Evidence map›Paper›PMID 32764878›Full record

Trial reportDrug design, development and therapy2020

Does an Earlier or Late Intravenous Injection of Ondansetron Affect the Dose of Phenylephrine Needed to Prevent Spinal-Anesthesia Induced Hypotension in Cesarean Sections?

Jing Qian, Lin Liu, Xiufeng Zheng, Fei Xiao

Registry-linked trialOpen access · goldAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Drug design, development and therapy, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04703088 (A PROSPECTIVE, RANDOMIZED, DOUBLE-BLINDED STUDY OF THE EFFECT OF A STANDARD DOSE OF INTRAVENOUS ONDANSETRON ON THE EFFECTIVE DOSE IN 50% OF SUBJECTS OF PROPHYLACTIC NOREPINEPHRINE INFUSIONS FOR PREVENTING SPINAL ANESTHESIA-INDUCED HYPOTENSION DURING CESAREAN DELIVERY), which is not on this map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.0field-weighted citation impact, top 23% 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.

NCT04703088 phase3unknown statusnot on this mapstarted 2021, after this paper: background citation

A prospective, randomized, double-blinded study of the effect of a standard dose of intravenous ondansetron on the effective dose in 50% of subjects of prophylactic norepinephrine infusions for preventing spinal anesthesia-induced hypotension during cesarean delivery

TypeinterventionalSponsorLaval UniversityRan2021 to 2021Enrolled60ConditionsHypotension, Anesthesia, Adverse Effect, Spinal and Epidural, Cesarean SectionArmsOndansetron 4 MG, 0.9% Saline
3 · Its place in the literature

Who cites it

5 citing papers in PubMed, 10 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Review
  4. Article
  5. Article
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

4 authors at 1 institution in 1 country.

Jing QianDepartment of Anesthesia, Jiaxing University Affiliated Women and Children Hospital, Jiaxing, People's Republic of China.
Lin LiuDepartment of Anesthesia, Jiaxing University Affiliated Women and Children Hospital, Jiaxing, People's Republic of China.
Xiufeng ZhengDepartment of Obstetrics, Jiaxing University Affiliated Women and Children Hospital, Jiaxing, People's Republic of China.
Fei XiaoDepartment of Anesthesia, Jiaxing University Affiliated Women and Children Hospital, Jiaxing, People's Republic of China.
Jiaxing University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThere was controversy about ondansetron can reduce the incidence of spinal-induced hypotension and decrease the consumption of vasopressor in cesarean delivery with spinal anesthesia. We hypothesized that different timing of ondansetron administration may contribute to the controversy. Therefore, we aimed to determine the effect of different timing of ondansetron administration on the dose requirement of preventing phenylephrine via comparing the ED

methodsSeventy-five parturients were finally enrolled in this prospective, randomized, double-blinded dose finding study. Ondansetron or placebo was administered 5 min or 15 min before intrathecal injection. Up-down allocation method was used to determine the dose of prophylactic phenylephrine for each parturient in the three groups. The initial infusion rate of first patient was 0.5 µg/kg/min. Then, the rate for next patient was varied with increasing or decreasing of 0.05 μg/kg/min according to the response of the previous patient. An effective dose was defined as no hypotension occurred during the study period. An ineffective dose was defined as hypotension occurred during the study period. Study period in this study is from intrathecal injection to neonatal delivery. ED

resultsThe ED

conclusionAn earlier administration of 4 mg prophylactic ondansetron contributed no benefits for lowing the dose of prophylactic phenylephrine compared to a late administration, but can decrease the dose of preventing phenylephrine in patients undergoing cesarean delivery with combined spinal-epidural anesthesia. This finding may be useful for clinical practice and further studies.

Indexed as

AdultAnesthesia, SpinalCesarean SectionDose-Response Relationship, DrugDouble-Blind MethodFemaleHumansHypotensionHypotension, ControlledInjections, IntravenousOndansetronPhenylephrinePregnancyProspective StudiesOndansetronPhenylephrinecesarean deliveryhypotensionondansetronphenylephrinespinal anesthesia

Identifiers

PMID32764878
PMCPMC7371998
OpenAlexW3042480880

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Registered trials

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.