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Incidence and Risk Factors for Respiratory Syncytial Virus and Human Metapneumovirus Infections among Children in the Remote Highlands of Peru

  • Andrew Wu,

    Affiliation School of Medicine, Vanderbilt University, Nashville, Tennessee, United States of America

  • Philip J. Budge,

    Affiliation Division of Infectious Diseases, Washington University School of Medicine, St. Louis, Missouri, United States of America

  • John Williams,

    Affiliations Department of Pediatrics, Vanderbilt University, Nashville, Tennessee, United States of America, Department of Pathology, Microbiology, and Immunology, Vanderbilt University, Nashville, Tennessee, United States of America

  • Marie R. Griffin,

    Affiliation Department of Health Policy, Vanderbilt University, Nashville, Tennessee, United States of America

  • Kathryn M. Edwards,

    Affiliations Department of Pediatrics, Vanderbilt University, Nashville, Tennessee, United States of America, Vanderbilt Vaccine Research Program, Division of Infectious Diseases, Department of Pediatrics, Vanderbilt University, Nashville, Tennessee, United States of America

  • Monika Johnson,

    Affiliation Department of Pediatrics, Vanderbilt University, Nashville, Tennessee, United States of America

  • Yuwei Zhu,

    Affiliation Department of Biostatistics, Vanderbilt University, Nashville, Tennessee, United States of America

  • Stella Hartinger,

    Affiliations Swiss Tropical and Public Health Institute, Basel, Switzerland, Instituto de Investigación Nutricional, Lima, Peru

  • Hector Verastegui,

    Affiliation Instituto de Investigación Nutricional, Lima, Peru

  • Ana I. Gil,

    Affiliation Instituto de Investigación Nutricional, Lima, Peru

  • Claudio F. Lanata,

    Affiliation Instituto de Investigación Nutricional, Lima, Peru

  • Carlos G. Grijalva

    Affiliation Department of Health Policy, Vanderbilt University, Nashville, Tennessee, United States of America

Incidence and Risk Factors for Respiratory Syncytial Virus and Human Metapneumovirus Infections among Children in the Remote Highlands of Peru

  • Andrew Wu, 
  • Philip J. Budge, 
  • John Williams, 
  • Marie R. Griffin, 
  • Kathryn M. Edwards, 
  • Monika Johnson, 
  • Yuwei Zhu, 
  • Stella Hartinger, 
  • Hector Verastegui, 
  • Ana I. Gil



The disease burden and risk factors for respiratory syncytial virus (RSV) and human metapneumovirus (MPV) infections among children living in remote, rural areas remain unclear.

Materials and Methods

We conducted a prospective, household-based cohort study of children aged <3 years living in remote rural highland communities in San Marcos, Cajamarca, Peru. Acute respiratory illnesses (ARI), including lower respiratory tract infection (LRTI), were monitored through weekly household visits from March 2009 through September 2011. Nasal swabs collected during ARI/LRTI were tested for RSV, MPV, and other respiratory viruses using real-time RT-PCR. Incidence rates and rate ratios were calculated using mixed effects Poisson regression.


Among 892 enrolled children, incidence rates of RSV and MPV ARI were 30 and 17 episodes per 100 child-years, respectively. The proportions of RSV and MPV ARI that presented as LRTI were 12.5% and 8.9%, respectively. Clinic visits for ARI and hospitalizations were significantly more frequent (all p values <0.05) among children with RSV (clinic 41% and hospital 5.3%) and MPV ARI (38% and 3.5%) when compared with other viral infections (23% and 0.7%) and infections without virus detected (24% and 0.6%). In multivariable analysis, risk factors for RSV detection included younger age (RR 1.02, 95% CI: 1.00-1.03), the presence of a smoker in the house (RR 1.63, 95% CI: 1.12-2.38), residing at higher altitudes (RR 1.93, 95% CI: 1.25-3.00 for 2nd compared to 1st quartile residents; RR 1.98, 95% CI: 1.26-3.13 for 3rd compared to 1st quartile residents). Having an unemployed household head was significantly associated with MPV risk (RR 2.11, 95% CI: 1.12-4.01).


In rural high altitude communities in Peru, childhood ARI due to RSV or MPV were common and associated with higher morbidity than ARI due to other viruses or with no viral detections. The risk factors identified in this study may be considered for interventional studies to control infections by these viruses among young children from developing countries.


Lower respiratory tract infection (LRTI) is the leading global cause of death in children between one month and five years of age [14]. Approximately 70% of LRTI deaths under five years of age are among children in developing regions [1, 3]. However, the precise reasons for this disparity in childhood mortality between developed and developing countries are not well understood.

Viruses are commonly detected in childhood respiratory disease in both developed and developing countries [48]. Among respiratory viruses, respiratory syncytial virus (RSV) [46, 922] and human metapneumovirus (MPV) [13, 2023] are the leading causes of LRTI among children. Although the epidemiology of these viruses has been well characterized in developed countries [24, 25], fewer data exist about their burden and risk factors for developing countries, where their disease burden and related-mortality seem to be the highest [1, 3, 11, 26]. The dearth of information is especially prominent for rural communities where research is typically difficult to conduct due to unique settings, such as high altitudes, that may also influence disease burden [2729].

Most of the current literature on childhood respiratory disease in developing countries focuses on populations from tropical climates [30], urban areas, or settings where healthcare access is available and information is gathered during healthcare visits [9, 13, 14, 18, 2124, 3033]. In rural communities with limited access to health centers, passive surveillance performed at healthcare centers may not reflect the overall disease burden, severity, or risk factors in the community [10, 34, 35]. In those settings, active household-based studies conducted within the community can provide a more comprehensive perspective on disease patterns. Our study sought to quantify the RSV- and MPV-specific burden of acute respiratory infections and to identify risk factors for these infections among children from rural communities in the remote highlands of Peru.

Materials and Methods

The present study was nested within the RESPIRA-PERU study [36], a prospective, household-based, active surveillance cohort study conducted in the rural highlands of San Marcos, Cajamarca, Peru during March 2009 –September 2011. This region is notably high altitude (1500–4000 meters above sea level) and remote with a population density of 38 persons/km2.

Ethics Statement

Written informed consent was obtained from all participants’ parents or guardians prior to enrollment. The RESPIRA-PERU project was approved by the IRB of both Vanderbilt University and the Instituto de Investigación Nutricional in Peru.

Study Population

Enrollment criteria have been previously described [37]. Briefly, the study population included children aged <3 years old whose families planned to remain in the study area for at least a year after enrollment.

The integrating home-based environmental interventions (IHIP) trial

Before the RESPIRA-PERU study, the IHIP trial, a clustered randomized controlled study, was conducted in the same study area [38]. The IHIP trial randomized children to improved cook stoves, solar water disinfection units, and kitchen sinks with running water in order to decrease the frequency of diarrhea and LRTI. Control families were given a mother-child psychomotor stimulation intervention. Children who had participated in the IHIP trial for either arm were eligible to participate in the RESPIRA-PERU study if they met our enrollment selection criteria.

Household Visits and Data Collection

Data were gathered by local field workers who were trained by study personnel according to the World Health Organization (WHO) Integrated Management of Childhood Illness (IMCI) protocol [3941]. Field workers visited study participants weekly at their homes to obtain information about any respiratory symptoms during the previous seven days. If one visit was missed, during the next visit information was recorded for the previous 14 days. If two or more consecutive visits were missed, data were recorded only for the 14 days prior to the successful visit.

Definitions of ARI and LRTI

ARI was defined as the presence of reported fever or cough; and LRTI as the presence of at least one of the following: age-specific tachypnea, audible wheezing, intercostal and subcostal retractions, nasal flaring, or stridor [40]. To distinguish separate episodes of ARI, at least seven days without fever or cough were required between episodes. Only children with ARI symptoms on the day of the visit or the day prior were further evaluated for signs of LRTI as previously defined.

Collection and analysis of specimens

When an ARI was reported within the previous seven days including the visit day, field workers collected a nasal swab, placed it into Remel M4RT viral transport media (Thermo Fisher Scientific Remel Products, Lenexa, KS) and delivered to the local research laboratory in San Marcos within 8 hours of collection for processing and storage. Samples were subsequently shipped to Vanderbilt University for testing using real-time RT-PCR targeting the following respiratory viruses: rhinovirus, adenovirus, parainfluenza (types 1, 2, 3), influenza (A, B, C), RSV and MPV. [36].

RSV and MPV Seasons

To assure that our risk factor assessment was restricted to periods at risk for RSV and MPV infections, risk factor analyses were only performed during seasons when RSV and MPV were circulating. The beginning of a specific season was defined as the first week of continuous RSV/MPV activity with one or more test positives in two consecutive weeks. The end of a season was defined as the last week of two consecutive weeks with at least one infection per week.

Statistical Analysis

Descriptive analysis was conducted and frequencies, means, medians, and proportions were reported for RSV episodes without MPV co-detection and for MPV episodes without RSV co-detection. Wilcoxon rank sum tests for continuous data and Chi-squared tests for contingency tables were used to examine differences in clinical attributes between RSV and MPV episodes in which only one virus was detected. For comparison purposes, we grouped non-study viruses as “Other Virus” encompassing rhinovirus, adenovirus, parainfluenza (types 1, 2, 3), or influenza (A, B, C) infections. A separate “No Virus Detected” group included those ARI in which none of the tested viruses were detected.

Incidence rates were calculated by dividing the number of new ARI’s by person-time of observation at risk with the rates expressed as ARI incidence per 100 child-years, while accounting for individual and village clustering to obtain robust standard errors, and 95% CI’s of ARI incidence rates were reported. Incidence rate comparisons were performed using incidence rate ratios. For the identification of risk factors, we fit virus-specific multivariable mixed effects Poisson regression models. Factors evaluated simultaneously included age, gender, calendar year, sharing a bed, the number of household members per bedroom, day care attendance, presence of a smoker, maternal education level, dirt flooring, the household head’s occupation, presence of electricity, water source, disposal services and sewage, altitude, and IHIP participation status. Multilevel multiple imputation was performed to account for observations with missing covariate data (<8%) [42]. Analyses were repeated in a complete case scenario (without data imputation). All statistical analyses were performed using Stata 13.1 software (STATACorp College Station, TX).


The RESPIRA-PERU study enrolled 892 children from 810 households in 58 communities in the San Marcos province. There were 4,475 ARI episodes during a total of 755.1 child-years at risk (median follow-up of 0.81 child-years per child), with 226 episodes involving RSV and 130 involving MPV. Co-infection with RSV and MPV occurred in only two ARI episodes. 202 (23%) children had at least 1 RSV infection and 127 (14%) children had at least 1 MPV infection. Of note, in 42% of RSV ARI and 33% of MPV ARI other study viruses were co-detected, with rhinovirus responsible for 75% of the RSV co-detections and 65% of the MPV co-detections.

The average age of participants across all infection categories was 15 months. Approximately half of all participants were female. Most participants had dirt floors in their houses (>91%), used a solid form (coal or wood) of cooking fuel (>91%), lived with a household member who worked in agriculture (>76%), and had mothers who did not complete secondary school (>84%) [36]. These characteristics reflect the rural setting and poverty in which these participants reside. Additionally, 3 out of 4 participants across all infection categories resided at altitudes higher than 2314 meters above sea levels. Demographics and characteristics associated with infections involving RSV, MPV, other viruses, and no viral detections are shown in Table 1.

Table 1. Demographics and characteristics associated with ARI episodes by virus type.

Although the mean age for both infections was similar (16 months), the risk of RSV and MPV infections differed by age. The incidence of RSV was highest in children under 12 months of age (34 per 100 child-years, 95% CI: 25–46) and lowest in children from 24–35 months (25, 95% CI: 19–32). In contrast, the highest rate of MPV infection was in children between 6–11 months (27, 95% CI: 19–37) and lowest in children under 6 months of age (12, 95% CI: 14–20). The RSV incidence rates were significantly higher than MPV rates for each age group except among children 6–11 months of age (p = 0.14) (Table 2).

Table 2. RSV and MPV incidence rates per 100 child-years stratified by age.

Table 3 describes the clinical manifestations of RSV and MPV infections. The reported days of fever among RSV and MPV infections were each longer than duration of fever in infections where no virus was detected. RSV ARI was more likely to present as an LRTI and to result in an ARI clinic visit or hospitalization compared with ARI due to other viral infections and ARI in which no virus was detected. Similarly, MPV infections were more likely to present with tachypnea and result in an ARI clinic visit or hospitalization when compared to other viral ARI and ARI with no virus detected. RSV and MPV accounted for approximately 30.4% and 13% of virus-positive hospitalizations where one virus was detected. The next most common virus–rhinovirus–was detected in approximately 21.8% of hospitalizations. Approximately 10.7% and 6.9% of RSV and MPV ARI were associated with LRTIs, yielding incidence rates of 1.8 and 0.8 LRTIs per 100 child-years, respectively. The clinical manifestations of the ARI with a single virus were not significantly different from ARI that included other viral co-detections.

The risk factors for RSV and MPV infections also differed. In multivariable analyses younger age, the presence of a smoker, and living at higher altitudes (specifically 2315–2865 meters above sea level compared to 1976–2314 meters) were identified as independent risk factors for RSV infection. The only significant risk factor for MPV in multivariable analysis was the occupation of the household head, which was not so for RSV. Specifically, higher MPV risk was associated with unemployed household heads when compared with household heads with some type of employment (Table 4). Separate analyses without data imputation yielded results similar to those from the main analyses (S1 Table).


In our study, ARI due to RSV and MPV were very common among young children living in rural communities of the Peruvian Andes. RSV and MPV ARI were also more likely to exhibit indicators of severe disease such as tachypnea, clinic visits, and hospitalizations than ARI from other viral causes or when no viruses were detected. Risk factors for RSV detection were younger age, presence of an indoor smoker, and living at high altitudes. Conversely, age, smoking, and altitude were not associated with MPV infection risk. The only significant risk factor for MPV ARI was the head of household’s occupation, with higher risk associated with unemployment.

Our RSV ARI incidence rate of 30 events per 100 child-years is similar to that of prospective, household-based studies conducted in two low resource settings at lower altitude (about 36 events per 100 child-years) [17, 30]. To our knowledge, the only other household-based study that has assessed the burden of MPV infections in young children found an incidence rate of 7 per 100 child-years among the urban poor of Bangladesh [21], which was much lower than our observed MPV rate of 17 per 100 child-years. Of note, that study in Bangladesh required one major or multiple minor criteria for physician referral where the final ARI diagnosis was made, which may explain this difference in incidence rates. In previous studies performed by our group among young U.S. children, the rates of outpatient clinic visits for RSV and MPV infections in infants were much higher than the rates in this household-based study [24, 25]. This may largely be a reflection of greater access to outpatient care.

The age distribution of RSV and MPV appeared to have distinct patterns. RSV incidence rates were highest in children less than 12 months whereas MPV rates were highest only in the 6–11 month age range. Consistent with our results, several studies conducted at health facilities in developed countries have reported that MPV tend to affect older infants whereas RSV affects both younger and older infants [13, 24]. For example, rates of RSV among outpatient children <6 months and 6–11 months were both high and similar to each other in a study conducted by our colleagues among US children [25]. In another study by our group, rates of MPV were higher for those 6–11 months than less than 6 months in that same population of US children [24]. Similar RSV and MPV studies conducted in developing regions only report LRTI rates, but demonstrate similar age patterns, with RSV LRTI incidence rates highest among infants 0–6 months and MPV LRTI rates highest in 6–12 month olds [21, 43]. Although these studies have been conducted in different settings and use different methodologies, it appears that the age distribution of RSV and MPV ARI may be similar between studies conducted in developing and developed regions.

There was substantial clinical overlap between RSV and MPV ARI regarding duration of different symptoms. This is not surprising since both viruses belong to the same viral subfamily, tend to circulate between December and April in the Northern hemisphere in developed countries [23, 24, 32], and both are associated with bronchiolitis [4, 13, 22, 23]. Furthermore, these viruses frequently co-circulate during respiratory seasons in our study region as well [36]. These two viruses have similar patterns of severity in our study. The overlap of certain clinical manifestations such as audible wheezing and tachypnea seen with bronchiolitis highlights the frequent involvement of the lower respiratory tract with these two viruses. Other studies in developing regions often cite RSV and MPV as the most common causes of LRTI compared to other common childhood respiratory pathogens [10, 2023]. Of note, some of those studies defined LRTI as hospitalization or presence of tachypnea alone. Therefore, our results seem consistent with those studies since RSV and MPV did have significantly stronger associations with hospitalization compared to non-RSV and non-MPV infections. Our percentages of virus-positive hospitalizations attributable to RSV and MPV were also consistent with similar studies. LRTI among hospitalized children in Brazil were associated with RSV and MPV in 86% of all the virus-positive cases, while the other viruses comprised 14% of episodes [20]. Other studies by our group in US health facilities found that 20% and 6% of children under 5 years who were hospitalized for ARI were due to RSV and MPV, respectively [24, 25]. Overall, it appears that RSV and MPV ARI are significantly associated with indicators of more severe disease in both developed and developing countries.

Previous studies in low-resource settings have found that crowding is a significant risk factor for severe childhood RSV infection [14, 30, 33, 44, 45]. In our study, RSV and MPV ARI were not significantly associated with crowding. This finding should be interpreted with caution. First, crowding likely presents more risk indoors than outdoors and our study is unable to differentiate between times spent in these two settings. Additionally, the number of persons per household in our study (median of 5) was low compared to similar studies that did detect an association with crowding. For example, a study conducted in rural Alaska [33], where it is common to have 6 people per household [44], found a significant relationship between crowding and RSV hospitalizations of children >6 months only when the number of people in the household was at least eight. Similarly, a study in Gambia [14] used a threshold of 10 household members to define crowding. It should be noted that these studies assessed for hospitalization as a primary outcome, whereas we focused on all respiratory disease episodes. The risk factor of crowding may be limited to RSV hospitalization risk. Consistent with this observation is the finding from a Kenyan study [30] that increasing numbers of children in the household were not associated with RSV ARI, but was associated with LRTI when the number of children exceeded ten. Unfortunately, evaluation of the relationship between hospitalizations and crowding was unable to be performed in our study due to the low number of hospitalizations from these rural isolated communities.

A number of studies conducted in developed [13, 18] and developing countries [31] have reported that having a smoker in the house increases the risk of RSV infection. Okiro et al [30] found that RSV ARI risk increased significantly if at least 2 smokers were present in the household. Other studies have specifically demonstrated an association between maternal smoking and LRTI in the first year of life [46, 47]. In our study, we observed a significant relationship between indoor smoking and RSV infection but the association with MPV infection did not reach statistical significance. Although the point estimates were similar to associations previously reported, the prevalence of smoking was relatively low in the study population and the precision of our MPV estimates was limited. Interestingly, we also noted that although the risk of RSV infections was not strongly associated with the household head’s occupation, we observed a significant association between a MPV infection rate and household head’s occupation. This observation is intriguing but requires subsequent assessment in other settings.

A previous article on risk factors for RSV ARI reported that children living above 2500 meters were 33% more likely to be hospitalized for RSV compared to those living below 2500 meters [29]. Similarly, a 2008 WHO report mentions “high altitude (cold air)” as a possible risk factor for childhood community-acquired pneumonia [28]. This is congruent with our results, which show that the risk of RSV ARI increases with increasing altitude beyond 2300 meters. Besides the temperature differences, higher altitudes generally have lower oxygen saturation levels, can induce pulmonary vasoconstriction secondary to hypoxia, and can cause impaired nasal mucociliary transport, all of which may affect susceptibility to respiratory infection [27, 48]. In our study, however MPV infection rates appear to be less affected by altitude, which may suggest unique aspects of MPV infection, such as the effects of temperature on viral replication, transmission, or virulence. To our knowledge, this is one of few studies that have specifically explored the association of MPV infection with high altitude in the literature.

Our findings must be interpreted in light of some limitations. Our risk factor analyses required restrictions such as stratifying the primary participant group that likely limited our sample size and statistical power to detect some associations. Second, other relevant variables such as time-varying nutritional or immunological status of the study children were not gathered as part of the study, and thus remained unaccounted for in our analyses. Third, samples were only gathered during ARI episodes, though virus could have been present during asymptomatic periods. Nevertheless, previous studies using molecular detection techniques have consistently shown that RSV and MPV were rarely detectable in asymptomatic young children [32, 49, 50], which should mitigate that concern. Fourth, although viruses account for a majority of respiratory disease in children, bacteria also play an important role in severe disease. The bacterial etiology of study ARIs was not assessed in this study. In a number of RSV and MPV infections we also detected other viruses, especially rhinovirus. Although these co-infections might impact disease severity, the majority of RSV and MPV infections in our study did not have viral co-detections and we did not find significant differences in clinical manifestations or healthcare use between those with and without co-detections. Finally, even though our study was conducted in the rural, highland communities of the Andes, these results may not represent other populations who also live in high altitudes. Nevertheless, these populations are typically excluded from traditional research, and information on the epidemiology of viral infections in this setting is lacking.

In conclusion, RSV and MPV ARI were very common among young Andean children. Both viruses shared many clinical symptoms between each other as well as with other viruses. RSV and MPV ARI notably presented with more indicators of severe disease than infections due to other viral causes. The risk factors identified in this study may be considered for further interventions to control infections by these viruses among young children from developing countries.

Supporting Information

S1 Table. Risk factors for specific viral infections without imputation.

Values that were significantly different (p<0.05) when compared to reference values are indicated by the symbol †. Numbers of RSV and MPV infections are smaller than Table 3 because analysis was restricted to infections occurring during the RSV or MPV season among children who were observed and at risk during each season.



On behalf of the study of Respiratory Infections in Andean Peruvian children (RESPIRA-PERU): Vanderbilt University, Marie R. Griffin, John V. Williams, Kathryn M. Edwards, Monika Johnson, Philip J. Budge, Yuwei Zhu, Carlos G. Grijalva; Emory University, Jorge E. Vidal, Keith P. Klugman; Swiss Tropical and Public Health Institute, Stella Hartinger, MSc, PhD; Instituto de Investigacion Nutricional, Hector Verastegui, Ana I. Gil, Claudio F. Lanata. We especially want to thank the communities and families of San Marcos, Cajamarca Peru for their participation and cooperation in this study. We sincerely appreciate the approval and continued support of the Cajamarca Health Region authorities, and we are indebted to the local health workers who persevered in harsh environments over two years to conduct this study to work for better health of children in their communities.

Author Contributions

Conceived and designed the experiments: JW MG KE MJ SH HV AG CL CG. Performed the experiments: MG KE SH CG. Analyzed the data: AW PB YZ CG. Contributed reagents/materials/analysis tools: JW HV AG CL. Wrote the paper: AW PB JW MG KE YZ HV CL CG.


  1. 1. Global Burden of Disease (GBD) Compare. In: Compare G, editor. Institute for Health Metrics and Evaluation (IHME): The Lancet; 2010.
  2. 2. Liu L, Johnson HL, Cousens S, Perin J, Scott S, Lawn JE, et al. Global, regional, and national causes of child mortality: an updated systematic analysis for 2010 with time trends since 2000. The Lancet. 2012;379(9832):2151–61.
  3. 3. Lozano R, Naghavi M, Foreman K, Lim S, Shibuya K, Aboyans V, et al. Global and regional mortality from 235 causes of death for 20 age groups in 1990 and 2010: a systematic analysis for the Global Burden of Disease Study 2010. The Lancet. 2012;380(9859):2095–128.
  4. 4. Simoes EC, T. Chow J. et al. Acute Respiratory Infections in Children. In: Jamison DB, JG. Measham AR. et al., editor. Disease Control Priorities in Developing Countries. 2nd edition ed. Washington (DC): World Bank; 2006.
  5. 5. Claesson BA, Trollfors B, Brolin I, Granstrom M, Henrichsen J, Jodal U, et al. Etiology of community-acquired pneumonia in children based on antibody responses to bacterial and viral antigens. The Pediatric Infectious Disease Journal. 1989;8(12):856–61. pmid:2516622
  6. 6. Juven T, Mertsola J, Waris M, Leinonen M, Meurman O, Roivainen M, et al. Etiology of community-acquired pneumonia in 254 hospitalized children. The Pediatric Infectious Disease Journal. 2000;19(4):293–8. pmid:10783017
  7. 7. Michelow IC, Olsen K, Lozano J, Rollins NK, Duffy LB, Ziegler T, et al. Epidemiology and Clinical Characteristics of Community-Acquired Pneumonia in Hospitalized Children. Pediatrics. 2004;113(4):701–7. pmid:15060215
  8. 8. Wubbel L, Muniz L, Ahmed A, Trujillo M, Carubelli C, McCoig C, et al. Etiology and treatment of community-acquired pneumonia in ambulatory children. The Pediatric Infectious Disease Journal. 1999;18(2):98–104. pmid:10048679
  9. 9. Law BJ, Carbonell-Estrany X, Simoes EAF. An update on respiratory syncytial virus epidemiology: a developed country perspective. Respiratory Medicine. 2002;96, Supplement 2(0):S1–S7.
  10. 10. Nair H, Nokes DJ, Gessner BD, Dherani M, Madhi SA, Singleton RJ, et al. Global burden of acute lower respiratory infections due to respiratory syncytial virus in young children: a systematic review and meta-analysis. The Lancet. 2010;(1474-547X (Electronic)).
  11. 11. Peltola V, Ruuskanen O. Respiratory Viral Infections in Developing Countries: Common, Severe, and Unrecognized. Clinical Infectious Diseases. 2008;46(1):58–60. pmid:18171214
  12. 12. Kwofie TB, Anane YA, Nkrumah B, Annan A, Nguah SB, Owusu M. Respiratory viruses in children hospitalized for acute lower respiratory tract infection in Ghana. Virology Journal. 2012;(1743-422X (Electronic)).
  13. 13. Papenburg J, Hamelin M-È, Ouhoummane N, Carbonneau J, Ouakki M, Raymond F, et al. Comparison of Risk Factors for Human Metapneumovirus and Respiratory Syncytial Virus Disease Severity in Young Children. Journal of Infectious Diseases. 2012;206(2):178–89. pmid:22551815
  14. 14. Weber MW, Milligan P, Hilton S, Lahai G, Whittle H, Mulholland EK, et al. Risk factors for severe respiratory syncytial virus infection leading to hospital admission in children in the Western Region of The Gambia. International Journal of Epidemiology. 1999;28(1):157–62. pmid:10195682
  15. 15. Infection and Incidence: Respiratory Syncytial Virus Infection: Centers for Disease Control and Prevention; 2010 [April 19, 2014].
  16. 16. Munywoki PK, Koech DC, Agoti CN, Lewa C, Cane PA, Medley GF, et al. The Source Of Respiratory Syncytial Virus Infection In Infants: A Household Cohort Study In Rural Kenya. Journal of Infectious Diseases. 2013. 10.1093/infdis/jit828.
  17. 17. Nokes DJ, Okiro EA, Ngama M, Ochola R, White LJ, Scott PD, et al. Respiratory syncytial virus infection and disease in infants and young children observed from birth in Kilifi District, Kenya. Clinical Infectious Diseases. 2008;(1537–6591 (Electronic)).
  18. 18. von Linstow ML, Hogh M, Nordbo SA, Eugen-Olsen J, Koch A, Hogh B. A community study of clinical traits and risk factors for human metapneumovirus and respiratory syncytial virus infection during the first year of life. European Journal of Pediatrics. 2008;(1432–1076 (Electronic)).
  19. 19. Hortal M, Mogdasy C, Russi JC, Deleon C, Suarez A. Microbial agents associated with pneumonia in children from Uruguay. Review of Infectious Diseases. 1990;(0162–0886 (Print)).
  20. 20. da Silva ER, Pitrez MC, Arruda E, Mattiello R, Sarria EE, de Paula FE, et al. Severe lower respiratory tract infection in infants and toddlers from a non-affluent population: viral etiology and co-detection as risk factors. BMC Infectious Diseases. 2013;(1471–2334 (Electronic)).
  21. 21. Homaira N LS, Petri WA, Vainionpaa R, Rahman M, et al. Incidence of Respiratory Virus-Associated Pneumonia in Urban Poor Young Children of Dhaka, Bangladesh, 2009–2011. PLoS ONE 2012;7(2).
  22. 22. Singleton RJ, Bulkow LR, Miernyk K, DeByle C, Pruitt L, Hummel KB, et al. Viral respiratory infections in hospitalized and community control children in Alaska. Journal of Medical Virology. 2010;82(7):1282–90. pmid:20513097
  23. 23. Foulongne V, Guyon G, Rodiere M, Segondy M. Human metapneumovirus infection in young children hospitalized with respiratory tract disease. Pediatric Infectious Disease Journal. 2007;(0891–3668 (Print)).
  24. 24. Edwards KM, Zhu Y, Griffin MR, Weinberg GA, Hall CB, Szilagyi PG, et al. Burden of human metapneumovirus infection in young children. New England Journal of Medicine. (1533–4406 (Electronic)).
  25. 25. Hall CB, Weinberg GA, Iwane MK, Blumkin AK, Edwards KM, Staat MA, et al. The Burden of Respiratory Syncytial Virus Infection in Young Children. New England Journal of Medicine. 2009;360(6):588–98. pmid:19196675.
  26. 26. Rudan I, Lawn J, Cousens S, Rowe AK, Boschi-Pinto C, Tomakovi L, et al. Gaps in policy-relevant information on burden of disease in children: a systematic review. The Lancet. 2005;365(9476):2031–40.
  27. 27. Barry P, Mason N, O'Callaghan C. Nasal mucociliary transport is impaired at altitude. European Respiratory Journal. 1997;10(1):35–7. pmid:9032488
  28. 28. Rudan I, Boschi-Pinto C, Biloglav Z, Mulholland K, Campbell H. Epidemiology and etiology of childhood pneumonia. Bulletin of the World Health Organization. 2008;(1564–0604 (Electronic)).
  29. 29. Sommer C, Resch B, Simoes EA. Open Microbiology Journal. 2011;(1874–2858 (Electronic)). D—NLM: PMC3258650 OTO—NOTNLM.
  30. 30. Okiro EA, Ngama M, Bett A, Cane PA, Medley GF, James Nokes D. Factors associated with increased risk of progression to respiratory syncytial virus-associated pneumonia in young Kenyan children. Tropical Medicine & International Health. 2008;13(7):914–26.
  31. 31. Al-Sonboli N HC, Al-Aghbari N, Al-Ansi A, Ashoor O, Cuevas LE. Human metapneumovirus and respiratory syncytial virus disease in children, Yemen. Emerging Infectious Diseases. 2006.
  32. 32. Williams JV, Harris PA, Tollefson SJ, Halburnt-Rush LL, Pingsterhaus JM, Edwards KM, et al. Human Metapneumovirus and Lower Respiratory Tract Disease in Otherwise Healthy Infants and Children. New England Journal of Medicine. 2004;350(5):443–50. pmid:14749452.
  33. 33. Bulkow LR, Singleton RJ, Karron RA, Harrison LH. Risk factors for severe respiratory syncytial virus infection among Alaska native children. Pediatrics. 2002;(1098–4275 (Electronic)).
  34. 34. Mulholland K. Global burden of acute respiratory infections in children: implications for interventions. Pediatric Pulmonology. 2003;(8755–6863 (Print)).
  35. 35. Smith KR, McCracken JP, Weber MW, Hubbard A, Jenny A, Thompson LM, et al. Effect of reduction in household air pollution on childhood pneumonia in Guatemala (RESPIRE): a randomised controlled trial. The Lancet. 2011;378(9804):1717–26.
  36. 36. Budge PJ, Griffin MR, Edwards KM, Williams JV, Verastegui HA, Hartinger SM, et al. A Household-based Study of Acute Viral Respiratory Illnesses in Andean Children. The Pediatric Infectious Disease Journal. 2014.
  37. 37. Grijalva CG, Griffin MR, Edwards KM, Williams JV, Gil AL, Verastegui HA, et al. The Study of Respiratory Pathogens in Andean Children. International Journal of Epidemiology. 2013;(1464–3685 (Electronic)).
  38. 38. Hartinger SM, Lanata CF, Hattendorf J, Gil AL, Verastegui HA, Ochoa T, et al. A community randomised controlled trial evaluating a home-based environmental intervention package of improved stoves, solar water disinfection and kitchen sinks in rural Peru: rationale, trial design and baseline findings. Contemporary Clinical Trials. 2011;(1559–2030 (Electronic)).
  39. 39. Integrated management of childhood illness: conclusions. WHO Division of Child Health and Development. 1997;(0042–9686 (Print)).
  40. 40. Gove S. Integrated management of childhood illness by outpatient health workers: technical basis and overview. The WHO Working Group on Guidelines for Integrated Management of the Sick Child. Bulletin of the World Health Organization. 1997;(0042–9686 (Print)).
  41. 41. Lambrechts T, Bryce J, Orinda V. Integrated management of childhood illness: a summary of first experiences. Bulletin of the World Health Organization. 1999;(0042–9686 (Print)).
  42. 42. Carpenter JR, Goldstein H, Kenward MG. REALCOM-IMPUTE Software for Multilevel Multiple Imputation with Mixed Response Types. Journal of Statistical Software. 2011;45(5).
  43. 43. Nokes DJ, Okiro EA, Ngama M, White LJ, Ochola R, Scott PD, et al. Respiratory Syncytial Virus Epidemiology in a Birth Cohort from Kilifi District, Kenya: Infection during the First Year of Life. Journal of Infectious Diseases. 2004;190(10):1828–32. pmid:15499540
  44. 44. Colosia AD, Masaquel A, Hall CB, Barrett AM, Mahadevia PJ, Yogev R. Residential crowding and severe respiratory syncytial virus disease among infants and young children: a systematic literature review. BMC Infectious Diseases. (1471–2334 (Electronic)).
  45. 45. Simoes EAF. Environmental and demographic risk factors for respiratory syncytial virus lower respiratory tract disease. The Journal of Pediatrics. 2003;143(5):118–26.
  46. 46. Duff AL, Pomeranz ES, Gelber LE, Price GW, Farris H, Hayden FG, et al. Risk factors for acute wheezing in infants and children: viruses, passive smoke, and IgE antibodies to inhalant allergens. Pediatrics. 1993;(0031–4005 (Print)).
  47. 47. McConnochie KM, Roghmann KJ. Parental smoking, presence of older siblings, and family history of asthma increase risk of bronchiolitis. American Journal of Diseases of Children. 1986;(0002-922X (Print)).
  48. 48. Niermeyer S, Shaffer EM, Thilo E, Corbin C, Moore LG. Arterial oxygenation and pulmonary arterial pressure in healthy neonates and infants at high altitude. The Journal of Pediatrics. 1993;123(5):767–72. pmid:8229488
  49. 49. Jansen RR, Wieringa J, Koekkoek SM, Visser CE, Pajkrt D, Molenkamp R, et al. Frequent Detection of Respiratory Viruses without Symptoms: Toward Defining Clinically Relevant Cutoff Values. Journal of Clinical Microbiology. 2011;49(7):2631–6. pmid:21543571
  50. 50. van der Zalm MM, van Ewijk BE, Wilbrink B, Uiterwaal CSPM, Wolfs TFW, van der Ent CK. Respiratory Pathogens in Children with and without Respiratory Symptoms. The Journal of Pediatrics. 2009;154(3):396–400.e1. pmid:18823911