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Reporting of Adverse Drug Reactions : a study among Clinicians. Lisha Jenny John, Mohamed Arifulla , Jenny Cheriathu and Jayadevan Sreedharan Journal of Applied Pharmaceutical Science 2012. By: Mohammed Almoslem Ibrahim Asiri. Introduction. Adverse drug reaction
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Reporting of Adverse Drug Reactions: a study among Clinicians Lisha Jenny John, Mohamed Arifulla, Jenny Cheriathuand JayadevanSreedharan Journal of Applied Pharmaceutical Science 2012 By: Mohammed Almoslem Ibrahim Asiri
Introduction • Adverse drug reaction • A reaction which is noxious and unintended and which occurs at doses normally used in humans for prevention, diagnosis or therapy of disease, or for the modification of physiological functions (WHO, 2000).
Introduction • Pharmacovigilance • It is the science and activities relating to the detection, assessment, understanding and prevention of adverse drug effects or any other drug-related problem (WHO, 2000).
Introduction • Serious ADR • An adverse drug reaction that requires hospitalization, prolongs hospitalization, is permanently disabling, or results in death of the patient (Lazarouet al., 1998).
Methods • Study propose • The aim of the study is to investigate knowledge, practice and factors affecting ADR reporting among clinicians. • Study design • Cross sectional study carried out among 55 doctors during study period. • Hospital in United Arab Emirates, Ajman
Methods • Sample procedure • 110 doctors were working in the institute • 50% (55 doctors) were randomly recruited • 76% was the response rate (42 questionnaire)
Methods • Research tool • Self-administered questionnaire • Demographics • Knowledge of ADR reporting • Attitude to report • Factor affecting reporting • Open-ended and close ended questions • Pilot study to randomly selected doctors
Methods • Statistical analysis • SPSS program • Chi-square test • Significance: P value <0.05
Results • Demographics • Response rate 76% (42/55) • 50% male and the mean age of 36±8 • Multiethnic population (Egyptian and Indian) • 22 clinicians were specialized (52.4%) • 41/42 had come across ADRs in their clinical practice included serious ADRs • 16.7% noticed serious ADRs in their patient on a monthly basis
Results • Demographics • The most frequent ADRs noticed are drug induced rashes, and diarrhea. • The commonly implicated drugs are antibiotics and analgesics • The observed serous ADRs are Steven Johnson’s syndrome and anaphylaxis
Steven Johnson’s syndrome Anaphylaxis
Results • Knowledge of ADR reporting • ADR that have to be reported • 97.6% for serious • 95% unusual • 88% new drugs and new reactions to existing drugs
Results • Knowledge of ADR reporting • Who can report ADR • 97.6% clinicians • 81% nurses and pharmacists • 42.9 patients
Results • Knowledge of ADR reporting • The awareness about pharmacovigilance centre • Only 19 (45.2%) aware of its existence • Only 6 had reported ADRs to pharmcovigilance centre • Only 28 (66.7%) felt ADR reporting was necessary
Results • Attitudes towards ADR reporting • 13 (31%) reporting is professional obligation • 24 (57%) reporting should be compulsory • 13 (31%) reporting is voluntary process
Results • Factors encouraging reporting of ADRs
Results • Factors discouraging reporting of ADRs
Results • Measures to improve ADR reporting
Results • Education and training on ADRs • Only 3 had received training on how to report ADR and all had received training from India. • 97.6% of the clinicians were willing to be trained in reporting of ADRs.
Conclusion • It is desirable to initiate workshops and training programs on ADR reporting to overcome the underreporting • ADR reporting should be considered as an integral part of the clinical activities by the health care providers.