<span class="elsevierStyleSup">e</span>"
"identificador" => "aff0025"
]
]
]
5 => array:3 [
"nombre" => "Jochen"
"apellidos" => "Dunkel"
"referencia" => array:1 [
0 => array:2 [
"etiqueta" => "<span class="elsevierStyleSup">f</span>"
"identificador" => "aff0030"
]
]
]
6 => array:3 [
"nombre" => "Esperanza"
"apellidos" => "Naredo"
"referencia" => array:1 [
0 => array:2 [
"etiqueta" => "<span class="elsevierStyleSup">g</span>"
"identificador" => "aff0035"
]
]
]
7 => array:1 [
"colaborador" => "on behalf of the SONAR Study Team"
]
]
"afiliaciones" => array:7 [
0 => array:3 [
"entidad" => "INIBIC-Complejo Hospitalario Universitario A Coruña, A Coruña, Spain"
"etiqueta" => "a"
"identificador" => "aff0005"
]
1 => array:3 [
"entidad" => "Hospital Universitario Virgen del Rocio, Sevilla, Spain"
"etiqueta" => "b"
"identificador" => "aff0010"
]
2 => array:3 [
"entidad" => "Hospital Clínic de Barcelona, Barcelona, Spain"
"etiqueta" => "c"
"identificador" => "aff0015"
]
3 => array:3 [
"entidad" => "Hospital de la Santa Cruz y San Pablo, Barcelona, Spain"
"etiqueta" => "d"
"identificador" => "aff0020"
]
4 => array:3 [
"entidad" => "UCB Pharma, Madrid, Spain"
"etiqueta" => "e"
"identificador" => "aff0025"
]
5 => array:3 [
"entidad" => "UCB Pharma, Monheim, Germany"
"etiqueta" => "f"
"identificador" => "aff0030"
]
6 => array:3 [
"entidad" => "Department of Rheumatology and Joint and Bone Research Unit, Hospital Fundación Jiménez Díaz, Madrid, Spain"
"etiqueta" => "g"
"identificador" => "aff0035"
]
]
"correspondencia" => array:1 [
0 => array:3 [
"identificador" => "cor0005"
"etiqueta" => "⁎"
"correspondencia" => "Corresponding author."
]
]
]
]
"titulosAlternativos" => array:1 [
"es" => array:1 [
"titulo" => "Estudio observacional con certolizumab pegol de 12 semanas de duración en pacientes con artritis reumatoide con y sin exposición previa a anti-TNF: resultados ecográficos, clínicos y reportados por los pacientes"
]
]
"resumenGrafico" => array:2 [
"original" => 0
"multimedia" => array:7 [
"identificador" => "fig0005"
"etiqueta" => "Fig. 1"
"tipo" => "MULTIMEDIAFIGURA"
"mostrarFloat" => true
"mostrarDisplay" => false
"figura" => array:1 [
0 => array:4 [
"imagen" => "gr1.jpeg"
"Alto" => 2499
"Ancho" => 2392
"Tamanyo" => 194010
]
]
"descripcion" => array:1 [
"en" => "<p id="spar0045" class="elsevierStyleSimplePara elsevierViewall">Clinical and patient-reported outcomes at baseline and Week 12. Data are presented for the full analysis set. Values are means and error bars represent the 95% confidence intervals. ***Statistically significant difference between baseline and Week 12 mean values; <span class="elsevierStyleItalic">p</span><span class="elsevierStyleHsp" style=""></span><<span class="elsevierStyleHsp" style=""></span>0.001. Patient's assessment of arthritis pain (PtAAP) was recorded on a visual analog scale (VAS) ranging from 0<span class="elsevierStyleHsp" style=""></span>mm (no pain) to 100<span class="elsevierStyleHsp" style=""></span>mm (maximum pain). DAS28: 28-joint count Disease Activity Score, ESR: erythrocyte sedimentation rate, HAQ-DI: health assessment questionnaire-disability index, MCS: mental component summary, PCS: physical component summary, PtAAP: patient's assessment of arthritis associated pain, VAS: visual analog scale.</p>"
]
]
]
"textoCompleto" => "<span class="elsevierStyleSections"><span id="sec0005" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0065">Introduction</span><p id="par0005" class="elsevierStylePara elsevierViewall">Rheumatoid arthritis (RA) is a chronic, typically progressive, autoimmune disorder characterized by polyarticular synovial inflammation. It is responsible for functional disability, joint destruction and significant physical pain.<a class="elsevierStyleCrossRef" href="#bib0175"><span class="elsevierStyleSup">1</span></a> Symptoms arise as a result of excessive production of pro-inflammatory cytokines such as tumor necrosis factor (TNF)-α, by activated T-cells.<a class="elsevierStyleCrossRef" href="#bib0180"><span class="elsevierStyleSup">2</span></a></p><p id="par0010" class="elsevierStylePara elsevierViewall">Treatment options for RA include biological agents and, during the period of the described trial, the biologics approved for the treatment of RA in Spain included abatacept, adalimumab, anakinra, certolizumab pegol (CZP), etanercept, golimumab, infliximab, rituximab and tocilizumab.<a class="elsevierStyleCrossRef" href="#bib0185"><span class="elsevierStyleSup">3</span></a> Improvements in clinical outcomes have been demonstrated in patients with RA using biologic agents including anti-TNFs.<a class="elsevierStyleCrossRefs" href="#bib0190"><span class="elsevierStyleSup">4–6</span></a> However, large proportions of patients still discontinue anti-TNF therapies as a result of failure to reach an adequate clinical response (primary failure), loss of clinical response (secondary failure), or as a result of adverse events.<a class="elsevierStyleCrossRef" href="#bib0205"><span class="elsevierStyleSup">7</span></a></p><p id="par0015" class="elsevierStylePara elsevierViewall">Patients experiencing a lack of effectiveness or adverse events may be switched to an alternative anti-TNF, however, the clinical practice guideline, available during the described trial, did not confirm whether a second anti-TNF, or a biologic with an alternative mechanistic route, would be favorable, due to insufficient data.<a class="elsevierStyleCrossRef" href="#bib0210"><span class="elsevierStyleSup">8</span></a> Establishing the effectiveness of anti-TNFs in patients who have experienced an inadequate response to prior treatment is of importance since reduced response to subsequent biological treatment has been shown to be proportional to increased prior use of biologics.<a class="elsevierStyleCrossRef" href="#bib0215"><span class="elsevierStyleSup">9</span></a> This could assist physicians in making the most appropriate next choice of treatment for their patients.</p><p id="par0020" class="elsevierStylePara elsevierViewall">Ultrasound (US) is a noninvasive, low-cost imaging technique which is well accepted by patients, not affected by metallic implants or prostheses, and can be repeated as many times as is necessary.<a class="elsevierStyleCrossRef" href="#bib0220"><span class="elsevierStyleSup">10</span></a> US is recommended for the detection of synovitis, effusion and erosions when this information is considered to be clinically relevant for the therapeutic management of patients. This recommendation is according to the clinical practice guideline for rheumatoid arthritis management (GUIPCAR), published in 2016, which was endorsed by the Spanish Society of Rheumatology.<a class="elsevierStyleCrossRef" href="#bib0225"><span class="elsevierStyleSup">11</span></a> Power Doppler ultrasound (PDUS) evaluates subclinical synovitis by visualizing synovial inflammatory joint changes that may previously have gone undetected by conventional clinical and radiographic examinations. This can facilitate physicians’ assessment of true inflammation, a typical precursor to the establishment of clinically detectable RA.<a class="elsevierStyleCrossRef" href="#bib0230"><span class="elsevierStyleSup">12</span></a></p><p id="par0025" class="elsevierStylePara elsevierViewall">This 12-week, open-label, observational study assessed the impact of treatment with CZP on clinical, patient-reported, and US outcomes in Spanish patients with active RA (with or without prior anti-TNF exposure).</p></span><span id="sec0010" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0070">Materials and methods</span><span id="sec0015" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0075">Patients</span><p id="par0030" class="elsevierStylePara elsevierViewall">Patients were aged ≥18 years old with active RA (determined according to ACR 1987 criteria)<a class="elsevierStyleCrossRef" href="#bib0235"><span class="elsevierStyleSup">13</span></a> of over 3 months duration, with 28-joint Disease Activity Score (DAS28) (erythrocyte sedimentation rate [ESR]) >4.5 and C-reactive protein (CRP) >1.0<span class="elsevierStyleHsp" style=""></span>mg/dL at baseline. Additionally, all patients had previously been treated with synthetic disease modifying anti-rheumatic drugs (DMARDs). Patients either had no other prior anti-TNF treatment (naïve patient) or CZP was administered after failure of the first anti-TNF treatment (first-switch patient). Patients enrolled onto the study were actively receiving CZP treatment and were not required to have a wash-out period prior to enrollment. The safety set (SS) consisted of all enrolled patients who took at least 1 dose of CZP. The full analysis set (FAS) consisted of all patients in the SS who had at least 1 valid baseline and post-baseline effectiveness assessment for any effectiveness variable and who had no important protocol deviations. Patients identified as having important protocol deviations were those not initiating CZP treatment, or not fulfilling the study inclusion criteria outlined above.</p></span><span id="sec0020" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0080">Study design</span><p id="par0035" class="elsevierStylePara elsevierViewall">SONAR (NCT01526434) was a 12-week, open-label, prospective, observational, multicenter, post-marketing study. Both naïve and first switch patients were treated with CZP (400<span class="elsevierStyleHsp" style=""></span>mg at Weeks 0, 2 and 4 followed by 200<span class="elsevierStyleHsp" style=""></span>mg every 2 weeks). CZP was administered subcutaneously, either by patients or according to the standard clinical setting for the prescribing physician and as defined by the Summary of Product Characteristics (SmPC). Permitted concomitant treatments included methotrexate, corticosteroids and analgesics including nonsteroidal anti-inflammatory drugs (NSAIDs). Assessments were carried out at weeks 0, and 12, with a 16-week safety follow-up visit. All patients provided written consent to participate in this study, which was carried out in accordance with local regulations, the Declaration of Helsinki and the local laws of Spain.</p></span><span id="sec0025" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0085">Study assessments</span><p id="par0040" class="elsevierStylePara elsevierViewall">The primary effectiveness endpoint was the mean change from baseline in Health Assessment Questionnaire-Disability Index (HAQ-DI) for RA,<a class="elsevierStyleCrossRef" href="#bib0240"><span class="elsevierStyleSup">14</span></a> at Week 12 in the FAS population; this population was also grouped by prior anti-TNF experience to compare HAQ-DI scores between anti-TNF naïve and first switch patients from baseline to Week 12. Other assessments included DAS28 (ESR),<a class="elsevierStyleCrossRef" href="#bib0245"><span class="elsevierStyleSup">15</span></a> Patient's Assessment of Arthritis Pain (PtAAP) – Visual Analog Scale (VAS)<a class="elsevierStyleCrossRef" href="#bib0250"><span class="elsevierStyleSup">16</span></a> and Short Form 36-item Health Survey (SF-36) physical component summary (PCS) and mental component summary (MCS).<a class="elsevierStyleCrossRef" href="#bib0255"><span class="elsevierStyleSup">17</span></a> For effectiveness assessments, the data were assigned to a visit based on the actual date of the routine clinical visit. Day was calculated relative to the baseline visit (recorded at Week 0). Any visit between Day ≥63 and ≤98 was assigned as Week 12 for the purposes of the analysis.</p><p id="par0045" class="elsevierStylePara elsevierViewall">PDUS assessment involved the detection and grading (from 0 to 3) of gray-scale synovitis and Power Doppler (PD) synovial signal of 24-joints (12-joint US assessment for RA<a class="elsevierStyleCrossRef" href="#bib0260"><span class="elsevierStyleSup">18</span></a> and the bilateral 4 and 5 metacarpophalangeal [MCP] joints and 2 to 5 metatarsophalangeal joints). Synovial hypertrophy and effusion were graded, semi-quantitatively, from 0 to 3, where 0<span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>absence; 1<span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>mild; 2<span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>moderate; and 3<span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>marked. PD signal was graded according to the following scale: 0<span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>absence, no synovial flow; 1<span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>mild, ≤3 isolated signals; 2<span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>moderate, ><span class="elsevierStyleHsp" style=""></span>3 isolated signals or confluent signal in less than half of the synovial area; 3<span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>marked, signals in more than half of the synovial area.<a class="elsevierStyleCrossRef" href="#bib0265"><span class="elsevierStyleSup">19</span></a> Assessments were made according to the Outcome Measures in Rheumatology definitions and published scoring systems.<a class="elsevierStyleCrossRef" href="#bib0270"><span class="elsevierStyleSup">20</span></a> An index for effusion, synovial hypertrophy and synovial PD signal was calculated by summing the corresponding scores from each assessed joint. PDUS outcomes measured included change from baseline to Week 12 in global US 24-joint indices (including synovial hypertrophy index, effusion index, and PD signal index). Intra-reader reliability was monitored by evaluating the first two patients at each center twice (2–4 days between evaluations) before the treatment period and was tested on representative images of joints included in the study. Intra-class correlation coefficients are reported for synovial hypertrophy index, effusion index, and PD signal index and were based on the repeated assessments at baseline for these patients.</p><p id="par0050" class="elsevierStylePara elsevierViewall">Adverse drug reactions (ADRs), were recorded and treatment-emergent adverse drug reactions (TEADRs) were defined as ADRs if they started on or after the date of first study medication and up to 70 days after the last (most recent) dose of CZP. Adverse events were classified as ADRs when a causal relationship between the product and the occurrence was suspected by the reviewing healthcare professional. TEADRs were coded using the Medical Dictionary for Regulatory Activities (MedDRA) Version 16.1.</p></span><span id="sec0030" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0090">Statistical analysis</span><p id="par0055" class="elsevierStylePara elsevierViewall">The sample size was calculated based on the precision of the 95% confidence interval (CI) around the expected HAQ-DI score mean change from Baseline to Week 12. A difference of at least ±0.22 was assumed to be sufficient to recognize a minimal clinically important difference (MCID) in HAQ-DI score, and the proportion of patients achieving MCID in HAQ-DI was calculated <span class="elsevierStyleItalic">post hoc</span>.<a class="elsevierStyleCrossRef" href="#bib0275"><span class="elsevierStyleSup">21</span></a> A sample size of 95 patients was estimated to provide at least 90% of statistical power to establish a difference of 0.22 as significant with a SD of 0.6 in a two-sided one-sample <span class="elsevierStyleItalic">t</span>-test, with a significance level of 0.05. A HAQ-DI difference greater than 0.22 could be confirmed with fewer patients.</p><p id="par0060" class="elsevierStylePara elsevierViewall">The mean changes in HAQ-DI scores from Baseline to Week 12 were analyzed by comparing the values at Baseline and Week 12 using a paired t-test. The primary analysis was run based on last observation carried forward (LOCF) imputation of missing data from dropouts. A paired t-test was also used to compare Baseline and Week 12 values for SF-36, PtAAP-VAS and DAS28(ESR). Apart from the <span class="elsevierStyleItalic">p</span>-value related to the primary endpoint, all <span class="elsevierStyleItalic">p</span>-values are nominal.</p><p id="par0065" class="elsevierStylePara elsevierViewall">Statistical analysis and generation of tables, figures and patient data listings were performed using Statistical Analysis System (SAS®) Version 9.4. <span class="elsevierStyleItalic">P</span>-values are only provided for the mean change from baseline, to Week 12, in HAQ-DI (the primary endpoint), DAS28(ESR), PtAAP and SF36 PCS and MCS, all other variables are represented by CIs. Nominal <span class="elsevierStyleItalic">p</span> values were not calculated for comparisons between the patients split by prior anti-TNF exposure, due to the small sample number, therefore data are shown as the mean and 95% CI for HAQ-DI and PDUS outcomes for each subgroup.</p></span></span><span id="sec0035" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0095">Results</span><span id="sec0040" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0100">Patient disposition and baseline characteristics</span><p id="par0070" class="elsevierStylePara elsevierViewall">A total of 77/80 enrolled patients received at least one dose of CZP during the trial and were included in the SS (<a class="elsevierStyleCrossRef" href="#tbl0005">Table 1</a>), of which 65 patients provided at least one valid baseline and post-baseline effectiveness assessment, without any important protocol deviations during the study (FAS); the remaining 12 recruited patients did not meet these criteria for inclusion within the FAS. The reasons for excluding these patients from the FAS were: 3 patients did not have active RA (defined as DAS28(ESR)<span class="elsevierStyleHsp" style=""></span>><span class="elsevierStyleHsp" style=""></span>4.5 and CRP<span class="elsevierStyleHsp" style=""></span>><span class="elsevierStyleHsp" style=""></span>1.0<span class="elsevierStyleHsp" style=""></span>mg/dL) at baseline, prior anti-TNF use was unknown for 1 patient, and 9 patients did not have a valid baseline and post-baseline effectiveness assessment. At baseline, 57/77 (74%) patients within the SS and 48/65 (73.8%) patients in the FAS were anti-TNF naïve. Of patients in the FAS, 17/65 (26.2%) patients were switched to CZP due to lack of effectiveness or adverse events. A large proportion of patients in the FAS completed CZP treatment to Week 12 of the study (60/65, 92.3%), 1 patient (1.5%) permanently withdrew CZP treatment before Week 12 due to an ADR, and 4 patients (6.2%) withdrew due to “other” reasons. “Other” reasons included the patient not attending the visit, patient decision, hospitalization, and temporary interruption of CZP due to vertigo. Among the 61 patients with a Week 16 visit, 56 patients (91.8%) opted to continue CZP treatment, and 1 patient (1.6%) withdrew due to an ADR, 1 patient (1.6%) withdrew due to ineffectiveness and 3 patients (4.9%) withdrew for “other” reasons. The mean duration of RA since diagnosis (SD) for enrolled patients was 7.8 (9.8) years. The mean age of patients was similar between the two study populations, 53.8 years (SS) and 53.7 years (FAS) (<a class="elsevierStyleCrossRef" href="#tbl0005">Table 1</a>). The gender of patients within the study population was predominantly female (SS: 74.0% and FAS: 73.8%) (<a class="elsevierStyleCrossRef" href="#tbl0005">Table 1</a>). Disease activity and patient-reported outcomes (PROs) were similar between the SS and the FAS (<a class="elsevierStyleCrossRef" href="#tbl0005">Table 1</a>). The SS had a greater median CRP (1.83<span class="elsevierStyleHsp" style=""></span>mg/dL) than the FAS (1.65<span class="elsevierStyleHsp" style=""></span>mg/dL) but a lower median ESR (SS: 31.0<span class="elsevierStyleHsp" style=""></span>mm/h, FAS: 34.0<span class="elsevierStyleHsp" style=""></span>mm/h) (<a class="elsevierStyleCrossRef" href="#tbl0005">Table 1</a>). US outcomes were similar between patients in the SS and the FAS (<a class="elsevierStyleCrossRef" href="#tbl0005">Table 1</a>) at baseline. At baseline, 57/65 (87.7%) patients in the FAS (69/77 [89.6%] patients in the SS) were taking concomitant DMARDs (<a class="elsevierStyleCrossRef" href="#tbl0005">Table 1</a>). At Week 12, 10 (15.4%) patients in the FAS were taking concomitant DMARDs, with 4 (6.2%) patients receiving a higher DMARD dose compared to baseline.</p><elsevierMultimedia ident="tbl0005"></elsevierMultimedia></span><span id="sec0045" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0105">Clinical and patient-reported outcomes</span><p id="par0075" class="elsevierStylePara elsevierViewall">Rapid improvements in clinical and PROs were observed between baseline and Week 12 (<a class="elsevierStyleCrossRef" href="#fig0005">Fig. 1</a>). An overall significant mean (SD) reduction of −0.6 (0.6) in HAQ-DI from baseline to Week 12 was achieved (<span class="elsevierStyleItalic">p</span><span class="elsevierStyleHsp" style=""></span><<span class="elsevierStyleHsp" style=""></span>0.001, <a class="elsevierStyleCrossRef" href="#fig0005">Fig. 1</a>A) and 33/65 (50.8%) patients achieved MCID in HAQ-DI at Week 12. A similar significant improvement was observed for DAS28 (ESR), with an overall mean reduction of −2.2 (1.5) from baseline to Week 12 (<span class="elsevierStyleItalic">p</span><span class="elsevierStyleHsp" style=""></span><<span class="elsevierStyleHsp" style=""></span>0.001, <a class="elsevierStyleCrossRef" href="#fig0005">Fig. 1</a>B). PROs also showed a significant improvement between baseline and Week 12, with a substantial reduction in PtAAP (VAS Scale 0–100) from 66.8 to 27.6 (<span class="elsevierStyleItalic">p</span><span class="elsevierStyleHsp" style=""></span><<span class="elsevierStyleHsp" style=""></span>0.001, <a class="elsevierStyleCrossRef" href="#fig0005">Fig. 1</a>C). Further to this an overall improvement in mean SF-36 PCS and SF-36 MCS was seen to rise from 32.2 at baseline to 38.4 by Week 12 (<a class="elsevierStyleCrossRef" href="#fig0005">Fig. 1</a>D) and from 42.4 at baseline to 50.1 at Week 12 (<a class="elsevierStyleCrossRef" href="#fig0005">Fig. 1</a>E) (both <span class="elsevierStyleItalic">p</span><span class="elsevierStyleHsp" style=""></span><<span class="elsevierStyleHsp" style=""></span>0.001), respectively.</p><elsevierMultimedia ident="fig0005"></elsevierMultimedia></span><span id="sec0050" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0110">HAQ-DI in anti-TNF naïve and first switch patients</span><p id="par0080" class="elsevierStylePara elsevierViewall">A comparison between anti-TNF naïve and anti-TNF first switch patient's HAQ-DI score indicated that functional improvements were seen in both anti-TNF naïve and first switch patients, although the patient numbers in these sub-group analyses were low (<a class="elsevierStyleCrossRef" href="#fig0010">Fig. 2</a>). The improvement seen in the naïve group (34 patients) was −0.67 (95% CI at Week 12: −0.86, −0.47) whereas the improvement in the first switch patients (13 patients) was numerically smaller, −0.28 (95% CI at Week 12: −0.65, 0.09). At Week 12, 27/34 anti-TNF naïve patients achieved MCID in HAQ-DI, compared to 6/13 first switch patients.</p><elsevierMultimedia ident="fig0010"></elsevierMultimedia></span><span id="sec0055" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0115">Ultrasound outcomes</span><p id="par0085" class="elsevierStylePara elsevierViewall">Reductions from baseline to Week 12 were seen in synovial hypertrophy index, from 19.3 to 12.3, effusion index, from 14.3 to 7.7, and PD signal index, from 8.9 to 4.6 (<a class="elsevierStyleCrossRef" href="#tbl0010">Table 2</a>). These reductions were observed in both anti-TNF naïve and first switch patients (<a class="elsevierStyleCrossRef" href="#fig0015">Fig. 3</a>). The mean [95% CI] effusion index for the naïve (13.5 [10.7, 16.3]) and first switch patients (16.8 [9.4, 24.1]) differed at baseline (<a class="elsevierStyleCrossRef" href="#fig0015">Fig. 3</a>D).</p><elsevierMultimedia ident="tbl0010"></elsevierMultimedia><elsevierMultimedia ident="fig0015"></elsevierMultimedia></span><span id="sec0060" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0120">Safety data</span><p id="par0090" class="elsevierStylePara elsevierViewall">The safety profile of CZP was consistent with other reports of CZP in RA; no new safety signals were identified (<a class="elsevierStyleCrossRef" href="#tbl0015">Table 3</a>). A total of 19 TEADRs were reported by 13/77 (16.9%) patients, 9 of which led to the discontinuation of 8/77 (10.4%) patients from the study. A total of 4 serious TEADRs were experienced by 3/77 (3.9%) patients. The serious TEADRs were lymphadenopathy mediastinal, tuberculosis, skin reaction and non-Hodgkin's lymphoma. The case of active tuberculosis was reported by the investigators to be related to CZP and the patient permanently discontinued CZP treatment. As the patient recovered after treatment with anti-tuberculosis therapy, with the disappearance of pulmonary nodules, the case was diagnosed clinically as tuberculosis, despite the absence of microbiological confirmation. The skin reaction was considered to be a medically important reaction and the patient permanently discontinued CZP treatment; the patient recovered from this event. Non-Hodgkin's lymphoma was reported 69 days after initiation of CZP in one patient, and was considered severe in intensity. The patient permanently discontinued CZP treatment due to non-Hodgkin's lymphoma. The event resulted in the death of the patient 64 days after onset. Because the study investigator stated that they were unable to confirm the relationship, UCB Pharmacovigilance Department, per protocol, classified the relationship of this adverse drug reaction conservatively as ‘related to study drug’.</p><elsevierMultimedia ident="tbl0015"></elsevierMultimedia></span></span><span id="sec0065" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0125">Discussion</span><p id="par0095" class="elsevierStylePara elsevierViewall">Treatment with anti-TNFs has been found to routinely manage patients’ RA symptoms. In the present 12-week, observational study, treatment with CZP led to significant improvements of both clinical outcomes and PROs. Similar improvements in clinical outcomes, in patients with RA, have been observed after 12 weeks, and up to 5 years of anti-TNF treatment, using data obtained from the Dutch and German biologic registers.<a class="elsevierStyleCrossRefs" href="#bib0280"><span class="elsevierStyleSup">22,23</span></a> However, as these observational studies were not conducted in Spain, these data are not directly comparable to the data from the present study. The recent preliminary findings from the IMPULSAR study, conducted in Barcelona, highlighted the value of US as a complimentary tool for treatment decisions.<a class="elsevierStyleCrossRef" href="#bib0290"><span class="elsevierStyleSup">24</span></a> These findings are complimented by the observations that US outcomes, but not clinical remission (measured by DAS28<span class="elsevierStyleHsp" style=""></span><<span class="elsevierStyleHsp" style=""></span>2.6, SDAI<span class="elsevierStyleHsp" style=""></span><<span class="elsevierStyleHsp" style=""></span>3.3, and CDAI<span class="elsevierStyleHsp" style=""></span><<span class="elsevierStyleHsp" style=""></span>2.8), were associated with prediction of 1-year X-ray progression of RA, and failure of biologic tapering in patients with RA.<a class="elsevierStyleCrossRefs" href="#bib0295"><span class="elsevierStyleSup">25,26</span></a></p><p id="par0100" class="elsevierStylePara elsevierViewall">The clinical findings of the present study aligned with a reduction in synovial hypertrophy, effusion and PD signal indices from baseline to Week 12, as determined by PDUS, both in the present study and from Week 8 to Week 52 in the CZP-SPEED trial.<a class="elsevierStyleCrossRef" href="#bib0305"><span class="elsevierStyleSup">27</span></a> Other anti-TNFs such as etanercept and adalimumab have also reported improvements in PDUS outcomes, which often accompany improvements in PROs.<a class="elsevierStyleCrossRefs" href="#bib0310"><span class="elsevierStyleSup">28–30</span></a> The clinical definition of RA remission is a DAS28 (ESR) <1.6 for at least 6 months, and low disease activity (LDA) is defined as DAS28 (ESR) <2.4 but >1.6 for at least 6 months, however, PDUS outcomes have identified that patients with RA, with apparent clinical remission, can still experience joint damage progression.<a class="elsevierStyleCrossRefs" href="#bib0325"><span class="elsevierStyleSup">31,32</span></a></p><p id="par0105" class="elsevierStylePara elsevierViewall">Observational studies have shown that many patients discontinue anti-TNF therapy for various reasons,<a class="elsevierStyleCrossRef" href="#bib0335"><span class="elsevierStyleSup">33</span></a> but patients discontinuing due to an initial lack of effect, or subsequent loss of effectiveness are less likely to achieve low disease activity or remission upon successive therapy, and are more likely to experience flares.<a class="elsevierStyleCrossRefs" href="#bib0335"><span class="elsevierStyleSup">33,34</span></a> However, in the present study, improvements in the HAQ-DI score of both anti-TNF naïve and first switch patients after 12 weeks of CZP treatment were observed, though patients who had never been treated with an anti-TNF showed a slightly stronger improvement. The number of patients in both subgroups was low, especially in the first-switch patient group (<span class="elsevierStyleItalic">n</span><span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>16), and this is likely the reason of a relatively large numerical difference for HAQ-DI being observed in this subgroup. Similarly, in the REALISTIC trial investigating the effect of CZP on clinical outcomes and PROs in a similar mixed population of naïve and switch RA patients, patients experienced comparable improvements in HAQ-DI, DAS28 (ESR) and PtAAP-VAS during the first 12 weeks of the 28-week study.<a class="elsevierStyleCrossRef" href="#bib0190"><span class="elsevierStyleSup">4</span></a></p><p id="par0110" class="elsevierStylePara elsevierViewall">The small number of patients enrolled in this study was a major limitation, however, 60/65 (92.3%) patients completed the treatment for the duration of the study (Week 12), and 56/61 (91.8%) of the patients that attended the visit at Week 16 opted to carry on with the treatment following the end of the study, providing data at Week 16. Nevertheless, the differences observed in primary analysis were larger than the minimally clinically significant change defined for the sample size calculation, thus the smaller population did not prevent the study from finding clinically significant differences. Another potential limitation, was that ultrasonographers were based at individual sites due to the multicenter nature of the study, which could have introduced variability between readers. However, to ensure consistency, all ultrasonographers were experts (>5 years of experience), used appropriate equipment and followed predefined recommendations to align the definition of scanning method and standardize scoring.</p><p id="par0115" class="elsevierStylePara elsevierViewall">One case of active tuberculosis was reported during this study, this was considered to be related to CZP, and the patient was permanently withdrawn from CZP treatment. The patient provided a negative Mantoux test result prior to receiving CZP, the positive Mantoux test result was reported 222 days after receiving CZP. One death was reported, as a result of non-Hodgkin's lymphoma, and the patient was permanently withdrawn from CZP treatment prior to their death. No new safety signals were identified within the present study and the safety profile of CZP was comparable to previous trials, including the REALISTIC trial which reported incidence of TEAEs up to Week 12, in a mixed population of patients with active RA, from multiple geographic locations.<a class="elsevierStyleCrossRef" href="#bib0190"><span class="elsevierStyleSup">4</span></a> This therefore provides further evidence that CZP has an acceptable safety profile in patients with active RA.</p><p id="par0120" class="elsevierStylePara elsevierViewall">In this observational study in Spain, patients with RA demonstrated improvements in clinical outcomes, PROs and PDUS outcomes over 12 weeks of CZP treatment. Improvements were observed regardless of whether patients had been previously treated with an anti-TNF, although the patient numbers in these sub-group analyses were low. The safety profile was consistent with previous CZP studies, with no new safety signals identified. These results from observational clinical practice add to the findings of previous clinical studies which demonstrate the impact of CZP on signs and symptoms of RA.</p></span><span id="sec0070" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0130">Funding</span><p id="par0125" class="elsevierStylePara elsevierViewall">UCB sponsored the study and the development of the manuscript/publication and reviewed the text to ensure that from UCB perspective, the data presented in the publication are scientifically, technically and medically supportable, that they do not contain any information that has the potential to damage the intellectual property of UCB, and that the publication complies with applicable laws, regulations, guidelines and good industry practice. The authors approved the final version to be published after critically revising the manuscript/publication for important intellectual content.</p><p id="par0130" class="elsevierStylePara elsevierViewall">This study and all costs associated with the development of this manuscript were funded by <span class="elsevierStyleGrantSponsor" id="gs1">UCB Pharma</span>.</p></span><span id="sec0075" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0135">Conflict of interest</span><p id="par0135" class="elsevierStylePara elsevierViewall">JD and PT are employees of UCB Pharma, and EN has received speaker fees from Abbvie, Roche, BMS, Pfizer, UC, Lilly, Novartis, Janssen, and Celgene GmbH.</p></span><span id="sec0080" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0140">Data availability</span><p id="par0145" class="elsevierStylePara elsevierViewall">Qualified researchers whose proposed use of the data has been approved by an independent review panel will be given access to anonymized individual participant data and redacted study documents. Additional information is available at <a href="http://www.clinicalstudydatarequest.com/">www.clinicalstudydatarequest.com</a></p></span></span>"
"textoCompletoSecciones" => array:1 [
"secciones" => array:13 [
0 => array:3 [
"identificador" => "xres1371370"
"titulo" => "Abstract"
"secciones" => array:4 [
0 => array:2 [
"identificador" => "abst0005"
"titulo" => "Objectives"
]
1 => array:2 [
"identificador" => "abst0010"
"titulo" => "Materials and methods"
]
2 => array:2 [
"identificador" => "abst0015"
"titulo" => "Results"
]
3 => array:2 [
"identificador" => "abst0020"
"titulo" => "Conclusions"
]
]
]
1 => array:2 [
"identificador" => "xpalclavsec1260356"
"titulo" => "Keywords"
]
2 => array:3 [
"identificador" => "xres1371371"
"titulo" => "Resumen"
"secciones" => array:4 [
0 => array:2 [
"identificador" => "abst0025"
"titulo" => "Objetivos"
]
1 => array:2 [
"identificador" => "abst0030"
"titulo" => "Materiales y métodos"
]
2 => array:2 [
"identificador" => "abst0035"
"titulo" => "Resultados"
]
3 => array:2 [
"identificador" => "abst0040"
"titulo" => "Conclusiones"
]
]
]
3 => array:2 [
"identificador" => "xpalclavsec1260357"
"titulo" => "Palabras clave"
]
4 => array:2 [
"identificador" => "sec0005"
"titulo" => "Introduction"
]
5 => array:3 [
"identificador" => "sec0010"
"titulo" => "Materials and methods"
"secciones" => array:4 [
0 => array:2 [
"identificador" => "sec0015"
"titulo" => "Patients"
]
1 => array:2 [
"identificador" => "sec0020"
"titulo" => "Study design"
]
2 => array:2 [
"identificador" => "sec0025"
"titulo" => "Study assessments"
]
3 => array:2 [
"identificador" => "sec0030"
"titulo" => "Statistical analysis"
]
]
]
6 => array:3 [
"identificador" => "sec0035"
"titulo" => "Results"
"secciones" => array:5 [
0 => array:2 [
"identificador" => "sec0040"
"titulo" => "Patient disposition and baseline characteristics"
]
1 => array:2 [
"identificador" => "sec0045"
"titulo" => "Clinical and patient-reported outcomes"
]
2 => array:2 [
"identificador" => "sec0050"
"titulo" => "HAQ-DI in anti-TNF naïve and first switch patients"
]
3 => array:2 [
"identificador" => "sec0055"
"titulo" => "Ultrasound outcomes"
]
4 => array:2 [
"identificador" => "sec0060"
"titulo" => "Safety data"
]
]
]
7 => array:2 [
"identificador" => "sec0065"
"titulo" => "Discussion"
]
8 => array:2 [
"identificador" => "sec0070"
"titulo" => "Funding"
]
9 => array:2 [
"identificador" => "sec0075"
"titulo" => "Conflict of interest"
]
10 => array:2 [
"identificador" => "sec0080"
"titulo" => "Data availability"
]
11 => array:2 [
"identificador" => "xack476248"
"titulo" => "Acknowledgements"
]
12 => array:1 [
"titulo" => "References"
]
]
]
"pdfFichero" => "main.pdf"
"tienePdf" => true
"fechaRecibido" => "2018-01-16"
"fechaAceptado" => "2018-07-11"
"PalabrasClave" => array:2 [
"en" => array:1 [
0 => array:4 [
"clase" => "keyword"
"titulo" => "Keywords"
"identificador" => "xpalclavsec1260356"
"palabras" => array:5 [
0 => "Certolizumab pegol"
1 => "Rheumatoid Arthritis"
2 => "Anti-TNF"
3 => "Observational"
4 => "Ultrasound"
]
]
]
"es" => array:1 [
0 => array:4 [
"clase" => "keyword"
"titulo" => "Palabras clave"
"identificador" => "xpalclavsec1260357"
"palabras" => array:5 [
0 => "Certolizumab pegol"
1 => "Artritis reumatoide"
2 => "Anti-TNF"
3 => "Observacional"
4 => "Ecografía"
]
]
]
]
"tieneResumen" => true
"resumen" => array:2 [
"en" => array:3 [
"titulo" => "Abstract"
"resumen" => "<span id="abst0005" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0010">Objectives</span><p id="spar0005" class="elsevierStyleSimplePara elsevierViewall">To assess the effectiveness and safety of certolizumab pegol (CZP) in Spanish patients with RA.</p></span> <span id="abst0010" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0015">Materials and methods</span><p id="spar0010" class="elsevierStyleSimplePara elsevierViewall">SONAR (NCT01526434), a 12-week, open-label, prospective, observational, multicenter study. Patients with active RA for ≥3 months, according to ACR criteria, were treated with CZP (400<span class="elsevierStyleHsp" style=""></span>mg at Weeks 0, 2 and 4, then 200<span class="elsevierStyleHsp" style=""></span>mg every 2 weeks). The primary effectiveness endpoint was change from baseline (CFB) in Health Assessment Questionnaire-Disability Index (HAQ-DI) at Week 12. Other assessments included DAS28(ESR), patient's assessment of arthritis pain (PtAAP-VAS) and Short Form 36-item Health Survey (SF-36) physical component summary (PCS) and mental component summary (MCS). Joint inflammation was investigated using Power Doppler (PD) ultrasound (US), to detect effusion, synovial hypertrophy and synovial PD signal. PDUS outcomes assessed CFB to Week 12 in synovial hypertrophy, effusion and PD signal indices.</p></span> <span id="abst0015" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0020">Results</span><p id="spar0015" class="elsevierStyleSimplePara elsevierViewall">A total of 77/80 enrolled patients received ≥1 dose of CZP. The 12-week mean reduction from baseline (SD) was −0.6 (0.6) for HAQ-DI and −2.2 (1.5) for DAS28(ESR). PtAAP-VAS was reduced from baseline (mean [SD]: −36.8 [26.8]) and improvements in SF-36 PCS and SF-36 MCS were reported. Synovial hypertrophy, effusion and PD signal indices were reduced from baseline to Week 12. One death was reported during the study.</p></span> <span id="abst0020" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0025">Conclusions</span><p id="spar0020" class="elsevierStyleSimplePara elsevierViewall">Spanish patients with RA demonstrated improvements in clinical, PDUS and patient-reported outcomes over 12 weeks of CZP treatment. No new safety signals were identified, and the safety profile was in line with previous CZP studies. These results support previous clinical trial findings investigating CZP treatment for active RA.</p></span>"
"secciones" => array:4 [
0 => array:2 [
"identificador" => "abst0005"
"titulo" => "Objectives"
]
1 => array:2 [
"identificador" => "abst0010"
"titulo" => "Materials and methods"
]
2 => array:2 [
"identificador" => "abst0015"
"titulo" => "Results"
]
3 => array:2 [
"identificador" => "abst0020"
"titulo" => "Conclusions"
]
]
]
"es" => array:3 [
"titulo" => "Resumen"
"resumen" => "<span id="abst0025" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0035">Objetivos</span><p id="spar0025" class="elsevierStyleSimplePara elsevierViewall">Evaluar la eficacia y la seguridad de certolizumab pegol (CZP) en pacientes españoles con artritis reumatoide (AR).</p></span> <span id="abst0030" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0040">Materiales y métodos</span><p id="spar0030" class="elsevierStyleSimplePara elsevierViewall">SONAR (NCT01526434), un estudio multicéntrico, observacional, prospectivo, abierto de 12 semanas. Pacientes con AR activa ≥3 meses, según criterios ACR, recibieron CZP (400<span class="elsevierStyleHsp" style=""></span>mg en las semanas 0, 2 y 4, seguido de 200<span class="elsevierStyleHsp" style=""></span>mg cada 2 semanas). La variable principal de eficacia fue el cambio desde el inicio (CDI) en el HAQ en la semana 12. Otras evaluaciones incluían el DAS28-VSG, la valoración del dolor (PtAAP-VAS) y el componente físico (PCS) y mental (MCS) del SF-36. La inflamación articular se estudió utilizando ecografía con Power Doppler (PDUS) midiendo derrame, hipertrofia sinovial y señal PD sinovial. Los resultados de PDUS evaluaron el CDI hasta la semana 12 en índices de hipertrofia sinovial, derrame y PD.</p></span> <span id="abst0035" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0045">Resultados</span><p id="spar0035" class="elsevierStyleSimplePara elsevierViewall">Un total de 77/80 pacientes recibieron ≥una dosis de CZP. La reducción media en 12 semanas desde el inicio (DE) fue de −0,6 (0,6) para HAQ y de −2,2 (1,5) para DAS28-VSG. La PtAAP-VAS disminuyó desde el inicio (media [DE]: −36,8 [26,8]) y hubo mejorías en los componentes PCS y MCS del SF-36. Los índices de señales de hipertrofia sinovial, derrame y PD disminuyeron desde el inicio hasta la semana 12. Se notificó una muerte durante el estudio.</p></span> <span id="abst0040" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0050">Conclusiones</span><p id="spar0040" class="elsevierStyleSimplePara elsevierViewall">Los pacientes españoles con AR mostraron mejoras en resultados clínicos, PDUS y notificados por el paciente durante 12 semanas de tratamiento con CZP. No hubo nuevas señales de seguridad, y el perfil de seguridad estaba en línea con estudios previos. Estos resultados respaldan los hallazgos de ensayos clínicos previos de CZP en AR.</p></span>"
"secciones" => array:4 [
0 => array:2 [
"identificador" => "abst0025"
"titulo" => "Objetivos"
]
1 => array:2 [
"identificador" => "abst0030"
"titulo" => "Materiales y métodos"
]
2 => array:2 [
"identificador" => "abst0035"
"titulo" => "Resultados"
]
3 => array:2 [
"identificador" => "abst0040"
"titulo" => "Conclusiones"
]
]
]
]
"multimedia" => array:6 [
0 => array:7 [
"identificador" => "fig0005"
"etiqueta" => "Fig. 1"
"tipo" => "MULTIMEDIAFIGURA"
"mostrarFloat" => true
"mostrarDisplay" => false
"figura" => array:1 [
0 => array:4 [
"imagen" => "gr1.jpeg"
"Alto" => 2499
"Ancho" => 2392
"Tamanyo" => 194010
]
]
"descripcion" => array:1 [
"en" => "<p id="spar0045" class="elsevierStyleSimplePara elsevierViewall">Clinical and patient-reported outcomes at baseline and Week 12. Data are presented for the full analysis set. Values are means and error bars represent the 95% confidence intervals. ***Statistically significant difference between baseline and Week 12 mean values; <span class="elsevierStyleItalic">p</span><span class="elsevierStyleHsp" style=""></span><<span class="elsevierStyleHsp" style=""></span>0.001. Patient's assessment of arthritis pain (PtAAP) was recorded on a visual analog scale (VAS) ranging from 0<span class="elsevierStyleHsp" style=""></span>mm (no pain) to 100<span class="elsevierStyleHsp" style=""></span>mm (maximum pain). DAS28: 28-joint count Disease Activity Score, ESR: erythrocyte sedimentation rate, HAQ-DI: health assessment questionnaire-disability index, MCS: mental component summary, PCS: physical component summary, PtAAP: patient's assessment of arthritis associated pain, VAS: visual analog scale.</p>"
]
]
1 => array:7 [
"identificador" => "fig0010"
"etiqueta" => "Fig. 2"
"tipo" => "MULTIMEDIAFIGURA"
"mostrarFloat" => true
"mostrarDisplay" => false
"figura" => array:1 [
0 => array:4 [
"imagen" => "gr2.jpeg"
"Alto" => 951
"Ancho" => 1612
"Tamanyo" => 57476
]
]
"descripcion" => array:1 [
"en" => "<p id="spar0050" class="elsevierStyleSimplePara elsevierViewall">Mean HAQ-DI in anti-TNF naïve and first switch patients at Week 12 <span class="elsevierStyleItalic">versus</span> baseline (observed data). Data are presented for the full analysis set (<span class="elsevierStyleItalic">n</span><span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>65) and patients are grouped by prior anti-TNF treatment (naïve or first-switch). Values are means and the error bars represent the 95% confidence intervals. For one patient within the first switch group the HAQ-DI score was not available at baseline. The Week 12 data are reported for the number of patients with HAQ-DI scores available at this time point.</p>"
]
]
2 => array:7 [
"identificador" => "fig0015"
"etiqueta" => "Fig. 3"
"tipo" => "MULTIMEDIAFIGURA"
"mostrarFloat" => true
"mostrarDisplay" => false
"figura" => array:1 [
0 => array:4 [
"imagen" => "gr3.jpeg"
"Alto" => 2112
"Ancho" => 3001
"Tamanyo" => 199606
]
]
"descripcion" => array:1 [
"en" => "<p id="spar0055" class="elsevierStyleSimplePara elsevierViewall">Power Doppler ultrasound scores at baseline and Week 12 for anti-TNF naïve and first-switch patients for (A) synovial hypertrophy index, (B) effusion index, and (C) Power Doppler signal index. Data are reported for the full analysis set. Values are means and the error bars represent the 95% confidence intervals.</p>"
]
]
3 => array:8 [
"identificador" => "tbl0005"
"etiqueta" => "Table 1"
"tipo" => "MULTIMEDIATABLA"
"mostrarFloat" => true
"mostrarDisplay" => false
"detalles" => array:1 [
0 => array:3 [
"identificador" => "at1"
"detalle" => "Table "
"rol" => "short"
]
]
"tabla" => array:3 [
"leyenda" => "<p id="spar0065" class="elsevierStyleSimplePara elsevierViewall">The full analysis set was defined as all patients who had a least one dose of CZP during the study, at least one valid baseline and post-baseline effectiveness assessment, and had no important protocol deviations. The safety set consisted of all patients that took at least one dose of CZP at any point during the study.</p>"
"tablatextoimagen" => array:1 [
0 => array:2 [
"tabla" => array:1 [
0 => """
<table border="0" frame="\n
\t\t\t\t\tvoid\n
\t\t\t\t" class=""><thead title="thead"><tr title="table-row"><th class="td" title="\n
\t\t\t\t\ttable-head\n
\t\t\t\t " align="" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t" scope="col" style="border-bottom: 2px solid black"> \t\t\t\t\t\t\n
\t\t\t\t\t\t</th><th class="td" title="\n
\t\t\t\t\ttable-head\n
\t\t\t\t " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t" scope="col" style="border-bottom: 2px solid black">Full analysis set, <span class="elsevierStyleItalic">N</span><span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>65Mean (SD) [<span class="elsevierStyleItalic">n</span>], unless otherwise stated \t\t\t\t\t\t\n
\t\t\t\t\t\t</th><th class="td" title="\n
\t\t\t\t\ttable-head\n
\t\t\t\t " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t" scope="col" style="border-bottom: 2px solid black">Safety set, <span class="elsevierStyleItalic">N</span><span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>77Mean (SD) [<span class="elsevierStyleItalic">n</span>], unless otherwise stated \t\t\t\t\t\t\n
\t\t\t\t\t\t</th></tr></thead><tbody title="tbody"><tr title="table-row"><td class="td-with-role" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t"><span class="elsevierStyleItalic">Age, years</span> \t\t\t\t\t\t\n
\t\t\t\t</td><td class="td" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t">53.7 (12.8) [64] \t\t\t\t\t\t\n
\t\t\t\t</td><td class="td" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t">53.8 (12.7) [76] \t\t\t\t\t\t\n
\t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t"><span class="elsevierStyleItalic">Female, n (%)</span> \t\t\t\t\t\t\n
\t\t\t\t</td><td class="td" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t">48 (73.8) \t\t\t\t\t\t\n
\t\t\t\t</td><td class="td" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t">57 (74.0) \t\t\t\t\t\t\n
\t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t"><span class="elsevierStyleItalic">BMI, kg/m</span><span class="elsevierStyleSup"><span class="elsevierStyleItalic">2</span></span> \t\t\t\t\t\t\n
\t\t\t\t</td><td class="td" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t">26.6 (5.0) [64] \t\t\t\t\t\t\n
\t\t\t\t</td><td class="td" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t">26.7 (5.3) [76] \t\t\t\t\t\t\n
\t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t"><span class="elsevierStyleItalic">HAQ-DI</span> \t\t\t\t\t\t\n
\t\t\t\t</td><td class="td" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t">1.4 (0.8) [64] \t\t\t\t\t\t\n
\t\t\t\t</td><td class="td" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t">1.4 (0.8) [76] \t\t\t\t\t\t\n
\t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t"><span class="elsevierStyleItalic">DAS28 (ESR)</span> \t\t\t\t\t\t\n
\t\t\t\t</td><td class="td" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t">5.8 (1.1) [65] \t\t\t\t\t\t\n
\t\t\t\t</td><td class="td" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t">5.6 (1.3) [76] \t\t\t\t\t\t\n
\t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t"><span class="elsevierStyleItalic">PtAAP-VAS</span><a class="elsevierStyleCrossRef" href="#tblfn0005"><span class="elsevierStyleSup">a</span></a> \t\t\t\t\t\t\n
\t\t\t\t</td><td class="td" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t">66.8 (22.1) [63] \t\t\t\t\t\t\n
\t\t\t\t</td><td class="td" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t">66.0 (23.8) [74] \t\t\t\t\t\t\n
\t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t"><span class="elsevierStyleItalic">SF-36 PCS</span> \t\t\t\t\t\t\n
\t\t\t\t</td><td class="td" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t">32.2 (7.7) [63] \t\t\t\t\t\t\n
\t\t\t\t</td><td class="td" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t">32.6 (7.6) [75] \t\t\t\t\t\t\n
\t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t"><span class="elsevierStyleItalic">SF-36 MCS</span> \t\t\t\t\t\t\n
\t\t\t\t</td><td class="td" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t">42.4 (12.8) [63] \t\t\t\t\t\t\n
\t\t\t\t</td><td class="td" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t">41.7 (12.6) [75] \t\t\t\t\t\t\n
\t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t"><span class="elsevierStyleItalic">ESR, median mm/h (min; max)</span><a class="elsevierStyleCrossRef" href="#tblfn0010"><span class="elsevierStyleSup">b</span></a> \t\t\t\t\t\t\n
\t\t\t\t</td><td class="td" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t">34.0 (4.0; 140.0) [65] \t\t\t\t\t\t\n
\t\t\t\t</td><td class="td" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t">31.0 (4.0; 140.0) [77] \t\t\t\t\t\t\n
\t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t"><span class="elsevierStyleItalic">CRP, median mg/dL (min; max)</span><a class="elsevierStyleCrossRef" href="#tblfn0010"><span class="elsevierStyleSup">b</span></a> \t\t\t\t\t\t\n
\t\t\t\t</td><td class="td" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t">1.65 (0.0; 14.5) [64] \t\t\t\t\t\t\n
\t\t\t\t</td><td class="td" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t">1.83 (0.0; 17.0) [76] \t\t\t\t\t\t\n
\t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t"><span class="elsevierStyleItalic">Synovial hypertrophy index</span> \t\t\t\t\t\t\n
\t\t\t\t</td><td class="td" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t">19.3 (10.9) [63] \t\t\t\t\t\t\n
\t\t\t\t</td><td class="td" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t">18.3 (10.8) [73] \t\t\t\t\t\t\n
\t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t"><span class="elsevierStyleItalic">Effusion index</span> \t\t\t\t\t\t\n
\t\t\t\t</td><td class="td" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t">14.3 (10.6) [63] \t\t\t\t\t\t\n
\t\t\t\t</td><td class="td" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t">13.8 (10.2) [73] \t\t\t\t\t\t\n
\t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t"><span class="elsevierStyleItalic">Power Doppler signal index</span> \t\t\t\t\t\t\n
\t\t\t\t</td><td class="td" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t">8.9 (7.0) [63] \t\t\t\t\t\t\n
\t\t\t\t</td><td class="td" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t">8.4 (6.9) [73] \t\t\t\t\t\t\n
\t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t " colspan="3" align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t"><span class="elsevierStyleVsp" style="height:0.5px"></span></td></tr><tr title="table-row"><td class="td-with-role" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t"><span class="elsevierStyleItalic">Concomitant DMARDs</span>,<a class="elsevierStyleCrossRef" href="#tblfn0015"><span class="elsevierStyleSup">c</span></a><span class="elsevierStyleItalic">n (%)</span> \t\t\t\t\t\t\n
\t\t\t\t</td><td class="td" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t">57 (87.7) \t\t\t\t\t\t\n
\t\t\t\t</td><td class="td" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t">69 (89.6) \t\t\t\t\t\t\n
\t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Sulfasalazine \t\t\t\t\t\t\n
\t\t\t\t</td><td class="td" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t">2 (3.1) \t\t\t\t\t\t\n
\t\t\t\t</td><td class="td" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t">3 (3.9) \t\t\t\t\t\t\n
\t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Leflunomide \t\t\t\t\t\t\n
\t\t\t\t</td><td class="td" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t">10 (15.4) \t\t\t\t\t\t\n
\t\t\t\t</td><td class="td" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t">15 (19.5) \t\t\t\t\t\t\n
\t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Hydroxychloroquine \t\t\t\t\t\t\n
\t\t\t\t</td><td class="td" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t">5 (7.7) \t\t\t\t\t\t\n
\t\t\t\t</td><td class="td" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t">8 (10.4) \t\t\t\t\t\t\n
\t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Indometacin \t\t\t\t\t\t\n
\t\t\t\t</td><td class="td" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t">1 (1.5) \t\t\t\t\t\t\n
\t\t\t\t</td><td class="td" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t">4 (5.2) \t\t\t\t\t\t\n
\t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Methotrexate \t\t\t\t\t\t\n
\t\t\t\t</td><td class="td" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t">45 (69.2) \t\t\t\t\t\t\n
\t\t\t\t</td><td class="td" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t">55 (71.4) \t\t\t\t\t\t\n
\t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Prednisone \t\t\t\t\t\t\n
\t\t\t\t</td><td class="td" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t">1 (1.5) \t\t\t\t\t\t\n
\t\t\t\t</td><td class="td" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t">30 (39.0) \t\t\t\t\t\t\n
\t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t " colspan="3" align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t"><span class="elsevierStyleVsp" style="height:0.5px"></span></td></tr><tr title="table-row"><td class="td-with-role" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t"><span class="elsevierStyleItalic">Prior anti-TNF treatment, n (%)</span> \t\t\t\t\t\t\n
\t\t\t\t</td><td class="td" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t">17 (26.2) \t\t\t\t\t\t\n
\t\t\t\t</td><td class="td" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t">20 (26.0) \t\t\t\t\t\t\n
\t\t\t\t</td></tr></tbody></table>
"""
]
"imagenFichero" => array:1 [
0 => "xTab2355021.png"
]
]
]
"notaPie" => array:3 [
0 => array:3 [
"identificador" => "tblfn0005"
"etiqueta" => "a"
"nota" => "<p class="elsevierStyleNotepara" id="npar0005">Patient's assessment of arthritis pain was recorded on a visual analog scale (VAS) ranging from 0<span class="elsevierStyleHsp" style=""></span>mm (no pain) to 100<span class="elsevierStyleHsp" style=""></span>mm (maximum pain).</p>"
]
1 => array:3 [
"identificador" => "tblfn0010"
"etiqueta" => "b"
"nota" => "<p class="elsevierStyleNotepara" id="npar0010">Median values (minimum, maximum) are reported.</p>"
]
2 => array:3 [
"identificador" => "tblfn0015"
"etiqueta" => "c"
"nota" => "<p class="elsevierStyleNotepara" id="npar0015">Patients receiving any concomitant disease modifying anti-rheumatic drugs. BMI: body mass index, CRP: C-reactive protein, DAS28: 28-joint disease activity score, DMARDs: disease modifying anti-rheumatic drugs, ESR: erythrocyte sedimentation rate, HAQ-DI: health assessment questionnaire disability index, MCS: mental component summary, NR: not reported, PCS: physical component summary, PtAAP: patient's assessment of arthritis pain, RF: rheumatoid factor, SD: standard deviation, SF-36: Short-Form 36-item Health Survey; TNF: tumor necrosis factor, VAS: visual analog scale.</p>"
]
]
]
"descripcion" => array:1 [
"en" => "<p id="spar0060" class="elsevierStyleSimplePara elsevierViewall">Patient baseline characteristics.</p>"
]
]
4 => array:8 [
"identificador" => "tbl0010"
"etiqueta" => "Table 2"
"tipo" => "MULTIMEDIATABLA"
"mostrarFloat" => true
"mostrarDisplay" => false
"detalles" => array:1 [
0 => array:3 [
"identificador" => "at2"
"detalle" => "Table "
"rol" => "short"
]
]
"tabla" => array:3 [
"leyenda" => "<p id="spar0075" class="elsevierStyleSimplePara elsevierViewall">Data are reported for the full analysis set, which was defined as the number of patients that received at least one dose of CZP and that provided at least one valid baseline and post-baseline effectiveness assessment and who had no important protocol deviations.</p>"
"tablatextoimagen" => array:1 [
0 => array:2 [
"tabla" => array:1 [
0 => """
<table border="0" frame="\n
\t\t\t\t\tvoid\n
\t\t\t\t" class=""><thead title="thead"><tr title="table-row"><th class="td" title="\n
\t\t\t\t\ttable-head\n
\t\t\t\t " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t" scope="col" style="border-bottom: 2px solid black">Values are means (95% CI)<a class="elsevierStyleCrossRef" href="#tblfn0020"><span class="elsevierStyleSup">a</span></a> \t\t\t\t\t\t\n
\t\t\t\t\t\t</th><th class="td" title="\n
\t\t\t\t\ttable-head\n
\t\t\t\t " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t" scope="col" style="border-bottom: 2px solid black">Baseline (<span class="elsevierStyleItalic">n</span><span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>63) \t\t\t\t\t\t\n
\t\t\t\t\t\t</th><th class="td" title="\n
\t\t\t\t\ttable-head\n
\t\t\t\t " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t" scope="col" style="border-bottom: 2px solid black">Week 12 (<span class="elsevierStyleItalic">n</span><span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>46) \t\t\t\t\t\t\n
\t\t\t\t\t\t</th></tr></thead><tbody title="tbody"><tr title="table-row"><td class="td-with-role" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t">Synovial hypertrophy index \t\t\t\t\t\t\n
\t\t\t\t</td><td class="td" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t " align="char" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t">19.3 (16.6; 22.1) \t\t\t\t\t\t\n
\t\t\t\t</td><td class="td" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t " align="char" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t">12.3 (9.5; 15.1) \t\t\t\t\t\t\n
\t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t">Effusion index \t\t\t\t\t\t\n
\t\t\t\t</td><td class="td" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t " align="char" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t">14.3 (11.7; 17.0) \t\t\t\t\t\t\n
\t\t\t\t</td><td class="td" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t " align="char" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t">7.7 (5.2; 10.2) \t\t\t\t\t\t\n
\t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t">PD signal index \t\t\t\t\t\t\n
\t\t\t\t</td><td class="td" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t " align="char" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t">8.9 (7.2; 10.7) \t\t\t\t\t\t\n
\t\t\t\t</td><td class="td" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t " align="char" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t">4.6 (3.1; 6.2) \t\t\t\t\t\t\n
\t\t\t\t</td></tr></tbody></table>
"""
]
"imagenFichero" => array:1 [
0 => "xTab2355022.png"
]
]
]
"notaPie" => array:1 [
0 => array:3 [
"identificador" => "tblfn0020"
"etiqueta" => "a"
"nota" => "<p class="elsevierStyleNotepara" id="npar0020">Univariate 95% CIs are shown as the lower bound of the 95% CI and the upper bound of the 95% CI (lower; upper). CI: confidence interval, PD: power Doppler.</p>"
]
]
]
"descripcion" => array:1 [
"en" => "<p id="spar0070" class="elsevierStyleSimplePara elsevierViewall">Ultrasound outcomes at baseline and Week 12.</p>"
]
]
5 => array:8 [
"identificador" => "tbl0015"
"etiqueta" => "Table 3"
"tipo" => "MULTIMEDIATABLA"
"mostrarFloat" => true
"mostrarDisplay" => false
"detalles" => array:1 [
0 => array:3 [
"identificador" => "at3"
"detalle" => "Table "
"rol" => "short"
]
]
"tabla" => array:2 [
"leyenda" => "<p id="spar0085" class="elsevierStyleSimplePara elsevierViewall">Data are reported for the safety set, which was defined as all patients that received at least one dose of CZP at any time during the study. Values are based on MedDRA preferred term. <span class="elsevierStyleItalic">n</span><span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>number of patients reporting at least 1 TEADR within the preferred term. TEADR: treatment emergent adverse drug reaction.</p>"
"tablatextoimagen" => array:1 [
0 => array:2 [
"tabla" => array:1 [
0 => """
<table border="0" frame="\n
\t\t\t\t\tvoid\n
\t\t\t\t" class=""><thead title="thead"><tr title="table-row"><th class="td-with-role" title="\n
\t\t\t\t\ttable-head\n
\t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t" scope="col">TEADR \t\t\t\t\t\t\n
\t\t\t\t\t\t</th><th class="td" title="\n
\t\t\t\t\ttable-head\n
\t\t\t\t " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t" scope="col">Safety set, <span class="elsevierStyleItalic">N</span><span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>77 \t\t\t\t\t\t\n
\t\t\t\t\t\t</th></tr><tr title="table-row"><th class="td" title="\n
\t\t\t\t\ttable-head\n
\t\t\t\t " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t" scope="col" style="border-bottom: 2px solid black">Preferred term \t\t\t\t\t\t\n
\t\t\t\t\t\t</th><th class="td" title="\n
\t\t\t\t\ttable-head\n
\t\t\t\t " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t" scope="col" style="border-bottom: 2px solid black"><span class="elsevierStyleItalic">n</span> (%) [# of events] \t\t\t\t\t\t\n
\t\t\t\t\t\t</th></tr></thead><tbody title="tbody"><tr title="table-row"><td class="td-with-role" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t"><span class="elsevierStyleItalic">Any TEADRs</span> \t\t\t\t\t\t\n
\t\t\t\t</td><td class="td" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t">13 (16.9) [19] \t\t\t\t\t\t\n
\t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Alopecia \t\t\t\t\t\t\n
\t\t\t\t</td><td class="td" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t">1 (1.3) [1] \t\t\t\t\t\t\n
\t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Hyperhidrosis \t\t\t\t\t\t\n
\t\t\t\t</td><td class="td" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t">1 (1.3) [1] \t\t\t\t\t\t\n
\t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Papule \t\t\t\t\t\t\n
\t\t\t\t</td><td class="td" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t">1 (1.3) [1] \t\t\t\t\t\t\n
\t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Rash \t\t\t\t\t\t\n
\t\t\t\t</td><td class="td" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t">1 (1.3) [1] \t\t\t\t\t\t\n
\t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Skin reaction \t\t\t\t\t\t\n
\t\t\t\t</td><td class="td" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t">2 (2.6) [2] \t\t\t\t\t\t\n
\t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Urticaria \t\t\t\t\t\t\n
\t\t\t\t</td><td class="td" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t">1 (1.3) [1] \t\t\t\t\t\t\n
\t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Escherichia urinary tract infection \t\t\t\t\t\t\n
\t\t\t\t</td><td class="td" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t">1 (1.3) [1] \t\t\t\t\t\t\n
\t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Respiratory tract infection \t\t\t\t\t\t\n
\t\t\t\t</td><td class="td" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t">1 (1.3) [1] \t\t\t\t\t\t\n
\t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Tuberculosis \t\t\t\t\t\t\n
\t\t\t\t</td><td class="td" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t">1 (1.3) [1] \t\t\t\t\t\t\n
\t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Conjunctivitis \t\t\t\t\t\t\n
\t\t\t\t</td><td class="td" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t">1 (1.3) [1] \t\t\t\t\t\t\n
\t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Vision blurred \t\t\t\t\t\t\n
\t\t\t\t</td><td class="td" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t">1 (1.3) [1] \t\t\t\t\t\t\n
\t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Lymphadenopathy mediastinal \t\t\t\t\t\t\n
\t\t\t\t</td><td class="td" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t">1 (1.3) [1] \t\t\t\t\t\t\n
\t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Gingival ulceration \t\t\t\t\t\t\n
\t\t\t\t</td><td class="td" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t">1 (1.3) [1] \t\t\t\t\t\t\n
\t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Pyrexia \t\t\t\t\t\t\n
\t\t\t\t</td><td class="td" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t">1 (1.3) [1] \t\t\t\t\t\t\n
\t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Non-Hodgkin's lymphoma \t\t\t\t\t\t\n
\t\t\t\t</td><td class="td" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t">1 (1.3) [1] \t\t\t\t\t\t\n
\t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Dizziness \t\t\t\t\t\t\n
\t\t\t\t</td><td class="td" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t">1 (1.3) [1] \t\t\t\t\t\t\n
\t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Bronchial hyperactivity \t\t\t\t\t\t\n
\t\t\t\t</td><td class="td" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t">1 (1.3) [1] \t\t\t\t\t\t\n
\t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Vasculitis \t\t\t\t\t\t\n
\t\t\t\t</td><td class="td" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t">1 (1.3) [1] \t\t\t\t\t\t\n
\t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t " colspan="2" align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t"><span class="elsevierStyleVsp" style="height:0.5px"></span></td></tr><tr title="table-row"><td class="td-with-role" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t"><span class="elsevierStyleItalic">Serious TEADRs</span> \t\t\t\t\t\t\n
\t\t\t\t</td><td class="td" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t">3 (3.9) [4] \t\t\t\t\t\t\n
\t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Lymphadenopathy mediastinal \t\t\t\t\t\t\n
\t\t\t\t</td><td class="td" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t">1 (1.3) [1] \t\t\t\t\t\t\n
\t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Tuberculosis \t\t\t\t\t\t\n
\t\t\t\t</td><td class="td" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t">1 (1.3) [1] \t\t\t\t\t\t\n
\t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Non-Hodgkin's lymphoma \t\t\t\t\t\t\n
\t\t\t\t</td><td class="td" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t">1 (1.3) [1] \t\t\t\t\t\t\n
\t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Skin reaction \t\t\t\t\t\t\n
\t\t\t\t</td><td class="td" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t">1 (1.3) [1] \t\t\t\t\t\t\n
\t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t " colspan="2" align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t"><span class="elsevierStyleVsp" style="height:0.5px"></span></td></tr><tr title="table-row"><td class="td-with-role" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t"><span class="elsevierStyleItalic">Discontinuations due to TEADRs</span> \t\t\t\t\t\t\n
\t\t\t\t</td><td class="td" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t">8 (10.4) [9] \t\t\t\t\t\t\n
\t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Bronchial hyperreactivity \t\t\t\t\t\t\n
\t\t\t\t</td><td class="td" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t">1 (1.3) [1] \t\t\t\t\t\t\n
\t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Respiratory tract infection \t\t\t\t\t\t\n
\t\t\t\t</td><td class="td" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t">1 (1.3) [1] \t\t\t\t\t\t\n
\t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Tuberculosis \t\t\t\t\t\t\n
\t\t\t\t</td><td class="td" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t">1 (1.3) [1] \t\t\t\t\t\t\n
\t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Skin reaction \t\t\t\t\t\t\n
\t\t\t\t</td><td class="td" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t">2 (2.6) [2] \t\t\t\t\t\t\n
\t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Lymphadenopathy mediastinal \t\t\t\t\t\t\n
\t\t\t\t</td><td class="td" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t">1 (1.3) [1] \t\t\t\t\t\t\n
\t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Gingival ulceration \t\t\t\t\t\t\n
\t\t\t\t</td><td class="td" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t">1 (1.3) [1] \t\t\t\t\t\t\n
\t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Non-Hodgkin's lymphoma \t\t\t\t\t\t\n
\t\t\t\t</td><td class="td" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t">1 (1.3) [1] \t\t\t\t\t\t\n
\t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Vasculitis \t\t\t\t\t\t\n
\t\t\t\t</td><td class="td" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t">1 (1.3) [1] \t\t\t\t\t\t\n
\t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t " colspan="2" align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t"><span class="elsevierStyleVsp" style="height:0.5px"></span></td></tr><tr title="table-row"><td class="td-with-role" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t"><span class="elsevierStyleItalic">Death</span> \t\t\t\t\t\t\n
\t\t\t\t</td><td class="td" title="\n
\t\t\t\t\ttable-entry\n
\t\t\t\t " align="left" valign="\n
\t\t\t\t\ttop\n
\t\t\t\t">1 (1.3) [1] \t\t\t\t\t\t\n
\t\t\t\t</td></tr></tbody></table>
"""
]
"imagenFichero" => array:1 [
0 => "xTab2355020.png"
]
]
]
]
"descripcion" => array:1 [
"en" => "<p id="spar0080" class="elsevierStyleSimplePara elsevierViewall">Summary of treatment-emergent adverse drug reactions.</p>"
]
]
]
"bibliografia" => array:2 [
"titulo" => "References"
"seccion" => array:1 [
0 => array:2 [
"identificador" => "bibs0015"
"bibliografiaReferencia" => array:34 [
0 => array:3 [
"identificador" => "bib0175"
"etiqueta" => "1"
"referencia" => array:1 [
0 => array:2 [
"contribucion" => array:1 [
0 => array:2 [
"titulo" => "Epidemiology and burden of illness of rheumatoid arthritis"
"autores" => array:1 [
0 => array:2 [
"etal" => false
"autores" => array:1 [
0 => "T.K. Kvien"
]
]
]
]
]
"host" => array:1 [
0 => array:2 [
"doi" => "10.2165/00019053-200422004-00002"
"Revista" => array:6 [
"tituloSerie" => "Pharmacoeconomics"
"fecha" => "2004"
"volumen" => "22"
"paginaInicial" => "1"
"paginaFinal" => "12"
"link" => array:1 [
0 => array:2 [
"url" => "https://www.ncbi.nlm.nih.gov/pubmed/15876006"
"web" => "Medline"
]
]
]
]
]
]
]
]
1 => array:3 [
"identificador" => "bib0180"
"etiqueta" => "2"
"referencia" => array:1 [
0 => array:2 [
"contribucion" => array:1 [
0 => array:2 [
"titulo" => "Risk of serious infections during rituximab, abatacept and anakinra treatments for rheumatoid arthritis: meta-analyses of randomised placebo-controlled trials"
"autores" => array:1 [
0 => array:2 [
"etal" => false
"autores" => array:3 [
0 => "C. Salliot"
1 => "M. Dougados"
2 => "L. Gossec"
]
]
]
]
]
"host" => array:1 [
0 => array:2 [
"doi" => "10.1136/ard.2007.083188"
"Revista" => array:6 [
"tituloSerie" => "Ann Rheum Dis"
"fecha" => "2009"
"volumen" => "68"
"paginaInicial" => "25"
"paginaFinal" => "32"
"link" => array:1 [
0 => array:2 [
"url" => "https://www.ncbi.nlm.nih.gov/pubmed/18203761"
"web" => "Medline"
]
]
]
]
]
]
]
]
2 => array:3 [
"identificador" => "bib0185"
"etiqueta" => "3"
"referencia" => array:1 [
0 => array:2 [
"contribucion" => array:1 [
0 => array:2 [
"titulo" => "[Consensus statement of the Spanish Society of Rheumatology on risk management of biologic therapy in rheumatic patients]"
"autores" => array:1 [
0 => array:2 [
"etal" => true
"autores" => array:6 [
0 => "J. Gomez Reino"
1 => "E. Loza"
2 => "J.L. Andreu"
3 => "A. Balsa"
4 => "E. Batlle"
5 => "J.D. Canete"
]
]
]
]
]
"host" => array:1 [
0 => array:2 [
"doi" => "10.1016/j.reuma.2011.05.002"
"Revista" => array:6 [
"tituloSerie" => "Reumatol Clin"
"fecha" => "2011"
"volumen" => "7"
"paginaInicial" => "284"
"paginaFinal" => "298"
"link" => array:1 [
0 => array:2 [
"url" => "https://www.ncbi.nlm.nih.gov/pubmed/21925444"
"web" => "Medline"
]
]
]
]
]
]
]
]
3 => array:3 [
"identificador" => "bib0190"
"etiqueta" => "4"
"referencia" => array:1 [
0 => array:2 [
"contribucion" => array:1 [
0 => array:2 [
"titulo" => "Efficacy and safety of certolizumab pegol in a broad population of patients with active rheumatoid arthritis: results from the REALISTIC phase IIIb study"
"autores" => array:1 [
0 => array:2 [
"etal" => true
"autores" => array:6 [
0 => "M.E. Weinblatt"
1 => "R. Fleischmann"
2 => "T.W. Huizinga"
3 => "P. Emery"
4 => "J. Pope"
5 => "E.M. Massarotti"
]
]
]
]
]
"host" => array:1 [
0 => array:1 [
"Revista" => array:5 [
"tituloSerie" => "Rheumatology (Oxford)"
"fecha" => "2012"
"volumen" => "51"
"paginaInicial" => "2204"
"paginaFinal" => "2214"
]
]
]
]
]
]
4 => array:3 [
"identificador" => "bib0195"
"etiqueta" => "5"
"referencia" => array:1 [
0 => array:2 [
"contribucion" => array:1 [
0 => array:2 [
"titulo" => "Effectiveness of adalimumab for rheumatoid arthritis in patients with a history of TNF-antagonist therapy in clinical practice"
"autores" => array:1 [
0 => array:2 [
"etal" => true
"autores" => array:6 [
0 => "S. Bombardieri"
1 => "A. Ruiz"
2 => "P. Fardellone"
3 => "P. Geusens"
4 => "F. McKenna"
5 => "K. Unnebrink"
]
]
]
]
]
"host" => array:1 [
0 => array:2 [
"doi" => "10.1093/rheumatology/kem091"
"Revista" => array:6 [
"tituloSerie" => "Rheumatology"
"fecha" => "2007"
"volumen" => "46"
"paginaInicial" => "1191"
"paginaFinal" => "1199"
"link" => array:1 [
0 => array:2 [
"url" => "https://www.ncbi.nlm.nih.gov/pubmed/17504821"
"web" => "Medline"
]
]
]
]
]
]
]
]
5 => array:3 [
"identificador" => "bib0200"
"etiqueta" => "6"
"referencia" => array:1 [
0 => array:2 [
"contribucion" => array:1 [
0 => array:2 [
"titulo" => "Etanercept versus methotrexate in patients with early rheumatoid arthritis: two-year radiographic and clinical outcomes"
"autores" => array:1 [
0 => array:2 [
"etal" => true
"autores" => array:6 [
0 => "M.C. Genovese"
1 => "J.M. Bathon"
2 => "R.W. Martin"
3 => "R.M. Fleischmann"
4 => "J.R. Tesser"
5 => "M.H. Schiff"
]
]
]
]
]
"host" => array:1 [
0 => array:1 [
"Revista" => array:5 [
"tituloSerie" => "Arthrit Rheumatol"
"fecha" => "2002"
"volumen" => "46"
"paginaInicial" => "1443"
"paginaFinal" => "1450"
]
]
]
]
]
]
6 => array:3 [
"identificador" => "bib0205"
"etiqueta" => "7"
"referencia" => array:1 [
0 => array:2 [
"contribucion" => array:1 [
0 => array:2 [
"titulo" => "When is switching warranted among biologic therapies in rheumatoid arthritis?"
"autores" => array:1 [
0 => array:2 [
"etal" => false
"autores" => array:4 [
0 => "A. Reynolds"
1 => "A.S. Koenig"
2 => "E. Bananis"
3 => "A. Singh"
]
]
]
]
]
"host" => array:1 [
0 => array:2 [
"doi" => "10.1586/erp.12.27"
"Revista" => array:6 [
"tituloSerie" => "Expert Rev Pharmacoecon Outcomes Res"
"fecha" => "2012"
"volumen" => "12"
"paginaInicial" => "319"
"paginaFinal" => "333"
"link" => array:1 [
0 => array:2 [
"url" => "https://www.ncbi.nlm.nih.gov/pubmed/22812556"
"web" => "Medline"
]
]
]
]
]
]
]
]
7 => array:3 [
"identificador" => "bib0210"
"etiqueta" => "8"
"referencia" => array:1 [
0 => array:2 [
"contribucion" => array:1 [
0 => array:1 [
"titulo" => "GUIPCAR Group Update of the clinical practice guideline for the management of rheumatoid arthritis in Spain"
]
]
"host" => array:1 [
0 => array:1 [
"Libro" => array:2 [
"fecha" => "2011"
"paginaInicial" => "367"
]
]
]
]
]
]
8 => array:3 [
"identificador" => "bib0215"
"etiqueta" => "9"
"referencia" => array:1 [
0 => array:2 [
"contribucion" => array:1 [
0 => array:2 [
"titulo" => "Evaluating the efficacy of sequential biologic therapies for rheumatoid arthritis patients with an inadequate response to tumor necrosis factor-α inhibitors"
"autores" => array:1 [
0 => array:2 [
"etal" => true
"autores" => array:6 [
0 => "R. Rendas-Baum"
1 => "G.V. Wallenstein"
2 => "T. Koncz"
3 => "M. Kosinski"
4 => "M. Yang"
5 => "J. Bradley"
]
]
]
]
]
"host" => array:1 [
0 => array:2 [
"doi" => "10.1186/ar3249"
"Revista" => array:5 [
"tituloSerie" => "Arthritis Res Ther"
"fecha" => "2011"
"volumen" => "13"
"paginaInicial" => "R25"
"link" => array:1 [
0 => array:2 [
"url" => "https://www.ncbi.nlm.nih.gov/pubmed/21324169"
"web" => "Medline"
]
]
]
]
]
]
]
]
9 => array:3 [
"identificador" => "bib0220"
"etiqueta" => "10"
"referencia" => array:1 [
0 => array:2 [
"contribucion" => array:1 [
0 => array:2 [
"titulo" => "Optimising ultrasonography in rheumatology"
"autores" => array:1 [
0 => array:2 [
"etal" => false
"autores" => array:3 [
0 => "H.I. Keen"
1 => "R. Wakefield"
2 => "P.G. Conaghan"
]
]
]
]
]
"host" => array:1 [
0 => array:1 [
"Revista" => array:5 [
"tituloSerie" => "Clin Exp Rheumatol"
"fecha" => "2014"
"volumen" => "32"
"paginaInicial" => "S-13"
"paginaFinal" => "S16"
]
]
]
]
]
]
10 => array:3 [
"identificador" => "bib0225"
"etiqueta" => "11"
"referencia" => array:1 [
0 => array:2 [
"contribucion" => array:1 [
0 => array:2 [
"titulo" => "Recomendaciones para el uso de la ecografía y la resonancia magnética en pacientes con artritis reumatoide"
"autores" => array:1 [
0 => array:2 [
"etal" => true
"autores" => array:6 [
0 => "I. Möller"
1 => "E. Loza"
2 => "J. Uson"
3 => "C. Acebes"
4 => "J.L. Andreu"
5 => "E. Batlle"
]
]
]
]
]
"host" => array:1 [
0 => array:2 [
"doi" => "10.1016/j.reuma.2016.08.010"
"Revista" => array:6 [
"tituloSerie" => "Reumatol Clin"
"fecha" => "2016"
"volumen" => "14"
"paginaInicial" => "9"
"paginaFinal" => "19"
"link" => array:1 [
0 => array:2 [
"url" => "https://www.ncbi.nlm.nih.gov/pubmed/28029551"
"web" => "Medline"
]
]
]
]
]
]
]
]
11 => array:3 [
"identificador" => "bib0230"
"etiqueta" => "12"
"referencia" => array:1 [
0 => array:2 [
"contribucion" => array:1 [
0 => array:2 [
"titulo" => "Contributions of ultrasound beyond clinical data in assessing inflammatory disease activity in rheumatoid arthritis: current insights and future prospects"
"autores" => array:1 [
0 => array:2 [
"etal" => false
"autores" => array:5 [
0 => "P. Mandl"
1 => "R. Kurucz"
2 => "D. Niedermayer"
3 => "P.V. Balint"
4 => "J.S. Smolen"
]
]
]
]
]
"host" => array:1 [
0 => array:1 [
"Revista" => array:5 [
"tituloSerie" => "Rheumatology (Oxford)"
"fecha" => "2014"
"volumen" => "53"
"paginaInicial" => "2136"
"paginaFinal" => "2142"
]
]
]
]
]
]
12 => array:3 [
"identificador" => "bib0235"
"etiqueta" => "13"
"referencia" => array:1 [
0 => array:2 [
"contribucion" => array:1 [
0 => array:2 [
"titulo" => "The American Rheumatism Association 1987 revised criteria for the classification of rheumatoid arthritis"
"autores" => array:1 [
0 => array:2 [
"etal" => true
"autores" => array:6 [
0 => "F.C. Arnett"
1 => "S.M. Edworthy"
2 => "D.A. Bloch"
3 => "D.J. McShane"
4 => "J.F. Fries"
5 => "N.S. Cooper"
]
]
]
]
]
"host" => array:1 [
0 => array:1 [
"Revista" => array:5 [
"tituloSerie" => "Arthritis Rheum"
"fecha" => "1988"
"volumen" => "31"
"paginaInicial" => "315"
"paginaFinal" => "324"
]
]
]
]
]
]
13 => array:3 [
"identificador" => "bib0240"
"etiqueta" => "14"
"referencia" => array:1 [
0 => array:2 [
"contribucion" => array:1 [
0 => array:2 [
"titulo" => "Measurement of patient outcome in arthritis"
"autores" => array:1 [
0 => array:2 [
"etal" => false
"autores" => array:4 [
0 => "J.F. Fries"
1 => "P. Spitz"
2 => "R.G. Kraines"
3 => "H.R. Holman"
]
]
]
]
]
"host" => array:1 [
0 => array:2 [
"doi" => "10.1002/art.1780230202"
"Revista" => array:6 [
"tituloSerie" => "Arthritis Rheum"
"fecha" => "1980"
"volumen" => "23"
"paginaInicial" => "137"
"paginaFinal" => "145"
"link" => array:1 [
0 => array:2 [
"url" => "https://www.ncbi.nlm.nih.gov/pubmed/7362664"
"web" => "Medline"
]
]
]
]
]
]
]
]
14 => array:3 [
"identificador" => "bib0245"
"etiqueta" => "15"
"referencia" => array:1 [
0 => array:2 [
"contribucion" => array:1 [
0 => array:2 [
"titulo" => "Modified disease activity scores that include twenty-eight-joint counts. Development and validation in a prospective longitudinal study of patients with rheumatoid arthritis"
"autores" => array:1 [
0 => array:2 [
"etal" => false
"autores" => array:6 [
0 => "M.L. Prevoo"
1 => "M.A. Van’T Hof"
2 => "H.H. Kuper"
3 => "M.A. van Leeuwen"
4 => "L.B. van de Putte"
5 => "P.L. van Riel"
]
]
]
]
]
"host" => array:1 [
0 => array:2 [
"doi" => "10.1002/art.1780380107"
"Revista" => array:6 [
"tituloSerie" => "Arthritis Rheum"
"fecha" => "1995"
"volumen" => "38"
"paginaInicial" => "44"
"paginaFinal" => "48"
"link" => array:1 [
0 => array:2 [
"url" => "https://www.ncbi.nlm.nih.gov/pubmed/7818570"
"web" => "Medline"
]
]
]
]
]
]
]
]
15 => array:3 [
"identificador" => "bib0250"
"etiqueta" => "16"
"referencia" => array:1 [
0 => array:2 [
"contribucion" => array:1 [
0 => array:2 [
"titulo" => "Measurement of pain"
"autores" => array:1 [
0 => array:2 [
"etal" => false
"autores" => array:1 [
0 => "E.C. Huskisson"
]
]
]
]
]
"host" => array:1 [
0 => array:1 [
"Revista" => array:6 [
"tituloSerie" => "Lancet"
"fecha" => "1974"
"volumen" => "2"
"paginaInicial" => "1127"
"paginaFinal" => "1131"
"link" => array:1 [
0 => array:2 [
"url" => "https://www.ncbi.nlm.nih.gov/pubmed/2890026"
"web" => "Medline"
]
]
]
]
]
]
]
]
16 => array:3 [
"identificador" => "bib0255"
"etiqueta" => "17"
"referencia" => array:1 [
0 => array:2 [
"contribucion" => array:1 [
0 => array:2 [
"titulo" => "The MOS 36-Item Short-Form Health Survey (SF-36): II. Psychometric and clinical tests of validity in measuring physical and mental health constructs"
"autores" => array:1 [
0 => array:2 [
"etal" => false
"autores" => array:3 [
0 => "C.A. McHorney"
1 => "J.E. Ware Jr."
2 => "A.E. Raczek"
]
]
]
]
]
"host" => array:1 [
0 => array:2 [
"doi" => "10.1097/00005650-199303000-00006"
"Revista" => array:6 [
"tituloSerie" => "Med Care"
"fecha" => "1993"
"volumen" => "31"
"paginaInicial" => "247"
"paginaFinal" => "263"
"link" => array:1 [
0 => array:2 [
"url" => "https://www.ncbi.nlm.nih.gov/pubmed/8450681"
"web" => "Medline"
]
]
]
]
]
]
]
]
17 => array:3 [
"identificador" => "bib0260"
"etiqueta" => "18"
"referencia" => array:1 [
0 => array:2 [
"contribucion" => array:1 [
0 => array:2 [
"titulo" => "[Are imaging techniques necessary for defining remission in rheumatoid arthritis?.]"
"autores" => array:1 [
0 => array:2 [
"etal" => false
"autores" => array:1 [
0 => "E. Naredo Sanchez"
]
]
]
]
]
"host" => array:1 [
0 => array:2 [
"doi" => "10.1016/j.reuma.2008.10.001"
"Revista" => array:8 [
"tituloSerie" => "Reumatol Clin"
"fecha" => "2009"
"volumen" => "5"
"numero" => "Suppl. 1"
"paginaInicial" => "17"
"paginaFinal" => "21"
"link" => array:1 [
0 => array:2 [
"url" => "https://www.ncbi.nlm.nih.gov/pubmed/21794637"
"web" => "Medline"
]
]
"itemHostRev" => array:3 [
"pii" => "S0140673605677045"
"estado" => "S300"
"issn" => "01406736"
]
]
]
]
]
]
]
18 => array:3 [
"identificador" => "bib0265"
"etiqueta" => "19"
"referencia" => array:1 [
0 => array:2 [
"contribucion" => array:1 [
0 => array:2 [
"titulo" => "Validity, reproducibility, and responsiveness of a twelve-joint simplified power doppler ultrasonographic assessment of joint inflammation in rheumatoid arthritis"
"autores" => array:1 [
0 => array:2 [
"etal" => true
"autores" => array:6 [
0 => "E. Naredo"
1 => "M. Rodriguez"
2 => "C. Campos"
3 => "J.M. Rodríguez-Heredia"
4 => "J.A. Medina"
5 => "E. Giner"
]
]
]
]
]
"host" => array:1 [
0 => array:1 [
"Revista" => array:5 [
"tituloSerie" => "Arthritis Care Res (Hoboken)"
"fecha" => "2008"
"volumen" => "59"
"paginaInicial" => "515"
"paginaFinal" => "522"
]
]
]
]
]
]
19 => array:3 [
"identificador" => "bib0270"
"etiqueta" => "20"
"referencia" => array:1 [
0 => array:2 [
"contribucion" => array:1 [
0 => array:2 [
"titulo" => "Musculoskeletal ultrasound including definitions for ultrasonographic pathology"
"autores" => array:1 [
0 => array:2 [
"etal" => true
"autores" => array:6 [
0 => "R.J. Wakefield"
1 => "P.V. Balint"
2 => "M. Szkudlarek"
3 => "E. Filippucci"
4 => "M. Backhaus"
5 => "M.A. D’Agostino"
]
]
]
]
]
"host" => array:1 [
0 => array:1 [
"Revista" => array:6 [
"tituloSerie" => "J Rheumatol"
"fecha" => "2005"
"volumen" => "32"
"paginaInicial" => "2485"
"paginaFinal" => "2487"
"link" => array:1 [
0 => array:2 [
"url" => "https://www.ncbi.nlm.nih.gov/pubmed/16331793"
"web" => "Medline"
]
]
]
]
]
]
]
]
20 => array:3 [
"identificador" => "bib0275"
"etiqueta" => "21"
"referencia" => array:1 [
0 => array:2 [
"contribucion" => array:1 [
0 => array:2 [
"titulo" => "The minimally important difference for the health assessment questionnaire in rheumatoid arthritis clinical practice is smaller than in randomized controlled trials"
"autores" => array:1 [
0 => array:2 [
"etal" => false
"autores" => array:4 [
0 => "J.E. Pope"
1 => "D. Khanna"
2 => "D. Norrie"
3 => "J.M. Ouimet"
]
]
]
]
]
"host" => array:1 [
0 => array:2 [
"doi" => "10.3899/jrheum.080479"
"Revista" => array:6 [
"tituloSerie" => "J Rheumatol"
"fecha" => "2009"
"volumen" => "36"
"paginaInicial" => "254"
"paginaFinal" => "259"
"link" => array:1 [
0 => array:2 [
"url" => "https://www.ncbi.nlm.nih.gov/pubmed/19132791"
"web" => "Medline"
]
]
]
]
]
]
]
]
21 => array:3 [
"identificador" => "bib0280"
"etiqueta" => "22"
"referencia" => array:1 [
0 => array:2 [
"contribucion" => array:1 [
0 => array:2 [
"titulo" => "Effectiveness of tumor necrosis factor inhibitors in rheumatoid arthritis in an observational cohort study: comparison of patients according to their eligibility for major randomized clinical trials"
"autores" => array:1 [
0 => array:2 [
"etal" => true
"autores" => array:6 [
0 => "A. Zink"
1 => "A. Strangfeld"
2 => "M. Schneider"
3 => "P. Herzer"
4 => "F. Hierse"
5 => "M. Stoyanova-Scholz"
]
]
]
]
]
"host" => array:1 [
0 => array:1 [
"Revista" => array:5 [
"tituloSerie" => "Arthrit Rheumatol"
"fecha" => "2006"
"volumen" => "54"
"paginaInicial" => "3399"
"paginaFinal" => "3407"
]
]
]
]
]
]
22 => array:3 [
"identificador" => "bib0285"
"etiqueta" => "23"
"referencia" => array:1 [
0 => array:2 [
"contribucion" => array:1 [
0 => array:2 [
"titulo" => "Long-term effectiveness and safety of TNF-blocking agents in daily clinical practice: results from the Dutch Rheumatoid Arthritis Monitoring register"
"autores" => array:1 [
0 => array:2 [
"etal" => true
"autores" => array:6 [
0 => "W. Kievit"
1 => "J. Fransen"
2 => "E.M. Adang"
3 => "A.A. den Broeder"
4 => "H.J. Bernelot Moens"
5 => "H. Visser"
]
]
]
]
]
"host" => array:1 [
0 => array:2 [
"doi" => "10.1093/rheumatology/keq325"
"Revista" => array:7 [
"tituloSerie" => "Rheumatology"
"fecha" => "2010"
"volumen" => "50"
"paginaInicial" => "196"
"paginaFinal" => "203"
"link" => array:1 [
0 => array:2 [
"url" => "https://www.ncbi.nlm.nih.gov/pubmed/21078625"
"web" => "Medline"
]
]
"itemHostRev" => array:3 [
"pii" => "S016752731736936X"
"estado" => "S300"
"issn" => "01675273"
]
]
]
]
]
]
]
23 => array:3 [
"identificador" => "bib0290"
"etiqueta" => "24"
"referencia" => array:1 [
0 => array:2 [
"contribucion" => array:1 [
0 => array:2 [
"titulo" => "Impact of ultrasonography on treatment decision in rheumatoid arthritis: the IMPULSAR study"
"autores" => array:1 [
0 => array:2 [
"etal" => true
"autores" => array:6 [
0 => "C. Díaz-Torné"
1 => "C. Moragues"
2 => "E. Toniolo"
3 => "C. Geli"
4 => "I. Castellví"
5 => "P. Moya"
]
]
]
]
]
"host" => array:1 [
0 => array:1 [
"Revista" => array:5 [
"tituloSerie" => "Rheumatol Int"
"fecha" => "2017"
"volumen" => "37"
"paginaInicial" => "891"
"paginaFinal" => "896"
]
]
]
]
]
]
24 => array:3 [
"identificador" => "bib0295"
"etiqueta" => "25"
"referencia" => array:1 [
0 => array:2 [
"contribucion" => array:1 [
0 => array:2 [
"titulo" => "A reduced 12-joint ultrasound examination predicts lack of X-ray progression better than clinical remission criteria in patients with rheumatoid arthritis"
"autores" => array:1 [
0 => array:2 [
"etal" => true
"autores" => array:6 [
0 => "E. de Miguel"
1 => "A. Pecondón-Español"
2 => "M. Castaño-Sánchez"
3 => "A. Corrales"
4 => "R. Gutierrez-Polo"
5 => "M. Rodriguez-Gomez"
]
]
]
]
]
"host" => array:1 [
0 => array:2 [
"doi" => "10.1007/s00296-017-3714-5"
"Revista" => array:6 [
"tituloSerie" => "Rheumatol Int"
"fecha" => "2017"
"volumen" => "37"
"paginaInicial" => "1347"
"paginaFinal" => "1356"
"link" => array:1 [
0 => array:2 [
"url" => "https://www.ncbi.nlm.nih.gov/pubmed/28389854"
"web" => "Medline"
]
]
]
]
]
]
]
]
25 => array:3 [
"identificador" => "bib0300"
"etiqueta" => "26"
"referencia" => array:1 [
0 => array:2 [
"contribucion" => array:1 [
0 => array:2 [
"titulo" => "Predictive value of Doppler ultrasound-detected synovitis in relation to failed tapering of biologic therapy in patients with rheumatoid arthritis"
"autores" => array:1 [
0 => array:2 [
"etal" => true
"autores" => array:6 [
0 => "E. Naredo"
1 => "L. Valor"
2 => "I. De la Torre"
3 => "M. Montoro"
4 => "N. Bello"
5 => "J. Martínez-Barrio"
]
]
]
]
]
"host" => array:1 [
0 => array:2 [
"doi" => "10.1093/rheumatology/kev006"
"Revista" => array:6 [
"tituloSerie" => "Rheumatology"
"fecha" => "2015"
"volumen" => "54"
"paginaInicial" => "1408"
"paginaFinal" => "1414"
"link" => array:1 [
0 => array:2 [
"url" => "https://www.ncbi.nlm.nih.gov/pubmed/25731769"
"web" => "Medline"
]
]
]
]
]
]
]
]
26 => array:3 [
"identificador" => "bib0305"
"etiqueta" => "27"
"referencia" => array:1 [
0 => array:2 [
"contribucion" => array:1 [
0 => array:2 [
"titulo" => "THU0151Multicenter open-label study to evaluate the predictability of disease control at week 52 based on early response to certolizumab pegol (in combination with methotrexate) in Italian patients with moderate to severe rheumatoid arthritis: the CZP-SPEED study"
"autores" => array:1 [
0 => array:2 [
"etal" => true
"autores" => array:6 [
0 => "P. Sarzi-Puttini"
1 => "E. Filippucci"
2 => "S. Adami"
3 => "P.L. Meroni"
4 => "P. Talavera"
5 => "T. Kumke"
]
]
]
]
]
"host" => array:1 [
0 => array:1 [
"Revista" => array:5 [
"tituloSerie" => "Ann Rheum Dis"
"fecha" => "2016"
"volumen" => "75"
"paginaInicial" => "236"
"paginaFinal" => "237"
]
]
]
]
]
]
27 => array:3 [
"identificador" => "bib0310"
"etiqueta" => "28"
"referencia" => array:1 [
0 => array:2 [
"contribucion" => array:1 [
0 => array:2 [
"titulo" => "Longitudinal power Doppler ultrasonographic assessment of joint inflammatory activity in early rheumatoid arthritis: predictive value in disease activity and radiologic progression"
"autores" => array:1 [
0 => array:2 [
"etal" => true
"autores" => array:6 [
0 => "E. Naredo"
1 => "P. Collado"
2 => "A. Cruz"
3 => "M.J. Palop"
4 => "F. Cabero"
5 => "P. Richi"
]
]
]
]
]
"host" => array:1 [
0 => array:2 [
"doi" => "10.1002/art.22461"
"Revista" => array:6 [
"tituloSerie" => "Arthritis Rheum"
"fecha" => "2007"
"volumen" => "57"
"paginaInicial" => "116"
"paginaFinal" => "124"
"link" => array:1 [
0 => array:2 [
"url" => "https://www.ncbi.nlm.nih.gov/pubmed/17266071"
"web" => "Medline"
]
]
]
]
]
]
]
]
28 => array:3 [
"identificador" => "bib0315"
"etiqueta" => "29"
"referencia" => array:1 [
0 => array:2 [
"contribucion" => array:1 [
0 => array:2 [
"titulo" => "Ultrasonography shows significant improvement in wrist and ankle tenosynovitis in rheumatoid arthritis patients treated with adalimumab"
"autores" => array:1 [
0 => array:2 [
"etal" => false
"autores" => array:2 [
0 => "H.B. Hammer"
1 => "T.K. Kvien"
]
]
]
]
]
"host" => array:1 [
0 => array:2 [
"doi" => "10.3109/03009742.2010.517549"
"Revista" => array:6 [
"tituloSerie" => "Scand J Rheumatol"
"fecha" => "2011"
"volumen" => "40"
"paginaInicial" => "178"
"paginaFinal" => "182"
"link" => array:1 [
0 => array:2 [
"url" => "https://www.ncbi.nlm.nih.gov/pubmed/21091275"
"web" => "Medline"
]
]
]
]
]
]
]
]
29 => array:3 [
"identificador" => "bib0320"
"etiqueta" => "30"
"referencia" => array:1 [
0 => array:2 [
"contribucion" => array:1 [
0 => array:2 [
"titulo" => "Power Doppler sonography monitoring of synovial perfusion at the wrist joints in patients with rheumatoid arthritis treated with adalimumab"
"autores" => array:1 [
0 => array:2 [
"etal" => false
"autores" => array:6 [
0 => "E. Filippucci"
1 => "A. Iagnocco"
2 => "F. Salaffi"
3 => "A. Cerioni"
4 => "G. Valesini"
5 => "W. Grassi"
]
]
]
]
]
"host" => array:1 [
0 => array:1 [
"Revista" => array:5 [
"tituloSerie" => "Ann Rheum Dis"
"fecha" => "2006"
"volumen" => "65"
"paginaInicial" => "1433"
"paginaFinal" => "1437"
]
]
]
]
]
]
30 => array:3 [
"identificador" => "bib0325"
"etiqueta" => "31"
"referencia" => array:1 [
0 => array:2 [
"contribucion" => array:1 [
0 => array:2 [
"titulo" => "Synovial features of patients with rheumatoid arthritis and psoriatic arthritis in clinical and ultrasound remission differ under anti-TNF therapy: a clue to interpret different chances of relapse after clinical remission?"
"autores" => array:1 [
0 => array:2 [
"etal" => true
"autores" => array:6 [
0 => "S. Alivernini"
1 => "B. Tolusso"
2 => "L. Petricca"
3 => "L. Bui"
4 => "G. Di Sante"
5 => "G. Peluso"
]
]
]
]
]
"host" => array:1 [
0 => array:1 [
"Revista" => array:5 [
"tituloSerie" => "Ann Rheum Dis"
"fecha" => "2017"
"volumen" => "76"
"paginaInicial" => "1228"
"paginaFinal" => "1236"
]
]
]
]
]
]
31 => array:3 [
"identificador" => "bib0330"
"etiqueta" => "32"
"referencia" => array:1 [
0 => array:2 [
"contribucion" => array:1 [
0 => array:2 [
"titulo" => "Ultrasonography is a potent tool for the prediction of progressive joint destruction during clinical remission of rheumatoid arthritis"
"autores" => array:1 [
0 => array:2 [
"etal" => true
"autores" => array:6 [
0 => "R. Yoshimi"
1 => "M. Hama"
2 => "K. Takase"
3 => "A. Ihata"
4 => "D. Kishimoto"
5 => "K. Terauchi"
]
]
]
]
]
"host" => array:1 [
0 => array:1 [
"Revista" => array:5 [
"tituloSerie" => "Mod Rheumatol"
"fecha" => "2013"
"volumen" => "23"
"paginaInicial" => "456"
"paginaFinal" => "465"
]
]
]
]
]
]
32 => array:3 [
"identificador" => "bib0335"
"etiqueta" => "33"
"referencia" => array:1 [
0 => array:2 [
"contribucion" => array:1 [
0 => array:2 [
"titulo" => "Effectiveness of TNF inhibitor switch in RA: results from the national Swedish register"
"autores" => array:1 [
0 => array:2 [
"etal" => false
"autores" => array:5 [
0 => "K. Chatzidionysiou"
1 => "J. Askling"
2 => "J. Eriksson"
3 => "L.E. Kristensen"
4 => "R. van Vollenhoven"
]
]
]
]
]
"host" => array:1 [
0 => array:2 [
"doi" => "10.1136/annrheumdis-2013-204714"
"Revista" => array:6 [
"tituloSerie" => "Ann Rheum Dis"
"fecha" => "2015"
"volumen" => "74"
"paginaInicial" => "890"
"paginaFinal" => "896"
"link" => array:1 [
0 => array:2 [
"url" => "https://www.ncbi.nlm.nih.gov/pubmed/24431398"
"web" => "Medline"
]
]
]
]
]
]
]
]
33 => array:3 [
"identificador" => "bib0340"
"etiqueta" => "34"
"referencia" => array:1 [
0 => array:2 [
"contribucion" => array:1 [
0 => array:2 [
"titulo" => "Clinical outcomes associated with switching or discontinuation from anti-TNF inhibitors for nonmedical reasons"
"autores" => array:1 [
0 => array:2 [
"etal" => true
"autores" => array:6 [
0 => "D. Wolf"
1 => "M. Skup"
2 => "H. Yang"
3 => "A.P. Fang"
4 => "A. Kageleiry"
5 => "J. Chao"
]
]
]
]
]
"host" => array:1 [
0 => array:2 [
"doi" => "10.1016/j.clinthera.2017.03.005"
"Revista" => array:6 [
"tituloSerie" => "Clin Ther"
"fecha" => "2017"
"volumen" => "39"
"paginaInicial" => "849"
"paginaFinal" => "862"
"link" => array:1 [
0 => array:2 [
"url" => "https://www.ncbi.nlm.nih.gov/pubmed/28363696"
"web" => "Medline"
]
]
]
]
]
]
]
]
]
]
]
]
"agradecimientos" => array:1 [
0 => array:4 [
"identificador" => "xack476248"
"titulo" => "Acknowledgements"
"texto" => "<p id="par0140" class="elsevierStylePara elsevierViewall">The authors thank the patients, the investigators and their teams who took part in this study. The authors also acknowledge Susanne Wiegratz, UCB Pharma GmbH, Monheim, Germany, for publication coordination and Maria Haughton, CMPP and Sarah Jayne Clements, PhD at Costello Medical, Cambridge, UK, for medical writing and editorial assistance in preparing this manuscript for publication, based on the authors’ input and direction.</p>"
"vista" => "all"
]
]
]
"idiomaDefecto" => "en"
"url" => "/1699258X/00000016000005P1/v1_202008070719/S1699258X18301682/v1_202008070719/en/main.assets"
"Apartado" => array:4 [
"identificador" => "17499"
"tipo" => "SECCION"
"es" => array:2 [
"titulo" => "Originales"
"idiomaDefecto" => true
]
"idiomaDefecto" => "es"
]
"PDF" => "https://static.elsevier.es/multimedia/1699258X/00000016000005P1/v1_202008070719/S1699258X18301682/v1_202008070719/en/main.pdf?idApp=UINPBA00004M&text.app=https://reumatologiaclinica.org/"
"EPUB" => "https://multimedia.elsevier.es/PublicationsMultimediaV1/item/epub/S1699258X18301682?idApp=UINPBA00004M"
]