Detection of venom after antivenom is not associated with persistent coagulopathy in a prospective cohort of Russell's viper (Daboia russelii) envenomings

PLoS Negl Trop Dis. 2014 Dec 18;8(12):e3304. doi: 10.1371/journal.pntd.0003304. eCollection 2014 Dec.

Abstract

Background: Venom recurrence or persistence in the circulation after antivenom treatment has been documented many times in viper envenoming. However, it has not been associated with clinical recurrence for many snakes, including Russell's viper (Daboia spp.). We compare the recovery of coagulopathy to the recurrence or persistence of venom in patients with Russell's viper envenoming.

Methodology/principal findings: The study included patients with Russell's viper (D. russelii) envenoming presenting over a 30 month period who had Russell's viper venom detected by enzyme immunoassay. Demographics, information on the snake bite, and clinical effects were collected for all patients. All patients had serum collected for venom specific enzyme immunoassay and citrate plasma to measure fibrinogen levels and prothrombin time (international normalised ratio; INR). Patients with venom recurrence/persistence were compared to those with no detectable recurrence of venom. There were 55 patients with confirmed Russell's viper envenoming and coagulopathy with low fibrinogen concentrations: 31 with venom recurrence/persistence, and 24 with no venom detected post-antivenom. Fibrinogen concentrations increased and INR decreased after antivenom in both the recurrence and non-recurrence patients. Clinical features, laboratory parameters, antivenom dose and length of hospital were similar for both groups. Pre-antivenom venom concentrations were higher in patients with venom recurrence/persistence with a median venom concentration of 385 ng/mL (16-1521 ng/mL) compared to 128 ng/mL (14-1492 ng/mL; p = 0.008).

Conclusion: Recurrence of Russell's viper venom was not associated with a recurrence of coagulopathy and length of hospital stay. Further work is required to determine if the detection of venom recurrence is due to the venom specific enzyme immunoassay detecting both venom-antivenom complexes as well as free venom.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Aged
  • Aged, 80 and over
  • Animals
  • Antivenins / therapeutic use*
  • Blood Coagulation Disorders / blood*
  • Blood Coagulation Disorders / drug therapy
  • Blood Coagulation Disorders / etiology
  • Cohort Studies
  • Daboia*
  • Female
  • Humans
  • Immunoenzyme Techniques
  • Male
  • Middle Aged
  • Prospective Studies
  • Snake Bites / blood*
  • Snake Bites / drug therapy*
  • Snake Venoms / blood*
  • Young Adult

Substances

  • Antivenins
  • Snake Venoms

Grants and funding

The study was supported in part by NHMRC Project Grant 631073. GKI is funded by an NHMRC Senior Research Fellowship ID1061041. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.