We thank the readers for their interest in our study [1]. Our
replies to the queries are as under:
(i)
Different clinical and laboratory parameters were already
described in table I and II of the article, and some of the
determinants are
similar to previous reports [2]. Reasons for discrepancy with
published literature were mentioned in the discussion section of
the article.
(ii)
Detailed baseline data were collected, but all of it
could not be presented due to limitation on the size of the
manuscript. Serum LDH and adrenal hemorrhage were not assessed
in our study. We appreciate your concern about cardiac
dysfunction, hemodynamic status etc, but different parameters
(requirement of ventilation, serum potassium level, requirement
of inotropes) mentioned in table I act as surrogate markers of
them. We used logistic regression and adjusted odds ratio to
remove confounders. Nephrotoxic drugs are avoided in viper-bite
patients according to unit protocol in our set-up.
(iii)
In a previous research project in the same setting, the
investigators noted some long-term toxicity of snakebite, as
also previously reported [2]. Hence we decided on a follow-up
period of 6 months.
(iv)
In the paper, we had mentioned the unit protocol for
dialysis. Opinion of a nephrologist was sought before starting
dialysis in all patients.
(v)
All study patients were followed up at our nephrology
specialty clinic after discharge from hospital.
(vi)
If at any point of time during the hospital stay, the
children developed AKI, we included them in the AKI group. The
initial version of the manuscript had information on AKI grades,
but it was later edited out on the suggestion of reviewers.
(vii)
We did not perform renal biopsy in AKI settings. We considered
renal biopsy in the children who developed permanent renal
damage, as per opinion of nephrologist. Before doing renal
biopsy, we took informed written consent from parents.
Snake bite, being a medicolegal case, autopsy is done in
every death. Samples from viscera are also routinely collected
by forensic expert. We could convince parents of all such
children for consent for renal histopathology examination.
(viii)
We used the study population as denominator because we want to
identify renal complication in children with hematotoxic bites,
not in the surviving children.
(ix)
As the data are skewed, we had summarized it as median
and interquartile range [1]. The mean (SD) number of vials
required were 12.3 (9.1) and 21.5 (18.9) in AKI and no AKI
groups, respectively.
(x)
It is the regression model used in the study.
(xi)
The mentioned time is only for those who did not develop
AKI; it was higher for those who developed AKI (74.5 minutes)
[1]. If we consider all children, mean time between bite and ASV
administration was 51.2 minutes. Moreover, many of the children
received the first dose of ASV at the place of initial medical
care, before referral to our center. The study referred to by
the readers was conducted in 2012-2016 and included both
children and adults [3]. Due to the sustained awareness
campaigns and easy availability of ASV, bite to needle time is
gradually decreasing. Transport vehicles are also easily
available for children under different government schemes.
Moreover, our study included children with viper-bite only,
which is symptomatic at early stage leading to early seeking of
healthcare.
REFERENCES
1.
Islam K, Seth S, Roy A, Datta AK. Predictors of renal
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Pediatr. 2020;57:427-30.
2.
Aye KP, Thanachartwet V, Soe C, Desakorn V, Thwin KT,
Chamnanchanunt S, et al. Clinical and laboratory
para-meters associated with acute kidney injury in patients with
snakebite envenomation: A prospective observational study from
Myanmar. BMC Nephrol. 2017;18:92.
3.
Jayawardana S, Arambepola C, Chang T, Gnanathasan A.
Long-term health complications following snake envenoming. J
Multidiscip Healthc. 2018;11:279-85.
4.
Sarkhel S, Ghosh R, Mana K, Gantait K. A hospital based
epidemiological study of snakebite in Paschim Medinipur
district, West Bengal, India. Toxicol Rep. 2017;4:415-9.