Exploring the clinical utility of blood ketone levels in the emergency department assessment of paediatric patients.
Journal: 2007/March - Emergency Medicine Journal
ISSN: 1472-0213
Abstract:
BACKGROUND
Ketonuria (on standard urine testing) is a frequent finding in children presenting to emergency departments. With the advent of hand-held ketone meters, blood ketone levels can now be rapidly quantified.
OBJECTIVE
Point of care testing (POCT) of blood ketone levels could provide clinically useful information on severity of illness in children and risk of hospital admission.
METHODS
A prospective study using POCT of blood ketone levels in a convenience sample of children <13 years old, with a typical case mix of medical problems.
RESULTS
186 children were studied. The range of ketone levels varied widely among this study population depending on the presenting complaint. Higher levels were noted in those presenting with anorexia or vomiting and fever. The median ketone level of the total study population was 0.2 (range 0-6.0, interquartile range 0.1-0.9) mmol/l. Ketone levels correlated poorly with discharge destination and duration of admission. However, receiver-operator characteristics for ketones as a predictor of admission were comparable to Pediatric Risk of Admission scores (area under the curve 0.64 and 0.72, respectively) and may represent an independent risk factor for admission. A ketone level >1.2 mmol/l has a positive predictive value of 66.7% for admission. Ketone levels correlated well with decreased oral intake (R2 = 0.25; p<0.001).
CONCLUSIONS
A strong association was found between ketone levels, decreased oral intake and fever. Although ketone levels do not correlate well with more traditional markers of illness severity, they can help to predict the requirement for admission to hospital when interpreted in the context of the presenting illness. They may have applications in both the emergency department and primary care settings. Further prospective testing is required to validate these findings.
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Emerg Med J 23(10): 783-787

Exploring the clinical utility of blood ketone levels in the emergency department assessment of paediatric patients

P B O'Donohoe, College of Medicine, University of Edinburgh, Edinburgh, UK
R Kessler, T F Beattie, Accident and Emergency Department, Royal Hospital for Sick Children, Edinburgh
Correspondence to: P B O'Donohoe
1f1, Grindlay Street, Edinburgh EH3 9AS, UK; p_od@yahoo.com
P B O'Donohoe, College of Medicine, University of Edinburgh, Edinburgh, UKR Kessler, T F Beattie, Accident and Emergency Department, Royal Hospital for Sick Children, EdinburghCorrespondence to: P B O'Donohoe
1f1, Grindlay Street, Edinburgh EH3 9AS, UK; p_od@yahoo.com
Accepted 2006 Jun 1.

Abstract

Background

Ketonuria (on standard urine testing) is a frequent finding in children presenting to emergency departments. With the advent of hand‐held ketone meters, blood ketone levels can now be rapidly quantified.

Hypothesis

Point of care testing (POCT) of blood ketone levels could provide clinically useful information on severity of illness in children and risk of hospital admission.

Methods

A prospective study using POCT of blood ketone levels in a convenience sample of children <13 years old, with a typical case mix of medical problems.

Findings

186 children were studied. The range of ketone levels varied widely among this study population depending on the presenting complaint. Higher levels were noted in those presenting with anorexia or vomiting and fever. The median ketone level of the total study population was 0.2 (range 0–6.0, interquartile range 0.1–0.9) mmol/l. Ketone levels correlated poorly with discharge destination and duration of admission. However, receiver–operator characteristics for ketones as a predictor of admission were comparable to Pediatric Risk of Admission scores (area under the curve 0.64 and 0.72, respectively) and may represent an independent risk factor for admission. A ketone level >1.2 mmol/l has a positive predictive value of 66.7% for admission. Ketone levels correlated well with decreased oral intake (R = 0.25; p<0.001).

Conclusions

A strong association was found between ketone levels, decreased oral intake and fever. Although ketone levels do not correlate well with more traditional markers of illness severity, they can help to predict the requirement for admission to hospital when interpreted in the context of the presenting illness. They may have applications in both the emergency department and primary care settings. Further prospective testing is required to validate these findings.

Abstract

Determining how sick a child is when he or she attends an emergency department can be challenging. Assessment is usually based on a “snap shot” built on history and examination findings. At the extremes of illness severity, the decision to admit or discharge is usually self‐evident. However, there is a group of children in whom this decision is difficult to make on the basis of history and examination findings alone.123 As clinicians, we are often looking for simple tools or tests that can help us in the assessment of these children.345678 These may include the use of scoring systems, bedside investigations or the judicious use of more sophisticated tests.

Scoring systems for severity of illness or risk of admission include the Paediatric Risk of Mortality Score,9 the Yale Observation Scale, Odyrons Score for Sick Children and, more recently, the Pediatric Risk of Admission (PRISA) score.1210 These scores are often complicated and time consuming or not easily used prospectively, making their use in the emergency department difficult.21011 Bedside or point of care testing (POCT; eg, pulse oximetry, blood glucose testing, electrocardiograms, bedside spirometry and urine analysis) is usually minimally invasive, easy to obtain, provides rapid and relatively accurate results that can influence management, and is cost effective. More sophisticated laboratory tests and imaging modalities are generally expensive and time consuming, and should be reserved for assessment of appropriate patients at the discretion of the attending doctor. Additional information about the scoring system using the PRISA score is available online at http://www.emj.bmjjournals.com/supplemental.

Anecdotally, we have noticed that ketonuria is a common finding in children who are ill, but have not been able to quantify this with accuracy. Ketone bodies are produced by fatty acid metabolism in hepatic mitochondria during a range of physiological and pathological conditions associated with either altered glucose metabolism or relative glucose or glycogen deficiency. There are three ketone bodies: acetoacetate (AcAc), acetone and β‐hydroxybutyrate (β‐HB). Ketones are used primarily by the heart, kidney, central nervous system and skeletal muscle. These tissues produce the enzyme succinyl coenzyme A‐oxoacid transferase.12 This enables the production of acetyl coenzyme A from ketone bodies and ultimately ATP via the tricarbocylic acid cycle. In toddlers and young children, hyperketonaemia becomes apparent within 12–24 h of a fast. Children of this age are more susceptible to ketosis because of their diminished stores of glycogen and their proportionately larger central nervous systems than adults.12

Standard dipstick urine analysis using Ketostix or Multistix (Bayer Diagnostics, Berkshire, UK) gives a semiquantitative measure of AcAc and, to a lesser degree, of acetone.12131415 It is, however, commonly assumed that β‐HB is quantitatively and clinically the more important ketone body. The ratio of β‐HB to AcAc can vary from 1:1 (postprandially) to 10:1 depending on the physiological status of the patient.12131415 Urine AcAc levels may underestimate the severity of ketosis.121415 Laboratory measurement of β‐HB is not routinely available and takes too long to be of practical use in the emergency department setting. The advent of hand‐held blood ketone meters, more commonly used for testing in patients with diabetes, provides a method for rapid and accurate quantification of blood β‐HB levels. Using techniques similar to that for bedside glucose estimation, one drop of blood on a test strip can provide a ketone level in about 30 s.

This is a simple test that has been well researched in people with diabetes,1214151617 but also has potential applications in the assessment of a much broader case mix of medical patients in the paediatric emergency department.

Acknowledgements

We thank Nancy Doleman, Abbott Laboratories, for providing us with MediSense Ketone Meters and reagents. We also thank the medical and nursing staff at the Royal Hospital for Sick Children for assistance in recruiting participants.

Acknowledgements

Abbreviations

AcAc - acetoacetate

β‐HB - β‐hydroxybutyrate

HDU - high‐dependency unit

IQR - interquartile range

ITU - intensive therapy unit

POCT - point of care testing

PRISA - Pediatric Risk of Admission

ROC - receiver–operator characteristic

Abbreviations

Footnotes

Competing interests: None.

Contributors: PBO'D planned the study, gained ethical approval, contributed to data collection, collated and analysed the data, and drafted the paper. RK contributed to data collection and drafted the paper. TFB initiated the idea, contacted Abbott Diagnostics, was associated with the ethical approval application process and drafted the paper.

Ethical approval: The Lothian Research Ethics Committee and the National Health Service approved the study.

Footnotes

References

  • 1. Chamberlain J M, Patel K M, Ruttimann U E. et al Pediatric risk of admission (PRISA): a measure of severity of illness for assessing the risk of hospitalization from the emergency department. Ann Emerg Med 199832161–169. [[PubMed]
  • 2. Chamberlain J M, Patel K M, Pollack M M. et al Recalibration of the pediatric risk of admission score using a multi‐institutional sample. Ann Emerg Med 200443461–468. [[PubMed]
  • 3. Knott J C, Meyer A DImpact of blood testing on patient disposition from the emergency department. Emerg Med (Fremantle) 200315121–125. [[PubMed][Google Scholar]
  • 4. Krishnan SEvaluation and management of the febrile infant in the emergency department. Indian J Pediatr 200370(Suppl 1)S45–S50. [[PubMed][Google Scholar]
  • 5. Keahey L, Bulloch B, Becker A B. et al Initial oxygen saturation as a predictor of admission in children presenting to the emergency department with acute asthma. Ann Emerg Med 200240300–307. [[PubMed]
  • 6. Twaddell S H, Henry R L, Francis J L. et al The prediction of hospital admission in children with acute asthma. J Paediatr Child Health 199632532–535. [[PubMed]
  • 7. Dean N C, Suchyta M R, Bateman K A. et al Implementation of admission decision support for community‐acquired pneumonia. Chest 20001171368–1377. [[PubMed]
  • 8. Armon K, Stephenson T, MacFaul R. et al An evidence and consensus based guideline for acute diarrhoea management. Arch Dis Child 200185132–142.
  • 9. Pollack M M, Patel K M, Ruttimann U EPRISM III: an updated Pediatric Risk of Mortality score. Crit Care Med 199624743–752. [[PubMed][Google Scholar]
  • 10. Gravel J, Gouin S, Amre D. et al Evaluation of the pediatric risk of admission score in a pediatric emergency department. Ann Emerg Med 200341630–638. [[PubMed]
  • 11. Gorelick M HSeverity of illness measures for pediatric emergency care: are we there yet? Ann Emerg Med 200341639–643. [[PubMed][Google Scholar]
  • 12. Laffel LKetone bodies: a review of physiology, pathophysiology and application of monitoring to diabetes. Diabetes Metab Res Rev 199915412–426. [[PubMed][Google Scholar]
  • 13. Porter W H, Yao H H, Karounos D GLaboratory and clinical evaluation of assays for beta‐hydroxybutyrate. Am J Clin Pathol 1997107353–358. [[PubMed][Google Scholar]
  • 14. Chiu R W, Ho C S, Tong S F. et al Evaluation of a new handheld biosensor for point‐of‐care testing of whole blood beta‐hydroxybutyrate concentration. Hong Kong Med J 20028172–176. [[PubMed]
  • 15. Byrne H A, Tieszen K L, Hollis S. et al Evaluation of an electrochemical sensor for measuring blood ketones. Diabetes Care 200023500–503. [[PubMed]
  • 16. Fulop M, Murthy V, Michilli A. et al Serum beta‐hydroxybutyrate measurement in patients with uncontrolled diabetes mellitus. Arch Intern Med 1999159381–384. [[PubMed]
  • 17. Wallace T M, Meston N M, Gardner S G. et al The hospital and home use of a 30‐second hand‐held blood ketone meter: guidelines for clinical practice. Diabetes Med 200118640–645. [[PubMed]
  • 18. VanItallie T B, Nufert T HKetones: metabolism's ugly duckling. Nutr Rev 200361327–341. [[PubMed][Google Scholar]
  • 19. Fukao T, Song X Q, Mitchell G A. et al Enzymes of ketone body utilization in human tissues: protein and messenger RNA levels of succinyl‐coenzyme A (CoA):3‐ketoacid CoA transferase and mitochondrial and cytosolic acetoacetyl‐CoA thiolases. Pediatr Res 199742498–502. [[PubMed]
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