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SAT0149 EVALUATION OF A PROSPECTIVE COHORT EVENT MONITORING MODEL FOR PATIENT-REPORTED ADVERSE DRUG REACTIONSATTRIBUTED TO BIOLOGICAL DMARDS: VALIDITY OF THE PATIENT-REPORTED INFORMATION AND REPRESENTATIVENESS OF THE PARTICIPANTS
  1. Leanne Kosse1,
  2. Naomi Jessurun1,
  3. Renske Hebing2,
  4. Victor Huiskes3,
  5. Karin Spijkers3,
  6. Michael Nurmohamed2,4
  1. 1Netherlands Pharmacovigilance Centre Lareb, ‘s-Hertogenbosch, Netherlands
  2. 2Amsterdam Rheumatology and Immunology Center, location Reade, Amsterdam, Netherlands
  3. 3Sint Maartenskliniek, Ubbergen, Netherlands
  4. 4Amsterdam Rheumatology and Immunology Center, location VU University Medical Center, Amsterdam, Netherlands

Abstract

Background: To gain knowledge on the prevalence, course and treatment of adverse drug reactions (ADRs) attributed to biological DMARDs (bDMARDs) and the experienced impact of ADRs on patients, an ADR-focused online questionnaire system was developed by Netherlands Pharmacovigilance Centre Lareb (Dutch Biologic Monitor). 898 consecutive patients of eight centers who used a bDMARD indicated for an inflammatory rheumatic disease were followed between 1 January 2017 and 31 December 2018.

Objectives: Validation of the quality of the patient-reported information in the Dutch Biologic Monitor and evaluation of the representativeness of the participants in relation to the source populations.

Methods: Patients of 18 years and older who used a bDMARD indicated for an inflammatory rheumatic disease were included by the participating hospitals. The patient-reported medical information (bDMARD, indication and concomitant DMARDs) of 479 patients with a rheumatic disease (Reade, Amsterdam: N=174; Sint Maartenskliniek, Nijmegen: N=305) was verified by comparing the patient-reported parameters to the patient’s electronic health record using percentage agreement and/or Cohen’s kappa. Representativeness was tested in 550 patients with an inflammatory rheumatic disease (Reade, Amsterdam: N=192; Sint Maartenskliniek, Nijmegen: N=358) by comparing their grouped age, grouped gender and prescribed bDMARD to the source populations of the respective hospitals using Mann-Whitney U test, Chi-Square Goodness-of-Fit and Fisher’s exact test with Monte Carlo simulation.

Results: 95.8% of the tested rheumatic disease patients correctly reported their bDMARD (active substance and brand name). Furthermore, agreement between patients and the electronic health record was strong for the reported indications (90.4% agreement, κ = 0.832) and moderate for the concomitant therapy (79.7% agreement; κ=0.725). The subpopulations were representative for their source populations based on grouped gender (38.4% vs. 38.8% male, χ2(df=1, N=550)=0.038; p>0.05) and bDMARD use (both p>0.05). Grouped median age was not representative (58.0 vs. 56.0 years; U=962872; p=0.04), since the male participants were older (58.5 vs. 55 years; p=0.001).

Conclusion: So far, the Dutch Biologic Monitor seems to be a valid tool to obtain knowledge on ADRs attributed to bDMARDs, since the reported medical information corresponded to the patients’ electronic health records and the participants generally represented their source populations regarding grouped gender and prescribed bDMARD.

Disclosure of Interests: Leanne Kosse: None declared, Naomi Jessurun: None declared, Renske Hebing: None declared, Victor Huiskes: None declared, Karin Spijkers: None declared, Michael Nurmohamed Grant/research support from: AbbVie, Bristol-Myers Squibb, Celgene, Eli Lilly, Janssen, Menarini, MSD, Mundipharma, Pfizer, Roche, Sanofi and UCB, Consultant for: AbbVie, Bristol-Myers Squibb, Celgene, Eli Lilly, Janssen, Menarini, MSD, Mundipharma, Pfizer, Roche, Sanofi and UCB, Speakers bureau: AbbVie, Bristol-Myers Squibb, Celgene, Eli Lilly, Janssen, Menarini, MSD, Mundipharma, Pfizer, Roche, Sanofi and UCB

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