Volume 17, Number 10—October 2011
Household Transmission of Pandemic (H1N1) 2009 Virus, Taiwan
Author affiliation: National Taiwan University, Taipei, Taiwan
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|EID||Chang L, Chen W, Lu C, Shao P, Fan T, Cheng A, et al. Household Transmission of Pandemic (H1N1) 2009 Virus, Taiwan. Emerg Infect Dis. 2011;17(10):1928-1931. https://dx.doi.org/10.3201/eid1710.101662|
|AMA||Chang L, Chen W, Lu C, et al. Household Transmission of Pandemic (H1N1) 2009 Virus, Taiwan. Emerging Infectious Diseases. 2011;17(10):1928-1931. doi:10.3201/eid1710.101662.|
|APA||Chang, L., Chen, W., Lu, C., Shao, P., Fan, T., Cheng, A....Huang, L. (2011). Household Transmission of Pandemic (H1N1) 2009 Virus, Taiwan. Emerging Infectious Diseases, 17(10), 1928-1931. https://dx.doi.org/10.3201/eid1710.101662.|
During August–November 2009, to investigate disease transmission within households in Taiwan, we recruited 87 pandemic (H1N1) 2009 patients and their household members. Overall, pandemic (H1N1) 2009 virus was transmitted to 60 (27%) of 223 household contacts. Transmission was 4× higher to children than to adults (61% vs. 15%; p<0.001).
Pandemic (H1N1) 2009 was first identified in 2 southern California counties in April 2009 (1), and the World Health Organization declared a global pandemic on June 11, 2009 (2). In Taiwan, the government suggested that persons with pandemic (H1N1) 2009 remain home until 24 hours after they were symptom free (3). In some influenza epidemics, ≈50% of households have >1 members who become infected (4). Further investigation into the transmission of pandemic (H1N1) 2009 virus among household members is needed to help control and prevent additional infections. We investigated the transmission of pandemic (H1N1) 2009 virus and clinical outcomes of infection within households of persons with laboratory-confirmed infection.
During August–November 2009, we enrolled patients at the National Taiwan University Hospital who were infected with pandemic (H1N1) 2009 virus and their household members. The following samples were obtained from patients with clinical signs and symptoms suggestive of pandemic (H1N1) 2009 infection who visited the emergency department, outpatient clinics, or inpatient wards: nasopharyngeal swab specimen for rapid influenza antigen testing (QuickVue A+B test; Quidel, San Diego, CA, USA), throat swab specimen for virus isolation and novel subtype H1N1 reverse transcription PCR (RT-PCR), and blood specimen for serum hemagglutination inhibition (HI) assays. Laboratory-confirmed pandemic (H1N1) 2009 infection was defined in 3 ways: 1) isolation of influenza A virus, followed by positive RT-PCR result for pandemic (H1N1) 2009 virus; 2) positive rapid influenza A test result, followed by positive RT-PCR result for pandemic (H1N1) 2009 virus; or 3) pandemic (H1N1) 2009 virus HI titer >40. None of the participants had received an influenza subtype H1N1 vaccine before this study.
Persons with laboratory-confirmed pandemic (H1N1) 2009 and their household members were sent a letter and/or received a telephone call inviting them to participate (Figure). After they accepted the invitation, we collected their case report forms, which contained data regarding the source of infection, final diagnosis, clinical manifestations, and course of the disease. The index patient was defined as the first person in a household to have laboratory-confirmed pandemic (H1N1) 2009 (body temperature >38.0°C and/or cough and/or sore throat). All enrolled index patients and their household members provided blood samples for further HI assays. A mean of 45 days (SD 26, median 36, range 12–107 days) elapsed between the first day of illness in the index patient and household investigations, including blood sampling. The household transmission rate (secondary attack rate) was defined as the percentage of household members who had laboratory-confirmed pandemic (H1N1) 2009 infection 1–7 days after the onset of symptoms in the index patient.
During August–November 2009, pandemic (H1N1) 2009 was confirmed for 399 patients at National Taiwan University Hospital. Of those 399 patients, 87 patients and their households were enrolled in the study; households included the 87 index patients and their 223 household contacts (172 adults and 138 children) (Figure). Of the 87 index patients, 72 (83%) had visited the hospital for illness and had laboratory-confirmed pandemic (H1N1) 2009 infection (PCR-positive test results, HI titer >40, or both); the remaining 15 (17%) index patients attended community clinics and were identified by having titers >40 for pandemic (H1N1) 2009 virus on HI test when household investigations were done. The possible source of infection was traced for 52 (60%) of the 87 households: 46 (53%) infections were traced to schools, 5 (6%) infections were traced to daycare centers or other child care situation (when 1 babysitter cared for a few children), and 1 (1%) infection was traced to a summer camp.
As shown in Table 1, the mean ages of the index patients and their household contacts were 10.6 and 33.8 years, respectively; only 6 (7%) of the 87 index patients were adults. Households contained a mean of 1.9 children (SD 0.8, median 2, range 0–4 children).
Pandemic (H1N1) 2009 virus was transmitted to 60 (27%) of the 223 household contacts. The virus was transmitted to 35 (63%) of 56 child-aged siblings (but not to 1 cousin), to none of 5 adult-aged siblings, to 20 (14%) of 138 parents, to 4 (22%) of 18 grandparents, and to 1 (20%) of 5 aunts and uncles. Percentage of transmission among the different groups of household contacts differed significantly: the virus was transmitted to 35 (61%) of the 57 children and to 25 (15%) of the 166 adults (p<0.01 by χ2 test). However, percentage of transmission among different adult groups did not differ significantly (p = 0.86 by χ2 test). Mean interval between the onset of illness in the index patient and household members was 3.3 days (SD 2.6, median 3, range 1–6 days).
Of the 147 patients with pandemic (H1N1) 2009, 119 (81%) received a diagnosis of influenza-like illness; 10% received a diagnosis of upper respiratory tract infection; 3% each received a diagnosis of bronchitis, bronchopneumonia, asthma, or acute gastroenteritis; and 2% received a diagnosis of pneumonia. Of the 147 patients (all children), 10 (7%) were hospitalized and discharged without sequelae. Seventy-seven (89%) of the 87 index patients and 29 (48%) of the 60 household members received oseltamivir.
Table 2 shows attack rates and odds ratios for pandemic (H1N1) 2009 virus infection among the 223 household contacts by patient characteristics (sex and age) and signs and symptoms. Age <18 years, fever, cough, sore throat, rhinorrhea, myalgia, and malaise were significantly associated with pandemic (H1N1) 2009 infection, but age <18 years, fever, and cough most significantly predicted the transmission of pandemic (H1N1) 2009 virus in multivariate analysis with a multiple logistic regression model. However, we did not find a significant relationship between index patient characteristics, specific symptoms, lower respiratory tract infection, or the need for hospitalization and the rate of household transmission of pandemic (H1N1) 2009 virus.
We found children to be >4× more susceptible than adults to the secondary transmission of pandemic (H1N1) 2009 virus within households (61% vs. 15%). Furthermore, 93% of our index patients were children, and for ≈60% of them, the source of exposure to the virus was a school or daycare center. Thus, children play major roles in the introduction and spread of influenza within families. Vaccination and other measures will prevent susceptible children from becoming infected and reduce influenza virus transmission among families and communities.
This study has limitations, however, for example, the potential for nonresponse bias and possible preferential recruitment of families with sick children as index patients. Thus, adults may be relatively underrepresented as index patients in this study. Also, some adults may be less likely to go to the hospital with influenza-like symptoms.
In our study, the secondary attack rate in households was 27%, which is similar to rates in studies by Komiya et al. (26%), Sikora et al. (30.2%), and Looker et al. (33%) but higher than rates in studies by Cauchemez et al. (13%) and Carcione et al. (14.5%) (5–9). The secondary attack rate found in this study may have been relatively high because, without a vaccine against pandemic (H1N1) 2009, there were more susceptible children in the households and because most index patients were children who may shed virus for a longer period (10). Our findings show the key role that children play in introducing and spreading pandemic (H1N1) 2009 virus within households. Public health measures, such as vaccination and community health education, can prevent infections among children and help reduce virus transmission among families and the larger community.
Prof Chang is a specialist in pediatric infectious diseases at National Taiwan University Hospital, College of Medicine, National Taiwan University. Her research interests include enterovirus 71, influenza, Kawasaki disease, and other pediatric infectious diseases.
This study was supported by grants from the National Research Program for Genomic Medicine, National Science Council, Taiwan (NSC 98-2321-B-002-016, 98-2314-B-002-008-MY2, and NSC 98-3112-B-002-029), and A1 Program from National Taiwan University Hospital.
- Centers for Disease Control and Prevention. Swine influenza A (H1N1) infection in two children—southern California, March–April 2009. MMWR. 2009;58:1–3.
- Epidemiological summary of pandemic influenza A (H1N1) 2009 virus—Ontario, Canada, June 2009 [in French]. Wkly Epidemiol Rec. 2009;84:485–91.
- Centers for Disease Control. Republic of China (Taiwan). Guidance for pandemic H1N1: patients and household members [in Chinese] [cited 2010 Jun 17]. http://www.cdc.gov.tw/public/Attachment/910159235071.doc
- Taber LH, Paredes A, Glezen WP, Couch RB. Infection with influenza A/Victoria virus in Houston families, 1976. J Hyg (Lond). 1981;86:303–13.
- Komiya N, Gu Y, Kamiya H, Yahata Y, Yasui Y, Taniguchi K, Household transmission of pandemic 2009 influenza A (H1N1) virus in Osaka, Japan in May 2009. J Infect. 2010;61:284–8.
- Sikora C, Fan S, Golonka R, Sturtevant D, Gratrix J, Lee BE, Transmission of pandemic influenza A (H1N1) 2009 within households: Edmonton, Canada. J Clin Virol. 2010;49:90–3.
- Looker C, Carville K, Grant K, Kelly H, Influenza A. H1N1) in Victoria, Australia: a community case series and analysis of household transmission. PLoS ONE. 2010;5:e13702.
- Cauchemez S, Donnelly CA, Reed C, Ghani AC, Fraser C, Kent CK, Household transmission of 2009 pandemic influenza A (H1N1) virus in the United States. N Engl J Med. 2009;361:2619–27.
- Carcione D, Giele CM, Goggin LS, Kwan KS, Smith DW, Dowse GK, Secondary attack rate of pandemic influenza A(H1N1) 2009 in Western Australian households, 29 May–7 August 2009. Euro Surveill. 2011;16:pii:19765 [cited 2011 Mar 10]. http://www.eurosurveillance.org/ViewArticle.aspx?ArticleId=19765
- Li CC, Wang L, Eng HL, You HL, Chang LS, Tang KS, Correlation of pandemic (H1N1) 2009 viral load with disease severity and prolonged viral shedding in children. Emerg Infect Dis. 2010;16:1265–72.
- Figure. Flowchart showing household transmission of pandemic (H1N1) 2009 virus infection, Taiwan, August–November 2009.
- Table 1. Demographic characteristics and pandemic (H1N1) 2009 infection rates among 223 household contacts of 87 index case-patients, by contact type, Taiwan, August–November 2009
- Table 2. Pandemic (H1N1) 2009 attack rates among 223 household contacts of 87 index patients, by patient characteristics and symptoms, Taiwan, August–November 2009
Please use the form below to submit correspondence to the authors or contact them at the following address:
Li-Min Huang, Division of Pediatric Infectious Diseases, Department of Pediatrics, National Taiwan University Hospital, No. 7, Chung-Shan South Rd, Taipei 100, Taiwan
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