# COVID‐19‐Related Hematological Abnormalities Among Adults; A Cross‐Sectional Study in a Resource‐Limited Setting

**Authors:** Charles Nkansah, Felix Osei‐Boakye, Samuel K. Appiah

PMC · DOI: 10.1002/iid3.70322 · Immunity, Inflammation and Disease · 2026-01-12

## TL;DR

This study found that many adults with COVID-19 in a resource-limited setting had blood-related issues like anemia and low platelet counts, which are linked to more severe disease.

## Contribution

The study provides insights into hematological abnormalities in a resource-limited setting, emphasizing their clinical relevance for managing severe COVID-19.

## Key findings

- Anemia was present in 60.4% of patients, with normocytic and macrocytic types being most common.
- Thrombocytopenia was detected in 56.2% of patients, and blood cell counts predicted severe disease.
- Older adults and rural residents were more likely to experience anemia.

## Abstract

Alterations in hematological parameters in SARS‐CoV‐2 infection may contribute to disease severity and poor outcomes. This study reports the hematological profile of COVID‐19 patients.

This was a cross‐sectional study involving 169 confirmed COVID‐19 patients conducted at Sunyani Teaching Hospital between January and August, 2022. Sociodemographic, clinical, and laboratory data were obtained. Full blood count was performed using an automated hematology analyzer, and systemic inflammatory indices were calculated.

Participants were mostly young adults (51.5%), females (53.8%), resided in urban settings (41.4%), and aged 20‐81 years with a median age of 35.0 (29.0–47.0) years. Overall, anemia was present in 60.4% of the COVID‐19 patients (56.4% in males and 63.7% in females), with 23.7%, 23.7%, and 13.0% experiencing mild, moderate, and severe anemia, respectively. The COVID‐19 patients mostly had normocytic normochromic anemia (50.3%), and 37.9% had macrocytic normochromic anemia. Older adults (6.600 times, p = 0.004), middle‐aged adults (4.435 times, p = 0.034), and rural dwellers (3.759 times, p = 0.012) were associated with anemia among the COVID‐19 patients. Thrombocytopenia was detected in 56.2% of the patients, and 36.7%, 16.0%, and 2.4% had mild, moderate and severe thrombocytopenia respectively. Leucocyte alterations among the patients included leucopenia (22.5%), leucocytosis (17.2%), neutropenia (40.8%), and lymphocytosis (39.6%). Total leucocyte count (AUC: 0.818, p < 0.001), absolute neutrophil count (AUC: 0.816, p < 0.001), and absolute lymphocyte count (AUC: 0.804, p < 0.001) predicted severe COVID‐19 among the participants. Bicytopenia and pancytopenia were observed in 37.3% and 17.8%, respectively.

COVID‐19 is associated with diverse and clinically relevant hematological abnormalities, remarkably anemia, thrombocytopenia, and leucocyte alterations, and usually relate with disease severity. Routine blood cell analysis is essential in the management of COVID‐19, particularly in resource‐limited settings.

## Linked entities

- **Diseases:** COVID-19 (MONDO:0100096)

## Full-text entities

- **Genes:** ACE2 (angiotensin converting enzyme 2) [NCBI Gene 59272] {aka ACEH}, EPO (erythropoietin) [NCBI Gene 2056] {aka DBAL, ECYT5, EP, MVCD2}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, IFNG (interferon gamma) [NCBI Gene 3458] {aka IFG, IFI, IMD69}, PMCH (pro-melanin concentrating hormone) [NCBI Gene 5367] {aka MCH, ppMCH}, REN (renin) [NCBI Gene 5972] {aka ADTKD4, HNFJ2, RTD}, IL1A (interleukin 1 alpha) [NCBI Gene 3552] {aka IL-1 alpha, IL-1A, IL1, IL1-ALPHA, IL1F1}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}
- **Diseases:** Anemia (MESH:D000740), Lymphocytosis (MESH:D008218), Blood cell abnormalities (MESH:D006402), Neutropenia (MESH:D009503), hypochromic anemia (MESH:D000747), immune dysregulation (OMIM:614878), infected (MESH:D007239), Microcytosis (OMIM:616959), iron (MESH:D000090463), Leucopenia (MESH:C536227), macrocytosis (MESH:C564004), neutrophilia (MESH:C563010), HIV (MESH:D015658), fatigue (MESH:D005221), Thrombocytopenia (MESH:D013921), respiratory failure (MESH:D012131), multi-organ dysfunction (MESH:D009102), coagulopathies (MESH:D001778), malignancies (MESH:D009369), disseminated intravascular coagulation (MESH:D004211), death (MESH:D003643), nutritional deficiencies (MESH:D044342), cough (MESH:D003371), malaria (MESH:D008288), monocytosis (MESH:C538328), immune (MESH:D007154), hypoxia (MESH:D000860), leucocyte abnormalities (MESH:D000014), Pancytopenia (MESH:D010198), loss of smell (MESH:D000086582), nausea (MESH:D009325), viral infections (MESH:D014777), beta-coronavirus (MESH:D018352), COVID-19 (MESH:D000086382), parasitic infections (MESH:D010272), headache (MESH:D006261), erythrocyte abnormalities (MESH:D012010), renal dysfunction (MESH:D007674), elevated (MESH:D006937), lung damage (MESH:D008171), pneumonia (MESH:D011014), bone marrow failure syndromes (MESH:D000080983), bone marrow dysfunction (MESH:D001855), lymphopenia (MESH:D008231), inflammation (MESH:D007249), loss of taste (MESH:D000370), Platelet abnormalities (MESH:D001791), chronic kidney disease (MESH:D051436), Cell (MESH:D002292), nutritional deficits (MESH:D009748), Fever (MESH:D005334)
- **Chemicals:** iron (MESH:D007501), oxygen (MESH:D010100), aldosterone (MESH:D000450)
- **Species:** Severe acute respiratory syndrome coronavirus 2 (no rank) [taxon 2697049], Meleagris gallopavo (common turkey, species) [taxon 9103], Homo sapiens (human, species) [taxon 9606]

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## References

44 references — full list in the complete paper: https://tomesphere.com/paper/PMC12796507/full.md

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Source: https://tomesphere.com/paper/PMC12796507