Cardiovascular Disease Events in Hemotoxic Snakebite Envenoming: A Prospective Observational Study from Himachal Pradesh, India
Akshit Gupta.1 Sujeet Raina.3 Bikram Shah.2 Manoj Thakur.2 Nikhil Kumar.1
.1Postgraduate student, Department of Internal Medicine, Dr. RPGMC, Tanda, Kangra
.2Assistant Professor, Department of Internal Medicine, Dr. RPGMC, Tanda, Kangra
.3Professor, Department of Internal Medicine, Dr. RPGMC, Tanda, Kangra
Correspondence: Sujeet Raina, Department of Internal Medicine, C-15, Type-V Quarters, Dr RPGMC Campus Tanda, Kangra (H.P.) India.
Received: December 23, 2025 Published: March 20,2026
Citation: Sujeet Raina, Cardiovascular Disease Events in Hemotoxic Snakebite Envenoming: A Prospective Observational Study from Himachal Pradesh, India. AOJ Emerg and Int Med. 2026;1(3):68–78.
Copyright: ©2026 Sujeet Raina. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and build upon your work non-commercially.
Abstract
Background: Cardiotoxicity as a feature of snake bite envenomation toxidrome is uncommonly described. The study was conducted to assess the prevalence of cardiovascular disease events in patients with hemotoxic venomous snakebites.
Material and Methods: This was a hospital based open cohort observational study conducted on patients diagnosed with hemotoxic envenoming. The study period was of one year using a nonprobability sampling method. Hemotoxic envenoming was defined as positive bedside 20 min whole blood clotting time (20 WBCT) following a history of snake bite. Cardiovascular events were recorded based on clinical history and examination, electrocardiography, high sensitivity (HS) troponin I levels and echocardiogram. Time frames to understand the sequential changes during the hospital stay were defined as less than 48 h, 48 to 96 hours, and at discharge.
Results: A total of 62 patients were included in the study. The prevalence of cardiovascular disease events was 16.1% (10/62). ECG changes were observed in nine patients. Three patients developed acute coronary syndrome, One patient had features of capillary leak syndrome. presented with shock and required inotropes.
Conclusion: The study demonstrated that cardiovascular disease events are not an uncommon entity due to hemotoxic snakebite envenoming in the geographical region of Himachal Pradesh, India.
Keywords: Cardiac, heart, myocardial infarction, snakes
References
1. World Health Organization. Guidelines for the Management of Snake Bites WHO. 2nd ed. Regional Office for South-East Asia. World Health Organization. 2016.
2. Liblik K, Byun J, Saldarriaga C, et al. Snakebite Envenomation and Heart: Systematic Review. Curr ProblCardiol. 2022;47:100861.
3. Simpson ID. Snakebite management in India, the first few hours: A guide for primary care physicians. J Indian Med Assoc. 2007;105:324.
4. Kumar KS, Joseph JK, Joseph S, et al. Cardiac involvement in vasculotoxic and neurotoxic snakebite A not so uncommon complication. J Assoc Physicians India. 2020;68:38–41.
5. John Binu A, Kumar Mishra A, Gunasekaran K, et al. Cardiovascular manifestations and patient outcomes following snake envenomation: a pilot study. Trop Doct. 2019;49:10–3.
6. Nayak KC, Jain AK, Sharda DP, et al. Profile of cardiac complications of snake bite. Indian Heart J. 1990;42:185–8.
7. Menon JC, Joseph JK, Jose MP. et al. Clinical Profile and Laboratory Parameters in 1051 Victims of Snakebite from a Single Centre in Kerala, South India. J Assoc Physicians India. 2016;64:22–9.
8. Gupta P, Mahajan N, Gupta R, et al. Cardiotoxicity profile of snake bite. JK Science. 2013;15:169-73.
9. Silva A, Pilapitiya S, Siribaddana S. Acute Myocardial Infarction following a possible direct intravenous bite of Russell’s viper (Daboia russelli). BMC Res Notes. 2012;5:500.
10. Niraj M, Jayaweera JL, Kumara WGDI. Acute myocardial infarction following a Russell’s viper bite: a case report. Int Arch Med. 2013;6:7.
11. Wanninayake WMDAS, Aponso T, Seneviratne. Dissanayake. A rare case of acute myocardial infarction with heart failure following hump-nosed viper bite in a Sri Lankan female. Trop Med Health. 2025;53:2.
12. Kim OH, Lee JW, Kim HI, et al. Adverse Cardiovascular Events after a Venomous Snakebite in Korea. Yonsei Med J. 2016;57:512–7.
13. Karaye KM, Mijinyawa MS, Yakasai AM, et al. Cardiac and hemodynamic features following snakebite in Nigeria. Int J Cardiol. 2012;156:326–8.
14. Ramakrishna CD, Kanattu PS. A Study of Cardiac Profile in Patients with Snake Envenomation and Its Complications. International Journal of Clinical Medicine. 2017;8:167-77.
15. Chakrabarti S, Biswas P, Patil S, et al. Acute Myocardial Infarction Following Viper Bite: A Rare Scenario. Heart India. 2015;3:18-20.
16. Cupo P, de Azevedo-Marques MM, Hering SE. Absence of Myocardial Involvement in Children Victims of Crotalus durissusterrificus Envenoming. Toxicon. 2003;42:741–5
17. Karlson-Stiber C, Salmonson H, Persson H. A Nationwide Study of Vipera berus Bites During One Year-Epidemiology and Morbidity of 231 Cases. Clin Toxicol (Phila). 2006;44:25–30.
18. Suchithra N, Pappachan JM, Sujathan P. Snakebite envenoming in Kerala, South India: Clinical Profile and Factors Involved in Adverse Outcomes. Emergency Medicine Journal. 2008;25:200–4.
19. Kim JS, Yang JW, Kim MS, et al. Coagulopathy in Patients Who Experience Snakebite. The Korean Journal of Internal Medicine. 2008;23:94–9.
20. Magdalan J, Trocha M, Merwid-Ląd A. Vipera berus Bites in the Region of Southwest Poland-A Clinical Analysis of 26 Cases. Wilderness Environ Med. 2010;21:114-9.
21. Hønge BL, Hedegaard SK, Cederstrøm S,et al. Hospital Contacts After Bite by the European adder (Vipera berus). Danish Medical Journal. 2015;62:A5022.
22. Johnston CI, Ryan NM, Leary MA, et al. Australian taipan (Oxyuranus spp.) Envenoming: Clinical Effects and Potential Benefits of Early Anti venom Therapy- Australian Snakebite Project (ASP-25). Clinical Toxicology (Phila delphia, Pa). 2017;55:115–22.
23. Tony JC, Bhat R. Acute myocardial infarction following snakebite. Trop Doct.1995; 25:137.
24. Blondheim DS, Plich M, Borman M, et al. Acute myocardial infarction complicating viper bite. Am J Cardiol. 1996;78:492–3.
25. Dissanayake P, Sellahewa KH. Acute myocardial infarction in a patient with Russell's viper bite. Ceylon Med J. 1996;41:67–8.
26. Maheshwari M, Mittal SR. Acute myocardial infarction complicating snakebite. J. Ass Phys India. 2004;52:63–4.
27. Gaballa M, Taher T, Brodin LA, et al. Myocardial Infarction as a Rare Consequence of a Snakebite. Circulation. 2005;112:140–142.
28. Gupta PN, Thomas J, Francis PK, Sajith VS. BMJ Case Rep. 2014.
29. Gomes RAF, Cantarelli FL, Vieira FA, et al. Gouveia MMA, Feitosa ADM. Myocardial infarction after snake bite. Int J Cardiovasc Sci. 2018;31:79-81.
30. Pirasath S, Gajan D, Guruparan M, et al. Saw scaled viper envenoming complicated with acute myocardial infarction. SAGE Open Med Case Rep. 2021;9:1-5.
31. Salem W, Abdelrahim MG, Majmaie LA, et al. Acute myocardial infarction(AMI) treated with snake antivenom. Case Rep Emerg Med. 2021: 9945296.
32. McCarthy CP, Steg G, Bhatt DL. The management of antiplatelet therapy in acute coronary syndrome patients with thrombocytopenia: a clinical conundrum. Eur Heart J. 2017;38:3488-92.
33. Thygesen K, Alpert JS, Jaffe AS, et al. Executive Group on behalf of the Joint European Society of Cardiology (ESC)/American College of Cardiology (ACC)/American Heart Association (AHA)/World Heart Federation (WHF) Task Force for the Universal Definition of Myocardial Infarction. Fourth Universal Definition of Myocardial Infarction. Circulation. 2018;138:618-651.
34. Johnston CI, Silva A, Hodgson W, et al. Investigating skeletal muscle biomarkers for the early detection of Australian myotoxic snake envenoming: an animal model pilot study. Clin Toxicol (Phila). 2024;62:2807.
35. Tasoulis T, Isbister GK. A current perspective on snake venom composition and constituent protein families. Arch Toxicol. 2023;97:133–153.
36. Warrell DA, Williams DJ. Clinical aspects of snakebite envenoming and its treatment in low resource settings. Lancet. 2023;401:1382-98.