Evidence map›Paper›PMID 41133084›Full record

ArticleCureus2025

Evaluating the Efficacy of Ropivacaine Instillation Through a Subgaleal Drain for Postcraniotomy Pain: A Randomized Controlled Trial.

Usha Shukla, Urvashi Yadav, Deepika Doneria, Priyanka Bhardwaj

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Article in Cureus, 2025. 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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0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Usha ShuklaAnesthesiology and Critical Care, Uttar Pradesh University of Medical Sciences, Saifai, IND.
Urvashi YadavAnesthesiology, Uttar Pradesh University of Medical Sciences, Saifai, IND.
Deepika DoneriaAnesthesiology, Uttar Pradesh University of Medical Sciences, Saifai, IND.
Priyanka BhardwajAnesthesiology and Critical Care, Uttar Pradesh University of Medical Sciences, Saifai, IND.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe majority of patients experience moderate to severe postcraniotomy pain, which causes several complications such as raised intracranial pressure, cerebral hemorrhage, chronic headache, etc. Therefore, this study aimed to assess the efficacy of ropivacaine instillation through subgaleal drain in patients undergoing elective craniotomy to reduce postcraniotomy pain. The primary objective of this study was to assess postoperative pain after craniotomy using the Numeric Rating Scale (NRS) score. MATERIALS AND

methodsA prospective, double-blinded, randomized controlled study was conducted in 120 patients posted for elective craniotomy, randomly allocated into three groups. Group A (n = 40) received 12 mL of 0.9% normal saline, Group B (n = 40) received 12 mL of 0.1% ropivacaine, and Group C (n = 40) received 12 mL of 0.2% ropivacaine. Postoperative NRS score, duration of analgesia, amount of rescue analgesia, patient satisfaction score, and hemodynamic parameters were compared in 24 hours among the three groups.

resultsThe NRS score was lowest in Group C compared to Group A and Group B at all time points, with significant differences observed at 30 minutes, 45 minutes, one hour, and two hours after drug instillation. The duration of analgesia was significantly prolonged in Group C (489.24 ± 204.5 minutes) compared to Group B (112.7 ± 156.5 minutes) and shortest in Group A (43.87 ± 24.2 minutes). The amount of rescue analgesic required was least in the 0.2% ropivacaine group (103.12 ± 36.3 mg) compared to the 0.1% ropivacaine group (144.37 ± 48.5 mg). It was in a substantial amount in the 0.9% normal saline group (176.2 ± 61.7 mg).

conclusionsWe concluded that for postcraniotomy pain, a single-dose 0.2% ropivacaine drug installation at the end of surgery through a surgical (subgaleal) drain had better pain control, a longer duration of analgesia, and a lower analgesic requirement compared to 0.1% ropivacaine and 0.9% normal saline.

Indexed as

brain draincraniotomydrug instillationpostcraniotomy painropivacaine

Identifiers

PMID41133084
PMCPMC12541271

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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.