Persistence of venom-induced consumption coagulopathy (VICC) associated with the late application of antivenom after snakebite by Bothrops complex: a retrospective cohort study

Abstract

Introduction Antivenom neutralizes the effects of snake venom toxins. Its timely administration can by critical in reducing the risk of complications, including serious clinical hemorrhage. The objective of this study was to evaluate the relationship between the late administration of antivenom and the persistence of venom-induced consumption coagulopathy (VICC) in patients with Bothrops snakebite envenomation.

Methods We conducted a retrospective observational study in three hospitals referent in the management of snakebite envenomation in a region of Colombia. Patients were identified through ICD10 codes. The information was extracted from patients’ clinical records. Late and early antivenom administration patients were compared; “late” was defined as a period between snakebite and antivenom administration >4h. Definition of persistence of VICC was as an International Normalized Ratio >1.5 between 25-72h after snakebite. The clinical bleeding (as reported by clinicians) was also explored. Groups were compared through X2 of association; binary and multiple logistic regressions were ran to estimate the magnitude of the crude and adjusted relative risk (RR) for the analyzed outcomes.

Results 304 patients with snakebite from Bothrops spp.were analyzed; 138 (45.3%) with late antivenom administration, and 166 (54.7%) early. The persistence of VICC was more frequent in the late antivenom group (2.06 [95% IC 1.11-3.83]), as well as for clinical bleeding and major bleeding (1.97[1.30-2.98]; 3.00 [1.19-7.54], respectively).

Discussion Late antivenom administration was associated with increased risk in the persistence of VICC and major bleeding in patients with envenomation by a Bothrops complex snakebite. The results reported in the literature are diverse; inter and intra species variability and definitions can influence the finding.

Conclusions The Timely administration of antivenom was associated with an increased risk in persistence of VICC.

Synopsis Snakebites can cause different levels of damage to humans, depending on the type of venom. The venom produced by pit vipers, specifically those of the genus Bothrops, can change blood clotting and cause bleeding that can be life-threatening. Most snakebites from these vipers occur in tropical areas where the most affected are farmers and rural people. There is often a lack of access to antivenom treatment, depending on access to and provision of health services. It seems that giving the antivenom at the right time can reduce the risk of complications. However, it is still unclear whether waiting to give the antivenom increases the risk of continued envenoming and bleeding. This study shows that waiting to treat a patient can lead to a higher chance of bleeding. This information can help doctors, decision makers, and lawmakers improve treatment options and access in remote areas.

Competing Interest Statement

The authors have declared no competing interest.

Funding Statement

The author(s) received no specific funding for this work.

Author Declarations

I confirm all relevant ethical guidelines have been followed, and any necessary IRB and/or ethics committee approvals have been obtained.

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The details of the IRB/oversight body that provided approval or exemption for the research described are given below:

This research was classified as no risk by Colombian regulatory laws (Resolution Number 8430 of 1993 from the Colombian Ministry of Health). The approval of the project and the waiver of informed consent to participate in the study were granted by the Research ethics committee of the Hospital San Vicente Fundación, Medellín, and the Research and Ethics Committee of the Hospital Pablo Tobón Uribe, evaluated and approved the investigation through Minute No.06-2022 of February 25, 2022, and Minute 05/2022 of March 17, 2022, respectively. This study was conducted in accordance with tenets of the Helsinki Declaration.

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Yes

I understand that all clinical trials and any other prospective interventional studies must be registered with an ICMJE-approved registry, such as ClinicalTrials.gov. I confirm that any such study reported in the manuscript has been registered and the trial registration ID is provided (note: if posting a prospective study registered retrospectively, please provide a statement in the trial ID field explaining why the study was not registered in advance).

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Data availability statement

Data is available for public consultation, as Supporting Information, as S1 Appendix.

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