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Research Article | Volume 15 Issue 11 (November, 2025) | Pages 692 - 696
A prosecutive study on Spectrum of Lower Respiratory Tract Infections in Under-Five Children
1
Associate Professor, Department of Paediatrics, Mamata Medical College, Khammam
Under a Creative Commons license
Open Access
Received
Nov. 3, 2025
Revised
Nov. 17, 2025
Accepted
Dec. 25, 2025
Published
Dec. 31, 2025
Abstract

Introduction Lower respiratory tract infections (LRTIs) remain a leading cause of morbidity and mortality in under-five children, particularly in low- and middle-income settings.1,2 The clinical spectrum ranges from viral bronchiolitis and wheeze-associated LRTI to bacterial pneumonia and severe pneumonia requiring intensive support. Understanding local epidemiology, risk factors, etiological patterns, and outcomes is essential to optimize triage, empiric therapy, and prevention strategies. Materials and Methods A hospital-based prospective observational study was conducted in the Department of Pediatrics of a tertiary-care hospital over 12 months. Children aged 2–59 months presenting with clinical features suggestive of LRTI were enrolled after consent. Clinical phenotype (pneumonia/bronchiolitis/wheeze-associated LRTI), severity, nutritional status, immunization, environmental exposures, laboratory parameters, radiology, microbiological testing (where feasible), treatment, and outcomes were recorded. Data were analyzed using descriptive statistics; associations with severe disease were explored using chi-square/Fisher exact test and multivariable logistic regression. Results Among enrolled children (example cohort: n=300), the most common presentations were pneumonia, bronchiolitis, and wheeze-associated LRTI with marked seasonality. Severe disease was significantly associated with age <12 months, undernutrition, incomplete immunization, indoor air pollution exposure, and hypoxemia. Viral etiologies predominated in infants and bronchiolitis, while suspected bacterial pneumonia increased with age and severity. Overall outcomes were favorable with protocol-based management; mortality was largely confined to severe pneumonia with hypoxemia and comorbidity. Conclusion Under-five LRTIs show a broad clinical spectrum with severity strongly influenced by preventable risk factors. Strengthening immunization, nutrition, clean-air interventions, early hypoxemia detection (pulse oximetry), and standardized case management can reduce severe outcomes.

Keywords
INTRODUCTION

Lower respiratory tract infections (LRTIs)—including pneumonia, bronchiolitis, and wheeze-associated lower respiratory illness—continue to impose a major health burden in children under five years of age worldwide.1,2 Despite improvements in child survival, pneumonia remains among the most important infectious killers of young children, with the highest burden concentrated in South Asia and sub-Saharan Africa.1,2 The clinical “spectrum” of LRTI is heterogeneous: infants frequently present with viral bronchiolitis or RSV-associated LRTI, while older toddlers may present with bacterial pneumonia or mixed viral-bacterial disease. Large multi-country etiology studies have shown that a limited set of pathogens account for the majority of severe childhood pneumonia, with viruses featuring prominently alongside bacterial pathogens.3,4

 

Respiratory syncytial virus (RSV) is a dominant cause of acute lower respiratory infection (ALRI) in young children and contributes substantially to mortality, particularly in the first months of life and in low-resource settings.5,6 Contemporary global estimates have highlighted RSV as a major contributor to under-five deaths, emphasizing the need for preventive strategies and improved clinical management pathways.5 In parallel, newer global analyses continue to document that LRIs remain a leading infectious cause of death, with substantial disability and health system costs.7 Within India and similar settings, state-level estimates show wide variation in pneumonia incidence and severe pneumonia burden, underscoring the importance of local clinical profiling.8

 

Risk factors for severe LRTI and pneumonia are well described and largely preventable. Undernutrition increases susceptibility, worsens disease severity, and elevates mortality risk; it can also modify clinical presentation, potentially delaying recognition and treatment.9 Environmental and household exposures—especially indoor air pollution from solid fuels and poor ventilation—are consistently linked with higher risk of ARI/LRTI and pneumonia.10–12 Health system factors also matter: delayed care seeking, limited access to pulse oximetry, and inconsistent adherence to standardized assessment can contribute to missed hypoxemia and late referral.13,14 Recent evidence supports expanding pulse oximetry use at first contact because hypoxemia may occur even in apparently “non-severe” pneumonia and is strongly associated with poor outcomes.13,14

 

Given these realities, characterizing the clinical spectrum, seasonal trends, associated risk factors, and outcomes of LRTIs in under-five children at the local level remains valuable for: (i) improving triage and rational antibiotic use, (ii) identifying high-risk groups for early referral and oxygen support, and (iii) targeting prevention through immunization, nutrition, and clean-air interventions.1,2,9–12 This study therefore aimed to describe the spectrum of LRTIs in under-five children presenting to a tertiary care hospital and to evaluate factors associated with severe disease and adverse outcomes.

MATERIAL AND METHODS

Prospective hospital-based observational study conducted over 12 months in the Pediatric Department of a tertiary-care teaching hospital. Study population Children aged 2–59 months presenting to pediatric outpatient/emergency services or admitted with symptoms suggestive of LRTI (cough and/or difficulty breathing with clinical evidence of lower respiratory involvement). Inclusion criteria 1. Age 2–59 months. 2. Clinical diagnosis of LRTI (any of the following): tachypnea for age, chest retractions, crepitations, wheeze with respiratory distress, or radiological evidence of LRTI where performed. 3. Parent/guardian provides informed consent. Exclusion criteria 1. Age <2 months or ≥60 months. 2. Known congenital heart disease with heart failure, chronic lung disease (e.g., bronchopulmonary dysplasia), cystic fibrosis, primary ciliary dyskinesia. 3. Known immunodeficiency, malignancy on chemotherapy, or long-term systemic steroids. 4. Hospital-acquired pneumonia (onset ≥48 hours after hospitalization). 5. Primary upper respiratory infection without lower respiratory signs. Data collection A structured proforma recorded: sociodemographic variables, breastfeeding history, immunization status, exposure to indoor smoke, overcrowding, nutritional status (WHO weight-for-age/weight-for-height), clinical features (fever, cough, feeding difficulty, respiratory rate, retractions, wheeze), oxygen saturation by pulse oximetry, and danger signs. Classification (operational definitions) • Pneumonia phenotype: cough/difficulty breathing with age-specific tachypnea and/or chest indrawing, with or without radiographic pneumonia. • Bronchiolitis: first episode of wheeze in infant with coryza/cough and diffuse wheeze/crepitations. • Wheeze-associated LRTI: recurrent wheeze or wheeze with respiratory distress requiring bronchodilator response assessment. • Severe LRTI: presence of hypoxemia (SpO₂ <90–92%), inability to feed, lethargy, severe respiratory distress, or need for ICU/ventilatory support.13,14 Investigations and treatment CBC/CRP, chest radiograph, and microbiological testing (e.g., viral testing where feasible) were performed as per clinician discretion and feasibility. Management followed institutional protocols: oxygen therapy, bronchodilators for wheeze, antibiotics for suspected bacterial pneumonia, fluids and feeding support, and ICU care if indicated. Outcomes Primary outcomes: spectrum of LRTI phenotypes and severity distribution. Secondary outcomes: length of stay, complications (e.g., empyema), ICU admission, need for respiratory support, and mortality. Statistical analysis Descriptive statistics summarized proportions/means. Associations with severe disease were evaluated using chi-square/Fisher exact test. Predictors were explored using multivariable logistic regression; p<0.05 was considered statistically significant.

RESULTS

Table 1. Baseline characteristics of enrolled children (n=300)

Variable

Category

n (%)

Age group

2–11 months

126 (42.0)

 

12–23 months

78 (26.0)

 

                               24–59 months

96 (32.0)

Sex

Male

174 (58.0)

 

Female

126 (42.0)

Nutritional status

Normal

162 (54.0)

 

Moderate acute malnutrition

84 (28.0)

 

Severe acute malnutrition

54 (18.0)

Immunization

Complete for age

198 (66.0)

 

Incomplete

102 (34.0)

Feeding (≤24 mo)

Exclusive breastfeeding ≥6 mo

132 (44.0)

Exposure

Indoor air pollution (biomass/secondhand smoke)

138 (46.0)

 

Overcrowding

156 (52.0)

Infants formed the largest group, with high prevalence of undernutrition and indoor air pollution exposure—both known contributors to pneumonia/LRTI severity.9–12

                                                                                                                                                                            

Table 2. Clinical spectrum of LRTI presentations

Clinical phenotype

n (%)

Pneumonia (clinical ± radiographic)

144 (48.0)

Bronchiolitis

84 (28.0)

Wheeze-associated LRTI

54 (18.0)

Other (e.g., laryngotracheobronchitis with LRT signs)

18 (6.0)

Pneumonia constituted about half of cases, while bronchiolitis and wheeze-associated illness contributed substantially—highlighting the need to differentiate phenotypes for rational antibiotic use and supportive care.

 

Table 3. Severity markers and supportive requirements

Parameter

n (%)

Hypoxemia at presentation (SpO₂ <92%)

96 (32.0)

Severe respiratory distress

72 (24.0)

ICU admission

42 (14.0)

HFNC/CPAP required

30 (10.0)

Mechanical ventilation

12 (4.0)

One-third presented with hypoxemia, reinforcing evidence that hypoxemia is common and may be missed without pulse oximetry, even in resource-limited settings.13,14

Table 4. Laboratory and radiological findings

Finding

n / N (%)

Leukocytosis (>15,000/mm³)

90/300 (30.0)

CRP elevated (≥20 mg/L)

78/240 (32.5)

Chest X-ray done

210/300 (70.0)

Radiographic pneumonia (consolidation/infiltrate)

102/210 (48.6)

Hyperinflation/peribronchial thickening

66/210 (31.4)

Pleural effusion/empyema

12/210 (5.7)

Nearly half of radiographs were consistent with pneumonia; bronchiolitic patterns were also frequent, consistent with mixed LRTI phenotypes seen in routine pediatric practice.

 

Table 5. Etiological pattern (where testing available)

Etiology (operational)

n (%)

Predominantly viral (clinical bronchiolitis/viral LRTI ± positive test)

108 (36.0)

Suspected bacterial pneumonia

120 (40.0)

Mixed/indeterminate

54 (18.0)

Atypical (suspected)

18 (6.0)

Viral disease dominated in infants/bronchiolitis, while suspected bacterial pneumonia increased among pneumonia phenotypes. This aligns with large etiology studies showing major viral contribution alongside bacteria in severe childhood pneumonia.3,4

Table 6. Outcomes and factors associated with severe LRTI

  1. A) Outcomes

Outcome

n (%)

Recovered and discharged

282 (94.0)

Complications (e.g., empyema, sepsis)

24 (8.0)

Median length of stay (IQR), days

4 (3–6)

Death

6 (2.0)

 

  1. B) Selected risk factors vs severe LRTI (ICU/HFNC/ventilation or hypoxemia)

Risk factor

Severe n/N (%)

Non-severe n/N (%)

p-value*

Age <12 months

54/126 (42.9)

72/126 (57.1)

<0.01

SAM

30/54 (55.6)

24/54 (44.4)

<0.001

Incomplete immunization

48/102 (47.1)

54/102 (52.9)

0.002

Indoor air pollution exposure

54/138 (39.1)

84/138 (60.9)

0.01

Hypoxemia (SpO₂ <92%)

96/96 (100)

0/96 (0)

<0.001

*Example statistics—recalculate with your dataset.

Severe disease clustered among infants, severely malnourished children, and those with incomplete immunization and indoor air pollution exposure—patterns strongly supported by the literature.9–12,14

DISCUSSION

This study highlights that under-five LRTIs present as a broad clinical spectrum, dominated by pneumonia and bronchiolitis with a substantial proportion of wheeze-associated illness. The prominence of viral phenotypes in infants is consistent with global evidence that RSV and other respiratory viruses account for a major share of ALRI burden in early life.5,6 Recent global estimates demonstrate RSV’s substantial contribution to under-five mortality, particularly in LMICs and in the first 6 months, supporting intensified prevention and early supportive management strategies.5,6

 

Our findings (template pattern) suggest that suspected bacterial pneumonia remains common, especially among older children and severe presentations. The PERCH multi-country study and related analyses showed that a limited number of pathogens explain much of severe childhood pneumonia and that viral detection is frequent, emphasizing diagnostic complexity and the risk of antibiotic overuse when phenotype differentiation is not performed.3,4 In practical settings where point-of-care etiology tests are limited, structured clinical assessment and risk stratification remain crucial.

 

A key observation is the high proportion of hypoxemia and the strong association between hypoxemia and severe outcomes. This aligns with contemporary evidence that hypoxemia can be prevalent even among children classified as non-severe at first contact and that pulse oximetry can improve identification and referral decisions.13,14 The operational implication is clear: strengthening pulse oximetry availability in emergency and peripheral settings, along with reliable oxygen systems, may reduce preventable deaths.

 

Preventable risk factors strongly influenced severity. Undernutrition—especially severe acute malnutrition—was associated with severe disease and complications, echoing evidence that malnutrition increases infection frequency, severity, and pneumonia mortality risk, while also potentially masking classic respiratory distress signs.9 Similarly, exposure to indoor air pollution and household crowding were associated with increased severity, consistent with systematic reviews and epidemiologic studies linking biomass smoke and indoor pollutants to childhood pneumonia and ARI.10–12 These findings support integrated interventions addressing nutrition, clean cooking fuels, and smoke-free homes alongside clinical care.

 

Immunization status also correlated with severity in this cohort template, reinforcing the protective role of vaccination programs against bacterial pneumonia and severe outcomes. Public health emphasis on complete age-appropriate immunization and early care seeking is aligned with ongoing national pneumonia control approaches and state-level pneumonia burden estimates.8 Overall, the study underscores that reducing severe LRTI outcomes requires both health-system strengthening (triage, pulse oximetry, oxygen, protocol-based care) and upstream prevention (vaccination, nutrition, clean air).

CONCLUSION

Under-five LRTIs show substantial heterogeneity in clinical presentation, with pneumonia and bronchiolitis comprising the major share. Severe disease is closely linked to hypoxemia, infancy, undernutrition, incomplete immunization, and indoor air pollution exposure. Strengthening early detection (including pulse oximetry), standardized management, and preventive interventions focused on immunization, nutrition, and clean household air can reduce severe outcomes and mortality.

REFERENCES

1.             World Health Organization. Pneumonia in children. 2022. (World Health Organization)

2.             UNICEF. Pneumonia in children statistics. 2025. (UNICEF DATA)

3.             O’Brien KL, Baggett HC, Brooks WA, et al. Causes of severe pneumonia requiring hospital admission in children without HIV infection from Africa and Asia: the PERCH multi-country case-control study. Lancet. 2019. (The Lancet)

4.             Duke T. What the PERCH study means for future pneumonia research and policy. Lancet. 2019. (The Lancet)

5.             Li Y, Wang X, Blau DM, et al. Global, regional, and national disease burden estimates of acute lower respiratory infections due to RSV in children aged 0–60 months. Lancet. 2022. (PubMed)

6.             Mazur NI, et al. Severe respiratory syncytial virus infection in children. Lancet. 2024. (ScienceDirect)

7.             Sirota SB, et al. Global burden of lower respiratory infections and attributable risk factors (GBD 2023 analysis). Lancet Infect Dis. 2025. (ScienceDirect)

8.             Wahl B, et al. National, regional, and state-level pneumonia and severe pneumonia in India (burden estimates). Lancet Child Adolesc Health. 2020. (The Lancet)

9.             Kirolos A, et al. The impact of childhood malnutrition on mortality from pneumonia. BMJ Global Health. 2021. (PMC)

10.          Adaji EE, et al. Understanding the effect of indoor air pollution on pneumonia in children: systematic review. 2018. (PMC)

11.          Nirmolia N, et al. Prevalence and risk factors of pneumonia in under-five children. Clin Epidemiol Glob Health. 2018. (CEGH)

12.          Mondal D, et al. Effects of indoor pollution on acute respiratory infections among under-five children. PLOS ONE. 2020. (PLOS)

13.          Rahman AE, et al. Introducing pulse oximetry for outpatient management of pneumonia in LMICs. EClinicalMedicine. 2022. (PMC)

14.          Rahman AE, et al. Prevalence of hypoxaemia in children with pneumonia in low-resource settings. 2022. (PMC)

15.          Bénet T, et al. Severity of pneumonia in under-5 children: predictors of hypoxemia and mortality (multicenter). 2017. (PMC)

16.          Yun KW, Wallihan R, et al. Community-acquired pneumonia in children: contemporary etiology and diagnosis. 2023. (e-cep.org)

17.          Wrotek A, et al. Etiology of community-acquired pneumonia in children (clinical classification and patterns). J Clin Med. 2022. (MDPI)

18.          Kumar KJ, et al. Etiology of community-acquired pneumonia among children with reference to atypical bacteria and viruses. 2018. (PMC)

19.          Chakraborty S, et al. Risk factors for pneumonia mortality in under-five children. Indian J Public Health. 2020. (Lippincott Journals)

20.          Wang X, et al. Global disease burden and risk factors for RSV-associated ALRI in infants and young children. 2024. (The Lancet)

21.          Ponce LJ, et al. RSV hospitalization costs, rates, and seasonality across Asia: systematic review. 2025. (The Lancet)

22.          Joseph J, et al. Disease burden due to RSV infection among under-five children in India (estimates). 2025. (PMC)

23.          Khan T, et al. Epidemiology and surveillance of influenza and RSV in under-five children. 2025. (PMC)

24.          Schuh HB, et al. Clinical hypoxemia score for outpatient child pneumonia and relevance of pulse oximetry. 2023. (Frontiers)

25.          Kumar P, et al. Chronicling the journey of pneumococcal conjugate vaccine introduction and implications for child health in India. 2025.

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