- Open Access
Pandemic influenza A (H1N1v) infection in pediatric population: a multicenter study in a North-East area of Italy
© Da Dalt et al; licensee BioMed Central Ltd. 2011
- Received: 28 February 2011
- Accepted: 19 May 2011
- Published: 19 May 2011
Data on clinical presentation, morbidity and mortality of 2009 pandemic influenza virus (H1N1v) in paediatric population are still emerging; most of the data so far available came from selected cohorts of children admitted to tertiary care paediatric hospitals.
An observational study involving all the 19 Divisions of Paediatrics of the Veneto Region was conducted with the aim of investigating into the demographic and clinical characteristics, the treatment, the outcome and the risk factors for disease severity of H1N1v infection occurring in children.
Two hundred children, median age of 4.15 years (range 0-15) were enrolled from the last week of October till the first week of January 2010 for an overall hospitalization rate of 23/100.000. At least one underlying medical condition was found in 44% of patients. Fever and cough were the most frequent symptoms (93% and 65% respectively). 11 patients (6%) were admitted to a PICU and 5 (2.5%) required mechanical ventilation. Antiviral therapy was administered in 103 patients (51.5%) Death occurred in 2 patients (1%); both had severe prior medical conditions. Pre-existing neurologic diseases (OR 7.82; 95%CI: 1.15-53.34), the presence of hypoxemia (OR 10.47; 95%CI: 2.12-51.70) and anemia (Haemoglobin < 10 g/dL) (OR 14.15; 95%CI: 2.36-84.64) were risk factor for Intensive Care Unit admission.
This observational study in a given area of North-East Italy confirms the rather favourable prognosis of children with influenza A H1N1 (2009). Pre-existing conditions, and which is new, significant anemia, are risk factors for a complicated course.
- Antiviral Therapy
- Paediatric Intensive Care Unit
- Hospitalization Rate
Compared to seasonal influenza, H1N1 2009 pandemic influenza virus (H1N1v) had an increased infection rate among children and adolescents [1–3]. Even though the illness has been mostly acute and self limited, a variable spectrum of disease severity has been reported from mild illness to death. Children with underlying chronic disease are at increased risk for complications and death from influenza [4–10].
However, data on clinical presentation, morbidity and mortality of novel influenza A H1N1v in paediatric population are still emerging. In fact, during weeks 49 to 52 of 2010, influenza activity in the Northern Hemisphere still increased, in particular in Europe, with A(H1N1) and B viruses predominating . The United Kingdom (U.K.) continues to report high rates of influenza. As February of 2011 approximately 25% of intensive care beds are occupied by influenza cases and 112 influenza-related deaths have been reported. 95 of 100 fatal cases from which the virus has been sub-typed have been H1N1 (2009) related and the other 5, influenza type B. The majority of severe and fatal cases have been between adolescent and adult population .
For all of these facts it is important to collect and critically analyze clinical information that may be useful for the correct management of patients in the near future.
As a matter of fact, there is a paucity in this field and those that exist are usually cohorts of children in tertiary care hospital [4, 12–16], thus not describing the actual severity of illness in all children admitted to any hospital.
The first cases of confirmed infection with the H1N1v virus in Italy were documented in Autumn 2009. By October 2010, 5.582.000 illnesses, 938 hospitalizations (455 in Intensive Care Units, ICU) and 228 deaths were estimated in Italy . In order to investigate the demographic and clinical characteristics, the treatment and the outcome of a large cohort of Italian children hospitalized because of the H1N1v Infection, we conducted an observational study in the Veneto region, a geographic area located in the North-East of Italy. The current study is also aimed to look into the risk factors for disease severity.
In Italy there is a system of seasonal flu epidemic surveillance, Influnet. Family doctors and paediatricians, called "sentinel physicians", representing all Italian Regions, insert the influenza cases observed during the epidemic season in a website. They share a common operative protocol. Every week the National Institute of Health makes provision to process data .
The study was a retrospective observational study involving all the 19 Divisions of Paediatrics of the Veneto Region, included two Paediatric Tertiary care centres with their own Paediatric Intensive Care Units (PICU). This area has a population of 867.521 subjects aged less than 15 years of age, representing 19% of all inhabitants.
Eligible patients were all children under 15 years of age hospitalized in paediatric wards for H1N1v infection documented by testing combined nasal and throat swabs. All samples were sent to the Microbiology and Virology Division of the University Hospital of Padua for the research of H1N1v virus using reverse-transcriptase Real-Time polymerase-chain-reaction assay (RT-PCR) . When required, the neuroaminidase (NA) gene of the viral isolates was also sequenced, by automated Applied Biosystems sequanator. Data collection started since the first week in which the virus was detected (October 2009) in a hospitalized child and extended through the last week the virus was detected (January 2010).
Demographic and clinical data for each study patient were collected using a standardized data collection form that included demographic information, influenza vaccination history, underlying medical conditions, clinical signs and symptoms, selected laboratory tests, radiographic findings, therapy, treatment course, complications and outcome in terms of duration of hospitalization, need for PICU, discharge or death.
All information was sent to the data-collection centre in Padua where a computerized database was created. The study was approved by the Research Ethics Committee of Padua Hospital and of the participating centres.
Continuous variables were expressed as median and interquartile range (IQR) due to the non-parametric distribution; categorical variables were expressed as percentages. Comparison for continuous variables was performed by means of Mann Whitney U test for non-normally distributed data. For categorical data, the X2 test with Yates correction for 2 × 2 tables was used. We used p < 0.05 as a threshold for statistical significance.
A multiple logistic regression model was used to identify variables independently associated with the outcome variable, namely admission to PICU. A stepwise regression procedure was used in obtaining the final model.
Epidemiological and clinical characteristics
Demographic features and pre-existing conditions of the study population.
Age groups (years): N° of patients (%)
Male sex, N° (%)
Race, N° (%)
Pre-existing conditions, N°. (%)
Type of pre-existing conditions N°
Chronic lung disease
H1N1 vaccine, N° (%)
Seasonal influenza vaccine, N° (%)
Clinical, laboratory and instrumental findings of the study population.
Clinical signs and symptoms, N° (%)
Hypoxemia (sat 02 <93%), N° (%)
Leukocyte count (mm3) - median (range)
Neutrophils (%) - median (range)
Haemoglobin (g/dl) - median (range)
Haemoglobin < 10 g/dL, N° (%)
Platelet count per mm3 - median (range)
PCR (mg/l) - median (range)
Procalcitonin (μg/L) - median (range)
Positive blood culture*- patients N°
Elevated aspartate aminotransferease, N°
Pneumonia - N°/total N° (%)
Interstitial pneumonia, N° (%)
Unilateral consolidation, N° (%)
Bilateral consolidation, N° (%)
Pleural effusion, N° (%)
Laboratory and instrumental findings
The laboratory and instrumental findings which were investigated are reported in Table 2.
Chest radiographs were suggestive of pneumonia in 104 patients, in most cases (76%) they showed lobar consolidation, unilateral or bilateral. In five cases pneumonia were associated with pleural effusion.
Laboratory confirmed co-infections were documented in nine children: four had a positive blood culture, respectively for Candida glabrata, Streptoccocus agalactiae, Neisseria meningitidis, and Staphylococcus aureus and 5 cases a positive serological test for recent Mycoplasma pneumoniae infection.
Antiviral therapy was administered in 103 patients (51.5%) after a median of 3 days (IQR 2-5) from the onset of symptoms; 46% of the children started antiviral therapy within 48 hours of the onset of symptoms. One-hundred-and-one children were treated with Oseltamivir and 2 with Zanamivir. In one case nebulized Zanamivir aqueous solution was administred for development of H1N1v viral mutation (H275Y), at the level of the NA gene, which conferred resistance to the initial treatment with Oseltamivir. The median duration of antiviral therapy was 4 days (IQR 4-5 days). Antiviral therapy was administered more frequently in patients with chronic diseases compared to healthy subjects (73% Vs. 37%, p < 0.0001) which explains why such therapy was administered more frequently in tertiary care centers compared with other pediatric institutions (84% versus 38%).
Eleven patients (5.5%), ten with a pre-existing clinical conditions, were admitted to PICU; 6 (3%) required mechanical ventilation for a median duration of 7 days (IQR 3.75-26.5) and 1 extracorporeal membrane oxygenation (ECMO). The median age of patients admitted to PICU was 3.8 years (IQR 2.4-4.6). The median length of hospital stay was 4 days (IQR 3-6.5) while the median length of stay in ICU was 6.5 days (IQR 4-8).
Two children with severe pre-existing clinical conditions died (1%); one, a 3-year old girl affected by a complex congenital heart disease, died of combined respiratory and cardiac failure despite 10 days therapy with Oseltamivir and aggressive respiratory support including ECMO. The other patient, also a 3-year old girl, affected by Niemann Pick disease and suffering of an important hepatosplenomegaly, died of respiratory failure and superimposed Staphylococcus bacteraemia after 73 days of hospitalization.
Comparison between clinical characteristics of children admitted to the Intensive Care Unit and to the regular ward.
Admitted to ICU (11 pts)
Admitted to regular ward (189 pts)
Age in years (range)
Pre-existing condition N° (%)
Other chronic lung disease
Clinical signs and symptoms, N° (%)
Hypoxemia at admission (Sat O2 <93%)
Laboratory Results (range)
Hb < 10 g/dL, N° (%)
Chest Radiograph (132 patients)
Abnormal Chest X-rays, N° (%)
Interstitial/focal consolidation, N°
Unilateral/Bilateral consolidation, N°
Pleural effusion, N° (%)
Antiviral treatment, N° (%)
Days from onset of symptoms to initiation
Multivariate logistic-regression analysis showed that the following were independent risk factors for admission to the ICU: pre-existing neurologic diseases (OR 7.82; 95%CI: 1.15 to 53.34), the presence at admission of hypoxemia (OR 10.47; 95%CI: 2.12 to 51.70) and anemia (Haemoglobin < 10 g/dL) (OR 14.15; 95%CI: 2.36 to 84.64).
This series of hospitalized children infected with the influenza A H1N1v virus, one of the largest so far published, provides complementary data about the natural history and the clinical management of this disease in children, to the amount of information provided in such a short period of time since the first case documented on April 2009. It includes patients all belonging to a well-defined area (the Veneto Region) and involves all paediatric institutions of any level. The hospitalization rate for children with influenza A H1N1v virus we documented, was equal to 23/100.000 with a peak in those aged between 2 and 5 years. It is difficult to compare these figures with the data available in the literature. In a series from California the hospitalization rate for all age groups was 2.8/100.000 ranging from 35.8/100.000 in infants 1 month old to 1.5/100.000 in patients aged 70 or older . In the Argentina study, the corresponding figure was 20/100.000 in children less than 18 years . Probably, differences in data collection and in the organization of the health system more than in the potential different clinical behaviour of the disease should be accounted to explain this geographic difference in the hospitalization rate. Certainly, influenza A H1N1v virus has affected more patients than seasonal influenza in a short time span worldwide . Also in Italy, during the peak period in November 2009, the incidence of the H1N1v virus infection was 12.92/1000 compared to 8.23/1000 for 2007-2008 seasonal influenza in the same population .
In our series the median age of those children who were hospitalized was 4 years, a finding which is comparable to what most of series have so far reported [6, 7, 11, 12, 14, 15, 20]. Only the group from Argentina describes a much younger median age of those children who were hospitalized .
In the present series, the prevalence of children affected by pre-existing chronic conditions was relatively low - 39% - in comparison with other series which report values as high as 80% [6, 7, 10, 12, 15]. These pre-existing conditions were, in order of frequency: chronic pulmonary diseases, haemoglobinopathies and neurological disorders. The fact that this is an unselected series accounting also for those children admitted to non tertiary care centres, thus less likely to be suffering of chronic conditions, could be accounted for explaining the low prevalence of predisposing conditions we documented in our study population. In this study in fact the proportion of patients affected by chronic diseases was significantly higher in third level centers compared with the other provincial and local hospitals (70.2% Vs 27.3%, p < 0.0001). Furthermore, the low incidence in this study of cases of chronic asthma, obesity, clinical conditions which have been counted as a pre-existing conditions and highly represented in the series from America has contributed to this discordance [4, 5]. Reading these data from a different point of view, the fact that slightly more than 60% of the children of this series were in a previous healthy status, underlines the potential severe clinical course which the disease may have in every children. In this regard it is worth highlighting the fact that one of the child of our cohort of young patients who ended-up in the PICU, was in a previously healthy status.
Despite these differences, the clinical, laboratory and radiographic manifestations of the H1N1v infection in this series were comparable to the ones reported by other studies.
As just said and described, the course of the H1N1v virus infection, despite generally very favourable, could be quite severe with even possible fatal outcomes. Severe pneumonia with respiratory distress syndrome, resulting in PICU admission, is the most common severe complication potentially bringing to death [4, 5, 9, 10].
In this series only 5.5% of hospitalized children were admitted to PICU, rate which goes up to almost 20% if we considered only those children admitted to tertiary care centres. In terms of PICU admission rate these figures are surprisingly equal to the ones produced by the other paediatric series [4, 6, 14].
It is universally accepted that the presence of pre-existing conditions mainly neurological and cardiac disorders and asthma, are associated with a higher rate of admission to the PICU and death [4, 7, 9, 11, 12, 14, 15]. In this regard it is worth noticing that none of our patients who ended up in the PICU were affected by asthma. This is a remarkable difference from other series which report incidences of asthma among the pre-existing conditions leading children to the PICU up to 85%.
The high quality of asthma control within the general population could be one of the reason why we did not document this detrimental effect of asthma on the disease outcome . In our cohort also anemia and hypoxemia resulted significant predictors of higher ICU admission rate. The rate of fatal outcomes in the cohort of children we studied is in the low range of the rates so far reported which varies from 1 to 5% [4, 6, 7, 12, 15]. Young age (less than 1 year) has been claimed as a risk factor for fatal outcome but the data has not been confirmed by our series as well as by others [4, 6].
The impact of therapy and of an early intervention on the outcome of the infection has been extensively discussed in the different reports [22, 23]. Half of the patients of this series were treated with neuroaminidase inhibitors including all the ones admitted to the PICU. At that time the principles which guided virus directed therapy were the following: to treat all children at risk; neonates and young infants, to rely on the clinical judgement for starting therapy in previously healthy children with uncomplicated diseases and ideally, to prolong treatment until complete virus clearance. However, from all the data so far produced no firm conclusions can be drawn on the role of this therapy and of an early intervention in reducing the length of hospital stay and/or the severity of the disease. The two patients of the present series who died were both affected by a sever pre-existing condition after having being treated for 10 and 73 days respectively with the appropriate therapy. Except for these two fatal outcomes, all other children had a full recovery which underlines once again the excellent prognosis of this viral infection.
It is worth mentioning the development, in a 3-year old severely immunocompromised patient, of resistance to oseltamivir, due to the appearance of H275Y mutation in the neuraminidase gene. A subsequent treatment with zanamivir was then able to clear the virus.
The main limits of this study were in the manner of data acquisition, since the collection was obtained by different clinicians, eventhough a uniformed report form was used and a good standardization of care exists in the Veneto Region and the fact that it relies on chart review.
In summary, this quite large series of Italian children infected by the influenza A H1N1v virus collected by pulling together the epidemiological and clinical information coming from the various paediatric divisions of the Veneto region confirms that the prognosis is quite favorable for 11 previously healthy children hospitalized with influenza H1N1. However, serious complication may rarely occur among low-risk children, and the total disease burden is high.
These conclusions appear to be relevant especially considering that we are likely to face a new wave of H1N1v infection and data guiding towards the best management of patients are required.
Participating Institutions and Members: Divisions of Pediatrics: Adria, Scolaro F, M.D; Arzignano, Trifirò G, M.D, Belluno, Memo L, M.D; Bussolengo, Dall'Agnola A, M.D; Camposampiero/Cittadella, Zorzi, M.D/Policicchio G, M.D; Castelfranco Veneto/Montebelluna, Tessariol D, M.D/Mesirca P, M.D; Chioggia-Piove di Sacco, Crivellaro C, M.D; Conegliano, Chiaffoni GP, M.D; Dolo, Miccoli R, M.D; Mestre, Pozzan GB, M.D; Monselice, Rossetti F, M.D; Portogruaro, Pulella A, M.D; Thiene, Bellettato M, M.D; Treviso, Agostini S, MD; Venezia, Santoro L, M.D; Verona Borgo Trento, Biban P, MD; Verona Borgo Roma, Boner A, MD, Cesaro S, MD; Vicenza, Colleselli P, M.D.
- Writing Committee of the WHO Consultation on Clinical Aspects of Pandemic (H1N1) 2009 Influenza, Bautista E, Chotpitayasunondh T, Gao Z, Harper SA, Shaw M: Clinical aspects of pandemic 2009 influenza A (H1N1) virus infection. N Engl J Med. 2010, 362 (18): 1708-1719.View ArticleGoogle Scholar
- Falagas ME, Cholevas NV, Kapaskelis AM, Vouloumanou EK, Michalopoulos A, Rafailidis PI: Epidemiological aspects of 2009 H1N1 influenza: the accumulating experience from the Northern Hemisphere. Eur J Microbiol:Infect Dis. 2010, 29 (11): 1327-47. 10.1007/s10096-010-1002-3. Epub 2010 Jul 13View ArticleGoogle Scholar
- Halasa NB: Update on the 2009 pandemic influenza A H1N1 in children. Curr Opin Pediatr. 2010, 22 (1): 83-87. 10.1097/MOP.0b013e3283350317.View ArticlePubMedGoogle Scholar
- Libster R, Bugna J, Coviello S, Hijano DR, Dunaiewsky M, Reynoso N: Pediatric hospitalizations associated with 2009 pandemic influenza A (H1N1) in Argentina. N Engl J Med. 2010, 362 (1): 45-55. 10.1056/NEJMoa0907673.View ArticlePubMedGoogle Scholar
- Centers for Disease Control and Prevention (CDC): Surveillance for pediatric deaths associated with 2009 pandemic influenza A (H1N1) virus infection - United States, April-August 2009. MMWR Morb Mortal Wkly Rep. 2009, 58 (34): 941-947.Google Scholar
- Kumar S, Havens PL, Chusid MJ, Willoughby RE, Simpson P, Henrickson KJ: Clinical and epidemiologic characteristics of children hospitalized with 2009 pandemic H1N1 influenza A infection. Pediatr Infect Dis J. 2010, 29 (7): 591-594. 10.1097/INF.0b013e3181d73e32.View ArticlePubMedGoogle Scholar
- Louie JK, Acosta M, Winter K, Jean C, Gavali S, Schechter R: Factors associated with death or hospitalization due to pandemic 2009 influenza A(H1N1) infection in California. JAMA. 2009, 302 (17): 1896-1902. 10.1001/jama.2009.1583.View ArticlePubMedGoogle Scholar
- Koliou M, Soteriades ES, Toumasi MM, Demosthenous A, Hadjidemetriou A: Epidemiological and clinical characteristics of influenza A(H1N1)v infection in children: The first 45 cases in Cyprus, June - August 2009. Euro Surveill. 2009, 14 (33): 19312-PubMedGoogle Scholar
- Lockman JL, Fischer WA, Perl TM, Valsamakis A, Nichols DG: The critically ill child with novel H1N1 influenza A: a case series. Pediatr Crit Care Med. 2010, 11 (2): 173-178. 10.1097/PCC.0b013e3181ccedae.View ArticlePubMedGoogle Scholar
- Campbell A, Rodin R, Kropp R, Mao Y, Hong Z, Vachon J: Risk of severe outcomes among patients admitted to hospital with pandemic (H1N1) influenza. CMAJ. 2010, 182 (4): 349-355.PubMed CentralView ArticlePubMedGoogle Scholar
- WorldHealthOrganization. Last access January 2011, [http://www.who.int/csr/disease/swineflu/updates/en/index.html]
- Hackett S, Hill L, Patel J, Ratnaraja N, Ifeyinwa A, Farooqi M: Clinical characteristics of paediatric H1N1 admissions in Birmingham, UK. Lancet. 2009, 374 (9690): 605-View ArticlePubMedGoogle Scholar
- Bettinger JA, Sauve LJ, Scheifele DW, Moore D, Vaudry W, Tran D: Pandemic influenza in Canadian children: a summary of hospitalized pediatric cases. Vaccine. 2010, 28 (18): 3180-4. 10.1016/j.vaccine.2010.02.044. Epub 2010 Feb 26View ArticlePubMedGoogle Scholar
- Calitri C, Gabiano C, Garazzino S, Pinon M, Zoppo M, Cuozzo M: Clinical features of hospitalised children with 2009 H1N1 influenza virus infection. Eur J Pediatr. 2010, 169 (12): 1511-5. 10.1007/s00431-010-1255-y. Epub 2010 Jul 22View ArticlePubMedGoogle Scholar
- Kumar A, Zarychanski R, Pinto R, Cook DJ, Marshall J, Lacroix J: Critically ill patients with 2009 influenza A(H1N1) infection in Canada. JAMA. 2009, 302 (17): 1872-1879. 10.1001/jama.2009.1496.View ArticlePubMedGoogle Scholar
- Miroballi Y, Baird JS, Zackai S, Cannon JM, Messina M, Ravindranath T: Novel influenza A(H1N1) in a pediatric health care facility in New York City during the first wave of the 2009 pandemic. Arch Pediatr Adolesc Med. 2010, 164 (1): 24-30. 10.1001/archpediatrics.2009.259.View ArticlePubMedGoogle Scholar
- ISS. Istituto Superiore della sanità. Last access January 2011, [http://www.epicentro.iss.it/focus/h1n1/aggiornamenti.asp]
- CDC (2009). H1N1 flu. Interim guidance on specimen collection, processing, and testing for patients with suspected novel influenza A (H1N1) (swine flu) virus infection. Last access January 2011, [http://www.cdc.gov/h1n1flu/specimencollection.htm]
- Novel Swine-Origin Influenza A (H1N1) Virus Investigation Team, Dawood FS, Jain S, Finelli L, Shaw MW, Lindstrom S: Emergence of a novel swine-origin influenza A (H1N1) virus in humans. N Engl J Med. 2009, 360 (25): 2605-2615.View ArticleGoogle Scholar
- Larcombe PJ, Moloney SE, Schmidt PA: Pandemic (H1N1) 2009: a clinical spectrum in the general paediatric population. Arch Dis Child. 2010,Google Scholar
- Leo G, Incorvaia C: Current management of allergic asthma in children. Minerva Pediatr. 2010, 62 (5): 475-84.PubMedGoogle Scholar
- Jain S, Kamimoto L, Bramley AM, Schmitz AM, Benoit SR, Louie J: Hospitalized patients with 2009 H1N1 influenza in the United States, April-June 2009. N Engl J Med. 2009, 361 (20): 1935-1944. 10.1056/NEJMoa0906695.View ArticlePubMedGoogle Scholar
- Shun-Shin M, Thompson M, Heneghan C, Perera R, Harnden A, Mant D: Neuraminidase inhibitors for treatment and prophylaxis of influenza in children: systematic review and meta-analysis of randomised controlled trials. BMJ. 2009, 339: b3172-10.1136/bmj.b3172.PubMed CentralView ArticlePubMedGoogle Scholar
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