TY - JOUR
T1 - Causes of DMARD withdrawal following ADR within 6 months of initiation among Indian rheumatoid arthritis patients
AU - Mittal, Niti
AU - Sharma, Aman
AU - Jose, Vinu
AU - Mittal, Rakesh
AU - Wanchu, Ajay
AU - Bambery, Pradeep
PY - 2012/3/1
Y1 - 2012/3/1
N2 - The present study was conducted in Indian rheumatoid arthritis (RA) patients prescribed disease-modifyinganti-rheumatic drugs (DMARDs) to determine theincidence and type of adverse drug reactions (ADRs) leading to their withdrawal in the initial 6 months of therapy. This was considered important as pharmacogenetic variations in the pattern of RA in different populations and genetic differences in efficacy and safety to drugs demand separate studies to be conducted in different populations. Hospital records were used to identify 1,000 consecutive patients with RA fulfilling the American College of Rheumatology criteria and having at least 6-month follow-up. Age, gender, duration of arthritis, drug usage and ADRrelated drug withdrawal were recorded from the charts. Most of the patients were put on single DMARD. Combineduse of DMARD was less frequent and non-use of DMARD was common; however, disease control wasgood. The commonest DMARD used in our hospital was hydroxychloroquine 444 (44%) and the commonest combination used was methotrexate with hydroxychloroquine by 55 (6%). Sulphasalazine use showed preference to young and males. Supportive drugs used were NSAIDs by 883 (88%), corticosteroids by 646 (65%), paracetamol by 594 (59%) and amitriptyline by 88 (9%). Incidence of ADRrelated DMARD withdrawal was maximum with leflunomide 2/15 (13.33%) followed by methotrexate 9/116 (7.76%), sulphasalazine 6/185 (3.24%), chloroquine 3/131 (2.29%) and hydroxychloroquine 8/444 (1.8%). Severity and symptomatology of disease, genetic pattern of patients, financial status, previous experience of the clinicians and patients, availability of drugs, patient expectations and compliance were the main factors that lead to a difference in pattern of therapy in our patients compared to other population.
AB - The present study was conducted in Indian rheumatoid arthritis (RA) patients prescribed disease-modifyinganti-rheumatic drugs (DMARDs) to determine theincidence and type of adverse drug reactions (ADRs) leading to their withdrawal in the initial 6 months of therapy. This was considered important as pharmacogenetic variations in the pattern of RA in different populations and genetic differences in efficacy and safety to drugs demand separate studies to be conducted in different populations. Hospital records were used to identify 1,000 consecutive patients with RA fulfilling the American College of Rheumatology criteria and having at least 6-month follow-up. Age, gender, duration of arthritis, drug usage and ADRrelated drug withdrawal were recorded from the charts. Most of the patients were put on single DMARD. Combineduse of DMARD was less frequent and non-use of DMARD was common; however, disease control wasgood. The commonest DMARD used in our hospital was hydroxychloroquine 444 (44%) and the commonest combination used was methotrexate with hydroxychloroquine by 55 (6%). Sulphasalazine use showed preference to young and males. Supportive drugs used were NSAIDs by 883 (88%), corticosteroids by 646 (65%), paracetamol by 594 (59%) and amitriptyline by 88 (9%). Incidence of ADRrelated DMARD withdrawal was maximum with leflunomide 2/15 (13.33%) followed by methotrexate 9/116 (7.76%), sulphasalazine 6/185 (3.24%), chloroquine 3/131 (2.29%) and hydroxychloroquine 8/444 (1.8%). Severity and symptomatology of disease, genetic pattern of patients, financial status, previous experience of the clinicians and patients, availability of drugs, patient expectations and compliance were the main factors that lead to a difference in pattern of therapy in our patients compared to other population.
KW - Adverse drug reactions
KW - Disease-modifying anti-rheumatic drugs
KW - Rheumatoid arthritis
KW - Withdrawal
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U2 - 10.1007/s00296-010-1646-4
DO - 10.1007/s00296-010-1646-4
M3 - Article
C2 - 21161534
AN - SCOPUS:84863302243
SN - 0172-8172
VL - 32
SP - 743
EP - 748
JO - Rheumatology International
JF - Rheumatology International
IS - 3
ER -