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Progression of Class 3 HELLP Syndrome: Biochemical Indicators Among Women in Port Harcourt, South-south Nigeria

Received: 25 October 2021    Accepted: 10 November 2021    Published: 23 November 2021
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Abstract

Background: Class 3 HELLP syndrome (c3HELLPs) is a mild transition stage of HELLP syndrome (HELLPs) with potential for rapid progression to more severe variants. Biochemical indicators of its progression are poorly understood. Hence, the current study evaluated the likely biochemical indicators of this progression among women in Port Harcourt, Nigeria. Methods: The current study was designed as a retrospective cross-sectional one and was conducted among women diagnosed with c3HELLPs in the University of Port Harcourt Teaching Hospital (UPTH) from 2011-2020. Relevant data from all eligible cases were abstracted from case notes, nurses’ charts, laboratory, and medical records using well-structured research pro forma and analyzed using the Statistical Package for Social Sciences version 25. Results: During the study period, 84 cases of c3HELLPs presented; 58 progressed while 26 did not progress while on management. The progressed cases had higher mean and abnormal levels of plasma uric acid (UA), creatinine, but low and abnormal levels of plasma albumin compared to the non-progressed c3HELLPs cases (p<0.05). The abnormally high UA, creatinine, and abnormally low albumin levels were associated with increased risk of c3HELLPs progression on crude/adjusted logistic regression (LR) and ROC analysis. However, the UA had a superior LR (crude=OR: 4.097; 95%CI: 2.917-5.753; p<0.001; adjusted=OR: 4.723; 95%CI: 3.199-5.763; p<0.001) and ROC (AUC: 0.978; 95%CI: 0.887-1.000; <0.001) predictive potentials. Conclusion: The study showed that rising plasma UA, creatinine levels but falling plasma albumin levels may indicate an increased risk of c3HELLPs progression. This finding should be considered along with clinical features and other HELLP-defined laboratory markers during the management of c3HELLPs. However, we recommend further studies to evaluate conclusions from this study.

Published in Science Journal of Clinical Medicine (Volume 10, Issue 4)
DOI 10.11648/j.sjcm.20211004.17
Page(s) 120-125
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, HELLP Syndrome, Class 3 HELLP Syndrome

References
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[2] Dusse LM, Alpoim PN, Silva JT, Rios DR, Brandão AH, Cabral AC. Revisiting HELLP syndrome. Clin Chim Acta. 2015; 451: 117-20. doi: 10.1016/j.cca.2015.10.024.
[3] Haram K, Svendsen E, Abildgaard U. The HELLP syndrome: clinical issues and management. A Review. BMC Pregnancy Childbirth. 2009; 9: 8. doi: 10.1186/1471-2393-9-8.
[4] Aloizos S, Seretis C, Liakos N, Aravosita P, Mystakelli C, Kanna E, et al. HELLP syndrome: understanding and management of a pregnancy-specific disease. J Obstet Gynaecol. 2013; 33 (4): 331-7. doi: 10.3109/01443615.2013.775231.
[5] Rahman H. Pinning down HELLP: a review. Biomed J Sci Tech Res. 2017; 1 (3): 646-50.
[6] Rimaitis K, Grauslyte L, Zavackiene A, Baliuliene V, Nadisauskiene R, Macas A. Diagnosis of HELLP syndrome: a 10-year survey in a perinatology centre. Int J Environ Res Public Health. 2019; 16 (1): 109.
[7] Martin Jr JN, Owens MY, Keiser SD, Parrish MR, Tam Tam KB, Brewer JM, Cushman JL, May WL. Standardized Mississippi Protocol treatment of 190 patients with HELLP syndrome: slowing disease progression and preventing new major maternal morbidity. Hypertension in pregnancy. 2012; 31 (1): 79-90.
[8] Sibai BM, Ramadan MK, Usta I, Salama M, Mercer BM, Friedman SA. Maternal morbidity and mortality in 442 pregnancies with hemolysis, elevated liver enzymes, and low platelets (HELLP syndrome). Am J Obstet gynecol. 1993; 169 (4): 1000-6.
[9] Abildgaard U, Heimdal K. Pathogenesis of the syndrome of hemolysis, elevated liver enzymes, and low platelet count (HELLP): a review. Eur J Obstet Gynecol Reprod Biol. 2013; 166 (2): 117-23.
[10] Wang L, Tang D, Zhao H, Lian M. Evaluation of Risk and Prognosis Factors of Acute Kidney Injury in Patients With HELLP Syndrome During Pregnancy. Front Physiol. 2021; 12: 650826. doi: 10.3389/fphys.2021.650826.
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[12] Ye W, Shu H, Yu Y, Li H, Chen L, Liu J, et al. Acute kidney injury in patients with HELLP syndrome. Nephrology. 2019; 51: 1199 – 206.
[13] Asghamia M, Mirblouk F, Kazemi S, Pourmarzi D, Keivani MM, Heirati SFD. Maternal serum uric acid and maternal and neonatal complications in preeclamptic women: A cross-sectional study. Int J Reprod Biomed. 2017; 15 (9): 583 – 588.
[14] Bellos I, Pergialiotis V, Loutradis D, Daskalakis G. The prognostic role of serum uric acid levels in preeclampsia: A meta-analysis. J Clin Hypertens. 2020; 22: 826 – 34.
[15] Gedik E, Yucei N, Salin T, Koca E, Colak YZ, Togal T. Hemolysis, elevated liver enzymes, and low platelet syndrome: outcomes for patients admitted to intensive care at a tertiary referral hospital. Hypertens Pregnancy. 2017; 36 (1): 21-29.
[16] Chen H, Tao F, Fang X, Wang X. Association of hypoproteinemia in preeclampsia with maternal and perinatal outcomes: A retrospective analysis of high-risk women. J Res Med Sci. 2016; 21; 98. Doi: 10.4103/1735-1995.193170.
[17] Seong WJ, Chong GO, Hong DG, Lee YS, Cho YL, Cheun SS, et al. Clinical significance of serum albumin levels in pregnancy-related hypertension. J Obstet Gynecol Res. 2010; 36 (6): 1165 – 72.
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  • APA Style

    Kinikanwo Green, Collins Amadi. (2021). Progression of Class 3 HELLP Syndrome: Biochemical Indicators Among Women in Port Harcourt, South-south Nigeria. Science Journal of Clinical Medicine, 10(4), 120-125. https://doi.org/10.11648/j.sjcm.20211004.17

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    ACS Style

    Kinikanwo Green; Collins Amadi. Progression of Class 3 HELLP Syndrome: Biochemical Indicators Among Women in Port Harcourt, South-south Nigeria. Sci. J. Clin. Med. 2021, 10(4), 120-125. doi: 10.11648/j.sjcm.20211004.17

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    AMA Style

    Kinikanwo Green, Collins Amadi. Progression of Class 3 HELLP Syndrome: Biochemical Indicators Among Women in Port Harcourt, South-south Nigeria. Sci J Clin Med. 2021;10(4):120-125. doi: 10.11648/j.sjcm.20211004.17

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  • @article{10.11648/j.sjcm.20211004.17,
      author = {Kinikanwo Green and Collins Amadi},
      title = {Progression of Class 3 HELLP Syndrome: Biochemical Indicators Among Women in Port Harcourt, South-south Nigeria},
      journal = {Science Journal of Clinical Medicine},
      volume = {10},
      number = {4},
      pages = {120-125},
      doi = {10.11648/j.sjcm.20211004.17},
      url = {https://doi.org/10.11648/j.sjcm.20211004.17},
      eprint = {https://article.sciencepublishinggroup.com/pdf/10.11648.j.sjcm.20211004.17},
      abstract = {Background: Class 3 HELLP syndrome (c3HELLPs) is a mild transition stage of HELLP syndrome (HELLPs) with potential for rapid progression to more severe variants. Biochemical indicators of its progression are poorly understood. Hence, the current study evaluated the likely biochemical indicators of this progression among women in Port Harcourt, Nigeria. Methods: The current study was designed as a retrospective cross-sectional one and was conducted among women diagnosed with c3HELLPs in the University of Port Harcourt Teaching Hospital (UPTH) from 2011-2020. Relevant data from all eligible cases were abstracted from case notes, nurses’ charts, laboratory, and medical records using well-structured research pro forma and analyzed using the Statistical Package for Social Sciences version 25. Results: During the study period, 84 cases of c3HELLPs presented; 58 progressed while 26 did not progress while on management. The progressed cases had higher mean and abnormal levels of plasma uric acid (UA), creatinine, but low and abnormal levels of plasma albumin compared to the non-progressed c3HELLPs cases (p<0.05). The abnormally high UA, creatinine, and abnormally low albumin levels were associated with increased risk of c3HELLPs progression on crude/adjusted logistic regression (LR) and ROC analysis. However, the UA had a superior LR (crude=OR: 4.097; 95%CI: 2.917-5.753; p<0.001; adjusted=OR: 4.723; 95%CI: 3.199-5.763; p<0.001) and ROC (AUC: 0.978; 95%CI: 0.887-1.000; <0.001) predictive potentials. Conclusion: The study showed that rising plasma UA, creatinine levels but falling plasma albumin levels may indicate an increased risk of c3HELLPs progression. This finding should be considered along with clinical features and other HELLP-defined laboratory markers during the management of c3HELLPs. However, we recommend further studies to evaluate conclusions from this study.},
     year = {2021}
    }
    

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  • TY  - JOUR
    T1  - Progression of Class 3 HELLP Syndrome: Biochemical Indicators Among Women in Port Harcourt, South-south Nigeria
    AU  - Kinikanwo Green
    AU  - Collins Amadi
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    N1  - https://doi.org/10.11648/j.sjcm.20211004.17
    DO  - 10.11648/j.sjcm.20211004.17
    T2  - Science Journal of Clinical Medicine
    JF  - Science Journal of Clinical Medicine
    JO  - Science Journal of Clinical Medicine
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    SN  - 2327-2732
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    AB  - Background: Class 3 HELLP syndrome (c3HELLPs) is a mild transition stage of HELLP syndrome (HELLPs) with potential for rapid progression to more severe variants. Biochemical indicators of its progression are poorly understood. Hence, the current study evaluated the likely biochemical indicators of this progression among women in Port Harcourt, Nigeria. Methods: The current study was designed as a retrospective cross-sectional one and was conducted among women diagnosed with c3HELLPs in the University of Port Harcourt Teaching Hospital (UPTH) from 2011-2020. Relevant data from all eligible cases were abstracted from case notes, nurses’ charts, laboratory, and medical records using well-structured research pro forma and analyzed using the Statistical Package for Social Sciences version 25. Results: During the study period, 84 cases of c3HELLPs presented; 58 progressed while 26 did not progress while on management. The progressed cases had higher mean and abnormal levels of plasma uric acid (UA), creatinine, but low and abnormal levels of plasma albumin compared to the non-progressed c3HELLPs cases (p<0.05). The abnormally high UA, creatinine, and abnormally low albumin levels were associated with increased risk of c3HELLPs progression on crude/adjusted logistic regression (LR) and ROC analysis. However, the UA had a superior LR (crude=OR: 4.097; 95%CI: 2.917-5.753; p<0.001; adjusted=OR: 4.723; 95%CI: 3.199-5.763; p<0.001) and ROC (AUC: 0.978; 95%CI: 0.887-1.000; <0.001) predictive potentials. Conclusion: The study showed that rising plasma UA, creatinine levels but falling plasma albumin levels may indicate an increased risk of c3HELLPs progression. This finding should be considered along with clinical features and other HELLP-defined laboratory markers during the management of c3HELLPs. However, we recommend further studies to evaluate conclusions from this study.
    VL  - 10
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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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