Figures
Abstract
Background
Snakebite envenoming is among the top five emergency health conditions in northern Ghana. Among the four genera of snake species classified to be of highest medical importance, species with haemotoxic venom are responsible for about 90% of all snakebite case presentations in the region. However, there is a dearth of clinical data on signs and symptoms of envenoming, treatment practices and health outcomes. We examined the signs and symptoms of envenoming and clinical management practices at referral hospitals in northern Ghana.
Methods
Medical records of patients reporting on account of snakebite between 2016 and 2020 at the Wa Municipal Hospital in the Upper West region and the Baptist Medical Centre in the North East region of Ghana were reviewed. Demographic characteristics, patients’ clinical data and management practices were analysed and evaluated taking into consideration the national standard treatment guideline.
Results
A total of 2,684 records of patients reporting on account of snakebite were accessed at both health facilities over the five-year period. 91% of the patients were admitted to the ward. Swelling, severe pain and bleeding were the most common clinical signs upon presentation. A total of 1,670 (64.7%) of all the patients tested had at least one abnormal blood clotting result suggesting haemotoxicity. Antivenom was administered to 84.3% of the patients. Antibiotics were administered to 70.5% with amoxicillin with clavulanic acid, flucloxacillin and metronidazole accounting for 59.2% of all antibiotics administered. The recorded case-fatality rate was 1.9%.
Conclusion
The annual hospital attendance rate on account of snakebite to the Wa Municipal Hospital and the Baptist Medical Centre is estimated at 55 persons per 100,000 population per year. Mortality was low, with antivenom available to most of the patients. More evidence is needed on the indication and dosing of antivenom and to improve appropriate ancillary care.
Author summary
Snakebite envenoming is among the top five emergency health conditions in northern Ghana. However, there is a dearth of clinical data on signs and symptoms of envenoming, treatment practices and health outcomes. We reviewed medical data of 2,684 patients reporting on account of snakebite to two referral health facilities in snakebite endemic regions in Ghana. The majority of patients presented with signs and symptoms suggesting haemotoxic envenoming with a two-days median length of hospitalisation. Over 80% of the patients were treated with antivenom and the mortality rate was below 2%. More context specific evidence is needed to guide the indication and dosing of antivenom and to reduce the delivery of unnecessary and ineffective ancillary care.
Citation: Aglanu LM, Amuasi JH, Duah IK, Agbogbatey MK, Steinhorst J, Adobasom-Anane AG, et al. (2025) Clinical presentation and management of snakebite envenoming in northern Ghana. PLoS Negl Trop Dis 19(12): e0013820. https://doi.org/10.1371/journal.pntd.0013820
Editor: Marcelo Larami Santoro, Instituto Butantan, BRAZIL
Received: April 26, 2025; Accepted: December 3, 2025; Published: December 12, 2025
Copyright: © 2025 Aglanu et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Data Availability: All relevant data are within the manuscript.
Funding: This study was funded by the Royal Society of Tropical Medicine and Hygiene (RSTMH) Early Career Grants Programme (LMA) https://rstmh.org/grants/grantawardees-2020/nihr-awardees-2020, the Hamish Ogston Foundation (JHA, LMA), the Buruli Ulcer Foundation Groningen (YS) https://buruli1ulcer2groningen3.wordpress.com/2014/01/27/60/ and the Global Health and Infectious Diseases Research Group of the Kumasi Centre for Collaborative Research in Tropical Medicine (JHA). The funders had no role in the study design, data collection and analysis, decision to publish or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exists.
Introduction
Limited access to adequately staffed and resourced healthcare facilities compounds the treatment challenges of common medical emergencies such as snakebite envenoming (SBE) in many rural tropical regions. Available estimates suggest Sub-Saharan Africa is among the regions with the highest snakebite morbidity and mortality rates [1–3]. Bites from different species in the region are associated with distinct clinical signs and symptoms, ranging from mild local effects such as pain and swelling to severe local tissue damage necessitating surgery and life-threatening systemic envenoming, including severe hypotension, neurotoxicity or even death [4,5]. Apart from the physical burden, SBE can also lead to severe psychosocial and economic consequences for patients and their families [6–8].
Upon presentation to a health facility, an accurate diagnosis and determination of the severity of envenomation is essential in guiding appropriate treatment. However, the lack of diagnostic tools for early detection and monitoring of envenoming presents a major impediment to effective management [9–11]. Healthcare workers in many rural tropical regions rely on patients’ history, knowledge on local snake species and basic laboratory investigations such as the 20-minute whole blood clotting test (20WBCT) to diagnose SBE and to estimate the most likely species responsible for the bite [12–14]. The complexity of clinical care for snakebite, combined with the limited attention given to SBE management in medical curricula suggest treatment may often be inadequate in many snakebite-endemic countries [15–17].
Although there are a number of medically important snake species in Ghana including the Black-necked Spitting Cobra (Naja nigricollis), Puff Adder (Bitis arietans), West African Green Mamba (Dendroaspis viridis), the Black Mamba (Dendroaspis polylepis) and the Night Adder (Causus maculatus), the West African Carpet Viper (Echis ocellatus) (S1 Appendix) is thought to cause about 90% of snakebite envenomings in northern Ghana [6,18–20]. Based on our assessment of health facility reported data between 2015–2020 from the District Health Information Management System of Ghana (DHIMS), the hospital attendance rate on account of snakebite in northern Ghana is estimated to be 76 persons per 100,000 population per year. In a community-based study involving household units in northern Ghana, a lifetime snakebite prevalence of 6% and a case-fatality ratio of about 3% was estimated [18]. Many studies have highlighted that a high number of rural snakebite patients do not visit or may not reach the formal healthcare system for treatment [21–23]. In a recent community survey in Ghana, about 40% of patients did not seek allopathic treatment from a health facility [6]. Access to well-resourced healthcare facilities, availability of antivenom and cost of treatment are among the factors influencing hospital attendance rate [24–26].
In Ghana, few studies on clinical manifestations and treatment practices in hospital settings have been undertaken to generate evidence needed to guide interventions at the health system level [19,20,27,28]. In this study, we present a comprehensive description of clinical features and management practices among patients presenting to the hospital on account of snakebite in northern Ghana by retrospectively evaluating patient medical records from two major health facilities.
Methods
Ethics statement
Ethics approval was obtained from the Ghana Health Service Ethics Review Committee (GHS-ERC010/03/20), the Medical Ethical Committee of the University Medical Centre Groningen, The Netherlands (NL-LTc201900047) and the Christian Health Association of Ghana Research Unit (CHAG-IRB 03062021). Access and permission to use the data was obtained from the medical directors of the participating hospitals.
Study design
A retrospective study design was used to examine the presentation and clinical management of snakebite patients over a five-year period in two hospitals in the Upper West and North East regions of Ghana (Fig 1). Selection of the study regions is based on data retrieved from the District Health Information Management System (DHIMS2) which estimates the hospital attendance rate on account of snakebite in Upper West and North East regions as 167 and 60 persons per 100,000 population per year respectively. These are above the estimated national average of 35 persons per 100,000 population per year [6].
Study population
Both regions are characterised by grassland with scattered drought-resistant trees, providing a habitat for similar snake species. About 2.9% and 2.2% of the total population of Ghana reside in the Upper West and North East regions, respectively [29]. Both regions are predominantly agrarian with most of the population engaged in rudimentary subsistence farming activities. Residential structures in these regions are mainly made of materials such as mud, reed, straw and thatch. The aforementioned occupation and residential structures in both regions have been found to contribute to an increased risk of snakebite [30,31].
The surveyed hospitals are located in their regional capitals and are among the major health facilities in the two regions, both offering specialist services including internal medicine, surgery, physiotherapy, obstetrics/gynaecology and paediatrics services. The Wa Municipal Hospital (WMH), which is located in the Wa Central Municipality of the Upper West region, is a public hospital with a capacity of about 210 beds and a medical staff of over 410. Until 2019, it served as the Upper West regional referral hospital and treats about 72,000 patients annually. The Baptist Medical Centre (BMC) is a faith-based healthcare provider that serves as the regional referral hospital in the North East region. The hospital has a bed capacity of about 310 and a workforce of about 340 healthcare workers. Located in Nalerigu in the East Mamprusi district, the BMC is the largest health facility in the North East region and attends to over 110,000 patients annually. Due to the specialist services provided in both the WMH and the BMC, they have been the preferred destination for patients as well as referral centres for peripheral health facilities for the management of snakebite in both regions.
Data collection
All records of patients reporting on account of snakebite and diagnosed based on the national Standard Treatment Guidelines (STG) [32] and the International Classification of Diseases codes from 2016 to 2020 inclusive in WMH and BMC were eligible for inclusion in the study. The identity numbers of folders containing patients’ medical records were retrieved from the electronic record systems by the Information Officer of the WMH and the Information Technology Officer of the BMC and the hard-copy folders and consulting room registers retrieved by the records unit of both hospitals. All patients whose medical records were not available or missing all the following variables were excluded: age, date the bite occurred, anatomical site of the bite, and symptoms upon admission. The data was collected in August 2019 and August 2022 at the BMC and between February and March 2021 at the WMH. On average, eight trained healthcare personnel affiliated to the hospitals conducted the data entry process at each hospital. The Research Electronic Data Capture (REDCap) tools (version 12.5.6) hosted by the Global Health and Infectious Diseases Research group at the KCCR, Ghana was used for the data collection process [33,34].
Data analysis
Demographic characteristics and patients’ clinical data were analysed using relative frequencies to describe the presenting clinical signs and symptoms, treatments received and the resulting health outcomes. Seasonal and monthly variations were assessed to identify periods during which the risk of snakebite envenoming is elevated. The seasons were defined as rainy (March to September) and dry (October to February) [35]. A nonparametric trend analysis using LOESS (Locally Estimated Scatterplot Smoothing) curves for the number of patients reporting on account of snakebite over the period under review was conducted. This technique uses local weighted regression to fit a smooth curve through the time series. The time of hospital presentation relative to the time of the bite, duration of hospitalisation, medications administered, medical complications, and health outcomes were compared between the two hospitals using relative frequency and relative risk. Patients with systolic blood pressure (SBP) < 90 mmHg were identified as having low SBP based on the national Standard Treatment Guidelines (STG) for shock by the Ghana Ministry of Health [32]. All clinical signs and symptoms not indicated in the patient’s record book were considered not present at the time of clinical examination. All other missing data were assumed to be missing completely at random. The pairwise deletion approach was used to handle missing data during the data analysis process. IBM SPSS Statistical software version 28 for Windows was used to conduct the data analysis.
Results
A total of 2,163 and 1,661 folder identity numbers of patients reporting on account of snakebite were retrieved from the record systems of the Wa Municipal Hospital (WMH) and the Baptist Medical Centre (BMC), respectively. Based on the cumulative total population of about 6.96 million in both regions over the study period and a total of 3,824 patients reporting on account of snakebite over the period in both hospitals, the annual hospital attendance rate on account of snakebite is estimated at 55 persons per 100,000 population per year in both health facilities. Due to instances of in-patients absconding with their folders to evade paying hospital bills prior to discharge, misplaced and missing folder details, and the random destruction of folders by insects and rodents, a total of 1,270 and 1,414 physical folders were retrieved and included in the study from the WMH and the BMC, respectively (Table 1).
In total, the records of 2,684 snakebite patients who presented to both health facilities between 2016 and 2020 were reviewed. Male patients accounted for 64.7%. The median (IQR) age of the patients at the time of bite was 20 (12.0 – 33.3) years. The LOESS smooth curves show a peak in snakebites from March to July (Fig 2). This correlates with the rainy season. The annual trend shows fairly constant case presentations until 2019, when the decline in case presentations started. The suspected snake species responsible for the bites were not indicated in the patients’ medical records.
a) Monthly trend with spikes in number of reported patients b) Annual trend of reported patients from January 2016 to December 2020.
Of the 2,684 patients, 11.7% were referred from peripheral health facilities (Table 2). 2,449 (91.2%) of the reporting patients were admitted to the ward after triage at the emergency departments. About 72% (1,923) of all the patients reported to the hospital on the same day the bite occurred. Within this group who reported on the same day of the bite, 70.6% reported directly to either of the study hospitals, 12.2% were referred from other health facilities on the same day the bite occurred and 17.3% did not have data on their referral status. Time to presentation to the hospital was recorded in days. Only 1.8% reported later than 5 days after the snakebite. The longest delay before reporting to a health facility was 22 days.
Only 2% of the records had data on first aid interventions administered before reporting to the hospital. These include visiting a traditional healer for treatment, making incisions at the bite site, applying herbs or blackstone (believed to have venom absorbing and healing effects) to the bite site, and using tourniquets. Patients who reported to the WMH in the Upper West region had a higher relative risk (RR, 1.10; 95% CI, 1.07–1.12) of being admitted compared to patients reporting to the BMC in the North East region. Swelling, severe pain and bleeding were the most common clinical signs upon presentation. Although 584 patients presented with some form of bleeding, only 9.6% had a low SBP. The site and extent of bleeding were not specified in the medical records.
At least one 20WBCT was conducted for 96.2% (2,581/2,684) of the patients. However, results were available for 2,526 patients. 1,670 (66.1%) of all the patients with 20WBCT results indicated had at least one abnormal clotting result; 93.2% had an abnormal clotting result on their first test while 6.8% had normal clotting results on the first test but recorded abnormal results on subsequent tests (Fig 3). The specific time for repeated clotting test is not often recorded. However, the general practice is to repeat the test between 4–6 hours.
Within the total population with at least one abnormal 20WBCT result, 24.1% (403/1,670) reported with bleeding and 23.1% (93/403) of this subgroup received blood transfusion. Among the patients who recorded normal 20WBCT results, 18% (154/856) reported with some form of bleeding, with 18.8% (29/154) of the patients in this subgroup receiving blood transfusion.
Of the 1,670 who had at least one abnormal clotting test result, 96.6% (1,614) were treated with antivenom compared to 64.3% (550/856) of those who did not record any abnormal clotting results. The median (IQR) number of antivenom vials received per patient was 2 (1–3) vials. However, 33 patients received 10 or more vials for their treatment. The specific type of antivenom administered was not recorded. A total of 73 (2.7%) patients experienced a rebound of abnormal clotting results and were retreated with antivenom, after ceasing treatment when normal clotting was achieved from initial treatment. Analgesics were the main ancillary medications administered for the management of snakebite induced pain (Fig 4). Paracetamol was administered to 73.3%, opioids to 13.9% and non-steroidal anti-inflammatory drugs (NSAIDS) to 12.3%. Steroids were given to 38.4% of the patients. Hydrocortisone accounted for over 99% of the steroids administrated, adjuvant to antivenom. Four patients received adrenaline but with unclear clinical indication.
Antibiotics were administered to 70.5% of the patients. Among whom, 59.2% received one antibiotic agent, 32.3% received two different agents and 8.5% received three to five different agents of antibiotics in the course of treatment. Amoxicillin with clavulanic acid, flucloxacillin and metronidazole were the most commonly administered antibiotics (Fig 5). Four out of the 14 administered antibiotics are on the World Health Organisation’s (WHO) watch list based on the Access, Watch and Reserve (AWaRE) classification.
Severe complications that were recorded included compartment syndrome (two patients), intraocular haemorrhage (two patients) and submandibular hematoma (two patients). Gangrene was diagnosed in eight patients and necrosis in four patients. Respiratory distress with dysphagia, hypoxia and seizures were observed in three patients. Cellulitis was reported for 28.8% of all patients without further description of the clinical signs. Anaemia was reported for 4.5% of the patients.
The total recorded case-fatality rate was 1.9% (Table 3). The Upper West recorded a case-fatality rate of 2.8% compared to 1.1% in the North East. However, in the North East region, 2.3% of the patients were referred from the BMC to other tertiary health facilities for advanced care and 0.1% discharged against medical advice. No referrals for advanced care were made from the WMH but 6% of patients absconded or were discharged against medical advice. The health outcomes of these patients are unknown. Furthermore, 22.6% of the patients reporting in the Upper West region were referred by other peripheral health facilities to the WMH compared to the 2% referrals received at the BMC in the North East region (Table 2). Patients who recorded abnormal clotting results but were not treated with antivenom were 56 in total. Out of this number, 16.1% reported with some form of bleeding, 48.2% with swelling and 30.4% with severe pain. Two patients within this group died and 9 were referred for advanced care.
The median age of the patients who died is 31 (15 – 45) years. The majority of them were male patients (62%). Four (8%) of the patients with fatal outcomes were referred from other health facilities to the WMH.
Discussion
The hospital attendance rate on account of snakebite is estimated at 55 persons per 100,000 population per year in the WMH and the BMC. The main clinical sign and symptoms exhibited by snakebite patients in these regions are clotting disorders, swelling and severe pain which are consistent with haemotoxins envenoming from species such as Echis ocellatus and Bitis arietans. The majority of the patients in the study were treated with antivenom. The main venom-induced medical complication recorded are compartment syndrome, intraocular haemorrhage, submandibular hematoma and amputation. The total facility-based fatality rate over the five-year period under review was 1.9%.
Existing evidence suggest snakebite envenoming exerts a high burden on the health system in northern Ghana [5,18,36], where the average doctor-to-patient ratio was estimated at about 1:14,200 in 2020 [37]. Our results show a similar trend with the two health facilities each handling an average annual case load of about 765 snakebite patients. In 2019 a new regional hospital was commissioned the Upper West regions. This may have accounted for the decrease in case presentations to the WMH. Diagnosis and treatment of snakebite patients was guided by the 20WBCT and presenting clinical signs and symptoms. This approach has been documented to be practiced in many resource-limited settings with poor diagnostic capabilities [12–14]. Although there was limited data on the type and brand of antivenom administered, only three polyvalent antivenom brands – PANAF-Premium (Pan Africa), AFRIVEN (Snake Venom Antiserum (African 10) I.H.S and ALS-SVAS (Snake Venom Anti Serum) (African)) – are listed on the Ghana Food and Drugs Authority Products Register [38]. Nevertheless, there are other brands and types of antivenoms in the open market, including ECHIVEN (Snake Venom Antiserum (ECHIS) I.H.S) a monovalent antivenom targeting Echis species as well as other antivenoms.
Generally, the length of hospitalisation was short in comparison with other studies in Ghana in which average length of hospitalisation ranged from 2.7 to 4.7 days [19,27,28,39]. The short length of hospitalisation may be linked to early presentation and most envenoming being haemotoxic and thus, may require shorter hospital stays compared to cytotoxic and neurotoxic bites from species such as Bitis arietans, Naja nigricollis, Dendroaspis viridis or Dendroaspis polylepis. Patients bitten by these species may require more extensive treatment and rehabilitation such as surgical procedures, wound care, respiratory support and physiotherapy [40,41]. Similar fatality rate was recorded in comparison with studies conducted in mid-and northern Ghana and north-eastern Nigeria in which recorded fatality rates ranged between zero to 1.6% [19,27,28,39,42]. However, the case-fatality rate in the Nigerian study increased more than two folds during the months of antivenom stock-out [42].
Repeating the 20WBCT is essential in averting complications of coagulopathic envenoming by detecting persistent or rebound coagulopathy [43,44]. In our study population, delayed and/or rebound coagulopathy was detected in more than 6% of the patients.
Among the patients who were not treated with antivenom, 56 (14%) recorded abnormal clotting results. Reasons for the non-administration of antivenom include stock-outs and patients’ inability to afford or access antivenom from the open market, patients absconding or discharged against medical advice or patients dying before antivenom could be administered. On the contrary, 648 (63.9%) of the patients with normal clotting results were treated with antivenom. In these patients, signs of systemic envenomation or severe local swelling are likely to be the primary reason for antivenom therapy [45]. Although a significant proportion of the patients in this study reported with swelling or bleeding, the extent and severity were not documented. It is therefore plausible that patients with dry bites or non-venomous bite may have been treated with antivenom. With the 20WBCT having a sensitivity of 82–89% and a specificity of 82–98%, some patients with coagulopathic envenoming may have gone undetected [40]. The 20WBCT may therefore be insufficient to identify all patients with coagulopathic envenoming in need of antivenom treatment. Although the national STG recommends 5–10 vials of antivenom depending on the severity of envenoming and repeating antivenom administration as required based on the patient’s response to treatment, we ascertained that clinicians often administer an average of two vials and repeat after about six hours depending on the severity or the persistence of clinical signs of envenoming and results of the repeated 20WBCT. This conservative approach is adopted due to the limited supply of antivenom in these high-risk settings. This highlights the need to ensure adequate stocking and judicious use of appropriate antivenom.
Aside antivenoms, ancillary medications are essential in treating other bite or venom induced signs and symptoms. Even though tetanus as a complication of snakebite is rare, the Ghanaian STG as well as the WHO guidelines recommends a prophylactic dose of anti-tetanus therapy for all snakebite patients [5,32]. However, less than 25% of the patients in this study population received anti-tetanus therapy. Paracetamol was the main medication used for pain management, although NSAIDs were administered to a considerable number of patients despite being identified as a relative contraindication particularly in patients with haemotoxic envenoming [46–48]. It is unclear whether adequate pain assessment was conducted, and management undertaken according to the WHO analgesic ladder [49]. Similarly, the national treatment guideline and prevailing evidence do not support the administration of antifibrinolytic agents, such as tranexamic acid or vitamin K for snakebite management [50–52].
Steroids, particularly hydrocortisone, are often administered by clinicians in our study setting. In the WHO guidelines, there is no indication for the use of steroids [5] and clinical trials have also showed no effect against a biphasic course of anaphylaxis in SBE patients [53–55]. In this study, only four patients were treated with adrenaline, but the exact indications are unclear. These four patients were among the deceased. The adrenaline may have been used as part of resuscitation efforts although anaphylactic shock was not recorded in their medical records. Training and making research evidence readily available to clinicians via updated STGs could improve clinical decision-making and help alleviate the socioeconomic and health system burden of SBE.
Even though most studies do not support the treatment of SBE patients with antibiotics [56–62], the majority of the patients in this study were treated with antibiotics. Four of the administered antibiotics are on the WHO AWaRE classification list, which is aimed at emphasizing the significance of appropriate use while also taking into account the impact of various antibiotics and antibiotic classes on antimicrobial resistance [63]. In the national STG, only amoxicillin has been recommended for the prevention of secondary infections. In the regional guideline for Africa, it is recommended that treatment with antibiotics should be delayed until definite signs of infection arise or when the bite site has been interfered with. Limited knowledge on the pathophysiology of infections such as cellulitis [64,65] may have contributed to the frequent administration of antibiotics, considering the high percentage of patients recorded to have developed cellulitis. Cellulitis was often diagnosed in less than 48 hours upon arrival to the health facility; a time frame within which a true bacterial infection is unlikely to establish itself in skin tissue. This suggests swelling or erythema after the bite was likely recorded as cellulitis in many cases. With limited indications documented in the medical records, the use of antibiotics, primarily as prophylaxis, demonstrates poor adherence to treatment guidelines.
There are limitations to this study given its retrospective nature, including that no data on snake species, specific antivenom utilised or systematic data on outcomes were available in the medical records. The misplacement or unavailability of patient’s medical records occurred at random. The non-standardisation of record-keeping between the health facilities and among clinicians may have also introduced procedural bias. Hence, the findings should be interpreted with caution. Nevertheless, the same data collection approach was employed in both health facilities to ensure uniformity in the structure and data collection process. Subsequently, all health facilities in the country have adopted the Lightwave Health Information Management System (LHIMS); an electronic medical information management platform that aims to standardise and improve medical data collection and storage.
Conclusion
With an estimated annual hospital attendance rate on account of snakebite being 55 persons per 100,000 population per year, snakebite is a major public health challenge and a burden to the Wa Municipal Hospital and the Baptist Medical Centre. Haemotoxic envenoming is the main clinical presentation but low mortality rates are recorded with a high number of patients treated with antivenom. More evidence on the clinical management of snakebite envenoming and better use of available evidence on ancillary care is needed to guide decisions.
Supporting information
S1 Appendix. West African Carpet Viper (Echis ocellatus).
https://doi.org/10.1371/journal.pntd.0013820.s001
(DOCX)
Acknowledgments
We are grateful to the Public Health and Records Units of the Wa Municipal Hospital and the ICT and Records Unit of the Baptist Medical Centre for their support in identifying and retrieving the medical records. We also appreciate Mr. Edward Addai, the Hospital Director of the Baptist Medical Centre for his support and all the health professionals who assisted with the data entry process at both hospitals.
References
- 1. Benjamin JM, Abo BN, Brandehoff N. Review article: snake envenomation in Africa. Curr Trop Med Rep. 2020;7(1):1–10.
- 2. Chippaux J-P. Estimate of the burden of snakebites in sub-Saharan Africa: a meta-analytic approach. Toxicon. 2011;57(4):586–99. pmid:21223975
- 3. GBD 2019 Snakebite Envenomation Collaborators. Global mortality of snakebite envenoming between 1990 and 2019. Nat Commun. 2022;13(1):6160. pmid:36284094
- 4.
WHO. Snakebite envenoming: a strategy for prevention and control. Geneva: World Health Organization; 2019. https://www.who.int/publications/i/item/9789241515641
- 5.
WHO. Guidelines for the prevention and clinical management of snakebite in Africa. Regional Office for Africa: World Health Organization; 2010. https://apps.who.int/iris/handle/10665/204458
- 6. Aglanu LM, Amuasi JH, Schut BA, Steinhorst J, Beyuo A, Dari CD, et al. What the snake leaves in its wake: Functional limitations and disabilities among snakebite victims in Ghanaian communities. PLoS Negl Trop Dis. 2022;16(5):e0010322. pmid:35604939
- 7. Tolboom J. The psychological impact of snakebite, a neglected aspect in WHO snakebite treatment guidelines for Africa: Lesson learnt from a historical case report from Zambia. mjz. 2021;48(1):67–9.
- 8. Kasturiratne A, Lalloo DG, Janaka de Silva H. Chronic health effects and cost of snakebite. Toxicon X. 2021;9–10:100074. pmid:34355162
- 9. Knudsen C, Jürgensen JA, Føns S, Haack AM, Friis RUW, Dam SH, et al. Snakebite envenoming diagnosis and diagnostics. Front Immunol. 2021;12:661457. pmid:33995385
- 10. Theakston RDG, Laing GD. Diagnosis of snakebite and the importance of immunological tests in venom research. Toxins (Basel). 2014;6(5):1667–95. pmid:24859244
- 11. Williams HF, Layfield HJ, Vallance T, Patel K, Bicknell AB, Trim SA, et al. The urgent need to develop novel strategies for the diagnosis and treatment of snakebites. Toxins (Basel). 2019;11(6):363. pmid:31226842
- 12. Wedasingha S, Isbister G, Silva A. Bedside coagulation tests in diagnosing venom-induced consumption coagulopathy in snakebite. Toxins (Basel). 2020;12(9):583. pmid:32927702
- 13. Hamza M, Knudsen C, Gnanathasan CA, Monteiro W, Lewin MR, Laustsen AH, et al. Clinical management of snakebite envenoming: future perspectives. Toxicon X. 2021;11:100079. pmid:34430847
- 14. Gerardo CJ, Vissoci JRN, Evans CS, Simel DL, Lavonas EJ. Does this patient have a severe snake envenomation?: The rational clinical examination systematic review. JAMA Surg. 2019;154(4):346–54. pmid:30758508
- 15. Barnes K, Ngari C, Parkurito S, Wood L, Otundo D, Harrison R, et al. Delays, fears and training needs: perspectives of health workers on clinical management of snakebite revealed by a qualitative study in Kitui County, Kenya. Toxicon X. 2021;11:100078. pmid:34401745
- 16. Taieb F, Dub T, Madec Y, Tondeur L, Chippaux JP, Lebreton M, et al. Knowledge, attitude and practices of snakebite management amongst health workers in Cameroon: need for continuous training and capacity building. PLoS Negl Trop Dis. 2018;12(10):e0006716. pmid:30359385
- 17. Ameade EPK, Bonney I, Boateng ET. Health professionals’ overestimation of knowledge on snakebite management, a threat to the survival of snakebite victims-A cross-sectional study in Ghana. PLoS Negl Trop Dis. 2021;15(1):e0008756. pmid:33465084
- 18. Musah Y, Ameade EPK, Attuquayefio DK, Holbech LH. Epidemiology, ecology and human perceptions of snakebites in a savanna community of northern Ghana. PLoS Negl Trop Dis. 2019;13(8):e0007221. pmid:31369551
- 19. Yakubu A-S, Abdul-Mumin A, Rivera O. Evaluation of management of snake bites in a teaching hospital in northern Ghana: a retrospective descriptive study. Int J Community Med Public Health. 2019;6(3):920.
- 20. Visser LE, Kyei-Faried S, Belcher DW, Geelhoed DW, van Leeuwen JS, van Roosmalen J. Failure of a new antivenom to treat Echis ocellatus snake bite in rural Ghana: the importance of quality surveillance. Trans R Soc Trop Med Hyg. 2008;102(5):445–50. pmid:18190937
- 21. Larson PS, Ndemwa M, Thomas AF, Tamari N, Diela P, Changoma M, et al. Snakebite victim profiles and treatment-seeking behaviors in two regions of Kenya: results from a health demographic surveillance system. Trop Med Health. 2022;50(1):31. pmid:35488352
- 22. Alcoba G, Sharma SK, Bolon I, Ochoa C, Babo Martins S, Subedi M, et al. Snakebite epidemiology in humans and domestic animals across the Terai region in Nepal: a multicluster random survey. Lancet Glob Health. 2022;10(3):e398–408. pmid:35180421
- 23. Francis MF, Vianney SJ-M, Heitz-Tokpa K, Kreppel K. Risks of snakebite and challenges to seeking and providing treatment for agro-pastoral communities in Tanzania. PLoS One. 2023;18(2):e0280836. pmid:36763599
- 24. Schioldann E, Mahmood MA, Kyaw MM, Halliday D, Thwin KT, Chit NN, et al. Why snakebite patients in Myanmar seek traditional healers despite availability of biomedical care at hospitals? Community perspectives on reasons. PLoS Negl Trop Dis. 2018;12(2):e0006299. pmid:29489824
- 25. Aglanu LM, Amuasi JH, Prokesh E, Beyuo A, Dari CD, Ravensbergen SJ, et al. Community members and healthcare workers’ priorities for the control and prevention of snakebite envenoming in Ghana. PLoS Negl Trop Dis. 2023;17(7):e0011504. pmid:37478151
- 26. Steinhorst J, Aglanu LM, Ravensbergen SJ, Dari CD, Abass KM, Mireku SO, et al. “The medicine is not for sale”: practices of traditional healers in snakebite envenoming in Ghana. PLoS Negl Trop Dis. 2021;15(4):e0009298. pmid:33861735
- 27. Yakubu A-S, Abdul-Mumin A, Adam A. Clinical and demographic profile of patients with snakebite in a tertiary hospital in Ghana. Sahel Med J. 2019;22(4):194.
- 28. Punguyire D, Baiden F, Nyuzaghl J, Hultgren A, Berko Y, Brenner S. Presentation, management, and outcome of snake-bite in two district hospitals in Ghana. The Pan African medical journal. 2014;19(1).
- 29. Ghana Statistical Service. Ghana 2021 Population and Housing Census Volume 3: General Report Highlights. 2022. https://census2021.statsghana.gov.gh/gssmain/fileUpload/reportthemelist/Volume%203%20Highlights.pdf
- 30. Kung’u PN, Chweya RN, Gachohi JM. Traditional remedies and other characteristics among human snakebite survivors in Baringo county, Kenya, 2010-2020: a case series. Int Health. 2023;15(3):242–9. pmid:35724263
- 31. Gutiérrez JM, Calvete JJ, Habib AG, Harrison RA, Williams DJ, Warrell DA. Snakebite envenoming. Nat Rev Dis Primers. 2017;3:17079. pmid:28980622
- 32.
Ghana National Drugs Programme (GNDP). Standard treatment guidelines. Ministry of Health, Republic of Ghana; 2017. https://www.moh.gov.gh/wp-content/uploads/2020/07/GHANA-STG-2017-1.pdf
- 33. Harris PA, Taylor R, Minor BL, Elliott V, Fernandez M, O’Neal L, et al. The REDCap consortium: building an international community of software platform partners. J Biomed Inform. 2019;95:103208. pmid:31078660
- 34. Harris PA, Taylor R, Thielke R, Payne J, Gonzalez N, Conde JG. Research electronic data capture (REDCap)--a metadata-driven methodology and workflow process for providing translational research informatics support. J Biomed Inform. 2009;42(2):377–81. pmid:18929686
- 35. Amekudzi L, Yamba E, Preko K, Asare E, Aryee J, Baidu M, et al. Variabilities in rainfall onset, cessation and length of rainy season for the various agro-ecological zones of Ghana. Climate. 2015;3(2):416–34.
- 36. Deikumah JP, Biney RP, Awoonor-Williams JK, Gyakobo MK. Compendium of medically important snakes, venom activity and clinical presentations in Ghana. PLoS Negl Trop Dis. 2023;17(7):e0011050. pmid:37506181
- 37. Ministry of Health. Health sector annual programme of work: 2021 holistic assessment report: mnistry of health, Republic of Ghana; 2022 [Cited 2025 November 25]. https://www.moh.gov.gh/wp-content/uploads/2022/08/2021-Holistic-Assessment-Report_v1.7.3.pdf
- 38. FDA. Food and drugs authority products register. Accessed 2025 November 25. https://verifypermit.fdaghana.gov.gh/publicsearch
- 39. Ketor CE, Benneh CK, Mensah KB, Sarkodie E, Mensah A, Somuah SO, et al. Snakebites and antisnake venom utilization in Ghana’s Oti Region: a 6-year retrospective study. Biomed Res Int. 2024;2024:6692421. pmid:39140000
- 40. Ralph R, Faiz MA, Sharma SK, Ribeiro I, Chappuis F. Managing snakebite. BMJ. 2022;376:e057926. pmid:34996773
- 41. Russell JJ, Schoenbrunner A, Janis JE. Snake bite management: a scoping review of the literature. Plast Reconstr Surg Glob Open. 2021;9(4):e3506. pmid:33936914
- 42. Habib AG, Abubakar SB. Factors affecting snakebite mortality in north-eastern Nigeria. Int Health. 2011;3(1):50–5. pmid:24038050
- 43. Tianyi F-L, Hamza M, Abubakar SB, Al Solaiss J, Trelfa A, Abdullahi HL, et al. Diagnostic characteristics of the 20-minute whole blood clotting test in detecting venom-induced consumptive coagulopathy following carpet viper envenoming. PLoS Negl Trop Dis. 2023;17(6):e0011442. pmid:37363905
- 44. Hamman NA, Ibrahim AD, Hamza M, Jahun MG, Micah M, Lawal HA, et al. A randomized controlled trial to optimize antivenom therapy for Carpet Viper (Echis romani)-envenomed children in Nigeria. Am J Trop Med Hyg. 2024;111(4):904–10. pmid:39106853
- 45. Ahmed SM, Ahmed M, Nadeem A, Mahajan J, Choudhary A, Pal J. Emergency treatment of a snake bite: Pearls from literature. J Emerg Trauma Shock. 2008;1(2):97–105. pmid:19561988
- 46. Villca-Corani H, Nieto-Ariza B, León R, Rocabado JA, Chippaux J-P, Urra FA. First reports of envenoming by South American water snakes Helicops angulatus and Hydrops triangularis from Bolivian Amazon: a one-year prospective study of non-front-fanged colubroid snakebites. Toxicon. 2021;202:53–9. pmid:34562494
- 47. Okumu MO, Patel MN, Bhogayata FR, Ochola FO, Olweny IA, Onono JO, et al. Management and cost of snakebite injuries at a teaching and referral hospital in Western Kenya. F1000Res. 2019;8:1588. pmid:31824667
- 48. Edgerton MT, Koepplinger ME. Management of Snakebites in the Upper Extremity. J Hand Surg Am. 2019;44(2):137–42. pmid:30057221
- 49. Anekar AA, Hendrix JM, Cascella M. WHO analgesic ladder. StatPearls. 2023. https://www.statpearls.com
- 50. Namal Rathnayaka R, Ranathunga PAN, Kularatne SA. Thrombotic microangiopathy, hemolytic uremic syndrome, and thrombotic thrombocytopenic purpura following hump-nosed pit viper (Genus: Hypnale) envenoming in Sri Lanka. Wilderness Environ Med. 2019;30(1):66–78. pmid:30711421
- 51. Wijewickrama ES, Gooneratne LV, Gnanathasan A, Gawarammana I, Gunatilake M, Isbister GK. Thrombotic microangiopathy and acute kidney injury following Sri Lankan Daboia russelii and Hypnale species envenoming. Clin Toxicol (Phila). 2020;58(10):997–1003. pmid:32067496
- 52. McCormack PL. Tranexamic acid: a review of its use in the treatment of hyperfibrinolysis. Drugs. 2012;72(5):585–617. pmid:22397329
- 53. Grunau BE, Wiens MO, Rowe BH, McKay R, Li J, Yi TW, et al. Emergency department corticosteroid use for allergy or anaphylaxis is not associated with decreased relapses. Ann Emerg Med. 2015;66(4):381–9. pmid:25820033
- 54. de Silva HA, Pathmeswaran A, Ranasinha CD, Jayamanne S, Samarakoon SB, Hittharage A, et al. Low-dose adrenaline, promethazine, and hydrocortisone in the prevention of acute adverse reactions to antivenom following snakebite: a randomised, double-blind, placebo-controlled trial. PLoS Med. 2011;8(5):e1000435. pmid:21572992
- 55. Kularatne SA, Weerakoon K, Silva A, Maduwage K, Walathara C, Rathnayake I, et al. Efficacy of intravenous hydrocortisone administered 2–4 h prior to antivenom as prophylaxis against adverse drug reactions to snake antivenom in Sri Lanka: An open labelled randomized controlled trial. Toxicon. 2016;120:159–65.
- 56. Wagener M, Naidoo M, Aldous C. Wound infection secondary to snakebite. S Afr Med J. 2017;107(4):315–9. pmid:28395682
- 57. Hardcastle T, Engelbrecht A, Lalloo V, Bell C, Toubkin M, Motara F, et al. Approach to the diagnosis and management of snakebite envenomation in South Africa in humans: special patient groups and surgical aspects. S Afr Med J. 2023;113(7):16–21. pmid:37882036
- 58. Warrell DA, Williams DJ. Clinical aspects of snakebite envenoming and its treatment in low-resource settings. Lancet. 2023;401(10385):1382–98. pmid:36931290
- 59. Patiño RSP, Salazar-Valenzuela D, Robles-Loaiza AA, Santacruz-Ortega P, Almeida JR. A retrospective study of clinical and epidemiological characteristics of snakebite in Napo Province, Ecuadorian Amazon. Trans R Soc Trop Med Hyg. 2023;117(2):118–27. pmid:35917814
- 60. Lertsakulbunlue S, Suebtuam R, Eamchotchawalit T, Chantkran W, Chaisakul J. Clinical profile and pharmacological management of snakebites in community care units: a retrospective study using two military hospital databases in South Thailand. Trop Med Infect Dis. 2023;8(7):346. pmid:37505642
- 61. Resiere D, Gutiérrez JM, Névière R, Cabié A, Hossein M, Kallel H. Antibiotic therapy for snakebite envenoming. J Venom Anim Toxins Incl Trop Dis. 2020;26:e20190098. pmid:32095137
- 62. August JA, Boesen KJ, Hurst NB, Shirazi FM, Klotz SA. Prophylactic antibiotics are not needed following rattlesnake bites. Am J Med. 2018;131(11):1367–71. pmid:30392637
- 63.
WHO. WHO Access, Watch, Reserve (AWaRe) classification of antibiotics for evaluation and monitoring of use. Geneva: World Health Organization; 2021.
- 64. David CV, Chira S, Eells SJ, Ladrigan M, Papier A, Miller LG, et al. Diagnostic accuracy in patients admitted to hospitals with cellulitis. Dermatol Online J. 2011;17(3):1. pmid:21426867
- 65. Pallin DJ, Bry L, Dwyer RC, Lipworth AD, Leung DY, Camargo CA Jr, et al. Toward an objective diagnostic test for bacterial cellulitis. PLoS One. 2016;11(9):e0162947. pmid:27656884