# Clinical Analysis of Neonatal Influenza in the Neonatal Intensive Care Unit: A Retrospective Study

**Authors:** Min Zhou, Jia Chen, Jing Zhao, Zhuli Yu, Mengjuan Feng, Xiang Qiu

PMC · DOI: 10.1002/iid3.70379 · Immunity, Inflammation and Disease · 2026-02-17

## TL;DR

This study examines the clinical features and treatment outcomes of 26 newborns with influenza admitted to a neonatal intensive care unit in China.

## Contribution

The study provides a detailed clinical analysis of neonatal influenza cases and confirms the safety and effectiveness of oseltamivir treatment in this population.

## Key findings

- Influenza A was the predominant type among 26 neonates, with one co-infected with influenza B.
- Common symptoms included fever, nasal congestion, and cough, with non-specific clinical presentations.
- Oseltamivir treatment was safe and effective, with all patients recovering.

## Abstract

To describe the clinical characteristics, treatment, and outcomes of neonatal influenza.

Retrospectively analyzed clinical data on 26 neonates who were diagnosed with neonatal influenza by positive influenza nasopharyngeal swab antigen tests, and admitted to the neonatal intensive care unit of Sichuan Province Chengdu Integrated TCM & Western Medicine Hospital in China, between January 2022 to December 2023.

Twenty‐six neonates were admitted, 25 with influenza A, whereas 1 co‐infected influenza A and B. Nine patients had close contact with family members showing respiratory symptoms prior to hospitalization. Common symptoms included fever (53.85%), nasal congestion (46.15%), cough, neonatal jaundice, and loss of appetite. The most frequent laboratory abnormalities were elevated CK‐MB (92.3%), lactic acid (80.77%), prominent lymphocytosis in both count and percentage, elevated monocyte percentage and AST. All patients treated with oseltamivir and recovered.

In this single‐year study, influenza A was the predominant type identified. The clinical symptoms are non‐specific, and main symptom is fever 14/26 (53.85%). Treatment with oseltamivir is safe and had favorable outcomes.

## Linked entities

- **Chemicals:** oseltamivir (PubChem CID 65028)
- **Diseases:** influenza (MONDO:0005812)

## Full-text entities

- **Genes:** CD44 (CD44 molecule (IN blood group)) [NCBI Gene 960] {aka CDW44, CSPG8, ECM-III, ECMR-III, H-CAM, HCELL}, UROD (uroporphyrinogen decarboxylase) [NCBI Gene 7389] {aka PCT, UPD}, GPT (glutamic--pyruvic transaminase) [NCBI Gene 2875] {aka AAT1, ALT, ALT1, GPT1, SGPT}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}, SLC17A5 (solute carrier family 17 member 5) [NCBI Gene 26503] {aka AST, ISSD, NSD, SD, SIALIN, SIASD}, CD8A (CD8 subunit alpha) [NCBI Gene 925] {aka CD8, CD8alpha, IMD116, Leu2, p32}, CMPK1 (cytidine/uridine monophosphate kinase 1) [NCBI Gene 51727] {aka CK, CMK, CMPK, UMK, UMP-CMPK, UMPK}
- **Diseases:** shock (MESH:D012769), respiratory infections (MESH:D012141), inflammation (MESH:D007249), gastrointestinal symptoms (MESH:D012817), congenital abnormalities (MESH:D000013), hemophagocytic syndrome (MESH:D051359), influenza (MESH:D007251), respiratory illness (MESH:D012140), breathlessness (MESH:D004417), oliguria (MESH:D009846), interstitial edema (MESH:D004487), unresponsiveness (MESH:C567934), respiratory (MESH:D012131), congenital or acquired immunodeficiency (MESH:D000163), neonatal sepsis (MESH:D000071074), multiple organ dysfunction (MESH:D009102), neonatal hyperbilirubinemia (MESH:D051556), febrile (MESH:D000071072), epigastric (MESH:C537170), diarrhea (MESH:D003967), acute renal failure (MESH:D058186), bacterial pneumonia (MESH:D018410), neonatal pneumonia (MESH:D011014), neurological abnormalities (MESH:D009461), genetic metabolic disease (MESH:D008659), convulsions (MESH:D012640), fever (MESH:D005334), milk vomiting (MESH:D014839), Nosocomial infection (MESH:D003428), co (MESH:D060085), rhinorrhea (MESH:D012818), blood disease (MESH:D006402), neonatal jaundice (MESH:D007567), bacterial or viral infections (MESH:D014777), preterm birth (MESH:D047928), agitation (MESH:D011595), infected (MESH:D007239), nasal congestion (MESH:D009668), cough (MESH:D003371), dehydration (MESH:D003681), lethargy (MESH:D053609), congenital heart disease (MESH:D006330), tachypnea (MESH:D059246), stillbirth (MESH:D050497), bacterial infection (MESH:D001424), spontaneous abortion (MESH:D000022), abdominal bloating (MESH:D000007), loss of appetite (MESH:D001068), ANE (OMIM:608033), lymphocytosis (MESH:D008218), sepsis (MESH:D018805)
- **Chemicals:** azithromycin (MESH:D017963), peramivir (MESH:C414210), oxygen (MESH:D010100), lactic acid (MESH:D019344), amoxicillin clavulanate potassium (MESH:D019980), neuraminidase inhibitor (-), cefotaxime sodium (MESH:D002439), Oseltamivir (MESH:D053139)
- **Species:** Escherichia coli (E. coli, species) [taxon 562], Mycoplasmoides pneumoniae (Filterable agent of primary atypical pneumonia, species) [taxon 2104], Klebsiella pneumoniae (species) [taxon 573], Severe acute respiratory syndrome coronavirus 2 (no rank) [taxon 2697049], human metapneumovirus (no rank) [taxon 162145], Orthomyxoviridae (family) [taxon 11308], Klebsiella oxytoca (species) [taxon 571], Staphylococcus aureus (species) [taxon 1280], Adenoviridae (family) [taxon 10508], Homo sapiens (human, species) [taxon 9606], Influenza A virus (no rank) [taxon 11320]

## Full text

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## Figures

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## References

49 references — full list in the complete paper: https://tomesphere.com/paper/PMC12914074/full.md

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Source: https://tomesphere.com/paper/PMC12914074