Evidence map›Paper›PMID 37635978›Full record

Trial reportFrontiers in endocrinology2023

Low-dose esketamine with sufentanil for postcesarean analgesia in women with gestational diabetes mellitus: a prospective, randomized, double-blind study.

Tao Han, Qin Chen, Jie Huang, Jie Zhang, Aiyuan Li, Wei Xu, Zheming Peng, Zhen Li, Liang Chen

Open access · goldAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Frontiers in endocrinology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
3.8field-weighted citation impact, top 6% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

8 citing papers in PubMed, 1 synthesis or guideline pooled it, 12 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Trial
  4. Trial
  5. Review
  6. Article
  7. Review
  8. Esketamine combined with sufentanilFrontiers in pharmacology · 2024
    Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 1 institution in 1 country.

Tao HanDepartment of Anesthesiology, Hunan Provincial Maternal and Child Health Care Hospital, Changsha, China.
Qin ChenDepartment of Anesthesiology, Hunan Provincial Maternal and Child Health Care Hospital, Changsha, China.
Jie HuangDepartment of Anesthesiology, Hunan Provincial Maternal and Child Health Care Hospital, Changsha, China.
Jie ZhangDepartment of Anesthesiology, Hunan Provincial Maternal and Child Health Care Hospital, Changsha, China.
Aiyuan LiDepartment of Anesthesiology, Hunan Provincial Maternal and Child Health Care Hospital, Changsha, China.
Wei XuDepartment of Anesthesiology, Hunan Provincial Maternal and Child Health Care Hospital, Changsha, China.
Zheming PengDepartment of Anesthesiology, Hunan Provincial Maternal and Child Health Care Hospital, Changsha, China.
Zhen LiDepartment of Anesthesiology, Hunan Provincial Maternal and Child Health Care Hospital, Changsha, China.
Liang ChenDepartment of Anesthesiology, Hunan Provincial Maternal and Child Health Care Hospital, Changsha, China.
Hunan Provincial Maternal and Child Health Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Pregnant women with gestational diabetes mellitus (GDM) require more analgesics after cesarean delivery than those who do not have GDM. Uncontrolled pain following cesarean delivery is a major problem in women with GDM. We investigate the efficacy of low-dose esketamine combined with sufentanil intravenous patient-controlled analgesia (PCA)for postcesarean analgesia in women with GDM. Methods: One hundred forty pregnant women with GDM were enrolled participate in this randomized controlled trial and were randomized into two groups (70 in each group). The esketamine (S) group was given esketamine +sufentanil + ondansetron, and the control (C) group was given sufentanil +ondansetron. The primary outcome is sufentanil consumption at 24 hours postoperatively, the secondary outcomes are sufentanil consumption at 6 hours postoperatively, pain scores at 6, 24 and 48 hours postoperatively. Results: Compared with group C, group S had significantly lower sufentanil consumption at 6 and 24 hours postoperatively (P= 0.049 and P<0.001), significantly lower activities VAS(pain during activities)scores at 6 hours postoperatively, rest and activities VAS (pain at rest and pain during activities)scores at 24 hours postoperatively, and activities VAS scores at 48 hours postoperatively(P=0.022, P =0.002, P=0.001 and P=0.007). Compared to group C, the time to bowel function return was significantly shorter in group S. There was no significant difference in rest VAS (pain at rest) scores at 6 and 48 hours postoperatively (P>0.05). The time to first lactation was not significantly different between the two groups (P>0.05). There was no significant difference in neonatal neurobehavioral scores between the two groups (P>0.05). Conclusion: Compared to sufentanil PCA, adding low dose of esketamine significantly reduced the consumption of sufentanil while providing equally effective post cesarean analgesia in the patients with gestational diabetes.

Indexed as

AnalgesiaDiabetes, GestationalDouble-Blind MethodFemaleHumansInfant, NewbornKetamineOndansetronPainPregnancyProspective StudiesSufentanilEsketamineKetamineOndansetronSufentanilcesarean deliveryesketaminegestational diabetesintravenous patient-controlled analgesiaprospective study

Identifiers

PMID37635978
PMCPMC10454896
OpenAlexW4385753850

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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 OpenQuestion graph.