Evidence map›Paper›PMID 40126848›Full record

ArticleIndian pediatrics2025

Diagnostic and Prognostic Performance of Proadrenomedullin Versus Procalcitonin in Children with Cancer and Febrile Neutropenia.

Jagdish Prasad Meena, Harshita Makkar, Aditya Kumar Gupta, Ashutosh Halder, Priyal Sharma, Rachna Seth

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Article in Indian pediatrics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Jagdish Prasad MeenaDivision of Pediatric Oncology, Department of Pediatrics, All India Institute of Medical Sciences, New Delhi, 110029, India. drjpmeena@yahoo.com.
Harshita MakkarDivision of Pediatric Oncology, Department of Pediatrics, All India Institute of Medical Sciences, New Delhi, 110029, India.
Aditya Kumar GuptaDivision of Pediatric Oncology, Department of Pediatrics, All India Institute of Medical Sciences, New Delhi, 110029, India.
Ashutosh HalderDepartment of Reproductive Biology, All India Institute of Medical Sciences, New Delhi, 110029, India.
Priyal SharmaDepartment of Reproductive Biology, All India Institute of Medical Sciences, New Delhi, 110029, India.
Rachna SethDivision of Pediatric Oncology, Department of Pediatrics, All India Institute of Medical Sciences, New Delhi, 110029, India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesPrimary objective was to compare the performance of proadrenomedullin (ProADM) and procalcitonin (PCT) for diagnosing clinically documented infections (CDI)/microbiologically documented infections (MDI)/fever without focus (NF) in children with cancer having febrile neutropenia (FN). The secondary objective was to compare the prognostic utility of PCT and ProADM for identifying adverse clinical outcome.

methodsCancer patients (aged ≤ 18 years) presenting with FN were included; those who had received antibiotics within the last 14 days were excluded. Serum PCT and ProADM were estimated on days 1, 3 and 7 of enrolment. Adverse outcome was defined in terms of clinical non-response and day 30 mortality.

resultsWe recruited 345 children. PCT in children with MDI were significantly higher than those with CDI on day 1 (P = 0.031) and day 7 (P < 0.001); PCT ≥ 0.21 ng/mL on day 1 had a 77% sensitivity and 44% specificity for diagnosis of MDI; the area under receiver operating characteristic curve (95 CI%) 0.601 (0.49, 0.71). ProADM did not differentiate between MDI and CDI. PCT and ProADM on day 1 did not predict the need for second line antibiotics. PCT ≥ 0.21 ng/mL on day 1 was predictive of MDI (P = 0.041) and PCT ≥ 1.77 ng/mL on day 7 was an independent predictor of day-30 mortality.

conclusionsPCT is effective in differentiating between MDI, CDI, and NF in children with FN, and also predicts the day 30 mortality.

Indexed as

AdrenomedullinFebrile NeutropeniaNeoplasmsProcalcitoninProtein PrecursorsAdolescentBiomarkersChildChild, PreschoolFemaleHumansInfantMalePrognosisAdrenomedullinBiomarkersproadrenomedullinProcalcitoninProtein PrecursorsBiomarkerChildMortalityOncologySepsis

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.