Evidence map›Paper›PMID 41645494›Full record

ArticleMedical science monitor : international medical journal of experimental and clinical research2026

Association of Preoperative Neutrophil-to-Lymphocyte Ratio With Post-Dural Puncture Headache After Cesarean Delivery.

Erkan Bayram, İlke Dolğun

Registry-linked trialAbstract read
In one paragraph

Article in Medical science monitor : international medical journal of experimental and clinical research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT07706751 (The Effectiveness of Inflammatory Indices in Predicting Postdural Puncture Headache), which is not on this map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

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.

NCT07706751 recruitingnot on this map

The Effectiveness of Inflammatory Indices in Predicting Postdural Puncture Headache

Typeobservational_patient_registrySponsorAmasya UniversityRan2026 to 2026Enrolled260ConditionsPregnancy, Headache After Spinal Puncture
3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

2 authors.

Erkan BayramDepartment of Anesthesiology and Reanimation, Istinye University Hospital Medical Park Gaziosmanpasa, Istinye University Faculty of Medicine, Istanbul, Turkey.ORCID 0000-0002-8527-8321
İlke DolğunDepartment of Anesthesiology and Reanimation, Haseki Training and Research Hospital, Istanbul, Turkey.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND Post-dural puncture headache (PDPH) is a common complication of spinal anesthesia in cesarean delivery. While demographic and procedural factors are well recognized, the role of systemic inflammatory indices in pregnant women has not been clearly defined. MATERIAL AND METHODS This retrospective cohort study included 821 pregnant women who underwent elective cesarean delivery under spinal anesthesia between January 2020 and December 2024. PDPH was diagnosed using the ICHD-3 criteria. Preoperative neutrophil-to-lymphocyte ratio (NLR), platelet-to-lymphocyte ratio (PLR), monocyte-to-lymphocyte ratio (MLR), and systemic inflammation response index (SIRI) were evaluated using correlation, logistic regression, and receiver operating characteristic (ROC) analyses. RESULTS PDPH occurred in 133 patients (16.2%). Median NLR values were lower in the PDPH group compared with controls (2.63 vs 3.82, P<0.001). NLR showed a moderate negative correlation with PDPH (ρ=-0.41, P<0.001). After adjustment for potential confounders, only NLR showed a significant association with PDPH (OR 0.51, 95% CI 0.39-0.66, P<0.001). ROC analysis demonstrated a moderate discriminatory performance (AUC 0.76), and a cutoff of ≤3.14 achieved 88.7% sensitivity and 92.1% negative predictive value. CONCLUSIONS Lower preoperative NLR values showed an association with PDPH after cesarean delivery under spinal anesthesia. Identification of a clinically relevant cutoff suggests that NLR may be a practical biomarker for perioperative risk assessment in obstetric anesthesia. Further prospective, multicenter studies are needed to confirm these findings.

Indexed as

Cesarean SectionLymphocytesNeutrophilsPost-Dural Puncture HeadacheAdultAnesthesia, SpinalFemaleHumansPregnancyPreoperative PeriodRetrospective StudiesRisk FactorsROC Curve

Identifiers

PMID41645494
PMCPMC12888405

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