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Journal of Venomous Animals and Toxins including Tropical Diseases

On-line version ISSN 1678-9199

J. Venom. Anim. Toxins incl. Trop. Dis vol.15 no.3 Botucatu  2009

http://dx.doi.org/10.1590/S1678-91992009000300009 

ORIGINAL PAPER

 

Appropriate antivenom doses for six types of envenomations caused by snakes in taiwan

 

 

Chieh-Fan CI; Tzeng-Jih LII; Wen-Chi HI; Hua-Wei YI

IDepartment of Emergency Medicine, Kaohsiung Municipal United Hospital, Kaohsiung, Taiwan
IIDepartment of Emergency Medicine, Kaohsiung Medical University, Chung-Ho Memorial Hospital, Kaohsiung, Taiwan

Correspondence to

 

 


ABSTRACT

Six of the 15 species of venomous snakes found in Taiwan are responsible for most of the clinically significant envenomations in the country. These species are: Trimeresurus mucrosquamatus, Trimeresurus stejnegeri, Naja atra, Bungarus multicinctus, Deinagkistrodon acutus and Daboia russelii siamensis, which together can be subdivided into three groups based on their venom effects. Primary treatment consists of rapid administration of appropriate antivenoms. The present study aimed to identify a proper dose of antivenom for each snake group as well as to describe hemorrhagic, neurotoxic, and mixed effects of their venoms. A retrospective chart review identified 72 snakebite cases referred to an emergency department. Data on epidemiology, examination findings, snake identification, treatment, antivenom dose and complications were collected. After excluding 14 patients, data from 58 victims were analyzed. Most studied cases were male (86%). Significantly higher doses of antivenom were administered against neurotoxic envenomations (mean dose: three vials) compared with the other two (p < 0.05). Moreover, patients affected by neurotoxic bites were more likely to develop blurred vision and other complications (p < 0.05). Multivariate logistic regression analysis indicated that neurotoxic envenomation was a risk factor for complications (OR: 8.84, 95% CI: 1.06-73.73). Neurotoxic envenomations and complication occurrence were positively correlated with antivenom dosage. In conclusion, patients affected by neurotoxic envenomations received higher doses of antivenom than others whereas incidence of complications was associated with higher antivenom doses.

Key words: antivenom, venomous snakes, snake envenomation, neurotoxic venom, hemorrhagic venom.


 

 

INTRODUCTION

Taiwan, located in the South Pacific, has a subtropical environment with more than 40 snake species; 15 of these are venomous snakes. Six of these 15 are responsible for most of the clinically significant snakebites (1). Two of these six species belong to the Elapidae family that includes cobra, coral and sea snakes, while the other four belong to the Viperidae family, vipers and adders.

These six species can be divided into three groups based on local or systemic clinical effects produced by their venoms, namely hemorrhagic, neurotoxic or mixed symptoms. The hemorrhagic venom causes disorders of the clotting cascade such as prolonged bleeding, primary fibrinolysis and disseminated intravascular coagulopathy (2, 3). Snakes that present hemorrhagic venom are Trimeresurus stejnegeri (Taiwan bamboo viper), Trimeresurus mucrosquamatus (turtle-designed snake) and Deinagkistrodon acutus.

The neurotoxic venom provokes respiratory distress from weakened respiratory muscles, blurred vision, diplopia, dysarthria, dysphagia, dysphonia and paralysis of extremity muscles (2, 4). Snakes that produce neurotoxic venom are Naja atra (Chinese common or Formosa Island cobra) and Bungarus multicinctus multicinctus (Taiwan banded krait).

The mixed envenomation manifests as a combination of neurotoxic and hemorrhagic effects previously described, as well as rhabdomyolysis and acute renal failure (5). Daboia russelii siamensis can inoculate this type of venom.

There are six snake species more involved in accidents with humans in Taiwan: Trimeresurus mucrosquamatus (32.9%), Trimeresurus stejnegeri (24.2%), Naja atra (12.1%), Bungarus multicinctus (10.1%), Deinagkistrodon acutus (3.9%) and Daboia russelii siamensis (1.6%) (1). There are four types of antivenoms available against these six more frequent snake envenomations, specifically: antivenom against T. stejnegeri and T. mucrosquamatus; antivenom against D. acutus; antivenom against N. atra and B. multicinctus multicinctus; and antivenom against D. russellii. The present study particularly compares three types of envenomations regarding dosages of antivenom and complications.

 

PATIENTS AND METHODS

Our medical center has a standard protocol for treatment of snakebite patients. A retrospective review was conducted based on records of the emergency department (ED) ranging from January 1993 to December 2002. Seventy-two patients who received medical treatment for snakebites were identified. Of them, 14 were unable to identify the snake species and were excluded. The following information of the remaining 58 patients was observed:

  • basic epidemiological characteristics including age, gender, the time of the bite, bitten area of the body, season when the bite occurred and clinical manifestations;
  • examination of  snakebite evidence (fang marks);
  • snake identification based on matching photographs, description, envenomation symptoms or the dead animal;
  • associated therapy including laboratory tests, antivenom administration, supportive care, debridement, respiratory support;
  • clinical outcomes.

This study was approved by the Institutional Review Board, Kaohsiung Medical University, protocol KMUH-IRB-960302.

Definitions

Each complication was defined according to associated venom effects. Complications consisted of tissue necrosis, compartment syndrome, coagulopathy, respiratory failure and acute renal failure. Coagulopathy and compartment syndrome were consequences of hemorrhagic venoms. Respiratory failure and tissue necrosis or fasciitis requiring debridement or fasciotomy were complications of neurotoxic venoms. Coagulopathy and acute renal failure resulted from mixed venoms.

Coagulopathy was defined as a prolonged prothrombin time (PT), activated partial thromboplastin time (aPTT) or thrombocytopenia.  Compartment syndrome comprised excessive pain with passive stretching, decreased sensation of pinprick or light touch, decreased discrimination of two points or necessity of fasciotomy. Measurement of intracompartmental pressure in affected limbs is required in an ideal situation; however, physical findings described above may substitute it in emergency circumstances. Acute renal failure was defined as a 50% decline in creatinine clearance or a 50% increase in serum creatinine from baseline. Acute respiratory failure was defined as arterial oxygen tension < 60 mmHg, arterial oxygen saturation < 90%, or arterial carbon dioxide tension > 45 to 55 mmHg.

Antivenom

Antivenoms employed in the treatment were produced by the Center for Disease Control, Department of Health, Taipei, Taiwan. Antivenoms were prepared by immunizing horses after snake envenomations. Each vial of antivenom contains over 1,000 Tanaka units (mean, 1200 TU). Each unit can neutralize one minimum lethal dose (MLD) of 12 to 14 g of mouse body weight (6). A skin test dose of 0.1 mL of a 1:100 solution was intradermally injected in the forearm of the patient. Epinephrine was available prior to test dose injection. Patients were given diphenhydramine and corticosteroids for evidence of allergic reaction. Before the administration, the antivenom was diluted in 300 to 500 mL of normal saline and infused over 30 to 60 minutes.

Statistical Analysis

The Kruskal-Wallis test was used for baseline comparisons of continuous variables, i.e., age and antivenom dosage. Chi-square and Fisher's exact tests were employed for analyses of categorical variables between risk factors and venomous types. Logistic and linear regression analyses were employed to establish a model for predicting the probability of complications and dosage of antivenom, respectively. SAS 9.0® (SAS Institute Inc., USA) was utilized to perform statistical analysis; p < 0.05 was significant.

 

RESULTS

Epidemiological and demographic characteristics of patients bitten by venomous snakes are presented in Table 1. The majority of the victims were male (86%), which was statistically significant (p < 0.05). More than half of the patients bitten by Viperidae and Elapidae serpents were attacked near their homes, in suburban areas. Fingers and palms were more frequently affected by Viperidae (hemorrhagic venom) and Elapidae snakes (neurotoxic venom), while toes and the lower leg were more commonly bitten by Viperidae (mixed venom). However, the locations of bitten areas were no statistically significant difference among the three venomous groups (Table 1).

 

Table 1. Epidemiological characteristics of 58 patients bitten by venomous snakes who received antivenom treatment in the medical center of Taiwan, from January 1993 to December 2002

Demographics/
other variables

Viperidae Familyª hemorrhagic venom

(n = 28)

Elapidae Familyª  neurotoxic venom

(n = 22)

Viperidae Familyª

 mixed venom

(n = 8)

p valueb,c

Age (years)

51.5 (15.0-93.0)

44.5 (22.0-67.0)

55.5 (19.0-78.0)

0.37

Median dose (vials)

1 (1.0-2.7)

3 (1.0-10.0)

2 (1.0-2.0)

0.005*

Gender

 

 

 

 

  Male

22 (78.6)

22 (100)

6 (75.0)

0.03*

  Female

6 (21.4)

0 (0.0)

2 (25.0)

 

Location

 

 

 

 

  Near house

15 (55.5)

15 (68.1)

3 (37.5)

0.29

  Suburban

12 (44.4)

7 (31.82)

5 (62.5)

 

Bitten area

 

 

 

 

  Fingers

9 (32.1)

12 (54.5)

1 (12.5)

0.13

  Palms

8 (28.6)

4 (18.2)

1 (12.5)

 

  Toes

4 (14.3)

0 (0.0)

2 (25.0)

 

  Lower legs

6 (21.4)

4 (18.2)

3 (37.5)

 

  Others

1 ( 3.6)

2 (9.1)

1 (12.5)

 

Symptomsd

 

 

 

 

  Local swelling

23 (46.9)

14 (28.0)

7 (36.9)

0.22

  Pain

18 (36.7)

12 (24.0)

5 (26.3)

0.82

  Local paralysis

2 (4.1)

9 (18.0)

3 (15.8)

2.00

  Blurred vision

0 (0.0)

4 (8.0)

0 (0.0)

0.04*

  Respiratory            distress

1 (2.0)

4 (8.0)

0 (0.0)

0.21

  Others

5 (17.9)

7 (31.9)

4 (50.0)

0.17

Complications 2 (7.1) 9 (40.9) 3 (37.5) 0.015*
Data are presented as mean for age and dosage of antivenom and number (percentage) for other variables.
ªViperidae family with hemorrhagic venom: T. stejnegeri, T. mucrosquamatus, D. acutus; Elapidae family with neurotoxic venom: N. atra, B. multicinctusmulticinctus; and Viperidae family with mixed venom: V. russellii.
bKruskal-Wallis for age and dosage of antivenom.
cChi-square test for gender, location, biting position, complaint and complications.
dNumber of subjects for data analysis of variables does not correspond to the total number of subjects because of more than one complaint from each subject.
* p < 0.05.

 

Local pain and swelling accounted for more than 50% of patients' complaints on the arrival at the ED in the three groups. Blurred vision was predominantly found among persons bitten by Elapidae snakes (neurotoxic venom) (p < 0.05), otherwise, there was no significant difference in symptoms among the three groups (Table 1). Complication rates and the dosage of antivenom required were significantly different for the three groups. Patients bitten by Elapidae serpents (neurotoxic venom) had higher complication rates (9/22; 40.9%) and required larger antivenom dosages compared to Viperidae (median dose: three vials, range: 1.0 to 10.0) (p < 0.05) (Table 1).

Further analysis using a univariate logistic regression model indicated important correlations among venom complications and venomous types, respiratory distress and duration of treatment (Table 2). However, after adjusting for gender, multivariate logistic regression analysis indicated only a significant correlation between complication rate and neurotoxic venom (OR: 8.84, 95% CI: 1.06-73.73, Table 2), suggesting that patients bitten by Elapidae snakes (neurotoxic venom) had greater chance for complications even after antivenom therapy, which included respiratory failure and flaccidity (4/9; 44.4%) and fasciitis requiring fasciotomy and debridement (3/9; 33.3%).

 

Table 2. Logistic regression analysis of complications derived from 58 cases of venomous snake bites, the medical center of Taiwan, January 1993 to December 2002

 

Univariate logistic regression

Multivariate logistic regressionª

Complication rate

Crude OR

95% CI

Adjusted OR

95% CI

Venom type

 

 

 

 

  Hemorrhagic

Ref.

b

Ref.

  Neurotoxic

7.29*

1.31-40.54

8.84*

1.06-73.73

  Mixed

7.50

0.98-57.14

3.53

0.28-45.26

Respiratory distress

 

 

 

 

  No

Ref.

Ref.

  Yes

13.67*

1.27-146.98

20.19

0.77-526.98

Treatment duration (hours)

 

 

 

 

  < 1

Ref.

Ref.

  < 2

2.17

0.24-19.28

4.42

0.25-77.80

  < 4

0.65

0.05-8.23

1.34

0.06-32.93

  < 10

8.13*

1.12-59.21

16.99

0.90-320.65

  > 10

1.44

0.17-12.23

1.55

0.10-24.80

OR: odds ratio; CI: confidence interval; Ref.: reference group.
ªAdjusted for sex and age.
bDashes represent no 95% CI for reference groups.
*p < 0.05.

 

Regression model results that analyzed the association among dose of antivenom and venom type, complications and blurred vision is presented in Table 3. After adjustment of age and gender, we found that patients affected by neurotoxic venom received a significantly greater dose of antivenom compared with those afflicted by hemorrhagic toxin (p < 0.05). Patients with complications received a considerably greater dose of antivenom compared with those who did not show any symptom (p < 0.05).  

 

Table 3. Linear regression analysis of the association between antivenom dose and effectors in 58 patients who received treatment in the medical center of Taiwan, from January 1993 to December 2002

Variable

Beta

p valueª

Venom type

 

 

  Hemorrhagic

Ref.

b

  Neurotoxic

1.33241

0.05*

  Mixed

0.27685

0.75

Complications

 

 

  No

Ref.

  Yes

1.57634

0.05*

Blurred vision

 

 

  No

Ref.

  Yes

1.42317

0.34

Ref.: reference group.
ªAdjusted for sex and age.
bDashes represent no p value for the reference groups.
* p < 0.05.

 

DISCUSSION

Roughly, one quarter of all the snake bite patients could not confirm the species of snake that had attacked them. Hung (1) found that of the 282 cases he studied, 50 patients were unable to identify the snake species that bite them. This may have clinical significance, as it could delay the antivenom administration. Based on this retrospective review, patients bitten by snakes of the family Elapidae (neurotoxic venom) required higher antivenom doses and had greater chances for complications, even after antivenom therapy. We found similar epidemiological patterns in previous studies including male predominance (86%), bites on distal extremities of the body (98%) and a large incidence of attacks occurring near the individual residence (57%) (3, 4, 7-9). Correct antivenom administration remains the mainstay of therapy, with a suggested elapsed time from the moment of the bite to the antivenom administration of six to eight hours (10). Most patients (72%) in our study received antivenom therapy within six hours from the time they were bitten.

The exact antivenom dose required remains a matter of discussion. Yeung et al. (11) in a study of 35 brown snake envenomations in Australia found that initial antivenom doses were very small, leading to a continued circulation of venom. Paul et al. (2) conducted a study with 100 patients bitten by snakes from three venom groups (hemorrhagic, neurotoxic and mixed). They further divided the patients into two groups; the first was treated with high doses of antivenom and the other group with low doses. There was no statistical difference in clinical outcomes between the two groups (2).

Antivenom can present adverse effects ranging from local skin reactions to severe anaphylaxis and death. Additionally, delayed reactions that include serum sickness may occur. Therefore, the goals of antivenom treatment comprise administration of an appropriate dose of antivenom to neutralize the toxin, avoidance of complications related to the envenomation and prevention of additional complications (12, 13).

In our study, the median dose of antivenom administered for the family Viperidae (hemorrhagic venom) was one vial and the complication rate was 7.14% (2/28), suggesting that the dose of antivenom may be suitable for most patients. Two of these victims had coagulopathy with compartment syndrome and required fasciotomies. Three victims were bitten by D. acutus and received antivenom for T. stejnegeri and T. mucrosquamatus since the antivenom against these two species presents weak cross-reactivity with D. acutus.

The median dose of antivenom administered for the family Elapidae (neurotoxic venom) was three vials, and the complication rate was 40.91%. This rate is consistent with the fact that neurotoxins cause paralysis that may not be reversible by antivenom. Pre-synaptic neurotoxins damage nerve endings at the neuromuscular junction while post-synaptic neurotoxins are short or long and bind to nicotinic acetylcholine receptors (14). Antivenom doses required in the Elapidae group were higher, although the suggested dose was one vial. Our findings suggest that the recommended dose of antivenom for treating these bites is insufficient.

Hung (7), in his work on neurotoxic envenomations, suggested that the level of serum venom detected by ELISA was connected with the severity of local tissue damage, with higher levels indicating higher damage. This author indicated that when this type of envenomation is suspected, patients may require ELISA tests in order to determine the correct dose of antivenom. Similarly, Agarwal et al. (4) analyzed low doses of antivenom for treating patients with neurotoxic envenomations. Patients were divided into two groups, one treated with high doses of antivenom, and the other treated with low doses. While there are apparent problems with the study design, they found a similar outcome between groups that received low or high doses of antivenom. Even though there were three deaths in the high dose group and none in the low dose group, the deaths were attributed to late presentation and complications related to pneumonia and sepsis (4).

The median dose of antivenom administered for envenomations provoked by Viperidae snakes (mixed venom) in our study was two vials, and the complication rate was 37.5% (3/8). The toxin from this family commonly causes coagulopathy with bleeding diathesis due to procoagulants contained in the venom that activate factor X, factor IX, and factor V leading to thrombosis and disseminated intravascular coagulation (6, 8, 9). In another study by Hung et al. (5), 13 patients received a mean dose of 3.3 vials. Among those patients, the mortality rate was 0% in 12 patients who received prompt treatment, compared to three deaths out of 19 cases in which treatment was delayed (5, 8). We found that antivenom may prevent hemorrhage, but appears to have no effect on progression to acute renal failure. Dialysis remains the preferred conduct for acute tubular necrosis in these patients.

Although improvements in the production and standardization of antivenom have occurred over the years, and resulted in highly efficient treatments, these changes have increased production costs, and several authors believe that the overall quality is similar to those from older methods when properly conducted (13). Additionally, new assay systems allow a very accurate assessment of antivenom efficacy, apart from changes in a patient clinical status (15). Though we may agree that improvements in quality, efficacy and consistency have resulted from enhanced methods of antivenom production, appropriate dosage and treatment duration are still decisive, and are based on clinician assessment of the patient condition.

There are some limitations to this study, specially being a retrospective chart review rather than a double blind, placebo-controlled trial of the antivenoms. Patients could have incorrectly identified the snakes that bit them and victims excluded from the present study due to the inability to identify the snake may have affected the results. Despite these limitations, important information regarding appropriate antivenom dosage and complication of envenomations caused by snake bites has been obtained.

 

CONCLUSION

Based on the present findings, patients affected by neurotoxic envenomation received higher doses of antivenom than other types of envenomation. However, they still presented higher rate of complication after antivenom therapy, suggesting that the dosage of antiserum may not be appropriate for them. Our study also indicated that the dosage of antivenom used for neutralizing venom may positively be connected with the occurrence of complications.

 

ACKNOWLEDGEMENTS

The authors would like to sincerely thank the staff of the Poison Control Center for their assistance in data collection and the members of the Division of Laboratory Resources Management, Center for Disease Control, Department of Health, Taiwan R.O.C. for provided information and research about the efficacy of antivenom.

 

INSTITUTION APPROVAL

The present study has been approved by the Institutional Review Board of Kaohsiung Medical University Hospital (KMUH-IRB-960302).

 

REFERENCES

1. Hung DZ. Taiwan's venomous snakebite: epidemiological, evolution and geographic differences. Trans R Soc Trop Med Hyg. 2004;98(2):96-101.         [ Links ]

2. Paul V, Pratibha S, Prahlad KA, Earali J, Francis S, Lewis F. High-dose anti-snake venom versus low-dose anti-snake venom in the treatment of poisonous snakebites: a critical study. J Assoc Physicians India. 2004;52:14-7.         [ Links ]

3. Srimannarayana J, Dutta TK, Sahai A, Badrinath S. Rational use of anti-snake venom (ASV): trial of various regimens in hemotoxic snake envenomation. J Assoc Physicians India. 2004;52:788-93.         [ Links ]

4. Agarwal R, Aggarwal AN, Gupta D, Behera D, Jindal SK. Low dose of snake antivenom is as effective as high dose in patients with severe neurotoxic snake envenoming. Emerg Med J. 2005;22(6):397-9.         [ Links ]      

5. Hung DZ, Yu YJ, Hsu CL, Lin TJ. Antivenom treatment and renal dysfunction in Russell's viper snakebite in Taiwan: a case series. Trans R Soc Trop Med Hyg. 2006; 100(5):489-94.         [ Links ]

6. Theakston RD, Warrell DA. Antivenoms: a list of hyperimmune sera currently available for the treatment of envenoming by bites and stings. Toxicon. 1991;29(12):1419-70.         [ Links ]

7. Hung DZ, Liau MY, Lin-Shiau SY. The clinical significance of venom detection in patients of cobra snakebite. Toxicon. 2003;41(4):409-15.         [ Links ]

8. Hung DZ, Wu ML, Deng JF, Lin-Shiau SY. Russell's viper snakebite in Taiwan: differences from other Asian countries. Toxicon. 2002;40(9):1291-8.         [ Links ] 

9. Liao WB, Lee CW, Tsai YS, Liu BM, Chung KJ. Influential factors affecting prognosis of snakebite patients management: Kaohsiung Chang Gung Memorial Hospital experience. Chang Gung Med J. 2000;23(10):577-83.         [ Links ]    

10. Gold BS, Dart RC, Barish RA. Bites of venomous snakes. N Engl J Med. 2002;347(5):347-56.         [ Links ]

11. Yeung JM, Little M, Murray LM, Jelinek GA, Daly FFS. Antivenom dosing in 35 patients with severe brown snake (Pseudonaja) envenoming in Western Australia over 10 years. Med J Aust. 2004;181(11-12):703-5.         [ Links ]   

12. Gold BS, Barish RA, Dart RC. North American snake envenomation: diagnosis treatment and management. Emerg Med Clin North Am. 2004;22(2):423-43.         [ Links ]

13. Krifi MN, El Ayeb M, Dellagi K. The improvement and standardization of antivenom production in developing countries: comparing antivenom quality, therapeutical efficiency and cost. J Venom Anim Toxins. 1999;5(2):128-41.         [ Links ]

14. Warrell DA. Bites by venomous snakes outside the Americas. In: Auerbach PS, editor. Wilderness Medicine. St. Louis: Mosby; 2007. p. 1086-1123.         [ Links ]

15. Theakston RDG, Kamiguti AS. Viper envenoming: evaluation of treatment by restoration of haemostasis and venom clearance. J Venom Anim Toxins. 1998;4(2):94-111.         [ Links ]

 

 

Correspondence to:
Lin Tzeng Jih
Department of Emergency Medicine
Kaohsiung Medical University Hospital, Kaohsiung, Taiwan
Phone: +886 7 3162631
Fax: +886 7 3162632
Email: tjlin@kmu.edu.tw

Received: November 25, 2008
Accepted: April 30, 2009
Abstract published online: June 1, 2009
Full paper published online: August 31, 2009
CONFLICTS OF INTEREST: There is no conflict.

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