Diagnostic utility of procalcitonin versus C-reactive protein as markers for early-onset neonatal sepsis at Korle-Bu Teaching Hospital

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Diagnostic utility of procalcitonin versus C-reactive protein as markers for early-onset neonatal sepsis at Korle-Bu Teaching Hospital. / Amponsah, Seth Kwabena; Adjei, George Obeng; Sulley, Abdul Malik; Woode, Joan; Kurtzhals, Jorgen Anders Lindholm; Enweronu-Laryea, Christabel.

In: Pan African Medical Journal, Vol. 27, 142, 28.06.2017.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Amponsah, SK, Adjei, GO, Sulley, AM, Woode, J, Kurtzhals, JAL & Enweronu-Laryea, C 2017, 'Diagnostic utility of procalcitonin versus C-reactive protein as markers for early-onset neonatal sepsis at Korle-Bu Teaching Hospital', Pan African Medical Journal, vol. 27, 142. https://doi.org/10.11604/pamj.2017.27.142.12209

APA

Amponsah, S. K., Adjei, G. O., Sulley, A. M., Woode, J., Kurtzhals, J. A. L., & Enweronu-Laryea, C. (2017). Diagnostic utility of procalcitonin versus C-reactive protein as markers for early-onset neonatal sepsis at Korle-Bu Teaching Hospital. Pan African Medical Journal, 27, [142]. https://doi.org/10.11604/pamj.2017.27.142.12209

Vancouver

Amponsah SK, Adjei GO, Sulley AM, Woode J, Kurtzhals JAL, Enweronu-Laryea C. Diagnostic utility of procalcitonin versus C-reactive protein as markers for early-onset neonatal sepsis at Korle-Bu Teaching Hospital. Pan African Medical Journal. 2017 Jun 28;27. 142. https://doi.org/10.11604/pamj.2017.27.142.12209

Author

Amponsah, Seth Kwabena ; Adjei, George Obeng ; Sulley, Abdul Malik ; Woode, Joan ; Kurtzhals, Jorgen Anders Lindholm ; Enweronu-Laryea, Christabel. / Diagnostic utility of procalcitonin versus C-reactive protein as markers for early-onset neonatal sepsis at Korle-Bu Teaching Hospital. In: Pan African Medical Journal. 2017 ; Vol. 27.

Bibtex

@article{8e554beb8590483d948e6255400f789d,
title = "Diagnostic utility of procalcitonin versus C-reactive protein as markers for early-onset neonatal sepsis at Korle-Bu Teaching Hospital",
abstract = "Introduction: Symptoms of sepsis are non-specific among neonates and diagnosis requires a high index of suspicion. The study sought to evaluate the utility of procalcitonin (PCT) versus C-reactive protein (CRP) in diagnosing early-onset neonatal sepsis. Methods: This was a cross-sectional study in which neonates admitted to the neonatal intensive care unit, with signs suggesting sepsis were categorized according to an adapted criteria from Tollner's sepsis score and case definition of bloodstream infection as: ''highly probable'', ''probable'' and ''less probable''. Laboratory investigations including blood culture, complete blood count, PCT and CRP levels were done before first antimicrobial drug administration. Results: A total of 62 neonates less than 12 hours postnatal age (0.16-9.82 hours) were recruited. Proportion of neonates with PCT>2 ng/mL was 91% (20/22) in the ''highly probable'' group compared to 31.6% (6/19) in the ''probable group'' (p<0.001). Neonates with CRP>5 mg/L was 54.4% (12/22) in the ''highly probable'' group compared to 26.3% (5/19) in the ''probable group'' (p = 0.07). The receiver operator characteristics for PCT and CRP were; sensitivity (87.5% vrs 50%), specificity (63.0% vrs 72.2%), positive predictive value (44.1% vrs 37.5%) and negative predictive value (93.8% vrs 81.3%), respectively. Conclusion: PCT was a better predictive marker for neonatal sepsis within the first 12 hours of life than CRP in this setting, however, its low specificity relative to CRP suggests that neonates without patent infection are more likely to be incorrectly diagnosed with sepsis using this test.",
keywords = "Diagnostic marker, Neonatal sepsis, Predictive value, Sensitivity, Specificity",
author = "Amponsah, {Seth Kwabena} and Adjei, {George Obeng} and Sulley, {Abdul Malik} and Joan Woode and Kurtzhals, {Jorgen Anders Lindholm} and Christabel Enweronu-Laryea",
year = "2017",
month = jun,
day = "28",
doi = "10.11604/pamj.2017.27.142.12209",
language = "English",
volume = "27",
journal = "Pan African Medical Journal",
issn = "1937-8688",
publisher = "African Field Epidemiology Network (A F E N E T)",

}

RIS

TY - JOUR

T1 - Diagnostic utility of procalcitonin versus C-reactive protein as markers for early-onset neonatal sepsis at Korle-Bu Teaching Hospital

AU - Amponsah, Seth Kwabena

AU - Adjei, George Obeng

AU - Sulley, Abdul Malik

AU - Woode, Joan

AU - Kurtzhals, Jorgen Anders Lindholm

AU - Enweronu-Laryea, Christabel

PY - 2017/6/28

Y1 - 2017/6/28

N2 - Introduction: Symptoms of sepsis are non-specific among neonates and diagnosis requires a high index of suspicion. The study sought to evaluate the utility of procalcitonin (PCT) versus C-reactive protein (CRP) in diagnosing early-onset neonatal sepsis. Methods: This was a cross-sectional study in which neonates admitted to the neonatal intensive care unit, with signs suggesting sepsis were categorized according to an adapted criteria from Tollner's sepsis score and case definition of bloodstream infection as: ''highly probable'', ''probable'' and ''less probable''. Laboratory investigations including blood culture, complete blood count, PCT and CRP levels were done before first antimicrobial drug administration. Results: A total of 62 neonates less than 12 hours postnatal age (0.16-9.82 hours) were recruited. Proportion of neonates with PCT>2 ng/mL was 91% (20/22) in the ''highly probable'' group compared to 31.6% (6/19) in the ''probable group'' (p<0.001). Neonates with CRP>5 mg/L was 54.4% (12/22) in the ''highly probable'' group compared to 26.3% (5/19) in the ''probable group'' (p = 0.07). The receiver operator characteristics for PCT and CRP were; sensitivity (87.5% vrs 50%), specificity (63.0% vrs 72.2%), positive predictive value (44.1% vrs 37.5%) and negative predictive value (93.8% vrs 81.3%), respectively. Conclusion: PCT was a better predictive marker for neonatal sepsis within the first 12 hours of life than CRP in this setting, however, its low specificity relative to CRP suggests that neonates without patent infection are more likely to be incorrectly diagnosed with sepsis using this test.

AB - Introduction: Symptoms of sepsis are non-specific among neonates and diagnosis requires a high index of suspicion. The study sought to evaluate the utility of procalcitonin (PCT) versus C-reactive protein (CRP) in diagnosing early-onset neonatal sepsis. Methods: This was a cross-sectional study in which neonates admitted to the neonatal intensive care unit, with signs suggesting sepsis were categorized according to an adapted criteria from Tollner's sepsis score and case definition of bloodstream infection as: ''highly probable'', ''probable'' and ''less probable''. Laboratory investigations including blood culture, complete blood count, PCT and CRP levels were done before first antimicrobial drug administration. Results: A total of 62 neonates less than 12 hours postnatal age (0.16-9.82 hours) were recruited. Proportion of neonates with PCT>2 ng/mL was 91% (20/22) in the ''highly probable'' group compared to 31.6% (6/19) in the ''probable group'' (p<0.001). Neonates with CRP>5 mg/L was 54.4% (12/22) in the ''highly probable'' group compared to 26.3% (5/19) in the ''probable group'' (p = 0.07). The receiver operator characteristics for PCT and CRP were; sensitivity (87.5% vrs 50%), specificity (63.0% vrs 72.2%), positive predictive value (44.1% vrs 37.5%) and negative predictive value (93.8% vrs 81.3%), respectively. Conclusion: PCT was a better predictive marker for neonatal sepsis within the first 12 hours of life than CRP in this setting, however, its low specificity relative to CRP suggests that neonates without patent infection are more likely to be incorrectly diagnosed with sepsis using this test.

KW - Diagnostic marker

KW - Neonatal sepsis

KW - Predictive value

KW - Sensitivity

KW - Specificity

U2 - 10.11604/pamj.2017.27.142.12209

DO - 10.11604/pamj.2017.27.142.12209

M3 - Journal article

AN - SCOPUS:85027551255

VL - 27

JO - Pan African Medical Journal

JF - Pan African Medical Journal

SN - 1937-8688

M1 - 142

ER -

ID: 188361429