This survey focused on evaluating the knowledge, attitudes and practices (KAP) regarding materiovigilance among Pharmacy students of Maharashtra. The aim was to identify gaps in their comprehension and reporting practices concerning adverse events associated with medical devices. Materiovigilance systematic monitoring and evaluation of adverse events and incidents linked to medical devices, playing a vital role in safeguarding patient well-being and improving device efficacy. In India, the Materiovigilance Programme of India (MvPI), operating under the Ministry of Health and Family Welfare, manages the secure utilization of medical devices while aligning with the pharmacovigilance system. Medical devices are essential for patient care, but they carry inherent risks. This highlights the need for materiovigilance to track and mitigate adverse events related to these devices. A self-administered questionnaire was developed and distributed via various social media platforms to ensure broad participation. This approach facilitated a diverse sample and encouraged participation across different educational institutions. Data collection was carried out online and responses were analysed using Microsoft Excel. In this study with 650 participants, the distribution across pharmacy programs was as follows: 25% (163 students) in D.Pharm, 35% (228 students) in B.Pharm, 29% (190 students each) in Pharm.D and Pharm.D (PB) and 10% (69 students) in M.Pharm. In terms of awareness, 390 students (60%) were unaware of MvPI, while 260 (40%) demonstrated a positive attitude towards MDAE reporting. Although 195 students (30%) correctly identified MvPI, only 98 students (15%) actively engaged in MDAE reporting, indicating a significant gap in practice. Additionally, 163 students (25%) reported having attended workshops related to this topic, highlighting the need for enhanced training and awareness initiatives. This survey reveals a critical knowledge gap among healthcare professionals regarding the Materiovigilance Programme of India, jeopardizing patient safety. Urgent training and awareness initiatives are essential to empower professionals and enhance the reporting of medical device adverse events.
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