Evidence map›Paper›PMID 42691939›Full record

ArticleHematology, transfusion and cell therapy2026

Effect of red blood cell processing on hemoglobin increment in oncology patients.

Kshitija Mittal, Manuru Sameer, Ravneet Kaur, Awadhesh Kumar Pandey, Paramjit Kaur, Gagandeep Kaur, Shivangi Sharma

Abstract read
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Article in Hematology, transfusion and cell therapy, 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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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

7 authors.

Kshitija MittalDepartment of Transfusion Medicine, Government Medical College and Hospital, Chandigarh, India. Electronic address: drkmittal@gmail.com.
Manuru SameerDepartment of Radiation and Oncology, Government Medical College and Hospital, Chandigarh, India.
Ravneet KaurGovernment Medical College and Hospital, Chandigarh, India.
Awadhesh Kumar PandeyDepartment of Radiation and Oncology, Government Medical College and Hospital, Chandigarh, India.
Paramjit KaurDepartment of Transfusion Medicine, Government Medical College and Hospital, Chandigarh, India.
Gagandeep KaurGovernment Medical College and Hospital, Chandigarh, India.
Shivangi SharmaGovernment Medical College and Hospital, Chandigarh, India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveThis study aimed to evaluate the effect of red blood cell processing on the hemoglobin increment in oncology patients requiring packed red blood cell transfusions. MATERIAL AND

methodsThe study population in this prospective, open-label, randomized controlled trial included healthy blood donors and oncology patients. Only first-time male donors aged 18 to 30 years with hemoglobin levels between 12.5 and 15 g/dL who were donating whole blood were included. Whole blood was collected in 450 mL triple or quintuple blood bag systems with integral leukoreduction filters. The triple bags were processed using the platelet-rich plasma method (non-Saline-Adenine-Glucose-Mannitol), whereas the quintuple bags were processed via the buffy coat method and leukoreduced using inline leukofilters (leukoreduced Saline-Adenine-Glucose-Mannitol). Enrolled patients were randomly allocated to two groups: Group I received non- Saline-Adenine-Glucose-Mannitol packed red blood units, and Group II received leukoreduced Saline-Adenine-Glucose-Mannitol packed red blood units.

resultsGroup II had red blood cell volume loss of 33.81 ± 3.49 mL during processing (p-value < 0.001). The calculated total hemoglobin content was significantly higher in Group I (67.75 ± 3.18 versus 62.47 ± 3.62 g/unit; p value < 0.001). No significant difference was observed between actual total hemoglobin content of Group I and Group II (47.51 ± 2.02 versus 46.44 ± 5.66 g/unit, p = 0.119). No significant difference was observed in the mean hemoglobin increment (Group I: 1.85 ± 0.91 g/dL versus Group II: 1.83 ± 0.64 g/dL, p = 0.887).

conclusionLoss of hemoglobin during processing did not affect the hemoglobin increment in oncology patients in our study.

Indexed as

Component processingHemoglobin incrementOncology patientsRed blood cells

Identifiers

PMID42691939
PMCPMC13571262

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