Evidence map›Paper›PMID 39294672›Full record

Observational studyArthritis research & therapy2024

Pain catastrophizing negatively impacts drug retention rate in patients with Psoriatic Arthritis and axial Spondyloarthritis: results from a 2-years perspective multicenter GIRRCS (Gruppo Italiano di Ricerca in Reumatologia Clinica) study.

Damiano Currado, Francesca Saracino, Piero Ruscitti, Annalisa Marino, Ilenia Pantano, Marta Vomero, Onorina Berardicurti, Viktoriya Pavlych, Claudio Di Vico, Francesco Caso and 22 more

Abstract readMulticenter StudyObservational Study
In one paragraph

Observational study in Arthritis research & therapy, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

13 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

32 authors.

Damiano CurradoClinical and Research Section of Rheumatology and Clinical Immunology, Fondazione Policlinico Universitario Campus Bio-Medico, Rome, Italy.
Francesca SaracinoClinical and Research Section of Rheumatology and Clinical Immunology, Fondazione Policlinico Universitario Campus Bio-Medico, Rome, Italy.
Piero RuscittiDepartment of Biotechnological and Applied Clinical Sciences, Rheumatology Unit, University of L'Aquila, L'Aquila, Italy.
Annalisa MarinoClinical and Research Section of Rheumatology and Clinical Immunology, Fondazione Policlinico Universitario Campus Bio-Medico, Rome, Italy.
Ilenia PantanoDepartment of Precision Medicine, Rheumatology Unit, University of Campania L. Vanvitelli, Caserta, Italy.
Marta VomeroClinical and Research Section of Rheumatology and Clinical Immunology, Fondazione Policlinico Universitario Campus Bio-Medico, Rome, Italy.
Onorina BerardicurtiClinical and Research Section of Rheumatology and Clinical Immunology, Fondazione Policlinico Universitario Campus Bio-Medico, Rome, Italy. o.berardicurti@policlinicocampus.it.ORCID 0000-0002-2808-1581
Viktoriya PavlychDepartment of Biotechnological and Applied Clinical Sciences, Rheumatology Unit, University of L'Aquila, L'Aquila, Italy.
Claudio Di VicoDepartment of Precision Medicine, Rheumatology Unit, University of Campania L. Vanvitelli, Caserta, Italy.
Francesco CasoDepartment of Clinical Medicine and Surgery, Rheumatology Research Unit, University of Naples Federico II, Naples, Italy.
Luisa CostaDepartment of Clinical Medicine and Surgery, Rheumatology Research Unit, University of Naples Federico II, Naples, Italy.
Marco TassoDepartment of Clinical Medicine and Surgery, Rheumatology Research Unit, University of Naples Federico II, Naples, Italy.
Federica CamardaDepartment of Health Promotion, Mother and Child Care, Rheumatology Section, Internal Medicine and Medical Specialties, University Hospital "P. Giaccone", Palermo, Italy.
Francesca MisceoDepartment of Biomedical Science and Human Oncology (DIMO), Rheumatic and Systemic Autoimmune Diseases Unit, University of Bari Medical School, Bari, Italy.
Francesco De VincenzoDepartment of Human Sciences, European University of Rome, Rome, Italy.
Addolorata CorradoDepartment of Medical and Surgical Sciences, Rheumatology Clinic, University of Foggia, Rione Biccari, Foggia, FG, 71122, Italy.
Luisa ArcareseClinical and Research Section of Rheumatology and Clinical Immunology, Fondazione Policlinico Universitario Campus Bio-Medico, Rome, Italy.
Amelia RigonClinical and Research Section of Rheumatology and Clinical Immunology, Fondazione Policlinico Universitario Campus Bio-Medico, Rome, Italy.
Marta VadaccaClinical and Research Section of Rheumatology and Clinical Immunology, Fondazione Policlinico Universitario Campus Bio-Medico, Rome, Italy.
Erika CorberiClinical and Research Section of Rheumatology and Clinical Immunology, Fondazione Policlinico Universitario Campus Bio-Medico, Rome, Italy.
Lyubomyra KunClinical and Research Section of Rheumatology and Clinical Immunology, Fondazione Policlinico Universitario Campus Bio-Medico, Rome, Italy.
Francesca TrunfioClinical and Research Section of Rheumatology and Clinical Immunology, Fondazione Policlinico Universitario Campus Bio-Medico, Rome, Italy.
Andrea PilatoClinical and Research Section of Rheumatology and Clinical Immunology, Fondazione Policlinico Universitario Campus Bio-Medico, Rome, Italy.
Ludovica LambertiClinical and Research Section of Rheumatology and Clinical Immunology, Fondazione Policlinico Universitario Campus Bio-Medico, Rome, Italy.
Francesco Paolo CantatoreDepartment of Medical and Surgical Sciences, Rheumatology Clinic, University of Foggia, Rione Biccari, Foggia, FG, 71122, Italy.
Federico PerosaDepartment of Biomedical Science and Human Oncology (DIMO), Rheumatic and Systemic Autoimmune Diseases Unit, University of Bari Medical School, Bari, Italy.
Giuliana GugginoDepartment of Health Promotion, Mother and Child Care, Rheumatology Section, Internal Medicine and Medical Specialties, University Hospital "P. Giaccone", Palermo, Italy.
Raffaele ScarpaDepartment of Clinical Medicine and Surgery, Rheumatology Research Unit, University of Naples Federico II, Naples, Italy.
Paola CiprianiDepartment of Biotechnological and Applied Clinical Sciences, Rheumatology Unit, University of L'Aquila, L'Aquila, Italy.
Francesco CicciaDepartment of Precision Medicine, Rheumatology Unit, University of Campania L. Vanvitelli, Caserta, Italy.
Roberto GiacomelliClinical and Research Section of Rheumatology and Clinical Immunology, Fondazione Policlinico Universitario Campus Bio-Medico, Rome, Italy.
Luca NavariniClinical and Research Section of Rheumatology and Clinical Immunology, Fondazione Policlinico Universitario Campus Bio-Medico, Rome, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundChronic pain and inflammation are common features of rheumatic conditions such as Psoriatic Arthritis (PsA) and Axial Spondyloarthritis (axSpA), often needing prolonged medication treatment for effective management. Maintaining drug retention is essential for both achieving disease control and improving patients' quality of life. This study investigates the influence of pain catastrophizing, a psychological response to pain, on the drug retention rates of PsA and axSpA patients.

methodsA two-year prospective multicenter observational study involved 135 PsA and 71 axSpA patients. Pain Catastrophizing Scale (PCS) was employed to assess pain catastrophizing. Univariable and multivariable regression analyses were utilized to identify factors associated with drug retention.

resultsIn the PsA group, patients early discontinuing therapy showed higher baseline disease activity as well as higher incidence of comorbid fibromyalgia. Notably, pain catastrophizing, specifically the domains of Helplessness, Magnification, and Rumination, were significantly elevated in PsA patients who interrupted the treatment. Multivariable analysis confirmed pain catastrophizing as an independent predictor of drug suspension within two years. In axSpA, drug discontinuation was associated with female gender, shorter disease duration, higher baseline disease activity as well as elevated levels of pain catastrophizing. Univariable analysis supported the role of pain catastrophizing, including its domains, as predictors of treatment interruption. However, limited events in axSpA patients precluded a multivariate analysis.

conclusionThis prospective study emphasizes the impact of pain catastrophizing on drug retention in patients with PsA and axSpA.

Indexed as

Arthritis, PsoriaticCatastrophizationAdultAgedAntirheumatic AgentsFemaleHumansMaleMedication AdherenceMiddle AgedPain MeasurementProspective StudiesQuality of LifeSpondylarthritisAntirheumatic AgentsAxial SpondyloarthritisPain CatastrophizingPsoriatic ArthritisRetention Rate

Identifiers

PMID39294672
PMCPMC11409633

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.