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Comparative Analysis Between Invalidated Biochemical Markers and the Well-established Markers of HELLP Syndrome

Received: 20 October 2021    Accepted: 8 November 2021    Published: 17 November 2021
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Abstract

Background: The use of the well-established markers of the Hemolysis, Elevated Liver enzymes and Low Platelet (HELLP) syndrome is very limited in the resource-poor settings of the developing populations. This study aimed to compare the readily available but invalidated biochemical markers with the well-established markers of HELLP syndrome. Methods: This was a retrospective cross-sectional study conducted among women diagnosed with HELLP syndrome in the University of Port Harcourt Teaching Hospital (UPTH) from 2011 to 2020. Data of each eligible case was acquired from the laboratory and medical records using a well-structured template and analyzed by standardized protocols. Results: A total of 230 cases of HELLP syndrome was identified; 200 complete HELLP (cHELLP) and 30 partial HELLP (pHELLP) variants. The cHELLP variants presented at an older age, higher gestational age, and had higher plasma bilirubin (PB), lactate dehydrogenase (LDH), creatinine, and uric acid (UA) but lower albumin concentration compared to those with pHELLP variant (p<0.05). With worsening severity, there was an increasing trend of plasma creatinine and UA but a decreasing trend of albumin among the cHELLP variants (p<0.05). UA level exhibited the strongest positive correlation with PB, LDH, aspartate, and alanine aminotransferases and maintained the strongest negative correlation with platelet count among those with cHELLP variants (p<0.05). At a cut-off value of 1.5 mmol/L, plasma UA (AUC:0.968; 95%CI:0.913-1.000;p<0.001) level had the most robust ROC values compared to those of plasma creatinine and albumin among the cHELLP variants. Conclusion: From the foregoing, plasma UA should be considered as an adjunct marker of cHELLP syndrome. However, further studies are highly recommended to evaluate conclusions from this study.

Published in Journal of Gynecology and Obstetrics (Volume 9, Issue 6)
DOI 10.11648/j.jgo.20210906.16
Page(s) 217-223
Creative Commons

This is an Open Access article, distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution and reproduction in any medium or format, provided the original work is properly cited.

Copyright

Copyright © The Author(s), 2024. Published by Science Publishing Group

Keywords

HELLP, Complete HELLP, Partial HELLP

References
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  • APA Style

    Kinikanwo Green, Collins Amadi. (2021). Comparative Analysis Between Invalidated Biochemical Markers and the Well-established Markers of HELLP Syndrome. Journal of Gynecology and Obstetrics, 9(6), 217-223. https://doi.org/10.11648/j.jgo.20210906.16

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    ACS Style

    Kinikanwo Green; Collins Amadi. Comparative Analysis Between Invalidated Biochemical Markers and the Well-established Markers of HELLP Syndrome. J. Gynecol. Obstet. 2021, 9(6), 217-223. doi: 10.11648/j.jgo.20210906.16

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    AMA Style

    Kinikanwo Green, Collins Amadi. Comparative Analysis Between Invalidated Biochemical Markers and the Well-established Markers of HELLP Syndrome. J Gynecol Obstet. 2021;9(6):217-223. doi: 10.11648/j.jgo.20210906.16

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  • @article{10.11648/j.jgo.20210906.16,
      author = {Kinikanwo Green and Collins Amadi},
      title = {Comparative Analysis Between Invalidated Biochemical Markers and the Well-established Markers of HELLP Syndrome},
      journal = {Journal of Gynecology and Obstetrics},
      volume = {9},
      number = {6},
      pages = {217-223},
      doi = {10.11648/j.jgo.20210906.16},
      url = {https://doi.org/10.11648/j.jgo.20210906.16},
      eprint = {https://article.sciencepublishinggroup.com/pdf/10.11648.j.jgo.20210906.16},
      abstract = {Background: The use of the well-established markers of the Hemolysis, Elevated Liver enzymes and Low Platelet (HELLP) syndrome is very limited in the resource-poor settings of the developing populations. This study aimed to compare the readily available but invalidated biochemical markers with the well-established markers of HELLP syndrome. Methods: This was a retrospective cross-sectional study conducted among women diagnosed with HELLP syndrome in the University of Port Harcourt Teaching Hospital (UPTH) from 2011 to 2020. Data of each eligible case was acquired from the laboratory and medical records using a well-structured template and analyzed by standardized protocols. Results: A total of 230 cases of HELLP syndrome was identified; 200 complete HELLP (cHELLP) and 30 partial HELLP (pHELLP) variants. The cHELLP variants presented at an older age, higher gestational age, and had higher plasma bilirubin (PB), lactate dehydrogenase (LDH), creatinine, and uric acid (UA) but lower albumin concentration compared to those with pHELLP variant (pConclusion: From the foregoing, plasma UA should be considered as an adjunct marker of cHELLP syndrome. However, further studies are highly recommended to evaluate conclusions from this study.},
     year = {2021}
    }
    

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    AU  - Collins Amadi
    Y1  - 2021/11/17
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    N1  - https://doi.org/10.11648/j.jgo.20210906.16
    DO  - 10.11648/j.jgo.20210906.16
    T2  - Journal of Gynecology and Obstetrics
    JF  - Journal of Gynecology and Obstetrics
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    AB  - Background: The use of the well-established markers of the Hemolysis, Elevated Liver enzymes and Low Platelet (HELLP) syndrome is very limited in the resource-poor settings of the developing populations. This study aimed to compare the readily available but invalidated biochemical markers with the well-established markers of HELLP syndrome. Methods: This was a retrospective cross-sectional study conducted among women diagnosed with HELLP syndrome in the University of Port Harcourt Teaching Hospital (UPTH) from 2011 to 2020. Data of each eligible case was acquired from the laboratory and medical records using a well-structured template and analyzed by standardized protocols. Results: A total of 230 cases of HELLP syndrome was identified; 200 complete HELLP (cHELLP) and 30 partial HELLP (pHELLP) variants. The cHELLP variants presented at an older age, higher gestational age, and had higher plasma bilirubin (PB), lactate dehydrogenase (LDH), creatinine, and uric acid (UA) but lower albumin concentration compared to those with pHELLP variant (pConclusion: From the foregoing, plasma UA should be considered as an adjunct marker of cHELLP syndrome. However, further studies are highly recommended to evaluate conclusions from this study.
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Author Information
  • Department of Obstetrics and Gynecology, University of Port Harcourt Teaching Hospital, Port Harcourt, Nigeria

  • Department of Chemical Pathology, Rivers State University Teaching Hospital, Port Harcourt, Nigeria

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