Evidence map›Paper›PMID 42328403›Full record

ArticleJournal of education and health promotion2026

Comparing additive effect of dexmedetomidine and neostigmine to bupivacaine on postspinal anesthesia cesarean section induced pain intensity: A health promotion Approach.

Alieh Zamani Kiasari, Iman Asdaghijahromi, Tahereh Galini Moghadam, Abbas Alipour, Goli Aezzi, Nahid Aghaei

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Article in Journal of education and health promotion, 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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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Alieh Zamani KiasariDepartment of Anaesthesiology, Faculty of Medicine, Mazandaran University of Medical Sciences, Sari, Iran.
Iman AsdaghijahromiDepartment of Anaesthesiology, Faculty of Medicine, Mazandaran University of Medical Sciences, Sari, Iran.
Tahereh Galini MoghadamDepartment of Obstetrics and Gynecology, School of Medicine, Mazandaran University of Medical Sciences, Sari, Iran.
Abbas AlipourDepartment of Community Medicine, School of Medicine, Mazandaran University of Medical Sciences, Sari, Iran.
Goli AezziFellowship Pain Medicine, Department of Anaesthesiology, Mazandaran University of Medical Sciences, Sari, Iran.
Nahid AghaeiDepartment of Anesthesiology, Operating Room and Emergencies, School of Allied Medical Sciences. Mazandaran University of Medical Sciences, Sari, Iran.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThis study pursued the goal to evaluate the effect of dexmedetomidine and neostigmine on pain, sedation, and locomotor properties during and after surgery in the patients receiving intrathecal bupivacaine for spinal anesthesia in women with elective cesarean section (CS) and to assess the effective dose of dexmedetomidine and neostigmine. MATERIALS AND

methodsThe present clinical trial study was performed on the women as the candidates for elective CS between 2022 and 2023 in Imam Khomeini Educational and Medical Center located in Mazandaran province. The patients for spinal anesthesia were divided into two groups: (1) receiving bupivacaine and dexmedetomidine (1 μg) and (2) receiving bupivacaine and neostigmine (10 μg). Bromage, Visual Analog Scale, and Ramsay scores were recorded in each patient at the intervention time, 2, 4, 8, and 12 h after the onset of anesthesia, along with the demographic and clinical baseline characteristics. The generalized statistical estimating model (GEE) was used to compare the variance of the aforementioned criteria between the two groups. The statistical significance level of 0.05 was used, and all statistical analyses were conducted using STATA/MP. 17: Stata|; M Statistical Software: Release 17. College Station, TX: StataCorp LLC.

resultsOne hundred ten individuals participated in this study. The study participants' mean age was 31.56 ± 5.92. The level of pain intensity in group 1 was lower than that of group 2, which was statistically significant (

conclusionUsing dexmedetomidine exerts a greater and better effect on reducing pain intensity and boosts the sedative effect of neostigmine in the patients undergoing CS. It is suggested to run a study with a larger statistical community to deal with this issue. The results of this study can be useful in making prevention decisions and maintaining performance of women.

Indexed as

Cesarean Sectiondexmedetomidinehealth promotionneostigminepainspinal anesthesia

Identifiers

PMID42328403
PMCPMC13278596

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LicenceCC BY-NC-ND
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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 Socratic graph.