Abstract
Background
Influenza is an important cause of respiratory illness in children, but data are limited on hospitalized children with laboratory‐confirmed influenza in China.
Methods
We conducted active surveillance for severe acute respiratory infection (SARI; fever and at least one sign or symptom of acute respiratory illness) among hospitalized pediatric patients in Jingzhou, Hubei Province, from April 2010 to April 2012. Data were collected from enrolled SARI patients on demographics, underlying health conditions, clinical course of illness, and outcomes. Nasal swabs were collected and tested for influenza viruses by reverse transcription polymerase chain reaction. We described the clinical and epidemiological characteristics of children with influenza and analyzed the association between potential risk factors and SARI patients with influenza.
Results
During the study period, 15 354 children aged <15 years with signs and symptoms of SARI were enrolled at hospital admission. severe acute respiratory infection patients aged 5–15 years with confirmed influenza (H3N2) infection were more likely than children without influenza to have radiographic diagnosis of pneumonia (11/31, 36% vs 15/105, 14%. P<.05). Only 16% (1116/7145) of enrolled patients had received seasonal trivalent influenza vaccination within 12 months of hospital admission. Non‐vaccinated influenza cases were more likely than vaccinated influenza cases to have pneumonia (31/133, 23% vs 37/256, 15%, P<.05). severe acute respiratory infection cases aged 5–15 years diagnosed with influenza were also more likely to have a household member who smoked cigarettes compared with SARI cases without a smoking household member (54/208, 26% vs 158/960, 16%, P<.05).
Conclusions
Influenza A (H3N2) virus infection was an important contributor to pneumonia requiring hospitalization. Our results highlight the importance of surveillance in identifying factors for influenza hospitalization, monitoring adherence to influenza prevention and treatment strategies, and evaluating the disease burden among hospitalized pediatric SARI patients. Influenza vaccination promotion should target children.
Keywords: children, influenza, risk factors, severe acute respiratory infection
1. Background
Influenza is an important vaccine‐preventable infectious disease that causes significant morbidity worldwide in persons of all ages. Studies conducted in North America, Europe, and Asia have documented that children have particularly high rates of morbidity and influenza‐related complications, particularly those aged <2 years.1, 2, 3 Although effectiveness varies by season through the interaction of viral and host factors, annual influenza vaccination remains the most effective method for preventing seasonal influenza and related complications.4, 5, 6, 7 In the United States, annual influenza vaccination is recommended for all persons aged ≥6 months of age.8 In China, availability and use of seasonal influenza vaccine has increased dramatically; nevertheless, the vast majority of Chinese children are not vaccinated annually.9
During 2010, in the post‐2009 H1N1 pandemic period, we initiated active surveillance for severe acute respiratory infection (SARI) and influenza in a central Chinese city. The highest influenza‐associated SARI rates occurred among children aged 6–11 months (3603 and 3805 hospitalizations per 100 000 during 2010–2011 and 2011–2012, respectively) and influenza‐associated SARI mostly affected children aged <5 years (2021 hospitalizations per 100 000 during 2010–2011 and 2349 per 100 000 during 2011–2012).10 We conducted active SARI surveillance in central China to analyze the clinical and epidemiological characteristic of influenza‐associated SARI cases, including pneumonia, among pediatric patients aged <15 years.
2. Methods
Surveillance was conducted in Jingzhou, Hubei Province, in three general hospitals and one pediatric hospital as previously described.10 All patients admitted to a surveillance hospital were screened by nurses and physicians for SARI and were considered eligible if the SARI case definition was met within 24 hours of hospital admission. Briefly, we collected demographic, clinical, and outcome data and performed influenza testing for all pediatric patients (aged <15 years) hospitalized for SARI to characterize the epidemiology of severe influenza in children.
2.1. Case definitions
Children <15 years of age met the case definition for SARI if they had measured elevated temperature (rectal or axillary) ≥37.3°C and at least one sign or symptom of acute respiratory illness, including cough, sore throat, tachypnea, difficulty breathing, abnormal breath sounds on auscultation, sputum production, hemoptysis, chest pain, or chest radiograph consistent with pneumonia. A laboratory‐confirmed influenza case was defined as a SARI patient with a documented positive result of real‐time reverse transcription polymerase chain reaction (RT‐PCR) assay for influenza, admitted to a participating hospital between April 5, 2010, and April 8, 2012. A pneumonia case was defined as a SARI patient with infiltrates noted on chest radiograph performed at any time during the hospitalization.
2.2. Data collection
Physicians screened potential case patients for SARI at hospital admission and obtained verbal consent from a parent or guardian for enrollment in the study. Physicians then abstracted data from the medical records of patients meeting the SARI case definition including basic demographic information, past medical history, signs, symptoms, and radiographic results on a structured case report form. At hospital discharge, physicians were required to update the form to include data about outcome and influenza testing results.
2.3. Laboratory
Nurses collected nasal swabs from pediatric SARI case patients within 24 hours of admission following standardized procedures and were transferred to the Jingzhou Center for Disease Control and Prevention (Jingzhou CDC). At Jingzhou CDC, laboratory confirmation of influenza virus infection was determined by real‐time RT‐PCR. Handling and testing of specimens has been described in detail elsewhere.10
2.4. Analysis
Data were entered into epidata (version 2.0, Odense, Denmark). Descriptive statistics including frequency analysis for categorical variables, medians, and interquartile ranges (IQRs) for continuous variables were calculated. To further examine the association between potential risk factors and SARI, we first performed univariate analysis. For multivariable logistic regression, we included variables with P<.10 in univariate analysis or those believed to be potential risk factors associated with the outcome of interest, such as “at least one tobacco smoker in household” and we conducted stepwise backwards variable selection, retaining variables with P<.05 after controlling for other risk factors in the logistic regression model. Data were analyzed with spss (v17.0; SPSS, Chicago, IL, USA).
2.5. Human subjects review
This project was approved by the ethical review committees at the Chinese Center for Disease Control and Prevention (China CDC, Beijing, China) and the Centers for Disease Control and Prevention (US CDC, Atlanta, GA, USA). In response to the 2009 H1N1 pandemic, China's Ministry of Health implemented the 2nd edition of the national protocol in October 2009 to conduct surveillance for influenza‐associated hospitalizations and authorized participating hospitals to collect individual patient data and specimens from patients hospitalized with acute respiratory infection. For this project, therefore, participation only required patients or their parent/guardian to provide brief verbal consent.
3. Results
3.1. Overall
From April 5, 2010, to April 8, 2012, a total of 37 607 patients aged <15 years were hospitalized in four surveillance hospitals in Jingzhou, and 15 354 (41%) of them met the SARI case definition and 15 354 were enrolled (0.05% refused; Fig. 1). Over the 24‐month period, there were increases in influenza activity during summer (August and September), winter (December–February), and spring (March–May) months.
3.2. SARI patients
The median age of all enrolled SARI patients was 1.9 years (interquartile range [IQR], 0.9–3.3 years), 80% were aged <5 years, and 57% were male. Only 2% of SARI patients had an underlying medical condition, the most common of which was prematurity (2%). Only 1% of influenza patient received monovalent pandemic H1N1 vaccination and 16% patient received seasonal trivalent influenza vaccination (Table 1). severe acute respiratory infection patients were admitted to the hospital a median of 2 days (IQR, 1–3 days) after illness onset. Cough (61%) and sore throat (27%) were the most frequent symptoms of SARI patients at hospital admission. A quarter of all SARI patients had high fever (temperature ≥39.0°C) at admission. The median length of hospitalization for SARI patients was 5 days (IQR, 3–6). Of these SARI patients, 3 (0.02%) died during hospitalization, and 5 (0.03%) died within 30 days after discharge (Table 2).
Table 1.
Characteristicsa | Confirmed Influenza (n=1774) (%) | Influenza negative (n=12 705) (%) | P‐valueb | Totalb (n=15 354) (%) |
---|---|---|---|---|
Male sex | 1024 (58) | 7248 (57) | .591 | 8789 (57) |
Median (IQR) age (years) | 2.5 (1.0–4.3) | 1.8 (0.9–3.2) | <.05 | 1.9 (0.9–3.3) |
Age group: | ||||
<6 mo | 156 (9) | 1099 (9) | 1318 (9) | |
6–11 mo | 263 (15) | 2684 (21) | 3121 (20) | |
12–23 mo | 339 (19) | 3042 (24) | 3596 (23) | |
2–4 y | 669 (38) | 4361 (34) | 5318 (35) | |
5–9 y | 300 (17) | 1300 (10) | 1710 (11) | |
10–15 y | 47 (3) | 219 (2) | 291 (2) | |
At least one underlying medical condition | 39 (2) | 283 (2) | .938 | 333 (2) |
Asthma | 3 (0.2) | 34 (0.3) | .617 | 39 (0.3) |
Chronic bronchitis | 0 | 8 (0.1) | .607 | 9 (0.1) |
Obesityc | 4/1016 (0.4) | 16/5880 (0.3) | .833 | 22/7319 (0.3) |
Prematurityd | 17/758 (2) | 97/6825 (1) | .507 | 117/8035 (2) |
Low birth‐weighte | 13/758 (2) | 67/6825 (1) | .862 | 82/8035 (1) |
Received Influenza vaccinationf | ||||
Received monovalent pandemic H1N1 vaccinationg | 5/407 (1) | 76/2299 (3) | .778 | 83/2826 (3) |
Received seasonal trivalent influenza vaccinationh | 151/959 (16) | 1116/7145 (16) | .907 | 1311/8528 (15) |
Exposure history | ||||
At least one tobacco smoker in household | 308/1182 (26) | 1865/8928 (21) | <.05 | 2294/10 640 (22) |
Sick contact with fever or respiratory symptomsi | 82/1083 (8) | 390/8078 (5) | <.05 | 497/9601 (5) |
More than one child living in household in past 3 mo | 60 (3) | 344 (3) | .106 | 422 (3) |
IQR, interquartile range.
Data presented as no. (%) of patients unless otherwise indicated. Denominators for testing of fewer patients than full group are indicated. Percentages may not total 100 because of rounding. Data did not include patients without specimens for influenza virus testing.
The P‐values are comparisons between “pediatric SARI patients with confirmed influenza infection” and “pediatric SARI patients without influenza infection”, and statistically significant as P<.05
There were 875 (6%) patients without NP/OP collection.
Body mass index (BMI) was calculated for patients with available height and weight data to assess obesity using Chinese criteria (BMI greater than the cutoff values for children aged 2–17 y). BMI was not calculated in children aged <2 y.11
Defined as gestational age <37 wk at birth for children aged <2 y.
Defined as birth weight of a live born infant of <2500 g for children aged <2 y.
Answered “Yes” to this question, “During the past 12 mo, have you had a flu shot?” which were asked during a face‐to‐face interview.
Of children aged ≥6 mo eligible to receive monovalent pandemic A (H1N1) influenza vaccine.
Of children aged ≥6 mo eligible to receive seasonal trivalent inactive influenza vaccine.
Contact with anyone else with fever or respiratory symptoms defined as having been in close contact (within 1 m) or direct contact of person with fever or respiratory symptoms in the previous 2 wk.
Table 2.
Characteristicsa | Confirmed Influenza (n=1774) (%) | Negative for Influenza (n=12 705) (%) | P‐value b | Total (n=15 354)c (%) |
---|---|---|---|---|
Symptoms at hospital admission | ||||
Cough | 1157 (65) | 7205 (57) | <.05 | 8836 (61) |
Sore throat | 401 (23) | 3531 (28) | <.05 | 4098 (27) |
Rhinorrhoea | 323 (18) | 1748 (14) | <.05 | 2192 (14) |
Sputum production | 135 (8) | 1089 (9) | .173 | 1304 (9) |
Dyspnoea | 39 (2) | 556 (4) | <.05 | 642 (4) |
Vomiting | 69 (4) | 721 (6) | <.05 | 859 (6) |
Diarrhea | 28 (2) | 540 (4) | <.05 | 609 (4) |
Abdominal pain | 27 (2) | 186 (2) | .849 | 228 (2) |
Signs at hospital admission | ||||
Temperature (T, °C) | ||||
T<36.0 | 0 | 6 (0.05) | <.05 | 7 (0.05) |
36.0≤T<37.0 | 251 (14) | 2071 (6) | 2460 (16) | |
37.0≤T<38.0 | 373 (21) | 3048 (24) | 3624 (24) | |
38.0≤T<39.0 | 676 (38) | 4461 (35) | 5459 (36) | |
T≥39.0 | 474 (27) | 3119 (25) | 3804 (25) | |
Abnormal breath sounds on auscultation | 537 (30) | 3799 (30) | .751 | 4579 (30) |
Tachypnea | 1 (0.1) | 25 (0.2) | .361 | 29 (0.2) |
Pneumonia Diagnosis | ||||
Clinically diagnosed as pneumonia at hospital admission | 238 (13) | 1911 (15) | .071 | 2291 (15) |
Clinically diagnosed as pneumonia at hospital admission and chest radiograph performed | 195/238 (82) | 1623/1911 (85) | .227 | 1938/2291 (85) |
Radiographic diagnosis of pneumonia | 161/195 (83) | 1401/1623 (86) | .154 | 1674/1938 (86) |
Chest radiograph performed at hospital admission and during hospitalization | 807 (46) | 5600 (44) | .262 | 6841 (45) |
Radiographic diagnosis of pneumonia | 246/807 (30) | 2188/5600 (39) | <.05 | 2583/6841 (38) |
Clinical laboratory findings | ||||
Leucopeniad | 165/1525 (11) | 557/11 055 (5) | <.05 | 777/13 299 (6) |
Leukocytosise | 282/1525 (19) | 3657/11 055 (33) | <.05 | 4188/13 299 (31) |
Anemiaf | 269/1520 (18) | 2313/11 014 (21) | <.05 | 2748/13 250 (21) |
Elevated erythrocyte Sedimentation rateg | 66/158 (42) | 641/1086 (59) | <.05 | 777/1349 (58) |
C‐reactive protein >8 mg/L | 117/476 (25) | 1431/3397 (42) | <.05 | 1622/4040 (40) |
Treatment | ||||
Received antibiotics before hospital admission | 670/1343 (50) | 4529/9831 (46) | <.05 | 5490/11 802 (47) |
Received antibiotics during hospitalization | 1750 (99) | 12 461 (98) | .097 | 15 056 (98) |
Received corticosteroids during hospitalization | 164 (9) | 1591 (13) | <.05 | 1880 (12) |
Received oseltamivir during hospitalization | 2 (0.1) | 21 (0.2) | 1.000 | 23 (0.1) |
Supplemental oxygen required | 16 (0.9) | 183 (1.4) | .086 | 216 (1) |
Mechanical ventilation | 1 (0.1) | 2 (0.05) | .324 | 5 (0.1) |
Admitted to ICU | 1 (0.1) | 18 (0.1) | .722 | 21 (0.1) |
Complications | ||||
Neurologic disorders | 3 (0.2) | 11 (0.1) | .241 | 20 (0.1) |
Respiratory failure | 1 (0.1) | 8 (0.1) | 1.000 | 10 (0.1) |
Cardiac failure | 1 (0.1) | 11 (0.1) | 1.000 | 14 (0.1) |
Hepatic dysfunction | 2 (0.1) | 3 (0.01) | .117 | 7 (0.1) |
Clinical course, median days (IQR) | ||||
From illness onset to hospital admission | 2 (1–3) | 2 (1–3) | .860 | 2 (1–3) |
From hospital admission to discharge or death | 5 (3–6) | 5 (3–6) | .936 | 5 (3–6) |
Clinical outcome | ||||
Died during hospitalization | 0 | 3 (0.02) | .221 | 3 (0.02) |
Died within 30 d after discharge | 1 (0.1) | 4 (0.03) | .480 | 5 (0.03) |
ICU, intensive care unit; IQR, interquartile range.
Data presented as no. (%) of patients unless otherwise indicated. Denominators for testing of fewer cases than full group are indicated. Percentages may not total 100 because of rounding. Data only include patients who provided specimens for influenza virus testing.
The P‐values are comparisons between “pediatric SARI patients with confirmed influenza infection” and “pediatric SARI patients without influenza infection”, and statistically significant as P<.05.
There were 875 (6%) patients without NP/OP collection.
Defined as a reduction in the circulating WBC count to <4000/μL.
Defined as a reduction in the circulating WBC count to >10 000/μL.
Defined as a reduction in the hemoglobin in grams per liter (Hb<110 g/L).
Raised erythrocyte sedimentation rate defined as >20 mm/h.
3.3. SARI patients with laboratory‐confirmed influenza
Of 14 479 (14 479/15 354, 94%) children who met the SARI case definition and had respiratory specimens collected, 1774 (17, 74/14, 479, 12%) tested positive for influenza viruses. Of the 1774 children with confirmed influenza, 58% were male and 88% were aged <5 years. Nearly all influenza‐associated SARI cases were previously healthy, and only 2% had at least one underlying medical condition, the most common of which were low birth weight (1%) and prematurity (1%) among children aged <2 years.
Influenza‐associated SARI cases were admitted to the hospital a median of 2 days (IQR, 1–3 days) after illness onset, and presented with fever (temperature ≥37.3°C; 82%), cough (65%), and sore throat (23%; Table 2). Other symptoms included rhinorrhea (18%) and sputum production (8%). Gastrointestinal symptoms (nausea, vomiting, and diarrhea) were uncommon. Twenty‐seven percent of influenza cases had high fever (temperature ≥39.0°C) at admission. Complications among influenza‐associated SARI patients were very uncommon, but included neurologic disorders (0.2%), respiratory failure (0.1%), cardiac failure (0.1%), and hepatic dysfunction (0.1%). Twenty‐one influenza patients were admitted to an intensive care unit, and five required mechanical ventilation. The median length of hospitalization for influenza‐associated SARI patients was 5 days (IQR, 3–6); of these, 1 (0.06%) died within 30 days after discharge.
3.4. SARI patients with and without laboratory‐confirmed influenza
Of 14 479 children who met the SARI case definition and had respiratory specimens collected during the study period, 12 705 (88%) tested negative for influenza viruses. The demographic characteristics of patients with and without influenza were similar except those without influenza had a lower median age and a younger age distribution (P<.05; Table 1). Influenza cases were more likely to have at least one tobacco smoker in the household and a sick contact with fever or respiratory symptoms than children without influenza (P<.05).
Clinical characteristics of pediatric influenza cases and children without influenza were similar. More pediatric influenza cases had cough and rhinorrhea than children without influenza (P<.05), while more SARI cases without influenza had gastrointestinal symptoms (nausea, vomiting, and diarrhea) than influenza cases (Table 2). More influenza cases had high fever at hospital admission than those without influenza (P<.05).
3.5. SARI cases with pneumonia
Of 2291 SARI patients clinically diagnosed with pneumonia at hospital admission, 1938 (85%) had chest radiography performed, and 1674 (86%) had evidence of pneumonia. The median length of hospitalization for pneumonia cases was 6 days (IQR, 5–8), which was longer (P<.05) than children without pneumonia (median 5 days, IQR, 3–6). Among influenza cases, the proportion with cough, sputum production, or Dyspnoea was higher in children with radiologic evidence of pneumonia compared with those without (P<.05; Table 3). However, children without radiologic evidence of pneumonia had higher temperatures (T>38°C) on admission than children with radiologic evidence of pneumonia, but more pneumonia cases had abnormal breath sounds on auscultation than children without pneumonia (P<.05).
Table 3.
Characteristics of influenza patientsa | Case patients with pneumonia (n=246) (%) | Case patients without pneumonia (n=561) (%) | P‐value b |
---|---|---|---|
Symptoms at hospital admission | |||
Cough | 209 (85) | 341 (61) | <.05 |
Sore throat | 48 (20) | 111 (20) | .928 |
Rhinorrhoea | 40 (16) | 103 (18) | .472 |
Sputum | 43 (18) | 56 (10) | <.05 |
Dyspnoea | 19 (8) | 11 (2) | <.05 |
Vomiting | 4 (2) | 25 (5) | .062 |
Diarrhea | 0 | 11 (2) | .022 |
Abdominal pain | 0 | 8 (1) | .115 |
Signs at hospital admission | |||
Temperature (T, °C) | |||
T<36.0 | 0 | 0 | <.05 |
36.0≤T<37.0 | 51 (21) | 100 (18) | |
37.0≤T<38.0 | 62 (25) | 124 (22) | |
38.0≤T<39.0 | 82 (33) | 202 (36) | |
T≥39.0 | 51 (21) | 135 (24) | |
Abnormal breath sounds on auscultation | 154 (63) | 191 (34) | <.05 |
Tachypnea | 1 (0.4) | 0 | .305 |
Clinical laboratory findings | |||
Leucopeniac | 14/228 (6) | 60/493 (12) | <.05 |
Leukocytosisd | 42/228 (18) | 85/493 (17) | .753 |
Anemiae | 50/229 (22) | 80/492 (16) | .070 |
Raised erythrocyte sedimentation ratef | 16/33 (49) | 28/72 (39) | .355 |
C‐reactive protein>8 mg/L | 24/94 (26) | 34/154 (22) | .533 |
Influenza virus type/subtype | |||
Influenza B | 101 (41) | 237 (42) | .753 |
A(H1N1)pdm09 | 46 (19) | 88 (16) | .290 |
A (H3N2) | 99 (40) | 236 (42) | .642 |
Treatment | |||
Received antibiotics before hospital admission | 112/177 (63) | 217/411 (53) | <.05 |
Received antibiotics during hospitalization | 245 (100) | 558 (100) | .811 |
Received corticosteroids during hospitalization | 35 (14) | 54 (10) | .055 |
Received oseltamivir during hospitalization | 1 (0.4) | 1 (0.2) | .517 |
Supplemental oxygen required | 4 (2) | 6 (1) | .503 |
Mechanical ventilation | 1 (0.4) | 0 | .131 |
Complications | |||
Neurologic disorders | 1 (0.4) | 1 (0.2) | .517 |
Respiratory failure | 1 (0.4) | 0 | .305 |
Cardiac failure | 1 (0.4) | 0 | .305 |
Hepatic dysfunction | 1 (0.4) | 0 | .305 |
Clinical course, median days (IQR) | |||
From illness onset to hospital admission | 3 (1–5) | 2 (0–3) | <.05 |
From hospital admission to discharge or death | 6 (5–8) | 5 (3–6) | <.05 |
Died during hospitalization | 0 | 0 | − |
Died within 30 d after discharge | 0 | 1 (0.2) | 1.000 |
ICU, intensive care unit; IQR, interquartile range.
Data presented as no. (%) of patients unless otherwise indicated. Denominators for testing of fewer cases than full group are indicated. Percentages may not total 100 because of rounding. Data only include patients with specimens for influenza virus testing.
The P‐values are comparisons between “pediatric influenza patients with pneumonia” and “pediatric influenza patients without pneumonia”, and statistically significant as P<.05.
Defined as a reduction in the circulating WBC count to <4000/μL.
Defined as a reduction in the circulating WBC count to >10 000/μL.
Defined as a reduction in the hemoglobin in grams per liter (Hb<110 g/L).
Raised erythrocyte sedimentation rate defined as exceed up limit as 20 mm/h.
Of 807 SARI cases with radiologic evidence of pneumonia that were tested for influenza viruses, 246 (30%) were positive, including 145 (59%) with influenza A and 101 (41%) with influenza B (Table 4). Among the influenza A cases, 46 (32%) were due to A(H1N1)pdm09 and 99 (68%) were due to A(H3N2). Among pneumonia cases aged 5–15 years, the proportion associated with A(H3N2) was significantly higher than either A(H1N1)pdm09 or influenza B (Table S3‐1).
Table 4.
Characteristics of influenza patientsa | Case patients with pneumonia (n=246) (%) | Case patients without pneumonia (n=561) (%) | P‐valueb |
---|---|---|---|
Male sex | 145 (59) | 332 (59) | .950 |
Median (IQR) age (years) | 2.3 (0.9–3.7) | 2.2 (1.0–4.0) | .542 |
Age group: | |||
<6 mo | 29 (12) | 50 (9) | |
6–11 mo | 38 (15) | 87 (16) | |
12–23 mo | 43 (18) | 124 (22) | |
2–4 y | 105 (43) | 195 (35) | |
5–9 y | 26 (11) | 90 (16) | |
10–15 y | 5 (2) | 15 (3) | |
At least one underlying medical condition | 7 (3) | 9 (2) | .275 |
Prematurityc | 2/110 (2) | 4/261 (2) | .744 |
Low birthweightd | 1/110 (1) | 5/261 (2) | .705 |
Vaccination historye | |||
Received monovalent pandemic H1N1 vaccinationf | 0 | 2/132 (2) | 1.000 |
Received seasonal trivalent influenza vaccinationg | 31/133 (23) | 37/256 (15) | <.05 |
Exposure history | |||
At least one tobacco smoker in household | 37/160 (23) | 102/322 (32) | .051 |
IQR, interquartile range.
Data presented as no. (%) of patients unless otherwise indicated. Denominators for testing of fewer patients than full group are indicated. Percentages may not total 100 because of rounding. Data did not include patients without specimens for influenza virus testing.
The P‐values are comparisons between “pediatric influenza patients with pneumonia” and “pediatric influenza patients without pneumonia”, and statistically significant as P<.05.
Defined as gestational age <37 wk at birth for children aged <2 y.
Defined as birth weight of a live born infant of <2500 g for children aged <2 y.
Answered “Yes” to this question, “During the past 12 mo, have you had a flu shot?” which were asked during a face‐to‐face interview.
Of children aged ≥6 mo eligible to receive seasonal trivalent inactive influenza vaccine.
Of children aged ≥6 mo eligible to receive monovalent pandemic A (H1N1) influenza vaccine.
3.6. Treatment
Forty‐seven percent of SARI patients had either been prescribed an antibiotic or self‐administered an antibiotic before hospitalization. A higher proportion of influenza‐associated SARI cases had been prescribed an antibiotic before admission than those without influenza (Table 2, P<.05). Nearly all SARI patients were treated with antibiotics after hospital admission regardless of influenza testing results. Fewer cases of influenza‐associated SARI were prescribed corticosteroids during hospitalization than those without influenza (P<.05) and 35 (21%) of them had developed X‐ray confirmed pneumonia (P<.05), which was significantly higher than those influenza cases without cortisosteroid treatment. Only 0.1% of SARI cases with laboratory‐confirmed influenza received oseltamivir treatment during hospitalization.
3.7. Risk factors associated with influenza
The results of univariate and multivariable analyses of potential factors associated with influenza among SARI patients are presented in Tables S1‐1–S8. The proportion of SARI cases with a household member who smokes cigarettes in the home or contact with anyone with fever or respiratory symptoms was significantly associated with influenza among young children aged 6–23 months. These two factors were also significantly associated with higher odds of influenza for children aged 2–4 years and children aged 5–15 years. In multivariable analyses, low birthweight (OR, 6.081; 95% CI, 1.308–28.266) and living with someone who smokes cigarettes in the household (OR, 1.363; 95% CI, 1.047–1.776) were independent risk factors for increased odds of influenza among children with SARI (Table S8).
4. Discussion
To our knowledge, this is one of the first prospective studies describing laboratory‐confirmed influenza among hospitalized children in China. We used data from an active, population‐based surveillance system to assess epidemiological and clinical characteristics of hospitalized children with influenza. Our results are consistent with our recent disease burden estimation, which found that influenza was associated with an estimated 2021 SARI hospitalizations per 100 000 during 2010–2011 and 2349 per 100 000 during 2011–2012 among children aged <5 years10 and other studies outside China.12, 13 In this study, we observed the low birth weight and living with someone who smokes cigarettes in the household were independent risk factors for increased odds of influenza among children with SARI. We also documented a low percentage (1%–16%) of SARI patients with influenza who had received influenza vaccine. Low antiviral treatment of influenza and high inappropriate use of antibiotics and corticosteroids were identified from the study.
In 2012, the WHO Strategic Advisory Group of Experts on immunization suggested that children up to 5 years of age should be considered as a target group for annual influenza vaccination.14 Several national guidelines recommend annual influenza immunization for children.15, 16, 17 However, the vast majority of the Chinese population is not vaccinated annually. Several studies have estimated vaccine effectiveness across influenza seasons and patient care settings using laboratory‐confirmed influenza cases and found a significant protective effect for children.18, 19, 20, 21, 22, 23 In our study, we did not document types or doses of vaccine administered, making it difficult to draw conclusions about vaccine effectiveness.
Almost no children with influenza were treated with oseltamivir, even though the drug is well tolerated in children and treatment started within 24 hours of symptom onset provides substantial benefits to children with influenza A infection.24 It is urgent to make oseltamivir more widely available for influenza patients, and educate Chinese clinicians about the clinical benefit of early oseltamivir treatment. More widespread use of rapid molecular assays with high sensitivity could also increase the proportion of children appropriately treated for influenza.
Corticosteroids were prescribed to 9% of influenza patients in this study. In a retrospective cohort study of hospitalized patients with A (H1N1)pdm09 influenza virus infection in China, the early use of glucocorticoids for fever reduction and pneumonia prevention was associated with the subsequent development of critical illnesses, even after adjusting for the presence of underlying diseases or risk factors.25, 26 Corticosteroids may also prolong influenza viral shedding in the respiratory tract.27 Based on available data, WHO does not currently recommend the use of systemic high‐dose corticosteroids for influenza‐associated pneumonia.28
While the infections (12%) in this study were caused by influenza viruses, clinicians prescribed antibiotics for almost all SARI patients. While we did not have data to assess the need for antibiotics in our study population, inappropriate antibiotic use is potentially harmful to the community, fostering the growth of antimicrobial‐resistant organisms.29 Reducing inappropriate antibiotic use among children in China may be challenging. Physicians may not be willing to wait for viral testing results, influenza testing is not widely available, and, even when widely available as in this study, physicians often did not receive results until at least 48 hours after specimen collection. Parents may also be less willing to accept waiting for test results before antibiotic administration. Indeed, over half of SARI patients were already treated with antibiotics before hospital admission.30
Severe acute respiratory infection patients exposed to tobacco smoke were more likely to have flu as an etiology of SARI. Environmental tobacco smoke or secondhand smoke causes ill health and mortality in children, especially among those under 5 years of age.31, 32, 33 Exposure to secondhand smoke kills approximately 100 000 people every year in China.34 Reducing secondhand smoke exposure is one of four priorities identified by the World Health Organization for global tobacco prevention and control. China's 12th 5‐Year Plan calls for smoke‐free public places as part of the major national goal to increase life expectancy. Despite the significant progress made in tobacco control in China, many children are still exposed to secondhand smoke in their home.
This study is subject to several limitations. First, our study only captured children who met our surveillance case definition for severe acute respiratory infections. Young infants might have fever only without any respiratory symptoms. Second, our study was only able to test for influenza virus infection, and only 12% of pediatric SARI patients had evidence of influenza virus infection. We do not know the etiology of illness among most pediatric SARI patients enrolled in our study.
5. Conclusions
Our results highlight the importance of surveillance in identifying factors associated with influenza in hospitalized SARI patients, monitoring adherence to influenza prevention and treatment strategies, and evaluating the year‐round disease burden during influenza seasons in central China. Additional research on pediatric SARI patients in China should also incorporate testing for other respiratory pathogens, further elucidate the connection between tobacco exposure and outcomes of SARI, and identify factors that can help clinicians rapidly start antiviral treatment of influenza while reducing inappropriate use of antibiotics and corticosteroids.
Financial Support
This study was supported by the Cooperative Agreement Number, 5U2GGH000018, funded by the Centers for Disease Control and Prevention. Its contents are solely the responsibility of the authors and do not necessarily represent the official views of the Centers for Disease Control and Prevention or the Department of Health and Human Services.
Conflicts of Interest
We declare that we have no conflict of interests.
Supporting information
Acknowledgements
We thank the participating hospitals and Jingzhou Health Bureau for assistance in coordinating data collection and supporting this study. We thank Danielle Iuliano, from the Influenza Division, National Center for Immunization and Respiratory Diseases, Centers for Disease Control and Prevention, Atlanta, USA, for comments on the manuscript. We thank Xiaojia Nie and Fang Ma from International Emerging Infections Program, US Centers for Disease Control and Prevention, Beijing, China; Jingping Ma, Aimin Li, and Jun Qin from Jingzhou Central Hospital, Xiaoxia Huang, Shaohua Zhou, and Hongzhu Lu from Jingzhou First People's Hospital, Zhangliang Hu and Daoyong Yuan from Jingzhou Second People's Hospital, and Hanbin Wu and Kewu Wang from Jingzhou Maternal and Children's Hospital for assistance in coordinating data collection and supporting this study. The views expressed are those of the authors and do not necessarily represent the policy of the China CDC or the U.S. Centers for Disease Control and Prevention.
Huai, Y., Guan, X., Liu, S., Uyeki, T. M., Jiang, H., Klena, J., Huang, J., Chen, M., Peng, Y., Yang, H., Luo, J., Zheng, J., Peng, Z., Huo, X., Xiao, L., Chen, H., Zhang, Y., Xing, X., Feng, L., Hu, D. J., Yu, H., Zhan, F. and Varma, J. K. (2017), Clinical characteristics and factors associated with severe acute respiratory infection and influenza among children in Jingzhou, China. Influenza and Other Respiratory Viruses 11, 148–156. doi: 10.1111/irv.12419
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