# Comparing Feto-Maternal Outcomes in Pregnant Women With Normal and Abnormal Liver Function Tests: A Prospective Observational Study

**Authors:** Jyotsna Pathak, Neeru Goel, Sanjeev Kumar Jha, Sweety Rani, Kanchan Kumari, Ranjana Ranjana

PMC · DOI: 10.7759/cureus.56811 · Cureus · 2024-03-24

## TL;DR

This study compares pregnancy outcomes in women with normal and abnormal liver function tests, finding higher maternal risks in those with abnormal tests.

## Contribution

The study identifies specific predictors of maternal mortality linked to abnormal liver function during pregnancy.

## Key findings

- Abnormal liver function tests were significantly associated with maternal mortality but not with fetal mortality.
- Hyperbilirubinemia and elevated ALT were significant predictors of maternal mortality.
- Intrahepatic cholestasis of pregnancy was the main cause of abnormal liver function in pregnant women.

## Abstract

Introduction: Pregnant women with abnormal liver function tests (LFTs) require proper evaluation and timely management to reduce maternal and fetal morbidity and mortality.

Objective: The present study was done with the objective of determining feto-maternal outcomes in antenatal women with abnormal LFTs and comparing them with antenatal women having normal liver function. The prevalence and possible causes of derangements in LFT were also identified.

Method: Pregnant women referred to an antenatal clinic for several reasons pertaining to abnormal liver functions, and those admitted to the labor room for delivery with abnormal LFTs were included in the study. The pregnant women with abnormal LFT were studied prospectively, and they were compared with pregnant women having normal LFT. The fetal and maternal outcomes were also noted.

Results: The pregnant women attending the antenatal clinic with a history of pruritus, abdominal pain, jaundice, nausea/vomiting, hypertension ascites, etc. and delivered at our facility were evaluated. One hundred and eight women had abnormal LFT defined by criteria laid down in material and methods. Eighty-seven women with normal LFT were taken for comparison. In the abnormal LFT, the main cause was intrahepatic cholestasis of pregnancy (IHCP). There were 6 (5.5%) maternal deaths in this group and none in the normal LFTs. There were 6 (5.6%) fetal deaths and 4 (4.6%) in the other group (p-value=1). The prevalence of abnormal LFT was 9.11% throughout pregnancy. Increased bilirubin and alkaline phosphatase (ALP) were significantly correlated with maternal mortality, while gestational age at birth, presence of meconium, appearance, pulse, grimace, activity, and respiration (APGAR) score, maternal mortality, and raised alkaline phosphatase level were found to be significantly associated with fetal mortality.

Conclusion: Patients with abnormal LFT were significantly associated with maternal morbidity and mortality. However, fetal outcomes in patients with abnormal and normal LFT were similar. Hyperbilirubinemia and raised alanine aminotransferase (ALT) were significant predictors of maternal mortality.

## Linked entities

- **Diseases:** intrahepatic cholestasis of pregnancy (MONDO:0100429), hyperbilirubinemia (MONDO:0002408)

## Full-text entities

- **Genes:** ALPP (alkaline phosphatase, placental) [NCBI Gene 250] {aka ALP, PALP, PLAP, PLAP-1}
- **Diseases:** pruritus (MESH:D011537), Hyperbilirubinemia (MESH:D006932), nausea/vomiting (MESH:D020250), deaths (MESH:D003643), abdominal pain (MESH:D015746), Abnormal Liver Function (MESH:D056486), Maternal (MESH:D000079262), IHCP (MESH:C535932), jaundice (MESH:D007565), fetal deaths (MESH:D005313), hypertension ascites (MESH:D001201)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC11036451/full.md

## Figures

1 figure with captions in the complete paper: https://tomesphere.com/paper/PMC11036451/full.md

## References

23 references — full list in the complete paper: https://tomesphere.com/paper/PMC11036451/full.md

---
Source: https://tomesphere.com/paper/PMC11036451