Abstract
Clinical incident reporting is a vital component of modern healthcare, enabling institutions to identify errors, enhance patient safety, and improve medical protocols. In Uzbekistan, while adverse drug reaction (ADR) reporting has been established, a comprehensive system for clinical incident reporting remains underdeveloped. This paper examines the current framework, highlighting challenges such as underreporting, the absence of a national database, inconsistent protocols, limited training, and a punitive workplace culture. To address these issues, recommendations include establishing a centralized reporting system, standardizing guidelines, fostering a non-punitive approach, enhancing training programs, strengthening internal monitoring, and encouraging patient involvement. Implementing these measures will contribute to a more transparent and effective healthcare system, ultimately improving patient outcomes and trust in Uzbekistan’s medical institutions.
References
1. Ministry of Health of Uzbekistan. "National Healthcare Regulations and Safety Measures." Tashkent, 2021.
2. Karimov, A. "The Role of Clinical Incident Reporting in Patient Safety." Journal of Medical Sciences, vol. 15, no. 2, 2022, pp. 56-72.
3. Rahmonov, N. "Developing Healthcare Quality Control Systems in Uzbekistan." Medical Policy Review, vol. 10, no. 4, 2023, pp. 89-104.
4. Saidova, L. "Adverse Drug Reaction Monitoring in Uzbekistan: Challenges and Perspectives." Uzbek Journal of Pharmacology, vol. 7, no. 1, 2021, pp. 33-45.
5. Yuldashev, O. "Medical Error Prevention Strategies in Post-Soviet Healthcare Systems." Central Asian Medical Journal, vol. 12, no. 3, 2020, pp. 21-38.