Evidence mapPaperPMID 42170484Full record

ArticleAmerican journal of translational research2026

Effect of ropivacaine-dexamethasone combination on postpartum uterine pain, inflammation, and breastfeeding in multiparous women.

Haiyun Ye, Xiaofei Wang, Dandan Zhou, Haiyan Huang

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Article in American journal of translational research, 2026. 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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1 · What the graph read from it

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Haiyun YeDepartment of Obstetrics, Xi'an Savaid Obstetrics-Gynecology Hospital No. 28, Jinhua North Road, Xincheng District, Xi'an 710000, Shaanxi, China.
Xiaofei WangDepartment of Anesthesiology, Northwest Women's and Children's Hospital No. 1616, Yanxiang Road, Yanta District, Xi'an 710000, Shaanxi, China.
Dandan ZhouDepartment of Anesthesiology, Northwest Women's and Children's Hospital No. 1616, Yanxiang Road, Yanta District, Xi'an 710000, Shaanxi, China.
Haiyan HuangDepartment of Anesthesiology, Shaanxi Provincial Nuclear Industry 215 Hospital No. 35, Weiyang West Road, Qindu District, Xianyang 712000, Shaanxi, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo investigate the effects of epidural ropivacaine combined with dexamethasone on postpartum uterine cramping pain, inflammatory markers, and breastfeeding behavior in multiparous women.

methodsThis retrospective cohort study included 336 women who underwent vaginal delivery and received postpartum epidural analgesia between May 2022 and November 2024, including 211 multiparous women. The observation group (n = 172) received 0.15% ropivacaine combined with 10 mg dexamethasone, while the control group (n = 164) received only 0.15% ropivacaine. The severity of uterine cramping pain was assessed using the Visual Analogue Scale (VAS) at 2, 6, 12, 24, and 48 hours postpartum. Serum levels of tumor necrosis factor-α (TNF-α), interleukin-6 (IL-6), and interleukin-10 (IL-10) were measured using ELISA, and C-reactive protein (CRP) was measured using a quantitative laboratory assay, at 6, 24, and 72 hours postpartum. Breastfeeding indicators and adverse events were recorded.

resultsThe VAS scores at all time points in the observation group were significantly lower than those of the control group (all P < 0.001), with a lower rescue analgesia rate (10.47% vs. 21.34%, P = 0.006). At 24 hours postpartum, the observation group showed significantly lower levels of TNF-α, IL-6, and CRP, and significantly higher levels of IL-10 (all P < 0.001); shorter first breastfeeding time (38.00 minutes vs. 52.00 minutes, P < 0.001); higher frequency of breastfeeding within 48 hours postpartum; and a higher rate of exclusive breastfeeding on day 7 postpartum (84.30% vs. 68.29%, P < 0.001). There were no significant differences in adverse events or neonatal outcome between the two groups (both P > 0.05).

conclusionsEpidural analgesia with ropivacaine combined with dexamethasone effectively alleviates postpartum uterine cramping pain in multiparous women, regulates the inflammatory responses, improves breastfeeding outcomes, and has a good safety profile.

Indexed as

breastfeedingdexamethasoneepidural analgesiainflammatory markersPostpartum analgesiaropivacaineuterine cramping pain

Identifiers

PMID42170484
PMCPMC13186759

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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 Socratic graph.