- Short Report
- Open Access
Educational sessions in pharmacovigilance: What do the doctors think?
BMC Research Notes volume 3, Article number: 311 (2010)
The aim of this study was to determine physicians' opinion regarding pharmacovigilance feedback sessions. A survey was conducted in a teaching hospital, and the physicians who attended the sessions were invited to participate by filling out a structured questionnaire. All sessions included a review of adverse drug reactions identified at the hospital and information on pharmacovigilance issues (news on warnings released by regulatory agencies or drug toxicity problems identified by recently published studies in medical journals). The survey questions were related to the interest, satisfaction, and belief in the utility of the sessions. A Likert scale (0-10 points) was used to assess physicians' opinions.
A total of 159 physicians attended the sessions and 115 (72.3%) participated in the survey. The mean (SD) age was 38.9 (12.1) years, and 72 (62.6%) were men. The mean (SD) scores of interest, satisfaction with the information provided, and belief in the utility of these sessions were 7.52 (1.61), 7.58 (1.46), and 8.05 (1.38) respectively. Significant differences were observed among physicians according to medical category and speciality in terms of interest, satisfaction, and belief in the utility of those sessions.
Educational activities for physicians, such as feedback sessions, can be integrated into the pharmacovigilance activities. Doctors who attend the sessions are interested in and satisfied with the information provided and consider the sessions to be useful. Additional studies on the development and effectiveness of educational activities in pharmacovigilance are necessary.
Spontaneous reporting of adverse drug reactions (ADR) is an important method of post-marketing surveillance [1, 2]. However, spontaneous ADR reporting is underused by physicians in primary health care and in hospitals [3, 4], and there is a need to promote pharmacovigilance activities. Several interventions to solve the problem of under-reporting of ADRs have been proposed . Some studies have evaluated the effectiveness of educational interventions aimed at increasing reporting among physicians [6–11]. However, there are no studies assessing the doctors' opinions about regular educational activities related to pharmacovigilance issues. We previously reported our experience related to an educational activity program that included regular pharmacovigilance sessions in different hospital departments intended to increase awareness about pharmacovigilance, to report on pharmacovigilance issues, and to promote spontaneous ADR reporting . The aim of our study was to understand hospital physicians' opinions regarding regular sessions on pharmacovigilance topics.
A voluntary, anonymous survey was conducted among doctors working at a teaching hospital in order to assess their opinion regarding the development of the regular pharmacovigilance sessions as part of the Pharmacovigilance Programme (PhVP) at the hospital. The survey was carried out from 8 February to 10 March 2006; all physicians who attended the sessions were invited to participate.
The pharmacovigilance sessions were held during scheduled staff sessions and lasted about 45 to 60 minutes to ensure that the greatest number of physicians could be present. The groups were made up of a variable number of physicians. The presentations were given by clinical pharmacologists and divided into three parts. The first part included a review of all identified and reported ADRs throughout the hospital (number of cases, type and severity of ADR, type of drug) between 1 January 2003 and 31 December 2005. The second part included a review of identified and reported ADRs in each specific medical department where the sessions were held. The main features of the cases and their contribution to the overall results of the PhVP were openly discussed. The third part provided general information on pharmacovigilance issues such as signals generated by the PhVP, news about ADR warnings released by regulatory agencies (Spanish Agency of Medicinal and Health Care Products, the European Medicines Agency, the U.S. Food and Drug Administration, and others), or drug toxicity problems identified by published studies in medical journals, and all topics were discussed openly.
Information was collected on the number of physicians who attended the session and the number of physicians who answered the survey. The physicians were interviewed using a structured questionnaire (one sheet in Spanish) that included demographic variables (age, sex, medical speciality, professional category) and asked seven questions about the sessions. The first three questions were general items on interest in the sessions, satisfaction with the information provided, and beliefs regarding the utility of the sessions. The last four questions were related to specific interest in each part of the presentation: review of ADRs observed throughout the hospital, review of ADRs observed in their medical department, information on signals generated by the PhVP, and information related to news and warnings released by regulatory agencies or published in the medical journals. To assess the doctors' opinions, a Likert scale (0-10 points) was used.
For the descriptive analysis, continuous variables were described by the mean, standard deviation (SD), median, and range. The statistical differences between the mean scores according to the medical specialities and professional categories were assessed by one-way analysis of variance (ANOVA) and Bonferroni post-hoc multiple comparison test. Categorical variables were described with percentages and statistical differences were assessed by the χ2 test. Significance was set at a level of 0.05 (two-tailed). The statistical analysis was performed using the SPSS version 14.0 statistical package.
A total of 159 physicians were present at the sessions, and 115 (72.3%) participated in the survey. The mean (SD) age was 38.9 (12.1) years, and 72 (62.6%) were men. A total of 61 (53%) were staff physicians, and 54 (47%) were in training (residents). The mean (SD) age of staff physicians was 47.9 (7.4) years, and 53 (86.9%) of them were men. The mean (SD) age of residents was 28.6 (7.1), and 35 (64.8%) of them were women. The medical specialities of the physicians who attended the sessions and participated in the survey are shown in Table 1.
The mean (SD) score of physicians' interest in the sessions was 7.52 (1.61) [median 8, minimum 0, maximum 10]. The mean (SD) score of the physicians' satisfaction with the information provided was 7.58 (1.46) [median 8, minimum 2, maximum 10]. The mean (SD) score of physicians' belief in the utility of these sessions was 8.05 (1.38) [median 8, minimum 4, maximum 10].
The mean (SD) score of physicians' interest in PhVP results was 7.38 (1.80) [median 8, minimum 0, maximum 10]. The mean (SD) score of physicians' interest in the pharmacovigilance results in their own departments was 7.91 (1.80) [median 8, minimum 0, maximum 10]. The mean (SD) score of physicians' interest in signals generated by the PhVP was 7.63 (1.63) [median 8, minimum 0, maximum 10]. The mean (SD) score of physicians' interest in news released by regulatory agencies or identified by publications was 7.97 (1.44) [median 8, minimum 4, maximum 10].
The mean scores for interest, satisfaction, and belief in the utility of the sessions were higher for staff physicians than for residents (Table 2). The mean score of interest in the information provided was also higher for staff physicians than for residents (Table 3). There were no statistically significant differences among medical specialities in the mean score of physicians' interest whereas the mean score of physicians' satisfaction and the mean score of physicians' belief in the utility of the sessions were statistically different among physicians with different specialities (Table 4).
The present study shows that most physicians who attend the pharmacovigilance sessions at the hospital are satisfied with them and consider them useful. The regular sessions enhance the relationship between health professionals responsible for the pharmacovigilance programme at the hospital and the medical doctors. At the sessions, the pharmacovigilance programme results at the hospital are presented, and the news and warnings about the risks of drug toxicities are discussed to provide drug safety information to the medical staff. Sessions are intended to increase physicians' awareness of pharmacovigilance topics and to explain the principles and demands of pharmacovigilance and the importance of reporting ADRs. Additionally, sessions improve interaction between the physicians responsible for the programme and those in the various specialities because the time encourages dialogue, opinion-sharing, and closer professional contact. Thus, the development of regular pharmacovigilance sessions, together with other interventions, has improved spontaneous ADR reporting by hospital physicians . Nevertheless, session preparation is specific to each medical department and requires considerable time and effort.
Pharmacovigilance activities are essential to ensure that doctors have enough information to prescribe drugs appropriately . Health care professionals usually have little basic knowledge of ADRs or the voluntary reporting system [13, 14]. Moreover, a lack of basic knowledge about ADRs and health professionals' attitudes regarding the voluntary reporting procedure has been associated with under-reporting . Health care professional education and training are needed to improve the current ADR reporting system. Previous experiences reported strategies in which spontaneous ADR reporting is integrated with training and continuous education . Therefore, we decided that our approach should integrate in-hospital ADR reporting with physician training and continuous education.
Educational interventions with feedback improve ADR reporting by physicians in both primary health care  and hospitals  and also enhance ADR reporting by pharmacists . Wallersted et al  reported that most physicians stated that feedback content to doctors reporting ADRs may influence ADR reporting rates. In fact, a distance-learning pharmacovigilance programme linked to educational credits was also associated with improved reporting of suspected ADRs by general practitioners and pharmacists . In a Dutch survey, general practitioners and specialists were asked about their experiences and expectations regarding feedback information from the pharmacovigilance centre. The feedback process contained information on whether the reported ADR was described and on the causal relationship between the drug and the ADR. Both general practitioners and specialists were satisfied with the feedback from the pharmacovigilance centre because they found it reliable, scientifically sound, and highly valuable . Educational activities in pharmacovigilance are necessary not only for physicians but for other health care professionals. A Swedish study reported an increase in the total number of ADR reports after pharmacovigilance teaching sessions were held for interested nurses. These results suggest that interested, well-instructed nurses could also play an important role in identifying and reporting suspected ADRs .
The development of ADR reporting and monitoring systems in the hospital setting has been described . Educational activities integrated in the hospital pharmacovigilance programme are necessary to build a culture of pharmacovigilance at the hospital and to raise awareness of spontaneous ADR reporting. However, educational activities with periodic dissemination of information have only been carried out on a few occasions. In a previous study, we reported that continuous intervention based on health care management agreements with educational activities was associated with a quantitative and qualitative improvement in spontaneous ADR reporting by hospital physicians .
The present study is the first to ask physicians about the development of pharmacovigilance educational activities at the hospital. The hospital's doctors valued the regular pharmacovigilance sessions positively, although we observed some differences among those interviewed, as staff physicians were more interested in the sessions than residents in training. The reasons for these differences are unknown, but perhaps medical staff is more familiar with the pharmacovigilance programme while residents are more interested in other topics of their medical specialisation. These results suggest that additional effort and research in pharmacovigilance education are needed to draw the interest of physicians still in training. Satisfaction and belief in the utility of sessions (but not in interest in sessions) differed according to medical speciality, in particular, they were higher in internal medicine than other medical specialities, although there are no other similar studies with which we can compare our results. In a previous study, specialists were more likely to expect information on ADRs than general physicians . Future studies should investigate speciality-related differences linked to pharmacovigilance educational activities.
The main limitations of our study were the low number of doctors who attended the sessions and participated in the survey and the problem with extrapolating our results to other settings. The study was conducted at the largest tertiary teaching hospital in Catalonia, which has a long tradition in pharmacovigilance activities. The sessions were only conducted for some medical specialities. Therefore, we do not know whether other settings or medical specialities would yield similar results. Other limitations are the reliability of answers -an inherent problem of surveys and interviews- and whether the physicians' answers are truly representative. Despite these limitations, our study provides information on hospital doctors' opinion about pharmacovigilance educational activities. Future studies should confirm these results in other settings and investigate the influence of the different types of educational activities on physicians' opinion. The survey could also be used to assess performance in the context of pharmacovigilance activities.
Pharmacovigilance educational and feedback sessions with physicians can be integrated into hospital pharmacovigilance activities. Physicians at our hospital stated that the sessions are useful and interesting and that they are satisfied with them. Further studies on the development and effectiveness of pharmacovigilance activities are necessary.
Wysowski DK, Swartz L: Adverse drug event surveillance and drug withdrawals in the United States, 1969-2002: the importance of reporting suspected reactions. Arch Intern Med. 2005, 165: 1363-1369. 10.1001/archinte.165.12.1363.
Lexchin J: Is there still a role for spontaneous reporting of adverse drug reactions?. CMAJ. 2006, 174: 191-192.
Hazell L, Shakir SA: Under-reporting of adverse drug reactions: a systematic review. Drug Saf. 2006, 29: 385-396. 10.2165/00002018-200629050-00003.
van der Hoft CS, Sturkenboom MC, van Grootheest K, Kingma HJ, Stricker BH: Adverse drug reaction-related hospitalisations: a nationwide study in The Netherlands. Drug Saf. 2006, 29: 161-168. 10.2165/00002018-200629020-00006.
Vallano A, Cereza G, Pedrós C, Agustí A, Danés I, Aguilera C, Arnau JM: Obstacles and solutions for spontaneous reporting of adverse drug reactions in the hospital. Br J Clin Pharmacol. 2005, 60: 653-658. 10.1111/j.1365-2125.2005.02504.x.
Fincham J: A statewide program to stimulate reporting of adverse drug reactions. J Pharm Pract. 1989, 2: 239-244. 10.1177/089719008900200407.
Scott HD, Thacher-Renshaw A, Rosenbaum SE, Waters WJ, Green M, Andrews LG, Faich GA: Physician reporting of adverse drug reactions. Results of the Rhode Island Adverse Drug Reaction Reporting Project. JAMA. 1990, 263: 1785-1788. 10.1001/jama.263.13.1785.
Nazario M, Feliu JF, Rivera GC: Adverse drug reactions: the San Juan Department of Veterans Affairs Medical Center experience. Hosp Pharm. 1994, 29: 244-250.
McGettigan P, Golden J, Conroy RM, Arthur N, Feely J: Reporting of adverse drug reactions by hospital doctors and the response to intervention. Br J Clin Pharmacol. 1997, 44: 98-100. 10.1046/j.1365-2125.1997.00616.x.
Figueiras A, Herdeiro MT, Polónia J, Gestal-Otero JJ: An educational intervention to improve physician reporting of adverse drug reactions: a cluster-randomized controlled trial. JAMA. 2006, 296: 1086-1093. 10.1001/jama.296.9.1086.
Pedrós C, Vallano A, Cereza G, Mendoza-Arán G, Agustí A, Aguilera C, Danés I, Vidal X, Arnau JM: An intervention to improve spontaneous adverse drug reaction reporting by hospital physicians. A time series analysis in Spain. Drug Saf. 2009, 32: 77-83. 10.2165/00002018-200932010-00007.
World Health Organisation: WHO Policy Perspective on Medicines. Pharmacovigilance: ensuring the safe use of medicines. (accessed 2010 Apr 22), [http://www.who-umc.org/graphics/7128.pdf]
Moride Y, Haramburu F, Requejo AA, Begaud B: Under-reporting of adverse drug reactions in general practice. Br J Clin Pharmacol. 1997, 43: 177-181. 10.1046/j.1365-2125.1997.05417.x.
Li Q, Zhang SM, Chen HT, Fang SP, Yu X, Liu D, Shi LY, Zeng FD: Awareness and attitudes of healthcare professionals in Wuhan, China to the reporting of adverse drug reactions. Chin Med J. 2004, 117: 856-861.
Lopez-Gonzalez E, Herdeiro MT, Figueiras A: Determinants of under-reporting of adverse drug reactions: a systematic review. Drug Saf. 2009, 32: 19-31. 10.2165/00002018-200932010-00002.
Debesa F, Jiménez G, Figueras A, Diogène E, Pérez Peña J, Avila J, Laporte JR: Spontaneous reporting of adverse drug reactions in Cuba: integrating continuous education, training and research in a network approach. Br J Clin Pharmacol. 2002, 54: 333-336. 10.1046/j.1365-2125.2002.01655.x.
Herdeiro MT, Polonia J, Gestal-Otero JJ, Figueiras A: Improving the reporting of adverse drug reactions: a cluster-randomized trial among pharmacists in Portugal. Drug Saf. 2008, 31: 335-344. 10.2165/00002018-200831040-00007.
Wallerstedt SM, Brunlöf G, Johansson ML, Tukukino C, Ny L: Reporting of adverse drug reactions may be influenced by feedback to the reporting doctor. Eur J Clin Pharmacol. 2007, 63: 505-508. 10.1007/s00228-007-0270-z.
Bracchi RC, Houghton J, Woods FJ, Thomas S, Smail SA, Routledge PA: A distance-learning programme in pharmacovigilance linked to educational credits is associated with improved reporting of suspected adverse drug reactions via the UK yellow card scheme. Br J Clin Pharmacol. 2005, 60: 221-223. 10.1111/j.1365-2125.2005.02419.x.
Cornelissen L, van Puijenbroek E, van Grootheest K: Expectations of general practitioners and specialist doctors regarding the feedback received after reporting an adverse drug reaction. Pharmacoepidemiol Drug Saf. 2008, 17: 76-81. 10.1002/pds.1516.
Bäckström M, Mjörndal T, Dahlqvist R: Spontaneous reporting of adverse drug reactions by nurses. Pharmacoepidemiol Drug Saf. 2002, 11: 647-650. 10.1002/pds.753.
Baniasadi S, Fahimi F, Shalviri G: Developing an adverse drug reaction reporting system at a teaching hospital. Basic Clin Pharmacol Toxicol. 2008, 102: 408-11. 10.1111/j.1742-7843.2008.00217.x.
The authors declare that they have no competing interests.
AV, CP, and AA contributed to the conception and design, data acquisition, and data analysis and interpretation processes and helped draft the manuscript. GC, ID, and CA contributed to data acquisition and participated in the critical review of the manuscript. JMA contributed to data interpretation and helped draft the manuscript. All authors read and approved the final manuscript.
About this article
Cite this article
Vallano, A., Pedrós, C., Agustí, A. et al. Educational sessions in pharmacovigilance: What do the doctors think?. BMC Res Notes 3, 311 (2010) doi:10.1186/1756-0500-3-311
- Adverse Drug Reaction
- Medical Speciality
- Educational Activity
- Adverse Drug Reaction Reporting
- Feedback Session