Kurup, et al. [1] recently published their study assessing the
validity of capillary b-hydroxybutyrate
(BOHB) for diagnosis and monitoring of ketonemia in pediatric diabetic
ketoacidosis (DKA). However, I would like authors to clarify certain
issues, which may help readers better interpret the study.
Lesser cost and availability of real-time results
(avoiding treatment delays while awaiting laboratory results) are the
potential advantages associated with the use of capillary BOHB in
clinical practice. While the authors have reported cost-effectiveness of
capillary measurement, it would be worthwhile mentioning the mean time
taken for availability of serum BOHB result once the sample had been
sent to the laboratory. This is important because the monitoring for
BOHB was repeated initially at every two hours in the study, and a lag
period close to or more than this time interval would probably indicate
the futility of serum BOHB measurement.
It has also been reported in the study that the bias
increased at values above 5 mmol/L, and results of capillary BOHB above
this threshold should be interpretated with caution. Could the authors
comment on total number of observations (>5 mmol/l) for which the bias
was estimated?
Finally, in the discussion, authors propose that
capillary BOHB may obviate the need for blood gas analysis in pediatric
DKA. However, one should be cognizant of the fact that blood BOHB serves
as a surrogate for high anion gap metabolic acidosis, and not normal
anion gap acidosis. Hyperchloremic metabolic acidosis (HCMA) may develop
during treatment of DKA due to urinary loss of bicarbonate precursors as
ketones and administration of excessive chloride in form of intravenous
fluids [2]. Such patients may fail to show recovery of serum pH and
bicarbonate despite resolution of ketoacidosis. In a retrospective
analysis of 59 pediatric DKA admissions, Mrozik, et al. [3]
reported that the difference in time period between recovery of
bicarbonate and closure of anion gap was >6 hours in one-fourth of
cases. Clearly, BOHB measurement may help to reduce the frequency of
blood gas analysis, but it would be largely ineffective in detecting
HCMA, a potential cause of persistent metabolic acidosis in patients
with DKA.
References
1. Kurup PM, Rameshkumar R, Soundravally R, Satheesh
P. Capillary versus serum
b-hydroxybutyrate
in pediatric diabetic ketoacidosis. Indian Pediatr. 2019;56:125-9.
2. Wolfsdorf JI, Allgrove J, Craig ME, Edge J, Glaser
N, Jain V, et al. ISPAD Clinical Practice Consensus Guidelines
2014. Diabetic Ketoacidosis and Hyperglycemic Hyperosmolar State.
Pediatr Diabetes. 2014;15:154-79.
3. Mrozik LT, Yung M. Hyperchloraemic metabolic
acidosis slows recovery in children with diabetic ketoacidosis: A
retrospective audit. Aust Crit Care. 2009;22:172-7.