Introduction
Acute bronchiolitis is a seasonal viral respiratory tract infection, affecting children aged 1 to 24 months [1]. Multiple respiratory viruses such as rhinovirus, human metapneumovirus and parainfluenza viruses can cause acute bronchiolitis, however, the most common virus is the human Respiratory Syncytial Virus (RSV), which is responsible for more than 60% of cases [2‐5]. Globally, RSV-caused infections affect roughly 33 million (21.6–50.3 million) of children under the age of five, and contribute to 3.2 million hospitalisations (range: 2.7–3.8 million), and 120,000 deaths (range: 94,000-149,000) each year [6]. The mean cost of hospitalisation is estimated at €3,973 per child < 1 year old [7]. It is clinically characterized by predominantly expiratory dyspnea, signs of respiratory distress, and wheezing which is sometimes audible at a distance [8]. The clinical course of this infection is variable, ranging from the mild forms managed on an ambulatory basis to more severe forms characterized by acute respiratory distress requiring hospitalization [8]. Mortality is less than 2% according to various reports [1, 9, 10].
In Cameroon, acute bronchiolitis has been reported as the third commonest lower respiratory infection [9]. Though consensual management guidelines for acute bronchiolitis are not yet known, the use of medications like bronchodilators and corticosteroids are not recommended [11‐13]. In 2003, in France, adherence to these guidelines was reported at 6% of cases, which improved to 52.5% in 2013 [14, 15] with subsequent reduction in mortality [16]. Non-adherence to these guidelines have been associated with increased hospital length of stay [17] with its corollary of increased cost of care.
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Only few reports in Sub-Saharan Africa have attempted to explore the burden and management of acute bronchiolitis. The aim of this work was to explore the hospital management practices with respect to recommended guidelines and analyse factors associated with prolonged length of stay and mortality in children hospitalized for acute bronchiolitis.
Methodology
Study design and study setting
This was a retrospective cohort study carried out in three hospitals in the city of Douala, the economic capital of Cameroon. Our study sites were the pediatric units of three hospitals: one is a second category hospital i.e. Laquintinie Hospital of Douala (HLD) and the two others are first category hospitals i.e., the General Hospital of Douala (HGD) and the Paediatric and Gynaecological Hospital of Douala (HGOPED).
Study period
The study involved hospital database over a period of 4 years from 1st January 2018 to 31st December 2022.
Population selection
All patients with a diagnosis acute bronchiolitis hospitalised in any of the three hospitals during the study period were eligible for the study. We included only patient aged 1–24 months. Patients with a diagnosis of asthma or who had 2 previous episodes of acute bronchiolitis were excluded. Records with missing data on demographic characteristics like age and sex as well as outcomes were also excluded.
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Outcome of interest
The main outcome of interest was prolonged hospital length of stay (LOS). Prolonged hospital stay was defined as at least one hospital stay of 5 or more days in a paediatric unit for acute bronchiolitis [18]. The secondary outcome of interest was death during hospitalisation.
Predictor of interest
The main predictors of interest were age, and initial oxygen saturation [18].
Sample size calculation
Rodriguez et al. [18] reported that mean initial oxygen saturation (%) was 86.4 ± 5.4SD in patients with prolonged hospital LOS while this was 88.4 ± 5.0SD in patients without prolonged hospital LOS. Based on these results, for a desired confidence interval of 95%, a power of 80%, the ratio of exposed samples to those not exposed of 1, a significance threshold of 5%, the minimum sample size is 107 patients in each exposure group, giving a total of 214 patients with acute bronchiolitis [19].
Data collection tools and procedures
Medical records of patients hospitalized for bronchiolitis were reviewed for the following demographic, clinical, and microbiologic information: month of admission, age in months, gender (male, female), presence of undernutrition and other comorbidities like trisomy 21, congenital heart disease (yes/no), initial peripheral oxygen saturation (%), and previous episode of bronchiolitis (yes/no). Data was collected using a pretested data collection form and entered in excel sheet for storage.
The diagnosis of acute bronchiolitis
Acute bronchiolitis was diagnosed based on history and physical exams alone as per recommendations [20]. Clinical diagnosis of acute bronchiolitis was retained in any infant presenting with any first episode of wheezing preceded by or associated with two-to-three-day viral prodrome of fever, cough, rhinorrhoea, and a variable degree of respiratory distress. Any second episode of wheezing with personal or familial history of atopy received a trial of salbutamol. If there was a clinically relevant response this was classified as asthma and if no response, it was classified as bronchiolitis [21]. Most if not all paediatric units in Cameroon, RSV rapid tests are not available and therefore no infant hospitalized for acute lower respiratory infections is tested for RSV.
The hospitalisation criteria for patients with acute bronchiolitis are: significant deterioration in general condition, apnea, cyanosis, respiratory rate > 60, age ≤ 6 weeks, history of prematurity ˂ 34 weeks of amenorrhea, corrected age of ˂3 months, underlying heart disease, transcutaneous arterial oxygen saturation below 94%, digestive disorders compromising hydration, psychosocial difficulties, ventilatory disorder on chest x-ray performed in the face of clinical arguments [15].
Management guidelines of acute bronchiolitis
In September 2000, a consensus conference (CC) organised by the HAS (Haute Autorité de Santé) in France recommended diagnostic and management guidelines for acute bronchiolitis [11]. Though these management guidelines have been updated in November 2019, both guidelines recommend comprehensive symptomatic therapy, with emphasis on nasopharyngeal wash (NPW) and prohibit the use of antibiotics (unless in cases when secondary bacterial infection is confirmed), corticosteroid therapy, or bronchodilators [13]. In Cameroon, no local management guidelines have been established and as such many consultants practicing in predominantly French-speaking cities like Douala, use guidelines from France. Our reference mainly relates to the guidelines from 2000 because our study covered hospitalisations in 2018–2019, which were prior to the release of these updated guidelines.
Statistical analysis
Data was entered and analysed using the SPSS version 28 software. Quantitative variables were presented as mean and standard deviations, while qualitative variables were presented as frequencies (counts) and percentages. Mean values were compared between patients with and without the outcomes of interest using the independent Student t-test. Multivariable linear regression analysis was then performed using variables with p ≤ 0.250 [22] on univariate analysis to identify independent factors associated with the outcomes of interest. Statistical significance was set at p ≤ 0.05 and the strength of the association was expressed as odds ratio with the 95% Confidence Interval (CI). Kaplan-Meier curves was displayed to depict survival time based on the most significant predictor of mortality event with subsequent log-rank test analysis.
Ethical considerations
Ethical clearance was obtained from the Institutional Ethics Committee for Research on Human Health of the University of Douala No 3527 CEI-UDo/03/2023/T. Our study was carried out in strict compliance with the fundamental principles of medical research.
Operational definitions
Fever
Temperature greater than or equal to 38 degrees.
Tachycardia
Abnormal respiratory rate
This is a broad term that refers to any respiratory rate that is not within normal limits i.e., 30–60 breaths per minute. Tachypnea referred to respiratory rate above 60 breaths per minute [23].
Hypoxia
Peripheral oxygen saturation below 94% [11].
Leukocytosis
White blood cell counts above 20 × 106 cells/uL [25].
Thrombocytosis
Platelet count above 450 × 106 cells/uL [26].
Severe anaemia
Haemoglobin level below 7 g/dL.
Undernutrition
Because of the retrospective nature of the study, only weight and age were correctly reported in files. We therefore considered undernutrition as any patient with Weight-for-Age Z scores below − 2.
Non-adherence to guidelines
Oxygen supplementation targets
Although most updated guidelines recommend < 90% as target for oxygen supplementation [6], the pediatric department at Laquintinie has adopted the level of < 94% as a safeguard measure. This is because some authors have reported that pulse oximetry overestimates oxygen saturation amongst blacks patients [28, 29].
Seasons
Dry season refers to the period running from November-February and July-August each year while the rainy season runs from March-June and September-October each year [30].
Results
Patient recruitment
In total, 7314, 6434 and 3653 patients were hospitalised at HLD, HGD and HGOPED respectively during the study period, of which 215 cases were diagnosed of acute bronchiolitis (HLD = 85, HGD = 59 and HGOPED = 71). The overall prevalence of acute bronchiolitis in these three major paediatric hospitals was 1.24% (n = 215/17,401) representing 1.2%, 0.92% and 1.94% for HLD, HGD and HGOPED respectively.
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Sociodemographic characteristics of patients and seasonal variations
Mean age of patients was 6.94 ± 5.71 months. Most represented age group was 3–11 months (n = 125, 58.14%) followed by less than 3 months (n = 49, 22.79%) and the 12–24 months (n = 41, 19.07%). Males constituted 58.14% (n = 125) of the sample while females made up 41.86% (n = 90) with a M/F sex ratio of 1.39. Most cases were hospitalised during the rainy season (n = 119, 55.35%) with peak hospitalisation months being March and October. These trends have been similar over the years as seen in Fig. 1.
Fig. 1
Monthly variations in acute bronchiolitis cases over the study period
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Prehospital management
Prior to admission, patients received antipyretics in 30.23% (n = 65), antibiotics in 26.05% (n = 56), cough suppressants in 3.26% (n = 7), and mucolytics in 3.26% (n = 7) of cases. Symptoms prior to admission included cough (n = 146, 67.91%), difficulty breathing (n = 93, 43.26%), refusal to feed (n = 74, 34.42%), rhinorrhoea (n = 74, 34.42%), vomiting (n = 23, 10.7%) and diarrhoea (n = 16, 7.44%) as shown in Table I.
Table 1
Comparison of selected variables between patients with or without prolonged hospitalisation
Variable | Prolonged hospitalizations (n = 101) | Without prolonged hospitalizations (n = 114) | Total | p value |
|---|---|---|---|---|
Age in months, mean ± SD | 7.04 ± 5.94 | 6.87 ± 5.51 | 6.94 ± 5.71 | 0.834 |
Gender, male/female | 53/48 | 72/42 | 125/90 | 0.113 |
Previous episode of bronchiolitis | 5 (4.95) | 13 (11.4) | 18 (8.37) | 0.088 |
Undernutrition | 18 (17.82) | 21 (18.42) | 39 (18.14) | 0.909 |
Presenting complaint | ||||
Refusal to feed | 37 (36.63) | 37 (32.46) | 74 (34.42) | 0.520 |
Cough | 76 (75.25) | 70 (61.40) | 146 (67.91) | 0.030 |
Dyspnea | 58 (57.43) | 64 (56.14) | 93 (43.26) | 0.849 |
Diarrhoea | 13 (12.87) | 3 (2.63) | 16 (7.44) | 0.004 |
Rhinorrhea | 33 (32.67) | 41 (35.96) | 74 (34.42) | 0.612 |
Fever | 52 (51.49) | 61 (53.51) | 113 (52.56) | 0.797 |
Hypoxia | 67 (66.34) | 60 (52.63) | 127 (59.07) | 0.041 |
Tachycardia | 56 (55.45) | 81 (71.05) | 137 (63.72) | 0.018 |
Abnormal respiratory rate | 31 (30.69) | 17 (14.91) | 48 (22.33) | 0.069 |
Alveolar opacities on CXR (n = 37/77) | 7/15 (46.67) | 11/22 (50.00) | 18/37 (48.65) | 0.842 |
Adherence to guidelines | 1 (0.99) | 9 (7.89) | 10 (4.65) | 0.016 |
Leukocytosis > 20x x106 | 5 (6.33) | 9 (10.71) | 14 (8.59) | 0.607 |
Severe anemia | 3 (3.85) | 1 (1.2) | 4 (2.48) | 0.282 |
Thrombocytosis | 25 (29.76) | 23 (29.11) | 48 (29.45) | 0.991 |
Oxygen administered | 80 (79.21) | 66 (57.89) | 146 (67.91) | 0.001 |
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Clinical characteristics
On admission, 3.26% (n = 7) of our patients had cyanosis, use of accessory muscles of respiration in 16.28% (n = 35), nasal flaring in 66.98% (n = 144), grunting in 33.49% (n = 72), thoraco-abdominal asynchrony in 44.19% (n = 95), intercostal recession in 60.74% (n = 130). Coarse and fine crackles were present in 48.84% (n = 105), rhonchi in 37.67% (n = 81). Silent chest was reported in one patient.
Mean initial temperature was 38.06 ± 0.94 SD ºC, mean initial peripheral oxygen saturation was 90.28 ± 9.99 SD %, mean initial heart rate was 145.9 ± 26.56 SD beats per minute and mean initial respiratory rate was 49.55 ± 15.48 SD breaths per minute. A total of 52.56% (n = 113) had fever, 59.97% (n = 127) had hypoxia, 63.72% (n = 137) had tachycardia, and 23.3% (n = 48) had abnormal respiratory rate as shown in Table I. Up to 34.42% of patients had comorbidities (n = 74) which were polymalformative syndromes (n = 2, 2.7%), congenital heart diseases (n = 12, 16.22%), trisomy 21 (n = 3, 4.95%), acute undernutrition (n = 39, 18.14%) and one case each of prematurity, laryngomalacia and HIV (n = 1, 1.35%).
In-hospital management
Corticosteroids were received in 75.81% (n = 163), antibiotics in 74.88% (n = 161). and salbutamol nebulization in 78.6% (n = 169). Nasal lavage was performed in 92.09% (n = 198), saline nebulization in 44.19% (n = 95), respiratory physiotherapy in 13.46% (n = 29), and nasogastric tube feeding in 35.35% (n = 76). About 5/16 (31.25%) children who had diarrhea in history of presenting complaint received IV fluid rehydration.
Laboratory and radiology results
Mean initial white blood cell count was 12.47 ± 6.74 SD x106 cells/uL, mean initial hemoglobin level was 10.4 ± 1.79 SD g/dL and mean initial platelet count was 371.76 ± 171.44 SD x103 cells/uL. Leukocytosis was present in 8.59% of patients, severe anemia in 2.48% and thrombocytosis in 29.45%. Chest X-ray was requested in 35.81% (n = 77/215) of patients and was abnormal in 48.05% (n = 37/77) of them. Alveolar opacities were present in 48.64% (n = 18/37) cases who performed a Chest X-ray as shown in Table I.
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Factors associated with prolonged length of stay (LOS) and mortality
Prolonged LOS was noted in 46.97% (n = 101) and mortality in 10.7% (n = 23) of patients. Mortality rate per age group was 16.33% (n = 8/49), 10.4% (n = 13/125) and 4.88% (n = 2/41) in patients aged less than 3 months, 3–11 months, and 12–24 months respectively. Prematurity, laryngomalacia, HIV and congenital heart diseases were insufficiently represented in outcome categories and therefor no sub analysis was conducted.
On univariate analysis, factors associated with prolonged hospital stay were female gender, previous episode of bronchiolitis, cough, diarrhoea, hypoxia, tachycardia, non-adherence to guidelines and oxygen administration as shown in Table I. On multivariable analysis, factors independently associated with prolonged hospital duration were oxygen administration [b = 0.36, OR = 2.35 (95% CI:1.16–4.74), p = 0.017], abnormal respiratory rate [b = 0.38, OR = 2.13 (1.00-4.55), p = 0.050] and patients presenting with cough [b = 0.33, OR = 2.35 (95% CI: 1.22–4.51), p = 0.011], and diarrhoea [b = 0.71, OR = 6.44 (95% CI: 1.6-25.86), p = 0.009] on admission as shown in Table II.
Factors associated with mortality on univariate analysis were age of the patient in months, cough as presenting complaint, fever, female gender, tachycardia, and oxygen administration as shown in Table III. On multivariable analysis, factors independently associated with mortality were age of the patient [b= -0.07, OR = 0.84 (95% CI: 0.74–0.97), p = 0.014] and oxygen administration [b = 1.08, OR = 9.64 (95% CI:1.16–79.85), p = 0.036] as shown in Table IV. A Kaplan-Meier survival curve was used to depict survival rates based on oxygen administration in Fig. 2. The log-rank test showed that there is a difference between oxygen administration status in terms of the distribution of time until the mortality event occurs, p = 0.009.
Table 2
Predictors of prolonged hospital duration on logistic regression analysis
Variable | OR (95% CI) | p value | b | aOR (95% CI) | p value |
|---|---|---|---|---|---|
Female gender | 1.55 (0.9–2.68) | 0.114 | 0.31 | 1.49 (0.81–2.74) | 0.200 |
Tachycardia | 0.51 (0.29–0.89) | 0.018 | 0.32 | 0.59 (0.31–1.120 | 0.105 |
Hypoxia | 1.77 (1.02–3.08) | 0.042 | 0.33 | 1.72 (0.9–3.28) | 0.103 |
Cough as presenting complaint | 1.91 (1.06–3.44) | 0.024 | 0.33 | 2.35 (1.22–4.51) | 0.011 |
Oxygen administered | 2.77 (1.51–5.09) | 0.001 | 0.36 | 2.35 (1.16–4.74) | 0.017 |
Abnormal respiratory rate | 1.85 (0.95–3.57) | 0.071 | 0.38 | 2.13 (1.00-4.55 | 0.050 |
Previous episode of bronchiolitis | 0.4 (0.14–1.18) | 0.097 | 0.62 | 0.48 (0.14–1.61) | 0.235 |
Diarrhoea as presenting complaint | 5.47 (1.51–19.78) | 0.010 | 0.71 | 6.44 (1.6-25.86) | 0.009 |
Non-adherence to guidelines | 8.57 (1.07–68.89) | 0.043 | 1.1 | 4.87 (0.56–42.17) | 0.151 |
Corticosteroids used | 1.17 (0.41–3.31) | 0.772 | - | - | - |
Antibiotics used* | 2.41 (0.69–8.46) | 0.169 | - | - | - |
Salbutamol nebulization used* | 6.73 (0.88–51.36) | 0.066 | - | - | - |
Table 3
Comparison of selected variables between patients alive and dead
Variable | Patients alive (n = 192) | Patient who died (n = 23) | Total (n = 215) | p value |
|---|---|---|---|---|
Age in months, mean ± SD | 7.42 ± 5.86 | 4.42 ± 3.37 | 6.94 ± 5.71 | 0.025 |
Gender, male/female | 109/83 | 16/7 | 125/90 | 0.240 |
Previous episode of bronchiolitis | 16 (8.33) | 2 (8.7) | 18 (8.37) | 0.953 |
Undernutrition | 35 (18.23) | 4 (17.39) | 39 (18.14) | 0.922 |
Presenting complaint | ||||
Refusal to feed | 68 (35.42) | 6 (26.09) | 74 (34.42) | 0.373 |
Cough | 134 (69.79) | 12 (52.17) | 146 (67.91) | 0.087 |
Dyspnea | 82 (42.71) | 11 (47.83) | 93 (43.26) | 0.640 |
Diarrhoea | 16 (8.33) | - | 16 (7.44) | 0.150 |
Rhinorrhea | 64 (33.3) | 10 (43.48) | 74 (34.42) | 0.333 |
Fever | 98 (51.04) | 15 (65.22) | 113 (52.56) | 0.198 |
Hypoxia | 114 (59.38) | 13 (56.52) | 127 (59.07) | 0.793 |
Tachycardia | 119 (61.98) | 18 (78.26) | 137 (63.72) | 0.125 |
Abnormal respiratory rate | 41 (21.35) | 7 (30.43) | 48 (23.33) | 0.323 |
Alveolar opacities on CXR (n = 37/77) | 17/35 (48.57) | 1/2 (50.00) | 18/37 (48.65) | 0.258 |
Adherence to guideline | 10 (5.2) | - | 10 (4.6) | 0.262 |
Corticosteroids used | 145 (75.52) | 18 (78.26) | 163 (75.81) | 0.772 |
Antibiotics used | 141 (73.44) | 20 (86.96) | 161 (74.88) | 0.158 |
Salbutamol nebulization used | 147 (76.56) | 22 (95.65) | 169 (78.6) | 0.035 |
Leukocytosis > 20x x106 | 12 (8.28) | 2 (11.11) | 14 (8.59) | 0.686 |
Severe anemia | 4 (2.8) | - | 4 (2.48) | 0.472 |
Thrombocytosis | 44 (30.34) | 4 (22.22) | 48 (29.45) | 0.748 |
Oxygen administered | 124 (64.58) | 22 (95.65) | 146 (67.91) | 0.003 |
Table 4
Predictors of mortality on logistic regression analysis
Variable | OR (95% CI) | p value | b | aOR (95% CI) | p value |
|---|---|---|---|---|---|
Age of the patient in months | 0.88 (0.78–0.99) | 0.031 | 0.07 | 0.84 (0.74–0.97) | 0.014 |
Cough as presenting complaint | 0.47 (0.2-1,13) | 0.093 | 0.50 | 0.69 (0.26–1.84) | 0.454 |
Fever | 1.8 (0.73–4.44) | 0.203 | 0.54 | 2.65 (0.93–7.57) | 0.069 |
Female gender | 0.57 (0.23–1.46) | 0.244 | 0.52 | 0.56 (0.20–1.55) | 0.266 |
Tachycardia | 2.21 (0.79–6.2) | 0.133 | 0.57 | 2.94 (0.95–9.06) | 0.061 |
Oxygen administered | 12.06(1.59–91.47) | 0.016 | 1.08 | 9.64 (1.16–79.85) | 0.036 |
Antibiotics used | 4.96 (2.38–10.3) | < 0.001 | 0.73 | 1.19 (0.29–4.96) | 0.812 |
Salbutamol nebulization used | 1.9 (0.96–3.74) | 0.064 | 1.09 | 7.87 (0.93–66.33) | 0.058 |
Fig. 2
Kaplan-Meier survival curve displaying mortality event rates over hospitalisation days (time) based on oxygen administration status
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Discussion
The predominance of male gender in our study has been reported before in Brazil, Senegal and Cameroon [1, 18, 31]. Though it is commonly recognised that females have smaller airways [32], regardless of age, females have been reported to have stronger antibody responses, baseline immunoglobulin levels, and B cell counts than males [33, 34]. Moreover, the Single Nucleotide Polymorphisms or SNP (rs2069885) in the interleukin (IL)-9 gene which has been associated with severe RSV infection requiring hospitalisation is associated with an increased susceptibility in boys [35]. All these factors may explain why males are more affected by respiratory infections than females [36, 37].
Bronchiolitis is caused by inflammation of the lining of the epithelial cells of the small airways of the lungs, which results mucus production, inflammation, and cellular necrosis [38]. This inflammation can restrict the airway and eventually cause cough, wheezing. and abnormal respiratory rate. These symptoms are less common in mild forms of the disease and therefore are surrogate measures of severity [4]. This may explain why cough and abnormal respiratory rate were associated with prolonged hospital stay in our study.
The administration of oxygen was the single most important factor associated with both prolonged LOS and mortality. It is well recognised that tissue hypoxia can lead to cell death. However, hyperoxaemia can also be dangerous for lung tissues [39]. Arterial PCO2 plays an important role in respiratory drive and therefore, high oxygen concentrations can compromise respiratory centre function and aggravate hypercapnia [40]. Oxygen administration must therefore be carefully codified, even in resource limited settings like ours. According to the Consensus Conference (CC) guidelines, all patients with peripheral oxygen saturation below 94% should be hospitalised and given oxygen [11]. Nonetheless, because of the potential dangers of excessive oxygen administration, increased cost of care and the potential increased risk in the transmission of nosocomial infections using oxygen delivery devices, some authors have proposed lower targets for oxygen saturation [41‐43]. Cunningham et al. [41], in a randomised controlled trial reported that the time taken for symptoms to resolve was the same whether in patients with acute bronchiolitis whether managed with a target oxygen saturation of 90% or 94%. Nonetheless, we believe that the main reason why oxygen administration was a significant factor associated with mortality and prolonged LOS in our study was because it is a marker of disease severity [44]. More studies are necessary in our setting to validate adequate targets of oxygen saturation in the management of acute bronchiolitis in infants and young children.
Diarrhea was present in 7.44% of our patients. It causes significant fluid losses, which in addition to fluid losses from increased respiratory efforts can predispose infants and children to clinically significant dehydration. Due to the retrospective nature of our study, dehydration was not evaluated. Nonetheless, we hypothesise that diarrhea was associated with prolonged LOS because it led to dehydration in these patients. Dehydration has been reported previously to increased LOS in patients with acute bronchiolitis [45],
In our study, an increase in age of the patient (in months) was associated with a decrease in the probability of mortality. Though the highest age group affected was 3–11 months, the highest mortality rate was reported in patients aged less than 3 months (16.33%). This finding has been similarly reported in other studies [46, 47] and is attributed to the rapid disease progression and immune fragility of younger infants [48, 49]. Because of these findings, some authors have suggested that vaccination strategies be focused on infants in their early life [50]. Nonetheless, other authors argue that this finding may represent survival bias as common risk factors for death like prematurity and neonatal infections might create a survival disadvantage at this age [51]. This is especially true in our study as we did not explore the contribution of prematurity, laryngomalacia, HIV and congenital heart diseases in these overall deaths.
In our study, 95.35% of the patients received either corticosteroids, antibiotics, or salbutamol nebulization, translating into poor adherence to management guidelines in only 4.65% of cases. Despite the fact that several authors [52, 53] and expert societies [14, 20] have reported that corticosteroids have no added benefits in the management of acute bronchiolitis, it was administered in more than 70% of patients in this study. According to an Italian study, four out of ten paediatricians are aware of recommended diagnostic criteria for acute bronchiolitis, however, 39.64% still prescribe bronchodilators, while 64.52% prescribe systemic corticosteroids [54]. The apparent severity, the associated anxiety from treating such severely ill children without medications, and personal reassurance or parental pressure are the reasons stated for this wrong practice [55]. Continuous Medical Education (CME) sessions need to be organised to harmonize practices in the management of acute bronchiolitis in Cameroon.
The study period spanning from 2018 to 2022 includes the period of the COVID-19 pandemic in Cameroon (1st case reported in March 2020). This could have contributed significantly in underestimating the real prevalence of acute bronchiolitis in our setting, as up to 27–47% drop in pediatric hospitalisation frequency in Cameroon has been reported [56]. This study was limited by its retrospective nature that prevented us from exploring all potential explanatory data like hydration status and prematurity. Moreover, mortality from RSV bronchiolitis has been reported to be different from mortality from other viral-induced bronchiolitis [18] and therefore, lack of viral testing in our study was a significant limitation. Moreover, although sometimes reported in all patients aged < 24 months [57], bronchiolitis typically affects infants aged 1-12months. Our sample also included patients aged 12–24 months and therefore our results may represent RSV induced Lower Respiratory Tract Infections (LRTI)) rather than bronchiolitis. A nationwide prospective study should be conducted to address the methodological flaws of this current study and explore nationwide trends in prevalence, and factors associated with hospitalisation, length of hospital stay and mortality.
Conclusion
Acute bronchiolitis represented 1.24% of pediatric hospitalisations, with peak admissions during the rainy season, particularly in March and October and this was consistent over the years. The most affected age group was 3–11 months, with males being more commonly affected. Management guidelines were poorly respected. Prolonged length of stay was reported in half of the patients and associated with oxygen administration, abnormal respiratory rate, cough, and diarrhea on admission. Mortality was high, with one out of ten patients dying, especially younger patients and patients receiving oxygen. Adequate implementation of management strategies may reduce hospital stays and improve outcomes for patients with acute bronchiolitis.
Acknowledgements
We thank the administration of the three hospitals involved and the personnel at the paediatric department for easing data collection procedures.
Declarations
Competing interests
The authors declare no potential conflicts of interest.
Consent for publication
Not applicable.
Ethics approval and consent to participate
Ethical clearance obtained from the Institutional Ethics Committee of the University of Douala No 3527 CEI-UDo/03/2023/T. In accordance with the Declaration of Helsinki, because of the retrospective design and impracticability, need for consent to participate was waived by Institutional Ethics Committee of the University of Douala No 3527 CEI-UDo/03/2023/T.
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