Evidence map›Paper›PMID 42800924›Full record

ArticleCureus2026

Delayed Adverse Reactions Following Whole-Blood and Plateletpheresis Donation: A Prospective Observational Study From a Tertiary-Care Blood Center.

Sunil Kumar, Tulika Chandra, Archana Solanki, Ashutosh Singh, Neelam Kumari

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Article in Cureus, 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

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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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

5 authors.

Sunil KumarTransfusion Medicine, King George's Medical University, Lucknow, IND.
Tulika ChandraTransfusion Medicine, King George's Medical University, Lucknow, IND.
Archana SolankiTransfusion Medicine, King George's Medical University, Lucknow, IND.
Ashutosh SinghTransfusion Medicine, King George's Medical University, Lucknow, IND.
Neelam KumariPhysical Medicine and Rehabilitation, King George's Medical University, Lucknow, IND.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

aimDelayed adverse reactions occurring after donors leave the blood center may be underrecognized by routine on-site hemovigilance. Comparative data on delayed reactions following whole-blood donation and plateletpheresis within the same institutional setting remain limited. This study aimed to determine the frequency and pattern of delayed adverse reactions and evaluate their associations with donor age, sex, donation status, and donation type.

methodsThis prospective observational study included 17,923 donors (17,633 whole-blood and 290 plateletpheresis) at a single tertiary-care blood center from June 2020 to May 2021. Four-week telephone follow-up was completed by 16,292/17,923 (90.9%) donors using a structured interview schedule. Reaction-specific proportions were calculated using the enrolled donation-group denominators. Associations were assessed using Pearson's chi-square or exact tests, as appropriate; odds ratios (ORs) were crude and unadjusted.

resultsWhole-blood donors most frequently reported fatigue (587/17,633 {3.33%}), bruising (390/17,633 {2.21%}), painful arm (283/17,633 {1.61%}), and hematoma (102/17,633 {0.58%}). Among plateletpheresis donors, hematoma (11/290 {3.79%}) and bruising (9/290 {3.10%}) were most frequent. Plateletpheresis was associated with higher unadjusted odds of hematoma (OR: 6.77, 95% CI: 3.57-12.84; p<0.001), allergy (OR: 14.12, 95% CI: 4.03-49.47; p=0.002), delayed bleeding (OR: 17.37, 95% CI: 3.59-84.09; p=0.009), and nerve irritation (OR: 13.58, 95% CI: 2.91-63.35; p=0.013). Among whole-blood donors, bruising, fatigue, and painful arm were more frequent among females (all p<0.001). Plateletpheresis subgroup findings were considered exploratory because of small subgroup numbers.

conclusionsDelayed-reaction profiles differed across donation modalities, with local venous-access complications more prominent after plateletpheresis. These unadjusted single-center findings require cautious interpretation and multicenter validation.

Indexed as

blood donationblood donor complicationsdelayed adverse reactionsdonor hemovigilancedonor safetyplateletpheresistelephonic follow-upwhole-blood donors

Identifiers

PMID42800924
PMCPMC13614916

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