Skip to main content
PLOS Neglected Tropical Diseases logoLink to PLOS Neglected Tropical Diseases
. 2022 Feb 9;16(2):e0010148. doi: 10.1371/journal.pntd.0010148

Treatment outcomes among snakebite patients in north-west Ethiopia—A retrospective analysis

Inge Steegemans 1,2,*, Kassaye Sisay 3, Ernest Nshimiyimana 3, Gashew Gebrewold 4, Turid Piening 5, Endale Menberu Tessema 5, Birhanu Sahelie 5, Gabriel Alcoba 6, Fikre Seife Gebretsadik 7, Dirk Essink 2, Simon Collin 8, Emiliano Lucero 1, Koert Ritmeijer 1
Editor: Stuart Robert Ainsworth9
PMCID: PMC8863263  PMID: 35139079

Abstract

Background

Millions of people are bitten by venomous snakes annually, causing high mortality and disability, but the true burden of this neglected health issue remains unknown. Since 2015, Médecins Sans Frontières has been treating snakebite patients in a field hospital in north-west Ethiopia. Due to the poor market situation for effective and safe antivenoms for Sub-Saharan Africa, preferred antivenom was not always available, forcing changes in choice of antivenom used. This study describes treatment outcomes and the effectiveness and safety of different antivenoms used.

Methodology / Principal findings

This retrospective observational study included 781 snakebite patients presenting at the field hospital between 2015 and 2019. Adjusted odds ratios, 95%-CI and p-values were used to compare the treatment outcome of patients treated with Fav-Afrique (n = 149), VacSera (n = 164), and EchiTAb-PLUS-ICP (n = 156) antivenom, and to identify the risk of adverse reactions for each antivenom. Whereas only incidental snakebite cases presented before 2015, after treatment was made available, cases rapidly increased to 1,431 in 2019. Envenomation was mainly attributed to North East African saw-scaled viper (Echis pyramidum) and puff adder (Bitis arietans). Patients treated with VacSera antivenom showed lower chance of uncomplicated treatment outcome (74.4%) compared to Fav-Afrique (93.2%) and EchiTAb-PLUS-ICP (90.4%). VacSera and EchiTAb-PLUS-ICP were associated with 16- and 6-fold adjusted odds of treatment reaction compared to Fav-Afrique, respectively, and VacSera was weakly associated with higher odds of death.

Conclusions / Significance

Snakebite frequency is grossly underreported unless treatment options are available. Although EchiTAb-PLUS-ICP showed favorable outcomes in this retrospective analysis, prospective randomized trials are needed to evaluate the effectiveness and safety of the most promising antivenoms for Sub-Saharan Africa. Structural investment in sustained production and supply of antivenom is urgently needed.

Author summary

Snakebite is an important but highly neglected medical problem, causing high morbidity and mortality in low-and-middle income countries all over the world, including Ethiopia. When bitten by a venomous snake, appropriate treatment with the correct antivenom is crucial. However, in Ethiopia the correct antivenom is not always available due to low access to health facilities in rural areas. Even if antivenom is available, patients can often not afford it due to the high costs of clinical effective antivenoms. This study explores the effectiveness of three different antivenoms, Fav-Afrique, VacSera and EchiTAb-PLUS-ICP, and provides insights in factors that might influence the outcome of the snakebite treatment. This study shows that patients treated with VacSera antivenom have a higher chance of an adverse outcome of the treatment. Much more research on snakebite epidemiology and the effectiveness of antivenoms should be conducted, aiming to alert governments and antivenom manufacturers that this is a serious problem which cannot be ignored any longer.

Introduction

Each year, around 5.5 million people worldwide are bitten by snakes, causing approximately 100,000 deaths and leaving 400,000 people disabled [1,2]. In Sub-Saharan Africa, snakebites are causing an estimated 435,000–580,000 envenomations and 20,000–32,000 deaths annually [3]. Snakebites mostly affect the poorest populations [4,5]. People living in rural areas are most susceptible as they live and work in areas where snakes reside [6]. In combination with poor access to health services, scarcity of safe and effective antivenoms and the economic impact of disabled young victims, snakebites put a high burden on the population and the economy of low-and-middle-income countries [7].

Data regarding the incidence and mortality of snakebites is often inaccurate due to the under-reporting of snakebites by patients and health institutions [2,8,9]. Snakebite victims often do not seek medical care in government dispensaries but go to traditional healers instead [2,9]. The reasons for this are low access to health facilities in rural areas and medical treatment being too expensive [2,10,11]. Moreover, antivenom treatment is often not available [12]. Antivenoms are the only effective treatment against envenomation when someone is bitten by a venomous snake [4]. They can prevent or reverse most toxic effects that occur during snakebite envenoming and they play a significant role in limiting the morbidity and mortality. However, at this moment antivenoms are mainly equine immunoglobulins, which are snake-specific and can cause serious adverse events; when an unsuitable product is used which has not been developed to neutralize venoms of relevant endemic snake species, it is ineffective [13,14]. Due to the high costs of clinical effective antivenoms, many cheaper but low-quality or even counterfeit antivenoms are circulating on the pharmaceutical market, posing a threat to populations of many low-and-middle-income countries [15]. The high costs of antivenoms also lead to a low demand, which makes it a non-profitable market for manufacturers which has resulted in a shortage in the supply of antivenoms [12].

In order to develop strategies for the management of snake antivenoms, epidemiological data is essential [1,8]. However, there is still a lack of reliable data concerning the incidence, burden and the management of snakebites in different regions of the world [1,2,8]. Moreover, limited data is available on the effectiveness and safety of different antivenoms in Sub-Saharan Africa [3]. With this information at hand, manufacturers of antivenoms will be able to better manage the production, and health authorities will be able to distribute the most effective antivenoms to the right places [12]. Recent literature states that population-based studies researching the incidence, morbidity, and mortality in high burden countries are required urgently [8].

Ethiopia is one of many countries facing a high incidence of snakebites and low access to treatment [16]. In the north-western lowlands of Ethiopia, snakebites occur regularly and present a sizeable health hazard. Since 2015, Médecins Sans Frontières (MSF) has been treating snakebite victims with antivenom in a field hospital in Abdurafi, in the lowlands of the Amhara region in north-west Ethiopia. The large commercial farming schemes in this region attract over 350,000 seasonal migrant workers from other parts of Ethiopia and neighboring countries [17,18]. Due to the poor conditions on these farms, migrant workers are particularly vulnerable to snakebites as they work, live, and sleep in the bare fields without protection.

MSF has been providing antivenom treatment for snakebite patients since March 2015. Before antivenom was available, standard care for snakebite patients consisted of first aid, supportive care and management, and mental support. In case a patient was in need of more intensive treatment, such as surgery, the clinic provided referral to a secondary or tertiary hospital. Since March 2015, four different antivenoms were used by MSF to treat snakebite envenoming: Fav-Afrique (March ‘15—Aug ‘16), VacSera (Jan ‘17 –Aug ‘18), and EchiTAb-PLUS-ICP and SAIMR (since Sep ‘18) (S1 Table). The different antivenoms were used based on accessibility and availability. First, the Fav-Afrique antivenom (Sanofi Pasteur, France) was used, which is a polyvalent antivenom and is effective against most bites of medically important snakes in sub-Saharan Africa (Bitis spp., Dendroaspis spp., Echis spp., Naja spp.) [19]. Because the production of Fav-Afrique was stopped in 2014, and the last batch expired in June 2016, another antivenom was urgently needed. At that time, the Egyptian VacSera antivenom (VACSERA, Egypt) was the only antivenom licensed for importation in Ethiopia. VacSera antivenom is also a polyvalent antivenom and is raised against endemic snakes in Egypt such as spitting cobras (Naja haje), horned vipers (Cerastes cerastes), saw-scaled vipers (Echis coloratus), and puff adders (Bitis arietans) [20]. However, it is not raised against the East African carpet viper (Echis pyramidum), which seems to be the most frequent causative species in the lowlands of north-west Ethiopia. The third antivenom protocol which is still being used includes EchiTAb-PLUS-ICP (ICP, Costa Rica) and SAIMR polyvalent antivenom (SAVP, South Africa). EchiTAb-PLUS-ICP antivenom is a polyvalent antivenom and is used in case of envenoming by puff adders (B. arietans), West African carpet vipers (Echis ocellatus), and spitting cobras (Naja nigricolis). SAIMR is an antivenom used in case of neurotoxic envenoming by mambas (Dendroaspis spp.), spitting and non-spitting cobras (Naja spp.) and in critical cases of severe cytotoxic envenomation by Bitis vipers.

Whether treatment of snakebite envenoming is effective depends highly on the early administration of adequate amounts of the correct antivenom to neutralize venom antigens and reverse its effects [2123]. However, in Ethiopia, antivenom is scarcely available in public hospitals, and if it is, it is expensive due to market failure and little attention to snakebite envenoming [2,9]. This study provides epidemiological data on the frequency and management of snakebites in north-west Ethiopia and aims to contribute to the current knowledge about the treatment of snakebites by describing which antivenom is most effective and safe, and what factors influence the treatment outcome. This context-specific information aims to contribute to the improvement of snakebite patient care and its medical management in Ethiopia.

Methods

Ethics statement

This research fulfills the exemption criteria set by the Médecins Sans Frontières Ethics Review Board (MSF ERB) for a posteriori analysis of routinely collected clinical data and therefore does not require MSF ERB review. The research was conducted with permission from MSF Holland. In addition, this research and the method of data collection has been approved by the Ethiopian Public Health Institute–Institutional Review Board (EPHI—IRB).

Design and research setting

In this descriptive retrospective cross-sectional study, secondary data analysis was performed with data from the MSF field hospital in Abdurafi, West Armachiho district, Amhara region in Ethiopia. In this hospital, snakebite patients are admitted for observation and treatment. A snakebite management algorithm is used to determine the treatment a patient requires. This algorithm is based on a syndromic approach as in most cases reliable snake information such as the species is unknown. There are three different types of snakebite syndromes: cytotoxic, haematotoxic, and neurotoxic. The cytotoxic syndrome affects skin and muscle cells, leading to extensive swelling, blistering, muscle damage, and possibly local tissue necrosis. The haematotoxic syndrome affects the cardiovascular system and blood functions and often causes internal and external bleeding. The neurotoxic syndrome affects the nervous system and causes flaccid muscular paralysis [24,25]. The algorithm indicates if antivenom should be administered or not and what kind of supportive care is recommended, based on the syndrome, its severity, and a blood clotting test. Antivenom is not administered when symptoms are mild, e.g. non-progressive swelling in the extremities or local bleeding, and when there are no critical signs.

Suspected snake species was assessed by patient description of the snake if possible, using a snake atlas with pictures and sizes. Snakes caught by a snake catcher of the Ethiopian Public Health Institute on the farms in Abdurafi area in 2017 identified Echis pyramidum and Bitis arietans as the main venomous snakes in the area.

Sampling procedure

The study population consists of patients who have attended the Abdurafi field hospital due to a snakebite incident between January 2015 and December 2019. Patients were divided into those who received antivenom and those who did not receive antivenom. Every patient who received antivenom between 2015 and 2019 was included in the study.

For the patient group who did not receive antivenom treatment, Grays’ systematic sampling strategy was used where every third chronological patient was included in the study [26]. Patients who were admitted to the clinic during the period from September 1st 2016 until December 31th 2016 were excluded from the analysis in order to exclude possible bias, since there was no antivenom available during this period. Patients who received antivenom were categorized based on the different antivenoms that were used during the research period: Fav-Afrique, VacSera, and EchiTAb-PLUS-ICP. Since there was only one patient during the research period who was treated with SAIMR antivenom, SAIMR antivenom was excluded from the analysis.

Treatment outcome and adverse event parameters

A patient was considered to have an adverse treatment outcome when the patient died, or has permanent physical damage or debilitation, for example, the amputation of a limb, or organ failure, or if the patient experienced an adverse treatment reaction, defined as an acute (anaphylactic or pyrogenic) reaction to antivenom presenting symptoms such as rash, itching, nausea, headache, fever, wheezing, body aches, hypotension, cyanosis, and altered level of consciousness, which develop up to one hour during or after the administration of antivenom [27]. All other patients were considered to have an uncomplicated outcome. Patients were classified into the two outcome groups using routinely collected data as described below.

Data collection and analysis

Routinely collected data were extracted from MSF standard snakebite patient forms (S1 Form) and corresponding patient files kept at the Abdurafi field hospital. Patients admitted to the field hospital were monitored until they were discharged. Anonymized data were digitalized and analyzed using IBM SPSS Statistics 23 and Stata 15 (StataCorp. 2017. Stata Statistical Software: Release 15. College Station, TX: StataCorp LLC). Epidemiological characteristics and outcomes were investigated using the following variables: age, gender, time between snakebite and admission to hospital, bite site, location, context of the bite, snake species, type of envenomation, number of antivenom vials received, time between admission and administration of antivenom, time between antivenom administration and restored blood coagulation, adverse reactions to antivenom, signs of severe envenomation, duration of hospitalization and whether the patient survived. Continuous variables were summarized using the median and interquartile range (IQR). Categorical and dichotomous variables are summarized using the number of patients (n) and percentages. Chi-squared tests (or Fisher’s exact tests if any frequency was <5) for categorical variables and Kruskal-Wallis tests for continuous variables were used to compare the differences between groups (alpha = 0.05). Odds ratios for adverse compared with uncomplicated outcomes among patients receiving different types of antivenom were estimated using logistic regression, adjusted for age, sex and time from bite to admission (as a priori confounders) and other variables with complete data and associated with antivenom type and adverse outcome (alpha = 0.10) and not considered to be on a causal pathway.

Results

The frequency of reported snakebites in the Abdurafi field hospital from 2015 to 2019 shows a seasonal pattern (Fig 1), peaking between June and November, which coincides with the agricultural season and presence of migrant workers. The number of admissions during 2016 was less than during 2015 due to a long rupture period of supply of antivenom in the hospital during the 2016 peak season after the expiry of Fav-Afrique. The annual drop in cases presenting in September is associated with the Ethiopian New Year (Enkutatash) when many migrant workers go back to their families for the celebrations. Overall, there is a clear increasing trend over the years in the total number of snakebite patients admitting to the field hospital. In 2015 this total was 330, in 2016 the total dropped to 159 as mentioned. In 2017 322 patients admitted to the clinic, in 2018 this doubled to 647 patients and in 2019 there was a total of 1,431 patients admitted to the clinic. During the period that Fav-Afrique was available (2015–2016) 32.9% of all snakebite admissions were treated with antivenom. This reduced to 27.6% during the VacSera period (2017–2018), and 20.5% during the EchiTAb-PLUS-ICP period (2018–2019).

Fig 1. Monthly snakebite admission to Abdurafi field hospital, 2015–2019.

Fig 1

Out of the 2,889 snakebite patients admitted in Abdurafi between 2015 and 2019, 781 patients were included in the study of which 149 in the Fav-Afrique group, 164 in the VacSera group, 156 in the EchiTAb-PLUS-ICP group, and 312 in the no-antivenom group. The characteristics of the patients and bites are presented in Table 1. The median ages of the different groups were between 24–26 years old (range 1–74 years) and 85 to 90 percent of the patients in the different antivenom groups were male. The median time between bite and admission was 10 hours, 7.4 hours, 7.7 hours, and 7 hours for the Fav-Afrique group, VacSera group, EchiTAb-PLUS-ICP group, and no-antivenom group respectively. In each group, most of the patients were bitten in the foot or leg (54–79%) and most bites occurred on the field (44–65%) while working (37–60%). Within each group, most victims did not know which snake had caused the bite, but most patients showed both cytotoxic and haematotoxic symptoms (57–99%). Patients in the no-antivenom group showed symptoms of envenoming as well, but only in mild forms: only local swelling and no signs of active bleeding. As shown in Table 2, the median time between admission to the clinic and the administration of antivenom for Fav-Afrique was 1.5 hours. For VacSera this time was 6 hours and for EchiTAb-PLUS-ICP this was almost 9 hours. The highest rate of adverse antivenom reactions occurred within the group of patients treated with VacSera (18.3% vs. 1.3% and 7.1% for patients treated with Fav-Afrique and EchiTAb-PLUS-ICP respectively). Also, patients treated with VacSera developed more signs of severe envenomation (22.0%) compared to Fav-Afrique (16.1%) and EchiTAb-PLUS-ICP (2.6%). In total, 63 patients experienced intense pain (requiring management with analgesics stronger than paracetamol), 61 patients experienced extensive internal or external bleeding (bleeding not only from the bite site but also from other sites of the body), 46 patients experienced intense swelling (swelling extending beyond one joint) and 29 patients experienced fever/infection. These were the main signs of severe envenomation during the treatment. There were no amputations recorded in the database in any treatment group. In this population, uncomplicated outcomes were observed less frequently for VacSera (74.4%) than for Fav-Afrique (93.2%) and EchiTAb-PLUS-ICP (90.4%). The mortality rate was highest in the group treated with VacSera (4.9%) compared to 1.9% and 1.3% in the EchiTAb-PLUS-ICP group and the Fav-Afrique group. In patients who did not receive antivenom 1.6% experienced an adverse outcome, but no deaths.

Table 1. Characteristics of snakebite patients admitted to Abdurafi field hospital between 2015 and 2019.

Fav-Afrique (n = 149) VacSera (n = 164) EchiTAb-PLUS-ICP (n = 156) No antivenom (n = 312)
Age (years) 24 (20–30) 24 (20–30) 26 (20–35) 24 (20–30)
Gender (m) n (%) 137 (91.9) 147 (89.6) 132 (84.6) 275 (88.1)
Bite site n (%)
    Foot 65 (43.6) 109 (66.5) 119 (76.3) 158 (50.6)
    Leg 16 (10.7) 10 (6.1) 4 (2.6) 29 (9.3)
    Hand 54 (36.2) 42 (25.6) 27 (17.3) 103 (33.0)
    Arm 7 (4.7) 0 (0.0) 0 (0.0) 9 (2.9)
    Other 7 (4.7) 3 (1.8) 6 (3.8) 13 (4.2)
Location of bite n (%)
    Field 66 (44.3) 97 (59.1) 101 (64.7) 180 (57.7)
    Compound 4 (2.7) 14 (8.5) 16 (10.3) 19 (6.1)
    Indoors 3 (2.0) 12 (7.3) 3 (1.9) 18 (5.8)
    Road 3 (2.0) 8 (4.9) 27 (17.3) 8 (2.6)
    Missing 73 (49.0) 33 (20.1) 9 (5.8) 87 (27.9)
Context of bite n (%)
    Working 55 (36.9) 98 (59.8) 74 (47.4) 168 (53.8)
    Walking 7 (4.7) 37 (22.6) 47 (30.1) 46 (14.7)
    Sleeping 12 (8.1) 11 (6.7) 21 (13.5) 26 (8.3)
    Playing 3 (2.0) 12 (7.3) 8 (5.1) 8 (2.6)
    Other 1 (0.7) 1 (0.6) 2 (1.3) 2 (0.6)
    Missing 71 (47.7) 5 (3.0) 4 (2.6) 62 (19.9)
Suspected snake species n (%)
    Echis 5 (3.4) 83 (50.6) 53 (34.0) 105 (33.7)
    Bitis 0 (0.0) 2 (1.2) 34 (21.8) 3 (1.0)
    Dendroaspis 1 (0.7) 8 (4.9) 0 (0.0) 6 (1.9)
    Other 0 (0.0) 3 (1.8) 7 (4.5) 28 (9.0)
    Unknown 26 (17.4) 60 (36.6) 60 (38.5) 102 (32.7)
    Missing 117 (78.5) 8 (4.9) 2 (1.3) 68 (21.8)
Type of envenomation n (%)
    Cytotoxic 2 (1.3) 17 (10.4) 51 (32.7) 113 (36.2)
    Haematotoxic 0 (0.0) 14 (8.5) 15 (9.6) 6 (1.9)
    Cytotoxic + haematotoxic 142 (95.3) 132 (80.5) 80 (51.3) 192 (61.5)
    Cytotoxic+ neurotoxic 0 (0.0) 0 (0.0) 5 (3.2) 0 (0.0)
    Cytotoxic + haematotoxic + neurotoxic 5 (3.4) 1 (0.6) 5 (3.2) 1 (0.3)

Table 2. Treatment and outcomes of snakebite patients admitted to Abdurafi field hospital between 2015 and 2019.

Fav-Afrique (n = 149) VacSera (n = 164) EchiTAb-PLUS-ICP (n = 156) No antivenom (n = 312) P-value*
Time from bite until admission in hours (IQR) 10.0 (3.9–21.0) 7.4 (3.8–21.0) 7.7 (3.8–18.7) 7.0 (4.0–17.0) 0.519
Time from admission to AV administration in hours (IQR) 1.5 (0.5–11.3), n = 54 6.0 (0.3–23.3), n = 131 8.8 (0.0–24.4), n = 136 - 0.319
Total time from bite to AV administration in hours (IQR) 18.4 (10.3–37.9), n = 54 25.0 (13.0–43.0), n = 131 22.2 (12.5–48.9), n = 136 - 0.284
Number vials of AV administered 2 (2–6)** 4 (4–22)*** 3 (3–9)** - <0.001
Time until blood clotting restoration in days (IQR) 2 (1–3) 2 (1–3) 1 (0–2) 1 (1–2) 0.066
Severe envenomation n (%) 24 (16.1) 36 (22.0) 4 (2.6) 17 (5.4) <0.001
Hospital duration in days (IQR) 4 (3–5) 4 (3–6) 4 (3–6) 2 (1–3) <0.001
Outcome n (%)
    Uncomplicated 138 (93.2) 122 (74.4) 141 (90.4) 299 (98.4)
    Antivenom reaction 2 (1.3) 30 (18.3) 11 (7.1) -
    Referred 6 (4.0) 9 (5.5) 1 (0.6) 5 (1.6)
    Died 2 (1.3) 8 (4.9) 3 (1.9) 0 (0.0) <0.001
Adverse outcome 10 (6.8) 42 (25.6) 15 (9.6) 5 (1.6) <0.001
Discharge against advice 1 (0.7) 0 (0.0) 0 (0.0) 8 (2.6)

* Chi-squared tests (or Fisher’s exact tests if any frequency was <5) for categorical variables and Kruskal-Wallis tests for continuous variables. Data complete for each variable in each group unless otherwise indicated

**Presenting the range instead of IQR, missing for 100/156 patients who received EchiTAb-PLUS-ICP.

Abbreviations: AV = Antivenom; IQR = Inter Quartile Range.

Among patients who received antivenom, those treated with VacSera or EchiTAb-PLUS-ICP had almost 6-fold and 3-fold odds respectively of experiencing an adverse outcome compared with those who received Fav-Afrique after adjusting for age, sex, signs of severe envenomation, body part bitten, heart rate and temperature on admission, and time from bite until admission (Table 3).

Table 3. Odds of adverse outcome in snakebite patients treated with different antivenoms at Abdurafi field hospital between 2015 and 2019.

Antivenom n Adverse outcome (%) Odds ratio (95% CI) p-value Adjusted odds ratio*** (95% CI) p-value
Fav-Afrique 148* 10 (6.8%) 1.00 (reference)
VacSera 164 42 (25.6%) 4.72 (2.27–9.80) <0.001 6.16 (2.64–14.4) <0.001
EchiTAb-PLUS-ICP 155** 15 (9.6%) 1.47 (0.64–3.38) 0.367 3.16 (1.12–8.00) 0.029

* excluding one patient who defaulted treatment (discharged against medical advice)

** excluding one patient who had missing data for heart rate

*** adjusted for age, sex, and time from bite until admission (a priori) and signs of severe envenomation, body part bitten, heart rate and temperature on admission (associated with outcome and antivenom)

The negative confounding of the effects of the different antivenoms observed in the multivariable model was cumulative and not attributable to any particular covariate. Of these, only severe envenomation was associated with odds of adverse outcome (odds ratio = 8.84, 95% CI 4.38–17.8). Complete data were available for all N = 466 patients. The model did not adjust for time from admission to administration of antivenom because these data were missing for 167/468 patients. Odds ratios for treatment reactions and death by antivenom type are shown in Table 4. VacSera and EchiTAb-PLUS-ICP were associated with 16- and 6-fold odds of treatment reaction, respectively, and VacSera was weakly associated with higher odds of death. However, all estimates were imprecise (very wide confidence intervals) because of the small numbers of patients experiencing these specific outcomes.

Table 4. Odds of treatment reaction and death in snakebite patients treated with different antivenoms at Abdurafi field hospital between 2015 and 2019.

Antivenom n Outcome (%) Odds ratio (95% CI) p-value Adjusted odds ratio** (95% CI) p-value
Treatment reaction
Fav-Afrique 148* 2 (1.4%) 1.00 (reference)
VacSera 164 30 (18.3%) 16.3 (3.83–69.7) <0.001 16.2 (3.79–69.2) <0.001
EchiTAb-PLUS-ICP 156 11 (7.1%) 5.54 (1.21–25.4) 0.028 5.78 (1.25–26.7) 0.024
Death
Fav-Afrique 148* 2 (1.4%) 1.00 (reference)
VacSera 164 8 (4.9%) 3.77 (0.79–18.0) 0.097 4.56 (0.90–23.0) 0.066
EchiTAb-PLUS-ICP 156 3 (1.9%) 1.44 (0.24–8.75) 0.691 1.16 (0.18–7.34) 0.871

* excluding one patient who defaulted treatment (discharged against medical advice)

** adjusted for age, sex, and time from bite until admission

Discussion

Over the past five years, much-needed information was gathered about the epidemiology of snakebites and the use of antivenoms in north-west Ethiopia. The results of this study show that over the years, there is an exponential growth of snakebite patients presenting at the MSF hospital since antivenom treatment was made available. This is a result of spreading awareness of treatment availability in Abdurafi among the migrant and resident population in the region, which led to an expanding catchment area. The improvement of communication networks, such as cell phone and internet services, and infrastructure (roads and vehicle availability) is also contributing to increased health-seeking behavior and improved access to Abdurafi MSF field hospital. But it also indicates massive underreporting of snakebites when comprehensive snakebite management is not available [28].

Monthly admissions to the hospital between 2015 and 2019 show a clear seasonal trend, with most patients admitted between June and November. These are the most labor-intensive months of the agricultural season when workers are in the fields for planting, weeding, and harvesting [22]. Protective means, like boots and gloves, are not made available, and would most likely have poor acceptability because of inconvenience due to the hot climate, with temperatures above 30°C. The significant relative decrease in patient numbers presenting in the period from July 2016 to January 2017 is associated with the expiry of Fav-Afrique antivenom in September 2016 and no suitable alternative antivenom being available until January 2017. This event demonstrated the quickly spreading awareness among the population that there was no antivenom available to treat snakebites anymore, leading to a change in the health-seeking behavior.

Most patients admitted to the hospital showed both cytotoxic and haematotoxic symptoms, which could indicate certain snake species being responsible for the bite, notably the Egyptian saw-scaled viper or Northeast African carpet viper (E. pyramidum) and puff adder (B. arietans). There were many patients who admitted to the hospital with both cytotoxic and haematotoxic symptoms who did not receive antivenom. In most of these cases, the envenomation was mild and no antivenom was required. Few patients admitted to the hospital with neurotoxic symptoms. However, the low number of patients presenting with neurotoxic symptoms does not necessarily indicate a low incidence of neurotoxic bites in the region. Because neurotoxic envenoming by elapids can cause respiratory paralysis and death within hours, patients may not have been able to access healthcare in time [29]. The presence of elapids (Egyptian cobra (N. haje) and black mamba (dendroaspis polylepis)) has been reported in the north-western Ethiopian lowlands [30]. In Table 1 there are six patients in the group who did not receive antivenom, who stated that they were bitten by a mamba. This is remarkable as these bites are typically very severe neurotoxic bites. An explanation might be that these were cases of misidentification of the snake species. This happens frequently, especially since many patients are bitten at night, which is also one of the reasons why it is difficult to identify the species of snakes in the area causing snakebites. To address this problem, a snake atlas was introduced in 2017 including pictures and descriptions of endemic venomous and non-venomous snakes to help patients identify the snake that bit them.

The results of this study are not representative for the whole of Ethiopia. Ethiopia has a wide topographical diversity, ranging from desert, savannah, grassland and tropical forests to alpine mountains. Therefore, the snake epidemiology in Ethiopia varies greatly between different regions [31]. However, the results are representative for the lowland savannah region in north-west Ethiopia.

The main signs of severe envenomation that occurred during the treatment were severe pain, extensive internal or external bleeding, severe swelling, and fever/infection of the bite site. However, in most cases, these severe manifestations can be attributed to the venom-induced syndrome. More severe complications such as massive hemorrhage, coma, respiratory distress, necrosis and organ failure were most frequent in the patient group which was treated with VacSera. Patients whose condition was very critical were referred to a tertiary hospital in Gondar.

We compared the occurrence of adverse outcomes according to the three different antivenoms used; Fav-Afrique, VacSera, and EchiTAb-PLUS-ICP. Fav-Afrique was found to be a safe and effective antivenom, which is in line with other authors’ findings [19], and the number of adverse reactions was lower than observed for VacSera and EchiTAb-PLUS-ICP.

VacSera had the highest rate of adverse reactions. This outcome corresponds with previous research by Larnyang, Salako & Alder et al., who found that VacSera caused adverse reactions in five out of six patients, and stated that VacSera did not fulfill the efficacy and safety criteria [28,32]. EchiTAb-PLUS-ICP showed to be safe due to the low rates of adverse reactions. This is in line with neutralization studies which have also demonstrated the safety and efficacy of EchiTAb-PLUS-ICP in African viperid envenoming [28,33]. However, more clinical trials evaluating the safety and effectiveness of the EchiTAb-PLUS-ICP antivenom need to be conducted to confirm these results [34,35].

Due to the low number of deaths it was not possible to compare the mortality rates between the antivenoms. There was no mortality in the group of patients who did not receive antivenom. This is explained by the fact that patients in the no-antivenom group by definition suffered from dry bites or mild envenoming. Patients treated with antivenom were more severely envenomed and therefore in need of antivenom. Out of 13 patients who died, 8 died within 48 hours after admission, indicating that these patients presented with severe envenoming syndrome on admission. Frequent signs and complications in the patients who died were organ failure, coma, hemorrhage and respiratory distress. Two patients who died experienced a shock after administration of VacSera antivenom.

The average time between bite and hospital admission decreased from 10 hours during the time that Fav-Afrique was available (2015–2016) to 7–8 hours in the later periods. This may reflect increased awareness among the communities and earlier presentation. However, in this study the time between the bite and admission to the hospital was not associated with odds of an adverse outcome of the treatment. This finding is contrary to previous studies which showed that delay in treatment is strongly associated with an adverse outcome of the treatment and that mortality is higher among patients who present late compared to patients who present within 24 hours after the bite [21,3640].

Interestingly, the median time between admission and antivenom administration increased over time from 1.5 hours in 2015–2016 to 8.8 hours during 2018–2019. However, in this study there was no association between the time between admission and the administration of antivenom and the development of an adverse outcome of the treatment. This could be explained by the improved clinical monitoring of envenoming effects and management of severe envenomation before administering antivenom. This may have resulted in reduced indications for antivenom treatment, without negatively impacting treatment outcome. This is reflected in the proportion of patients admitted that received treatment with antivenom, which decreased significantly over time, from 32.9% during the Fav-Afrique period (2015–2016) to 27.6% during the VacSera period (2017–2018) and 20.5% during the EchiTAb-PLUS-ICP period (2018–2019). Although there were no major changes in first aid care over the years, over time patients did present earlier due to community awareness. This allowed the healthcare workers at the clinic to take more time for patient observation and to decide whether the patient needed antivenom or not.

Other characteristics, such as bite site, the context of the bite, snake species responsible, and type of envenomation, were not association with adverse outcomes of the treatment. The fact that snake species had no effect could be explained by the fact that the antivenoms used are effective against the toxins of the specific snakes living in this certain geographical area. Snake species that are causing the greatest burden in this area are the Egyptian saw-scaled viper (E. pyramidum) and puff adder (B. arietans) [2]. The outcome of the treatment and the effectiveness of the antivenom can vary between different geographical areas as the venom composition can differ greatly within one certain snake species. These variations can introduce major medical implications to the treatment of snakebite victims. Also, depending on the snake species, different symptoms of envenoming can appear [41,42]. This is also the reason why it is important to know which species caused the envenoming since the antivenom might not be raised against the venom of certain snake species from that region. However, in all three groups of antivenom, there was a large proportion of patients who were not able to identify the type of snake species from the atlas.

Despite the production of Fav-Afrique antivenom was ceased by Sanofi-Pasteur in 2014, it remains a relevant product since MicroPharm (UK) announced its intention to relaunch the product after Sanofi-Pasteur signed an agreement to divest its antivenom immunoglobulin range to MicroPharm in December 2017 [43] Micropharm and Sanofi-Pasteur are currently working on the technology transfer.

Although antivenom affordability is a major factor in patient access to appropriate snakebite treatment, affordability was not an issue in this study. All antivenom treatment and supportive care and hospitalization were provided free of charge at the MSF clinic.

This is one of few studies on epidemiology of snakebites and treatment outcomes of various antivenoms in clinical practice in Ethiopia using a relatively large patient cohort. However, as this study is not a randomized controlled trial evaluating different antivenoms, it is important to acknowledge limitations. Firstly, since this is mainly a descriptive study, any comparisons between the antivenoms are indications since the antivenoms were used in different periods, introducing possible bias to the comparisons by differences in patient population or snakebite management practices over time. Although we adjusted for a priori and actual confounders, our estimates will still be subject to residual and unmeasured confounding. Similarly, although data were mostly complete for all variables in our final model, our analytical dataset represented a modest proportion of all patients treated during the study period.

Secondly, since this is a retrospective study with routinely collected data, there may have been factors that could have a possible influence on the outcome of the treatment which were not captured by the routine data collection. For example, in the data, there is no information about the consultation of traditional healers or the use of traditional remedies by the patients. Common traditional healing practices may include cutting, suction, tourniquets, black stones, local incisions, and herbal-based medicines which are put inside the wound or are taken orally by the patient [2]. For further research, it is recommended to include this in the data collection. While the use of traditional first aid may not directly predict an adverse outcome or mortality, some of these practices are harmful, and in addition cause a delay in seeking treatment, which could result in an increased occurrence of complications [2,4,21,36,37].

With the results of this research, a piece of the burden of snakebites in Ethiopia is revealed which shows that snakebites are a huge public health problem that deserves more attention. It gives an overview of the size of the problem in this part of Ethiopia and provides information necessary for improving access to antivenom treatment, and training of health staff on appropriate first aid and management of signs of severe envenoming and adverse reactions. Antivenom protocols can be adapted based on the information provided and snakebite management can be improved. Also, health promotion and advocacy among the communities at risk is essential to prevent snakebites, and to improve health-seeking behavior in the case of snakebites. However, in order to address the large public health problem caused by snake envenoming across Sub-Saharan Africa, further research is needed to determine the efficacy, safety, and regional specificity of existing antivenoms for Sub-Saharan Africa, linked with structural investments in sustained production and supply of antivenom.

Supporting information

S1 Table. Table of antivenoms.

(PDF)

S2 Table. Full analyses Table 3.

(PDF)

S3 Table. Full analyses Table 4.

(PDF)

S1 Form. Snakebite Patient Form.

(PDF)

Acknowledgments

We gratefully acknowledge the assistance of the Ethiopia Public Health Institute and the Federal Ministry of Health of Ethiopia. In addition, we wish to acknowledge the following individuals.

We would like to thank the nurses: Mekuanint Anagaw, Kasanesh Cherie, Umer Ibrahim, Woldegebriel, Teferi Molla, Taddelu Ajamu, Muluken Alemu, Molla Dessie, Fikremariam Yibabie, Tewodrose Dagnew and Eshetie Gobie, and the clinical officers: Leya Haileyesus and Seble Bihonegen who were working at the ward treating snakebite patients. They were able to provide us with valuable inside information on snakebite treatment and shared patient experiences. The PI would like to thank Gijs Hovenkamp for his continuous support during the writing of this manuscript.

Data Availability

MSF has a managed access system for data sharing that respects MSF’s legal and ethical obligations to its patients to collect, manage and protect their data responsibility. Ethical risks include, but are not limited to, the nature of MSF operations and target populations being such that data collected are often highly sensitive. Data are available on request in accordance with MSF’s data sharing policy (available at: http://fieldresearch.msf.org/msf/handle/10144/306501). Requests for access to data should be made to data.sharing@msf.org.

Funding Statement

The author(s) received no specific funding for this work. There were no extra costs involved.

References

  • 1.Kasturiratne A, Wickremasinghe AR, De Silva N, Gunawardena NK, Pathmeswaran A, Premaratna R, et al. The global burden of snakebite: A literature analysis and modelling based on regional estimates of envenoming and deaths. PLoS Med. 2008;5(11):1591–604. doi: 10.1371/journal.pmed.0050218 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 2.Birhanu Hurisa AMA. Epidemiological Survey of Snake Bite in Ethiopia. Epidemiol Open Access. 2014;04(04). [Google Scholar]
  • 3.Potet J, Smith J, McIver L. Reviewing evidence of the clinical effectiveness of commercially available antivenoms in sub-saharan africa identifies the need for a multi-centre, multi-antivenom clinical trial. PLoS Negl Trop Dis. 2019;13(6). doi: 10.1371/journal.pntd.0007551 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 4.Chippaux JP. Snakebite envenomation turns again into a neglected tropical disease! J Venom Anim Toxins Incl Trop Dis. 2017;23(1). doi: 10.1186/s40409-017-0127-6 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 5.Lancet The. Snake-bite envenoming: a priority neglected tropical disease. Lancet. 2017. Jul 1;390(10089):2. doi: 10.1016/S0140-6736(17)31751-8 [DOI] [PubMed] [Google Scholar]
  • 6.Ruha AM, Kleinschmidt KC, Greene S, Spyres MB, Brent J, Wax P, et al. The Epidemiology, Clinical Course, and Management of Snakebites in the North American Snakebite Registry. J Med Toxicol. 2017;13(4):309–20. doi: 10.1007/s13181-017-0633-5 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 7.de Silva HJ, Kasturiratne A, Pathmeswaran A, Lalloo DG. Snakebite: the true disease burden has yet to be determined. Ceylon Med J. 2013;58(3):93–5. doi: 10.4038/cmj.v58i3.6101 [DOI] [PubMed] [Google Scholar]
  • 8.Chippaux JP. Estimate of the burden of snakebites in sub-Saharan Africa: A meta-analytic approach. Toxicon. 2011;57(4):586–99. doi: 10.1016/j.toxicon.2010.12.022 [DOI] [PubMed] [Google Scholar]
  • 9.Chippaux J-P. Snake-bites: appraisal of the global situation. Bull World Heal Organ. 1998;76(5):515–24. [PMC free article] [PubMed] [Google Scholar]
  • 10.Warrell DA. Snake bite [Internet]. Vol. 375, The Lancet. 2010. [DOI] [PubMed] [Google Scholar]
  • 11.Bagcchi S. Experts call for snakebite to be re-established as a neglected tropical disease. BMJ. 2015. Oct 5;351:h5313. doi: 10.1136/bmj.h5313 [DOI] [PubMed] [Google Scholar]
  • 12.Chippaux J-P. Estimating the Global Burden of Snakebite Can Help To Improve Management Lack of Antivenom: A Market Failure. PLoS Med | www.plosmedicine.org. 2008;5(11):221. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 13.Warrell DA. Unscrupulous marketing of snake bite antivenoms in Africa and Papua New Guinea: choosing the right product-’What’s in a name?’. Trans R Soc Trop Med Hyg. 2008;102(5):397–9. doi: 10.1016/j.trstmh.2007.12.005 [DOI] [PubMed] [Google Scholar]
  • 14.Brown NI. Consequences of neglect: Analysis of the sub-saharan african snake antivenom market and the global context. PLoS Negl Trop Dis. 2012;6(6). doi: 10.1371/journal.pntd.0001670 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 15.Williams DJ, Habib AG, Warrell DA. Clinical studies of the effectiveness and safety of antivenoms. Toxicon. 2018;150:1–10. doi: 10.1016/j.toxicon.2018.05.001 [DOI] [PubMed] [Google Scholar]
  • 16.Yirgu A, Chippaux JP. Ethnomedicinal plants used for snakebite treatments in Ethiopia: A comprehensive overview. J Venom Anim Toxins Incl Trop Dis. 2019;25:20190017. doi: 10.1590/1678-9199-JVATITD-2019-0017 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 17.Schicker RS, Hiruy N, Melak B, Gelaye W, Bezabih B, Stephenson R, et al. A venue-based survey of malaria, anemia and mobility patterns among migrant farm workers in amhara region, Ethiopia. PLoS One. 2015;10(11). doi: 10.1371/journal.pone.0143829 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 18.Argaw D, Mulugeta A, Herrero M, Nombela N, Teklu T, Tefera T, et al. Risk factors for visceral Leishmaniasis among residents and migrants in Kafta-Humera, Ethiopia. Ghedin E, editor. PLoS Negl Trop Dis. 2013. Nov 7;7(11):e2543. doi: 10.1371/journal.pntd.0002543 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 19.Alirol E, Lechevalier P, Zamatto F, Chappuis F, Alcoba G, Potet J. Antivenoms for Snakebite Envenoming: What Is in the Research Pipeline? PLoS Negl Trop Dis. 2015;9(9). doi: 10.1371/journal.pntd.0003896 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 20.Gouda A, Elnabarawy N, Badawy S. A study of snakebite envenomation cases admitted to egyptian national poisoning center. Acta Medica Int. 2017;4(2):34. [Google Scholar]
  • 21.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. May 1;102(5):445–50. doi: 10.1016/j.trstmh.2007.11.006 [DOI] [PubMed] [Google Scholar]
  • 22.Visser LE, Kyei-Faried S, Belcher DW. Protocol and monitoring to improve snake bite outcomes in rural Ghana. Trans R Soc Trop Med Hyg. 2004;98(5):278–83. doi: 10.1016/S0035-9203(03)00065-8 [DOI] [PubMed] [Google Scholar]
  • 23.Mise YF, Lira-da-Silva RM, Carvalho FM. Time to treatment and severity of snake envenoming in Brazil. Rev Panam Salud Publica/Pan Am J Public Heal. 2018;42. doi: 10.26633/RPSP.2018.52 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 24.Kalam Y, Isbister GK, Mirtschin P, Hodgson WC, Konstantakopoulos N. Validation of a cell-based assay to differentiate between the cytotoxic effects of elapid snake venoms. J Pharmacol Toxicol Methods. 2011;63(2):137–42. doi: 10.1016/j.vascn.2010.09.001 [DOI] [PubMed] [Google Scholar]
  • 25.Vyas VK, Brahmbhatt K, Bhatt H, Parmar U. Therapeutic potential of snake venom in cancer therapy: Current perspectives. Asian Pac J Trop Biomed. 2013;3(2):156–62. doi: 10.1016/S2221-1691(13)60042-8 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 26.Gray DE. Doing research in the real world. First edit. London: SAGE Publications; 2014. [Google Scholar]
  • 27.De Silva HA, Ryan NM, De Silva HJ. Adverse reactions to snake antivenom, and their prevention and treatment. Br J Clin Pharmacol. 2016;81(3):446–52. doi: 10.1111/bcp.12739 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 28.Habib AG. Public health aspects of snakebite care in West Africa: Perspectives from Nigeria [Internet]. Vol. 19, Journal of Venomous Animals and Toxins Including Tropical Diseases. 2013. doi: 10.1186/1678-9199-19-27 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 29.WHO Regional Office for Africa. Guidelines for the prevention and clinical management of snakebite in Africa. World Health Organization. Regional Office for Africa. 2010;1–145. [Google Scholar]
  • 30.WHO. Venomous snakes distribution and species risk categories [Internet]. Venomous snakes distribution and species risk categories. 2021. [Google Scholar]
  • 31.Largen MJ, Rasmussen MJ. Catalogue of the snakes of ethiopia (reptilia serpentes), including identification keys. Trop Zool. 1993;6(2):313–434. [Google Scholar]
  • 32.Abubakar SB, Abubakar IS, Habib AG, Nasidi A, Durfa N, Yusuf PO, et al. Pre-clinical and preliminary dose-finding and safety studies to identify candidate antivenoms for treatment of envenoming by saw-scaled or carpet vipers (Echis ocellatus) in northern Nigeria. Toxicon. 2010;55(4):719–23. doi: 10.1016/j.toxicon.2009.10.024 [DOI] [PubMed] [Google Scholar]
  • 33.Abubakar IS, Abubakar SB, Habib AG, Nasidi A, Durfa N, Yusuf PO, et al. Randomised controlled double-blind non-inferiority trial of two antivenoms for Saw-scaled or carpet viper (Echis ocellatus) envenoming in Nigeria. PLoS Negl Trop Dis. 2010;4(7). doi: 10.1371/journal.pntd.0000767 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 34.Petras D, Sanz L, Segura Á, Herrera M, Villalta M, Solano D, et al. Snake venomics of African spitting cobras: Toxin composition and assessment of congeneric cross-reactivity of the Pan-African EchiTAb-Plus-ICP antivenom by antivenomics and neutralization approaches. J Proteome Res. 2011;10(3):1266–80. doi: 10.1021/pr101040f [DOI] [PubMed] [Google Scholar]
  • 35.Gutiérrez JM, Williams D, Fan HW, Warrell DA. Snakebite envenoming from a global perspective: Towards an integrated approach. Toxicon. 2010;56(7):1223–35. doi: 10.1016/j.toxicon.2009.11.020 [DOI] [PubMed] [Google Scholar]
  • 36.Iliyasu G, Tiamiyu AB, Daiyab FM, Tambuwal SH, Habib ZG, Habib AG. Effect of distance and delay in access to care on outcome of snakebite in rural north-eastern Nigeria. Rural Remote Health. 2015;15(4):1–6. [PubMed] [Google Scholar]
  • 37.Habib AG, Abubakar SB. Factors affecting snakebite mortality in north-eastern Nigeria. Int Health. 2011;3(1):50–5. doi: 10.1016/j.inhe.2010.08.001 [DOI] [PubMed] [Google Scholar]
  • 38.Ogunfowokan O. Bite-to-hospital time and morbidity in victims of viper bite in a rural hospital in Nigeria. African J Prim Heal Care Fam Med. 2012;4(1). [PubMed] [Google Scholar]
  • 39.Narvencar K. Correlation between timing of ASV administration and complications in snake bites. J Assoc Physicians India. 2006;54(SEP.):717–9. [PubMed] [Google Scholar]
  • 40.David S, Matathia S, Christopher S. Mortality Predictors of Snake Bite Envenomation in Southern India-A Ten-Year Retrospective Audit of 533 Patients. J Med Toxicol. 2012;8(2):118–23. doi: 10.1007/s13181-011-0204-0 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 41.Alirol E, Sharma SK, Bawaskar HS, Kuch U, Chappuis F. Snake bite in south asia: A review. de Silva J, editor. PLoS Negl Trop Dis. 2010. Jan 26;4(1):e603. doi: 10.1371/journal.pntd.0000603 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 42.Sharma SK, Kuch U, Höde P, Bruhse L, Pandey DP, Ghimire A, et al. Use of Molecular Diagnostic Tools for the Identification of Species Responsible for Snakebite in Nepal: A Pilot Study. de Silva HJ, editor. PLoS Negl Trop Dis. 2016. Apr 22;10(4):e0004620. doi: 10.1371/journal.pntd.0004620 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 43.Sanofi. NOTICE OF MEETING 2018 [Internet]. Paris; 2018.
PLoS Negl Trop Dis. doi: 10.1371/journal.pntd.0010148.r001

Decision Letter 0

Janaka de Silva, Stuart Robert Ainsworth

27 Jul 2021

Dear Dr Steegemans,

Thank you very much for submitting your manuscript "Epidemiology, treatment outcomes and antivenom effectiveness in snakebite patients in north-west Ethiopia – a retrospective analysis." for consideration at PLOS Neglected Tropical Diseases. As with all papers reviewed by the journal, your manuscript was reviewed by members of the editorial board and by several independent reviewers. In light of the reviews (below this email), we would like to invite the resubmission of a significantly-revised version that takes into account the reviewers' comments.

In particular, two reviewers have noted concerns about the statistical analysis/presentation of the results and multiple inconsistencies were noted in results tables.

We cannot make any decision about publication until we have seen the revised manuscript and your response to the reviewers' comments. Your revised manuscript is also likely to be sent to reviewers for further evaluation.

When you are ready to resubmit, please upload the following:

[1] A letter containing a detailed list of your responses to the review comments and a description of the changes you have made in the manuscript. Please note while forming your response, if your article is accepted, you may have the opportunity to make the peer review history publicly available. The record will include editor decision letters (with reviews) and your responses to reviewer comments. If eligible, we will contact you to opt in or out.

[2] Two versions of the revised manuscript: one with either highlights or tracked changes denoting where the text has been changed; the other a clean version (uploaded as the manuscript file).

Important additional instructions are given below your reviewer comments.

Please prepare and submit your revised manuscript within 60 days. If you anticipate any delay, please let us know the expected resubmission date by replying to this email. Please note that revised manuscripts received after the 60-day due date may require evaluation and peer review similar to newly submitted manuscripts.

Thank you again for your submission. We hope that our editorial process has been constructive so far, and we welcome your feedback at any time. Please don't hesitate to contact us if you have any questions or comments.

Sincerely,

Stuart Robert Ainsworth

Associate Editor

PLOS Neglected Tropical Diseases

Janaka de Silva

Deputy Editor

PLOS Neglected Tropical Diseases

***********************

Reviewer's Responses to Questions

Key Review Criteria Required for Acceptance?

As you describe the new analyses required for acceptance, please consider the following:

Methods

-Are the objectives of the study clearly articulated with a clear testable hypothesis stated?

-Is the study design appropriate to address the stated objectives?

-Is the population clearly described and appropriate for the hypothesis being tested?

-Is the sample size sufficient to ensure adequate power to address the hypothesis being tested?

-Were correct statistical analysis used to support conclusions?

-Are there concerns about ethical or regulatory requirements being met?

Reviewer #1: (No Response)

Reviewer #2: The objectives of the study were clearly stated. The study was appropriately designed to address the stated objectives and the study population was clearly described and appropriate to to test the hypothesis. Correct statistical analysis were used to arrived at the conclusion. All the ethical and regulatory requirement were met.

Reviewer #3: The objectives and study design are articulated and appropriate statistics used for analysis. Ethics approval in place.

That said the following needs attention:

1. The data collection tool needs to be provided - perhaps as a supplementary table

2. Patient inclusion/exclusion criteria need to be carefully described

3. the SAVP product - SAIMR poly is described in the introduction as being used by MSF in this hospital but is not included in the analysis - an explanation for this exlucsion is needed

4. A table describing the antivenoms used is needed (akin to that used by the Potet et al review of antivenoms) particularly with regards the venoms used for manufacture - as a supplementary table

--------------------

Results

-Does the analysis presented match the analysis plan?

-Are the results clearly and completely presented?

-Are the figures (Tables, Images) of sufficient quality for clarity?

Reviewer #1: (No Response)

Reviewer #2: The analysis presented matched the analysis plan, and the results were clearly and completely presented. The tables and figures were of sufficient quality and clarity.

Reviewer #3: This is a very important paper that makes several important points about snakebite management in sub-Saharan Africa but it requires careful editing to maximise its impact. The grammar, spelling and phrasing needs attention:

1. the name of the ICP antivenom is EchiTAb-PLUS-ICP - correct this throughout.

2. antivenoms are often described as 'incorrect' or 'wrong' - please correct this inadequate description throughout and make it understandable to a non-snakebite audience - using a reference to the 'antivenoms' table suggested elsewhere in this review.

I have the following questions regarding data management and results presentation:

3. I'm not a statistician but isn't a probability of 0.000 meaningless? Should it be p<0.005?

4. much of the data/analysis is upon 'complications' but this term is inadequately defined - the methods section would benefit from a section defining this, and subsequent analyses.

5. Table 7 focuses upon 'complications' but includes only 1 distinct analysis criteria from those in Table 6, which focuses upon Rx outcomes - why is this duplication needed?

6. And why are the figures for many of these identical criteria different in Tables 6 and 7?

7. In fact- please review both these Tables VERY carefully - because Table 6 (Rx outcome analysis) has a 'complications' analysis criteria but not a 'poor outcome' criteria, whereas Table 7 (Rx complications analysis) does NOT have a 'complications' analysis criteria. Please fix this major confusion and remove duplicated data (that are numerically inconsistent between the tables).

8. The bar charts for Figure 1 should be in colour to enable greater clarity of the change in annual admission rates - this is an important part of the study's finding and deserves greater clarity

--------------------

Conclusions

-Are the conclusions supported by the data presented?

-Are the limitations of analysis clearly described?

-Do the authors discuss how these data can be helpful to advance our understanding of the topic under study?

-Is public health relevance addressed?

Reviewer #1: (No Response)

Reviewer #2: The conclusions were supported by the data presented. The manuscript and the data presented are elaborate and help in advancing the understanding of the subject matter. The public health relevance has been addressed.

Reviewer #3: The conclusions are supported by the data analysis, with the exception that assigning snake species to hospital admissions (Table 1) is not supported by identification methods. If the authors want to include this (which I suggest they don't because it weakens the study's accuracy - see very speculative assumptions Abstract line 48/9), this entry should read 'Suspected snake species responsible for admission'). In this context - please be more careful using snake species names - the saw-scaled vipers in Egypt are either Echis coloratus or E. pyramidum - only the later is present in Ethiopia. It is correctly termed the North East African saw-scaled viper.

Antivenom affordability is correctly described as a major issue in snakebite management - but is not analysed here. Can this data and analysis be included here, especially in terms of patient admission, outcome and adverse effects?

The higher rate of complications when using FavAfrique (line 349) deserves a much more comprehensive discussion - and was lower than Vacsera (Table 7).

Cite ref 35 for high adverse effects of the Vacsera product.

Paragraph starting line 304. The NE Nigeria snakebite-research team led by Prof Habib has also noted that admission rates increase when availability of antivenom becomes known in communities - I suggest you seriously consider citing ref 39 here (or other papers by this research team) to emphasise that this aspect of health seeking behaviour is evident in different settings. Its an important point to improve snakebite management.

I have made several critical comments but only in an attempt to improve the impact and uptake of this very important paper that delivers many important points - that hopefully will receive attention and action from appropriate national, regional and international agencies.

--------------------

Editorial and Data Presentation Modifications?

Use this section for editorial suggestions as well as relatively minor modifications of existing data that would enhance clarity. If the only modifications needed are minor and/or editorial, you may wish to recommend “Minor Revision” or “Accept”.

Reviewer #1: (No Response)

Reviewer #2: The authors looked at the effectiveness of 3 different antivenoms that were used at different periods on outcome of snakebite envenoming. Differences in time between admission and antivenom administration were reported across the three groups, however, it was not shown if this difference is statistically significant. This is relevant because time delay between hospital admission and antivenom administration negatively affect outcome. The authors need to address this and provide information on how the confounder effect was addressed.

Reviewer #3: Please review the grammar, spelling and phrasing throughout.

In addition to the many points already made:

Line 131 - SAIMR is manufactured with, and effective against, venoms from many Bitis vipers, including puff adders

I really dislike the inclusion of several non-authorative, non peer-reviewed, internet references in the list of citations. This seems lazy referencing to me - especially refs 10, 15. There exist several other, peer-reviewed papers that make the points that the authors seek to support their themes.

--------------------

Summary and General Comments

Use this section to provide overall comments, discuss strengths/weaknesses of the study, novelty, significance, general execution and scholarship. You may also include additional comments for the author, including concerns about dual publication, research ethics, or publication ethics. If requesting major revision, please articulate the new experiments that are needed.

Reviewer #1: Thank you for the opportunity to review “Epidemiology, treatment outcomes and antivenom effectiveness in snakebite patients in north-west Ethiopia – a retrospective analysis”. This is an important topic in an understudied area, and I think this paper will make a good addition to the literature. Although I think it’s quite interesting, I do have some problems with the statistics and feel revisiting this section with different tools would make these results more useful for clinicians and policy makers.

Major comments:

Using Pearsons correlation is an unusual test to compare independent variables and your outcome of treatment (poor/ recovered). Pearsons works for normally distributed variables, and isn’t a great choice for binary outcomes; are you sure the variables meet these conditions? The correlation coefficient you present in Table 6 is hard to interpret and thus not very useful. Because you have a limited number of outcomes, you don’t have much statistical power for multivariable modeling, but I would recommend instead presenting the results from a logistic regression to show the associations between patient characteristics and outcome (i.e. one variable at a time). Presenting this as an odds ratio (or prevalence ratio, which is preferred though perhaps less common) with the 95% CI (and perhaps p value if you wish) will give the reader more informative data on the magnitude, precision, and significance of the association between each set of variables. You may wish to consider a limited multivariable analysis (e.g., one predictor variable, controlling for antivenom type and maybe time/year?) but you have a limited number of outcomes, so this may not be feasible.

Regarding using ANOVA and your post-hoc tests, the post hoc tests use a selective component of the shared variance for all the groups taken from the overall F statistic. That said, the sample sizes in the groups are different, and Tukey-HSD test is for samples of the same size. You may wish to consult with your statistician, I think you probably should have used a Tukey-Kramer test.

Line 237: Can you say anything about the significance of differences across groups of patients? It looks like the FAV-Afrique patients took longer to come in to the hospital. Is this a ‘statistically significant’ difference that you may wish to control for, or are these means and medians not meaningfully different? Since you have so few outcomes as to make multivariable analysis quite limited, I would urge you to compare your populations (i.e., show a p value across groups) so the reader can be aware of where differences lie.

Table 3: I’d recommend showing the number and percent of persons with the outcome of interest, rather than the “mean” or proportion as is currently shown (i.e., first column shows total persons who received treatment, second column shows total number with positive outcome, third column shows the percentage XX.X% of persons with positive outcome). Same recommendation applies to Tables 4 and 5.

Minor comments:

When in 2015 did you begin providing antivenom (i.e., what month did you start administering Fav-Afrique)? It would be appreciated if you could make more precise your duration-of-use estimates in line 115-116. Could you also specify in this section of the Introduction: what was the standard of care prior to MSF’s arrival?

Line 162: Please describe a bit more about those who did not receive antivenom. Did all in this category demonstrate symptoms (Table 1 suggests this is the case)? Is there anyone in this category who should have received antivenom but did not for whatever reason? What about patients who come who do not exhibit symptoms (e.g., they were bitten, but the envenomation was mild/nonexistent) – were there any patients who really didn’t need much help at all, but were just worried? Does this category also draw on patients admitted during the gap after Fav-Afrique expired and no treatment was available? I would assume this would then bias the type of patient included as a comparison (they’d be more likely to be in high need of antivenom even though they could not get it)

You mention the SAIMR polyvalent antivenom in line 127, but this is not shown as one of the antivenoms used in lines 115-116. Please clarify, or add this antivenom. (edit: I see you mention this in line 166. I would recommend that you clarify that too few patients were treated with SAIMR to be included in the analysis in lines 115-6)

Table 2: what is “defaulted”? Is that lost to follow up/unknown? Could you edit this last variable to match your outcome as defined in the methods (i.e., “cured” vs. “poor” – but including death as one of the “poor” outcomes as that’s informative)

Minor grammatical issues throughout, e.g., Line 36+: “Since 2015 Médecins Sans Frontières is treating” could be changed to “Since 2015 Médecins Sans Frontières has been treating”; Line 70 (and same comment for line 71): “This study shows that patients treated with VacSera antivenom have a higher chance on a poor outcome” should be “have a higher chance of a poor outcome” Lines 260 and 267 “Tuckey” should be “Tukey”. These are mostly minor, as I did not see any grammatical issues that interfered with my ability to interpret your message.

Reviewer #2: Data on the effectiveness and safety of the many antivenoms available in Africa is sparse and this has a huge implication on the management of snakebite envenoming in the continent. The manuscript therefore, provides a vital information on this subject matter. However, the retrospective nature of the study is a weakness as some vital information were not captured. Nevertheless, the authors must be recommended by providing an insight on this important issue and pave a way for further prospective study.

Reviewer #3: As stated before, I think this is an important paper to our filed, whose findings need to be widely disseminated and acted upon.

I have made several critical comments but only in an attempt to improve the impact and uptake of this very important paper that delivers many important points - that hopefully will receive attention and action from appropriate national, regional and international agencies.

--------------------

PLOS authors have the option to publish the peer review history of their article (what does this mean?). If published, this will include your full peer review and any attached files.

If you choose “no”, your identity will remain anonymous but your review may still be made public.

Do you want your identity to be public for this peer review? For information about this choice, including consent withdrawal, please see our Privacy Policy.

Reviewer #1: Yes: Matt A Price

Reviewer #2: No

Reviewer #3: No

Figure Files:

While revising your submission, please upload your figure files to the Preflight Analysis and Conversion Engine (PACE) digital diagnostic tool, https://pacev2.apexcovantage.com. PACE helps ensure that figures meet PLOS requirements. To use PACE, you must first register as a user. Then, login and navigate to the UPLOAD tab, where you will find detailed instructions on how to use the tool. If you encounter any issues or have any questions when using PACE, please email us at figures@plos.org.

Data Requirements:

Please note that, as a condition of publication, PLOS' data policy requires that you make available all data used to draw the conclusions outlined in your manuscript. Data must be deposited in an appropriate repository, included within the body of the manuscript, or uploaded as supporting information. This includes all numerical values that were used to generate graphs, histograms etc.. For an example see here: http://www.plosbiology.org/article/info%3Adoi%2F10.1371%2Fjournal.pbio.1001908#s5.

Reproducibility:

To enhance the reproducibility of your results, we recommend that you deposit your laboratory protocols in protocols.io, where a protocol can be assigned its own identifier (DOI) such that it can be cited independently in the future. Additionally, PLOS ONE offers an option to publish peer-reviewed clinical study protocols. Read more information on sharing protocols at https://plos.org/protocols?utm_medium=editorial-email&utm_source=authorletters&utm_campaign=protocols

Attachment

Submitted filename: Reviewers comment plos NTD.docx

PLoS Negl Trop Dis. doi: 10.1371/journal.pntd.0010148.r003

Decision Letter 1

Janaka de Silva, Stuart Robert Ainsworth

1 Nov 2021

Dear Dr Steegemans,

Thank you very much for resubmitting your manuscript "Epidemiology, treatment outcomes and antivenom effectiveness in snakebite patients in north-west Ethiopia – a retrospective analysis." for consideration at PLOS Neglected Tropical Diseases. As with all papers reviewed by the journal, your manuscript was reviewed by members of the editorial board and by several independent reviewers. In light of the reviews (below this email), we would like to invite a further re-submission of a significantly-revised version that takes into account reviewer #2's comments.

We cannot make any decision about publication until we have seen the revised manuscript and your response to the reviewers' comments. Your revised manuscript is also likely to be sent to reviewers for further evaluation.

When you are ready to resubmit, please upload the following:

[1] A letter containing a detailed list of your responses to the review comments and a description of the changes you have made in the manuscript. Please note while forming your response, if your article is accepted, you may have the opportunity to make the peer review history publicly available. The record will include editor decision letters (with reviews) and your responses to reviewer comments. If eligible, we will contact you to opt in or out.

[2] Two versions of the revised manuscript: one with either highlights or tracked changes denoting where the text has been changed; the other a clean version (uploaded as the manuscript file).

Important additional instructions are given below your reviewer comments.

Please prepare and submit your revised manuscript within 60 days. If you anticipate any delay, please let us know the expected resubmission date by replying to this email. Please note that revised manuscripts received after the 60-day due date may require evaluation and peer review similar to newly submitted manuscripts.

Thank you again for your submission. We hope that our editorial process has been constructive so far, and we welcome your feedback at any time. Please don't hesitate to contact us if you have any questions or comments.

Sincerely,

Stuart Robert Ainsworth

Associate Editor

PLOS Neglected Tropical Diseases

Janaka de Silva

Deputy Editor

PLOS Neglected Tropical Diseases

***********************

Reviewer's Responses to Questions

Key Review Criteria Required for Acceptance?

As you describe the new analyses required for acceptance, please consider the following:

Methods

-Are the objectives of the study clearly articulated with a clear testable hypothesis stated?

-Is the study design appropriate to address the stated objectives?

-Is the population clearly described and appropriate for the hypothesis being tested?

-Is the sample size sufficient to ensure adequate power to address the hypothesis being tested?

-Were correct statistical analysis used to support conclusions?

-Are there concerns about ethical or regulatory requirements being met?

Reviewer #1: - yes

- yes

- yes

- yes

- yes

- no concerns

Reviewer #4: Aims could be more clear:

It is stated this study provides data on incidence - I don't think this is correct as there is no denominator data. The numbers presenting to hospital with snakebite is defined.

As this is a non-randomised study that aims to comapre safety and effectiveness of 3 antivenoms, much more needs to be done to adjust for baseline differences/confounders. The statistical analysis is basic and there is no adjustment for baseline differences between the groups.

There is insufficient information on how the outcomes were allocated as 'cured' vs 'poor outcome.' Was this a single person or two independent people? Was this person blinded to the treatment outcome? More information on how 'cured' was defined is needed: in particular, whether this was objective or open to interpretation.

--------------------

Results

-Does the analysis presented match the analysis plan?

-Are the results clearly and completely presented?

-Are the figures (Tables, Images) of sufficient quality for clarity?

Reviewer #1: - yes

- yes

- yes

Reviewer #4: As highlighted above, major changes are required in the analysis. Table 1 should list all confounders that may account for differences in treatment outcome: particularly any differences in severity of envenoming at baseline. Degree of swelling, proprortion with systemic bleeding, and proportion with abnormal 20WBCT at baseline are important.

If there are differences betweent the groups at baseline then either comparisons of the antivenoms should not be done, or adjustment for the baseline differences between the groups needs to be undertaken. Consider matching, or more advanced statistical techniques for adjusting for baseline differences. As this is a non-randomised study, it is highly vulnerable to bias and this needs to be made up for with carefully considered analysis. I would suggest seeking further support from an experienced statistician.

As this is retrospective, there must have been missing and innacurate data. This needs to be detailed.

I don’t think Spearman's Rho is the best analysis for Table 5. Multivariate logistic regression analysis would be preferrable. Reduce the number of predictor variables if there are issues with small numbers. Have missing data prevented undertaking multivariate logistic regression analysis?

--------------------

Conclusions

-Are the conclusions supported by the data presented?

-Are the limitations of analysis clearly described?

-Do the authors discuss how these data can be helpful to advance our understanding of the topic under study?

-Is public health relevance addressed?

Reviewer #1: - yes

- yes

- yes

- yes

Reviewer #4: This may change when the analysis is updated.

--------------------

Editorial and Data Presentation Modifications?

Use this section for editorial suggestions as well as relatively minor modifications of existing data that would enhance clarity. If the only modifications needed are minor and/or editorial, you may wish to recommend “Minor Revision” or “Accept”.

Reviewer #1: N/A

Reviewer #4: Suggest revising cited articles in first paragraph:

Reference 1 – avoid referencing opinion type articles for epidemiology. Consider Kasturiratne 2008.

Reference 3 seems incorrect for epidemiological statement?

--------------------

Summary and General Comments

Use this section to provide overall comments, discuss strengths/weaknesses of the study, novelty, significance, general execution and scholarship. You may also include additional comments for the author, including concerns about dual publication, research ethics, or publication ethics. If requesting major revision, please articulate the new experiments that are needed.

Reviewer #1: N/A

Reviewer #4: Overall this is an important and well written paper. The dataset is of a reasonable sample size and seems to be of good quality. Unfortunately I think the study cannot be published without making fairly major changes to the analysis. Non-randomsied studies such as this are highly vulnerable to bias and careful analysis is needed to overcome this. This could change the main finding of the paper. Comparing crude proportions with 'cure' vs 'poor outcome' can be misleading. Once this is done, the paper would be of high quality and would certainly be suitable for publications in PLOS NTD.

--------------------

PLOS authors have the option to publish the peer review history of their article (what does this mean?). If published, this will include your full peer review and any attached files.

If you choose “no”, your identity will remain anonymous but your review may still be made public.

Do you want your identity to be public for this peer review? For information about this choice, including consent withdrawal, please see our Privacy Policy.

Reviewer #1: Yes: Matt Price

Reviewer #4: Yes: Michael Abouyannis

Figure Files:

While revising your submission, please upload your figure files to the Preflight Analysis and Conversion Engine (PACE) digital diagnostic tool, https://pacev2.apexcovantage.com. PACE helps ensure that figures meet PLOS requirements. To use PACE, you must first register as a user. Then, login and navigate to the UPLOAD tab, where you will find detailed instructions on how to use the tool. If you encounter any issues or have any questions when using PACE, please email us at figures@plos.org.

Data Requirements:

Please note that, as a condition of publication, PLOS' data policy requires that you make available all data used to draw the conclusions outlined in your manuscript. Data must be deposited in an appropriate repository, included within the body of the manuscript, or uploaded as supporting information. This includes all numerical values that were used to generate graphs, histograms etc.. For an example see here: http://www.plosbiology.org/article/info%3Adoi%2F10.1371%2Fjournal.pbio.1001908#s5.

Reproducibility:

To enhance the reproducibility of your results, we recommend that you deposit your laboratory protocols in protocols.io, where a protocol can be assigned its own identifier (DOI) such that it can be cited independently in the future. Additionally, PLOS ONE offers an option to publish peer-reviewed clinical study protocols. Read more information on sharing protocols at https://plos.org/protocols?utm_medium=editorial-email&utm_source=authorletters&utm_campaign=protocols

PLoS Negl Trop Dis. doi: 10.1371/journal.pntd.0010148.r005

Decision Letter 2

Janaka de Silva, Stuart Robert Ainsworth

5 Jan 2022

Dear Dr Steegemans,

We are pleased to inform you that your manuscript 'Treatment outcomes among snakebite patients in north-west Ethiopia – a retrospective analysis.' has been provisionally accepted for publication in PLOS Neglected Tropical Diseases.

Before your manuscript can be formally accepted you will need to complete some formatting changes, which you will receive in a follow up email. A member of our team will be in touch with a set of requests.

Please note that your manuscript will not be scheduled for publication until you have made the required changes, so a swift response is appreciated.

IMPORTANT: The editorial review process is now complete. PLOS will only permit corrections to spelling, formatting or significant scientific errors from this point onwards. Requests for major changes, or any which affect the scientific understanding of your work, will cause delays to the publication date of your manuscript.

Should you, your institution's press office or the journal office choose to press release your paper, you will automatically be opted out of early publication. We ask that you notify us now if you or your institution is planning to press release the article. All press must be co-ordinated with PLOS.

Thank you again for supporting Open Access publishing; we are looking forward to publishing your work in PLOS Neglected Tropical Diseases.

Best regards,

Stuart Robert Ainsworth

Associate Editor

PLOS Neglected Tropical Diseases

Janaka de Silva

Deputy Editor

PLOS Neglected Tropical Diseases

***********************************************************

Reviewer's Responses to Questions

Key Review Criteria Required for Acceptance?

As you describe the new analyses required for acceptance, please consider the following:

Methods

-Are the objectives of the study clearly articulated with a clear testable hypothesis stated?

-Is the study design appropriate to address the stated objectives?

-Is the population clearly described and appropriate for the hypothesis being tested?

-Is the sample size sufficient to ensure adequate power to address the hypothesis being tested?

-Were correct statistical analysis used to support conclusions?

-Are there concerns about ethical or regulatory requirements being met?

Reviewer #4: Yes

**********

Results

-Does the analysis presented match the analysis plan?

-Are the results clearly and completely presented?

-Are the figures (Tables, Images) of sufficient quality for clarity?

Reviewer #4: Yes

**********

Conclusions

-Are the conclusions supported by the data presented?

-Are the limitations of analysis clearly described?

-Do the authors discuss how these data can be helpful to advance our understanding of the topic under study?

-Is public health relevance addressed?

Reviewer #4: Yes

**********

Editorial and Data Presentation Modifications?

Use this section for editorial suggestions as well as relatively minor modifications of existing data that would enhance clarity. If the only modifications needed are minor and/or editorial, you may wish to recommend “Minor Revision” or “Accept”.

Reviewer #4: Nil

**********

Summary and General Comments

Use this section to provide overall comments, discuss strengths/weaknesses of the study, novelty, significance, general execution and scholarship. You may also include additional comments for the author, including concerns about dual publication, research ethics, or publication ethics. If requesting major revision, please articulate the new experiments that are needed.

Reviewer #4: This is a well written and important study, which provides key insight into the burden of snakebite in this region of Ethiopia. I commend the authors for updating the analysis, which is greatly improved. The comparisons between the antivenom products are fair and valid, with the inherent limitations of non-randomized data clearly defined in the discussion.

My only minor reccomendation would be to include the full results of the univariate and multivariate logistic regression analyses that are summarized in Tables 3 and 4. The unadjusted +/- adjusted ORs and CIs for each covariate should be listed, as many readers will be interested in this. This can be as a supplementary table in the appendices.

With this minor addition, I would suggest this paper is accepted for publication.

**********

PLOS authors have the option to publish the peer review history of their article (what does this mean?). If published, this will include your full peer review and any attached files.

If you choose “no”, your identity will remain anonymous but your review may still be made public.

Do you want your identity to be public for this peer review? For information about this choice, including consent withdrawal, please see our Privacy Policy.

Reviewer #4: Yes: Michael Abouyannis

PLoS Negl Trop Dis. doi: 10.1371/journal.pntd.0010148.r006

Acceptance letter

Janaka de Silva, Stuart Robert Ainsworth

4 Feb 2022

Dear mrs Steegemans,

We are delighted to inform you that your manuscript, "Treatment outcomes among snakebite patients in north-west Ethiopia – a retrospective analysis," has been formally accepted for publication in PLOS Neglected Tropical Diseases.

We have now passed your article onto the PLOS Production Department who will complete the rest of the publication process. All authors will receive a confirmation email upon publication.

The corresponding author will soon be receiving a typeset proof for review, to ensure errors have not been introduced during production. Please review the PDF proof of your manuscript carefully, as this is the last chance to correct any scientific or type-setting errors. Please note that major changes, or those which affect the scientific understanding of the work, will likely cause delays to the publication date of your manuscript. Note: Proofs for Front Matter articles (Editorial, Viewpoint, Symposium, Review, etc...) are generated on a different schedule and may not be made available as quickly.

Soon after your final files are uploaded, the early version of your manuscript will be published online unless you opted out of this process. The date of the early version will be your article's publication date. The final article will be published to the same URL, and all versions of the paper will be accessible to readers.

Thank you again for supporting open-access publishing; we are looking forward to publishing your work in PLOS Neglected Tropical Diseases.

Best regards,

Shaden Kamhawi

co-Editor-in-Chief

PLOS Neglected Tropical Diseases

Paul Brindley

co-Editor-in-Chief

PLOS Neglected Tropical Diseases

Associated Data

    This section collects any data citations, data availability statements, or supplementary materials included in this article.

    Supplementary Materials

    S1 Table. Table of antivenoms.

    (PDF)

    S2 Table. Full analyses Table 3.

    (PDF)

    S3 Table. Full analyses Table 4.

    (PDF)

    S1 Form. Snakebite Patient Form.

    (PDF)

    Attachment

    Submitted filename: Reviewers comment plos NTD.docx

    Attachment

    Submitted filename: 20210924 Reponse Letter Snakebite research Ethiopia.pdf

    Attachment

    Submitted filename: 20211213 Response letter snakebite research Ethiopia.pdf

    Data Availability Statement

    MSF has a managed access system for data sharing that respects MSF’s legal and ethical obligations to its patients to collect, manage and protect their data responsibility. Ethical risks include, but are not limited to, the nature of MSF operations and target populations being such that data collected are often highly sensitive. Data are available on request in accordance with MSF’s data sharing policy (available at: http://fieldresearch.msf.org/msf/handle/10144/306501). Requests for access to data should be made to data.sharing@msf.org.


    Articles from PLoS Neglected Tropical Diseases are provided here courtesy of PLOS

    RESOURCES