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Alterations and diagnostic performance of capillary ketonemia in pediatric acute appendicitis: a pilot study

INTRODUCTION: The diagnostic performance of capillary ketonemia (CK) has been previously evaluated in context of pediatric acute gastroenteritis. To our knowledge, there is no literature on its performance in the setting of pediatric acute appendicitis (PAA). MATERIALS AND METHODS: In this study, 15...

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Autores principales: Arredondo Montero, Javier, Bronte Anaut, Mónica, Bardají Pascual, Carlos, Antona, Giuseppa, López-Andrés, Natalia, Martín-Calvo, Nerea
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9741565/
https://www.ncbi.nlm.nih.gov/pubmed/36495332
http://dx.doi.org/10.1007/s00383-022-05332-7
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author Arredondo Montero, Javier
Bronte Anaut, Mónica
Bardají Pascual, Carlos
Antona, Giuseppa
López-Andrés, Natalia
Martín-Calvo, Nerea
author_facet Arredondo Montero, Javier
Bronte Anaut, Mónica
Bardají Pascual, Carlos
Antona, Giuseppa
López-Andrés, Natalia
Martín-Calvo, Nerea
author_sort Arredondo Montero, Javier
collection PubMed
description INTRODUCTION: The diagnostic performance of capillary ketonemia (CK) has been previously evaluated in context of pediatric acute gastroenteritis. To our knowledge, there is no literature on its performance in the setting of pediatric acute appendicitis (PAA). MATERIALS AND METHODS: In this study, 151 patients were prospectively included and divided into two groups: (1) patients with non-surgical abdominal pain in whom the diagnosis of PAA was excluded (n = 53) and (2) patients with a confirmed diagnosis of PAA (n = 98). In 80 patients (Group 1, n = 23 and group 2, n = 57) a CK was measured at the time of diagnosis. The PAA group was further classified into complicated (n = 18) and uncomplicated PAA (n = 39). Quantitative variables were compared between groups using the Mann–Whitney U test. Diagnostic performance of CK was evaluated with ROC curves. RESULTS: CK values were 0.3 [0.1–0.9] mmol/L in group 1 and 0.7 [0.4–1.4] mmol/L in group 2 (p = 0.01). Regarding the type of PAA, CK values were 0.6 [0.4–0.9] mmol/L in uncomplicated PAA and 1.2 [0.8–1.4] mmol/L in complicated PAA (p = 0.02). The AUC for the discrimination between groups 1 and 2 was 0.68 (95% IC 0.53–0.82) (p = 0.24) and the AUC for the discrimination between uncomplicated PAA and complicated PAA was 0.69 (95% IC 0.54–0.85) (p = 0.04). The best cut-off point (group 1 vs group 2) resulted in 0.4 mmol/L, with a sensitivity of 80.7% and a specificity of 52.2%. The best cut-off point (non-complicated vs complicated PAA) resulted in 1.1 mmol/L, with a sensitivity of 61.1% and a specificity of 76.9%. CONCLUSIONS: This study found significantly higher levels of CK in patients with PAA than in those with NSAP. Similarly, significantly higher levels were observed in patients with complicated than in those with uncomplicated PAA. Nevertheless, the diagnostic performance of CK was only moderate in the two settings analyzed. The potential usefulness of CK determination as a tool to guide the preoperative rehydration regimen of patients with PAA to prevent postoperative hyporexia and vomiting is a promising line of research and should be evaluated in future studies. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00383-022-05332-7.
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spelling pubmed-97415652022-12-12 Alterations and diagnostic performance of capillary ketonemia in pediatric acute appendicitis: a pilot study Arredondo Montero, Javier Bronte Anaut, Mónica Bardají Pascual, Carlos Antona, Giuseppa López-Andrés, Natalia Martín-Calvo, Nerea Pediatr Surg Int Original Article INTRODUCTION: The diagnostic performance of capillary ketonemia (CK) has been previously evaluated in context of pediatric acute gastroenteritis. To our knowledge, there is no literature on its performance in the setting of pediatric acute appendicitis (PAA). MATERIALS AND METHODS: In this study, 151 patients were prospectively included and divided into two groups: (1) patients with non-surgical abdominal pain in whom the diagnosis of PAA was excluded (n = 53) and (2) patients with a confirmed diagnosis of PAA (n = 98). In 80 patients (Group 1, n = 23 and group 2, n = 57) a CK was measured at the time of diagnosis. The PAA group was further classified into complicated (n = 18) and uncomplicated PAA (n = 39). Quantitative variables were compared between groups using the Mann–Whitney U test. Diagnostic performance of CK was evaluated with ROC curves. RESULTS: CK values were 0.3 [0.1–0.9] mmol/L in group 1 and 0.7 [0.4–1.4] mmol/L in group 2 (p = 0.01). Regarding the type of PAA, CK values were 0.6 [0.4–0.9] mmol/L in uncomplicated PAA and 1.2 [0.8–1.4] mmol/L in complicated PAA (p = 0.02). The AUC for the discrimination between groups 1 and 2 was 0.68 (95% IC 0.53–0.82) (p = 0.24) and the AUC for the discrimination between uncomplicated PAA and complicated PAA was 0.69 (95% IC 0.54–0.85) (p = 0.04). The best cut-off point (group 1 vs group 2) resulted in 0.4 mmol/L, with a sensitivity of 80.7% and a specificity of 52.2%. The best cut-off point (non-complicated vs complicated PAA) resulted in 1.1 mmol/L, with a sensitivity of 61.1% and a specificity of 76.9%. CONCLUSIONS: This study found significantly higher levels of CK in patients with PAA than in those with NSAP. Similarly, significantly higher levels were observed in patients with complicated than in those with uncomplicated PAA. Nevertheless, the diagnostic performance of CK was only moderate in the two settings analyzed. The potential usefulness of CK determination as a tool to guide the preoperative rehydration regimen of patients with PAA to prevent postoperative hyporexia and vomiting is a promising line of research and should be evaluated in future studies. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00383-022-05332-7. Springer Berlin Heidelberg 2022-12-10 2023 /pmc/articles/PMC9741565/ /pubmed/36495332 http://dx.doi.org/10.1007/s00383-022-05332-7 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Original Article
Arredondo Montero, Javier
Bronte Anaut, Mónica
Bardají Pascual, Carlos
Antona, Giuseppa
López-Andrés, Natalia
Martín-Calvo, Nerea
Alterations and diagnostic performance of capillary ketonemia in pediatric acute appendicitis: a pilot study
title Alterations and diagnostic performance of capillary ketonemia in pediatric acute appendicitis: a pilot study
title_full Alterations and diagnostic performance of capillary ketonemia in pediatric acute appendicitis: a pilot study
title_fullStr Alterations and diagnostic performance of capillary ketonemia in pediatric acute appendicitis: a pilot study
title_full_unstemmed Alterations and diagnostic performance of capillary ketonemia in pediatric acute appendicitis: a pilot study
title_short Alterations and diagnostic performance of capillary ketonemia in pediatric acute appendicitis: a pilot study
title_sort alterations and diagnostic performance of capillary ketonemia in pediatric acute appendicitis: a pilot study
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9741565/
https://www.ncbi.nlm.nih.gov/pubmed/36495332
http://dx.doi.org/10.1007/s00383-022-05332-7
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