Risk factors for hospitalisation and poor outcome with pandemic A/H1N1 influenza: United Kingdom first wave (May-September 2009).

BACKGROUND: During the first wave of pandemic H1N1 influenza in 2009, most cases outside North America occurred in the UK. The clinical characteristics of UK patients hospitalised with pandemic H1N1 infection and risk factors for severe outcome are described.
METHODS: A case note-based investigation was performed of patients admitted with confirmed pandemic H1N1 infection.
RESULTS: From 27 April to 30 September 2009, 631 cases from 55 hospitals were investigated. 13% were admitted to a high dependency or intensive care unit and 5% died; 36% were aged <16 years and 5% were aged > or = 65 years. Non-white and pregnant patients were over-represented. 45% of patients had at least one underlying condition, mainly asthma, and 13% received antiviral drugs before admission. Of 349 with documented chest x-rays on admission, 29% had evidence of pneumonia, but bacterial co-infection was uncommon. Multivariate analyses showed that physician-recorded obesity on admission and pulmonary conditions other than asthma or chronic obstructive pulmonary disease (COPD) were associated with a severe outcome, as were radiologically-confirmed pneumonia and a raised C-reactive protein (CRP) level (> or = 100 mg/l). 59% of all in-hospital deaths occurred in previously healthy people.
CONCLUSIONS: Pandemic H1N1 infection causes disease requiring hospitalisation of previously fit individuals as well as those with underlying conditions. An abnormal chest x-ray or a raised CRP level, especially in patients who are recorded as obese or who have pulmonary conditions other than asthma or COPD, indicate a potentially serious outcome. These findings support the use of pandemic vaccine in pregnant women, children <5 years of age and those with chronic lung disease.

Introduction

On 11 June 2009 the World Health Organization announced the first influenza pandemic of the 21st century.1 2 While most pandemic H1N1 infections were mild or subclinical, the case fatality rate was 0.1–0.7%.3 4 Early reports suggested a case hospitalisation rate of 2–8%,5–9 later moderated to approximately 1% in view of under-ascertainment of mild cases.10 Although atypical, patients with severe disease imposed a considerable burden on hospital systems. Hospitalisation due to pandemic H1N1 infection was most common in children, teenagers and younger adults. At least half had underlying medical conditions.1 2 8–12 Relatively few studies have examined the risk factors associated with a severe outcome.7 13

Methods

Data collection

The Influenza Clinical Information Network (FLU-CIN) surveillance network was established by the Department of Health in England on 11 May 2009. Clinical data were collected from 55 hospitals in 20 cities or towns (see figure 1 in online supplement). Trained FLU-CIN data collectors gathered information from the case notes of patients hospitalised with pandemic H1N1 infection without pre-selection. All patients had acute respiratory illness and pandemic H1N1 infection confirmed by real-time reverse-transcriptase PCR. Diagnostic tests were performed as dictated by clinical management.

Data were extracted using a standard form that included demographic characteristics, past medical history, prehospital medication, clinical presentation, care timelines, initial assessment (emergency department and/or acute medical unit), investigations and care escalation from levels 0 to 3,i discharge and death. Since height and weight are not uniformly recorded in UK hospital notes, obesity based on physicians' observations was captured when recorded on admission.

Analysis of data

Anonymised data were analysed using STATA Version 10 (StataCorp). χ2 or Fisher exact tests were used to assess differences in proportions and the Mann–Whitney test was used for continuous variables. The demographic data were compared with those of the combined populations of London, East Midlands and Northern Ireland because these areas provided >75% of the FLU-CIN cases. As paediatric normal reference ranges for respiratory rate and blood pressure vary with age, and heart rate also varies with body temperature, abnormal values in children (aged <16 years) were defined after appropriate adjustment.14–17

Univariate analysis was performed using logistic regression to identify factors affecting the risk of requiring enhanced care (levels 2 or 3) or death in hospital (or both) as a combined measure of severe outcome. Unadjusted odds ratios (Wald test) and 95% CIs were computed. A multivariable regression technique was applied using all statistically significant variables identified during univariate analysis, including exploration for robustness and interactions using likelihood ratio tests. Age (continuous variable) was forced into each model, being an a priori confounder for comorbid conditions and case fatality. Two separate models were constructed—one for demography, comorbidities and clinical characteristics and one for selected investigations and other prognostic indicators. Where continuous variables (eg, serum C-reactive protein (CRP)) were found to be significant, these were converted into categorical variables to facilitate clinical interpretation. A peripheral oxygen saturation threshold of 94% (breathing air) was selected based on British Thoracic Society recommendations for the instigation of supplemental oxygen therapy.18

Results

A total of 631 hospitalised cases with H1N1 infection (226 children, 405 adults; median age 23 years; range 3 months–90 years) admitted between 27 April and 30 September 2009 are described. The onset of illness, available for 522 patients, occurred from April 25 to September 29 (see figure 2 in online supplement). Most cases were non-white (table 1) and the distribution of age and ethnicity differed substantially from the source population. Of the 631 patients, 284 (45% overall; 34% children and 51% adults) had one or more underlying medical conditions (table 2), of which asthma was most common in children (16%) and adults (31%). Of 159 subjects with asthma, 88 (55%) regularly used oral or inhaled steroids. Twenty-seven patients were pregnant, representing 4% of total admissions and 18% of admissions among women aged 16–44 years (table 2). Two, 13 and 8 pregnancies were in the first, second and third trimesters, respectively (missing data, n=4), and 8 (30%) had one or more underlying medical conditions. Obesity was recorded on admission in 8 (2%) of 405 adults; no child was noted to be obese.

Table 1

Demographic characteristics of 631 UK patients hospitalised with pandemic H1N1 infection during the first pandemic wave compared with source population data

	n (%)	Population comparison* (%)
Sex: female	320 (51)	51.3
Age (years)
<1	42 (7)	1.2
1–4	59 (9)	5.2
5–15	125 (20)	14.2
16–24	114 (18)	11.7
25–34	83 (13)	16.9
35–44	75 (12)	15.4
45–54	68 (11)	12.3
55–64	32 (5)	9.4
65–74	22 (3)	7.3
>75	11 (2)	6.4
Ethnicity†
White	202 (38)	81.9
Mixed	7 (1)	2.1
Asian/Asian British	169 (31)	8.0
Black/Black British	100 (19)	6.3
Chinese and other	59 (11)	1.7

Data are number (%) unless otherwise indicated.

Data for comparison of sex, age structure and ethnicity (London, East Midlands and Northern Ireland combined) were obtained from the Office for National Statistics (www.statistics.gov.uk) and Northern Ireland Statistics and Research Agency (www.nisra.gov.uk): National Census 2001 data: KS01 sex, KS02 age structure, KS06 ethnicity and corresponding census area statistics (CAS) data: UV03, UV04 and UV09 (available on Neighbourhood Statistics and www.nomis.co.uk) for further subdivisional data.

Information on ethnicity was unavailable for 94 cases; assessments of ethnicity are based on 537 cases.

Table 2

Prehospital comorbidity in 631 patients hospitalised with pandemic H1N1 infection during the first pandemic wave compared with national prevalence data

	Children (n=226)	Adults (n=405)	All admissions (n=631)	Background prevalence* (%)
No. of comorbidities†
0	149 (66)	198 (49)	347 (55)	–
1	66 (29)	138 (34)	204 (32)	–
≥2	11 (5)	69 (17)	80 (13)	–
Comorbidity
Cardiovascular disease	5 (2)	64 (16)	69 (11)	3.5
Pulmonary disease
COPD	0 (0)	25 (6)	25 (4)	1.5
Asthma	35 (16)	124 (31)	159 (25)	5.9
Other pulmonary disease	8 (3)	13 (3)	21 (3)	-
Diabetes	3 (1)	48 (12)	51 (8)	4.1
Other metabolic disease	4 (2)	2 (<1)	6 (1)	-
Neurological disease	9 (4)	10 (3)	19 (3)	-
Cerebrovascular disease	0 (0)	3 (<1)	3 (<1)	1.7
Obesity recorded on admission	0 (0)	8 (2)	8 (1)	8.1‡
Pregnancy	0 (0)	27 (7)§	27 (4)	6.2¶

Data are number (%) unless otherwise indicated.

National prevalence data on comorbidity were obtained from the Quality and Outcomes Framework (QOF) primary care data for 2009 (www.qof.ic.nhs.uk) and are based on all ages except for pregnancy.

Recorded obesity and pregnancy are excluded from the number of comorbidities in the upper portion of the table.

National prevalence data on obesity based on QOF obesity registers defined as body mass index ≥30 kg/m2.

27 pregnancies represent 7% of all adults but 18% of women aged 16–44 years in the study.

6.2% of females aged 15–44 years estimated to be pregnant in source population: in addition to 207 474 live births in London, East Midlands and Northern Ireland in 2008, we assumed that 4% of females aged 15–44 years experienced miscarriage or abortion in the same time period (119 668). To calculate the prevalence of pregnancy we took 9/12 of annual live births (assuming 9-month duration of pregnancy) and 3/12 of miscarriages/abortions (assuming 3-month duration), divided by the total female population aged 15–44 years.

COPD, chronic obstructive pulmonary disease.

Preadmission care

The median interval between onset of illness and admission recorded for 522 cases was 2 days (range 0–33; interquartile range 0–24). It was shorter in children than in adults (1 day vs 2 days, p<0.001) but was unaffected by comorbid conditions (median 2 vs 2 days; p=0.42). Twenty children (9%) and 62 adults (15%) received antiviral drugs before admission (p=0.02). Preadmission antiviral drugs were given to 35 patients (12%) with comorbidity and to 47 patients (14%) without comorbidity (p=0.80).

Clinical presentation, treatment and outcome

Patients presented most frequently with fever (71%), cough (68%), breathlessness (36%), headache (27%), sore throat (23%) and nausea or vomiting (22%) in adults; and fever (74%), cough (50%) and nausea or vomiting (27%) in children. Overall, 11% presented with diarrhoea, which was almost twice as common in white ethnic groups (15.4% vs 8.1%; p=0.008) in both adults (16% vs 9%) and children (14% vs 7%).

Upon presentation, 63% of children and 87% of adults had tachycardia and 30% of children and 33% of adults had tachypnoea (table 3). About half had fever (≥38°C); 16% of children and 24% of adults had a peripheral oxygen saturation of <94% breathing air, and 13% of children and 24% of adults had systolic hypotension. Alanine aminotransferase was raised in 19% of children and 34% of adults. Increased levels of CRP of <100 mg/l occurred in 19% of children and 31% of adults; increases of ≥100 mg/l occurred in 8% of children and 18% of adults. Eighteen patients (3%) presented with symptoms of encephalitis (new behavioural change, meningism, focal signs, seizures or confusion), one of whom died. Twenty-nine patients (5%) presented with muscle weakness or tenderness suggestive of myositis, of whom one died.

Table 3

Presenting signs and initial investigations and the percentage that were abnormal in patients hospitalised with pandemic H1N1 infection during the first pandemic wave

Observations	n	Mean	Range	Interquartile range	Level of abnormality	%
Temperature (°C)
Children	183	38.0	35.3–41.4	36.0–40.1	37.1–37.9	22
					≥38.0	50
Adults	344	39.0	35.1–40.2	35.9–40.3	37.1–37.9	24
					≥38.0	53
Pulse (rate/min)
Children	97	137	54–240	89–184	> Normal*	63
Adults	218	107	54–184	62–155	>85	87
Pulse (respirations/min)
Children	94	37	18–98	20–66	> Normal	30
Adults	205	23	10–44	14–40	>30	33
Systolic BP (mmHg)
Children	32	106	83–126	93–119	< Normal	13
Adults	216	125	68–191	84–185	<110	24
Diastolic BP (mmHg)
Children	33	60	39–90	42–77	< Normal	36
Adults	217	71	32–121	43–100	<65	32
C-reactive protein (mg/l)
Children	98	60	1–322	4–146	31–99	19
					≥100	8
Adults	208	57	1–322	1.5–274	31–99	31
					≥100	18
White cell count (×109/l)
Adults and children	425	9.0	1.1–38.0	1.1–32.9	>11.0	17
Children	102	44	3–163	19–82	>195	0
Adults	285	91	5–800	7–611	>200	3
Urea (μmol/l)
Children	104	7.2	0.6–106	1.1–40	>6.4	14
Adults	286	7.3	0.9–130	1.5–56	>6.7	18
Alanine transaminase (IU/l)
Children	70	42.7	2–393	7–177	>40	19
Adults	179	36.3	8–167	10–127	>35	34
Spo2 (%, breathing room air)
Children	175	95.9	54–100	80–100	<94%	16
Adults	334	95.1	66–100	60–100	<94%	24

See Methods for derivation of abnormal values in children.

Spo2, peripheral oxygen saturation.

Pneumonia

Chest radiographic results were recorded in the notes in 349 cases (106 children, 243 adults), of which 37 children (35%) and 65 adults (27%) had findings consistent with pneumonia. Thirty-seven of 65 adults had sufficient data to derive a CURB65 score of 0, 1 and 2 in 15 (41%), 17 (46%) and 5 (14%) cases, respectively. The median age of patients with pneumonia was 26 years; 46 (45%) had one or more underlying medical conditions, 4 were pregnant and 2 were obese. Initial arterial blood gas analysis readings (while breathing room air) were available from 34 patients with pneumonia; 1/23 (4%) with an arterial oxygen tension ≥8 kPa died compared with 3/11 (27%) with an initial reading <8 kPa (p=0.085).

The occurrence of radiological pneumonia was unrelated to the presence of underlying medical conditions (p=0.09). Of the 102 cases with radiological pneumonia, 14 (6 children) had received preadmission antiviral drugs (14%) compared with 28/247 (11%) patients (2 children) without pneumonia on the chest x-ray (p=0.53). The median length of stay for patients with pneumonia was 6 days compared with 3 days for patients without pneumonia (p=0.0001). Thirty-seven of 102 patients (36%) required level 2 (n=6) or level 3 (n=31) care, 21 (21%) underwent mechanical ventilation (intubated) and 12 (12%) died, of whom 11 were ventilated. Mortality in cases with radiographic pneumonia was significantly higher than in cases without (OR 4.57, 95% CI 1.71 to 12.18; p=0.0008). Four cases of pneumonia (4%) had positive bacteriological findings. Two children with severe developmental delay and extreme prematurity, respectively, grew methicillin-resistant Staphylococcus aureus (MRSA) and one adult grew Streptococcus pneumoniae in sputum; all three died. One adult had S aureus bacteraemia and survived.

Inpatient treatment

After admission, antiviral drugs were prescribed to 474 patients (75%) and 366 (58%) received antibiotics. One hundred and forty-seven of 157 cases (93%) who did not receive an antiviral drug in hospital did not receive an antiviral agent before hospitalisation. One hundred and fourteen patients (18%) received steroids as an acute intervention; of these, 71 had underlying asthma, 57 of whom were previously maintained on steroids. The 43 patients without asthma treated in hospital with steroids included 13 with COPD or other chronic lung disease on long-term steroids; 7 on steroids for other long-term conditions (eg, myeloma); 8 with sudden deterioration (of whom 4 were pregnant or recently post-partum); 5 with wheeze on admission; 2 obese patients; 2 with suspected new asthma; and 1 suspected allergic reaction (the reason for steroid treatment was unclear in 5 cases).

Length of stay

The median length of hospital stay was 3 days in children (range 1–32; interquartile range 1–28) and 4 days in adults (range 1–41; interquartile range 1–29; p=0.004); it was unaffected by comorbidity or treatment with antiviral drugs before hospitalisation.

Deaths, severity criteria and requirement for critical care

Overall, 85 of the 631 cases (14%) had a severe outcome. Eighty patients received level 2 (n=27) or level 3 (n=53) care and 29 died. The recorded case fatality rate was 4.6%, 3.5% in children and 5.2% in adults (likelihood ratio=1.5, p=0.34). Seventeen of the 29 fatalities (59%) were previously healthy. The median age of those who died was 49 years in adults and 7 years in children. There were no significant differences in use of level 2 or level 3 care with age; however, the in-hospital case fatality rate increased with age (<5 years (3%), 5–15 years (4%), 16–44 years (3.7%), 45–64 years (9%), ≥65 years (6.0%)) and was significantly higher in patients aged ≥45 years (3.6% vs 8.3%; p=0.02). Twenty-five patients (31%) died while in level 2 or level 3 care. A further two deaths occurred on standard wards (a patient with metastatic carcinoma and another with severe chronic lung disease), one in the emergency room (after 4 h resuscitation) and one after transfer to another hospital (no subsequent information). Of cases receiving level 2 or level 3 care, those who died received a median of 10 days care at this level whereas survivors received 3 days of care (p=0.001). No patients were declined level 2 or level 3 care for non-clinical reasons during the study period.

Recipients of antiviral drugs before admission were less likely to require level 2 or level 3 care (8/82 (9.8%) vs 72/549 (13%); likelihood ratio=0.72, p=0.394) or to die (2/82 (2.4%) vs 27/549 (4.9%); likelihood ratio=0.48, p=0.31) than non-recipients, but both trends were non-significant. Two of 27 pregnant women (7%) died in hospital while in level 3 care; four others (15%) received level 2 (n=1) or level 3 (n=3) care and survived.

Table 4 shows the association between admission variables and severe outcome. Altered conscious level, dyspnoea, requirements for intravenous fluids or supplementary oxygen, radiologically-confirmed pneumonia and CRP levels ≥100 mg/l were each associated with a severe outcome, as were obesity recorded on admission and chronic pulmonary disease other than asthma or COPD (eg, cystic fibrosis, fibrosing alveolitis and congenital lung defects). In a multivariable model of demography, comorbidities and clinical characteristics, obesity recorded on admission and pulmonary conditions other than asthma or COPD were found to be associated with a severe outcome (table 5). An additional multivariable analysis of selected investigations and possible prognostic indicators showed that radiologically-confirmed pneumonia and a CRP level ≥100 mg/l were independently significant (table 5). The addition of further variables did not significantly alter either model.

Table 4

Analysis of comorbidity, demography, clinical characteristics and selected investigations as risk factors for severe outcome in patients hospitalised with pandemic H1N1 infection during the first pandemic wave

	People affected by condition or feature (number with severe outcome)	Likelihood ratio (95% CI)	p Value
Age (years)	–	1.01* (0.99 to 1.02)	0.089
Asthma	159 (18)	0.77 (0.44 to 1.34)	0.360
COPD	25 (6)	2.10 (0.81 to 5.43)	0.123
Chronic pulmonary conditions, excluding asthma or COPD	21 (7)	3.41 (1.33 to 8.71)	0.010
Cardiovascular disease	69 (12)	1.41 (0.72 to 2.75)	0.314
Diabetes	51 (7)	1.02 (0.44 to 2.35)	0.956
Neurological disorders	19 (3)	1.21 (0.34 to 4.25)	0.764
Hepatic disease	7 (2)	2.60 (0.49 to 13.65)	0.257
Obesity recorded on admission	8 (4)	6.96 (1.46 to 27.28)	0.008
Smoker (current and former)‡	103 (16)	1.01 (0.53 to 1.91)	0.972
Pregnancy	27 (6)	1.87 (0.73 to 4.77)	0.190
White ethnicity†‡	202 (29)	1.08 (0.65 to 1.78)	0.764
Altered conscious level	10 (6)	1.11 (1.04 to 1.17)	0.001
Dyspnoea	181 (44)	1.32 (1.81 to 1.49)	0.001
Heart rate (abnormal)†	198 (31)	1.62 (0.80 to 3.30)	0.180
Respiratory rate (abnormal)†	89 (16)	1.78 (0.89 to 3.56)	0.102
Required supplemental oxygen on admission	99 (33)	4.51 (2.72 to 7.40)	0.001
Intravenous fluid replacement on admission	145 (28)	1.76 (1.07 to 2.89)	0.005
Radiologically-confirmed pneumonia	102 (37)	5.28 (2.95 to 9.47)	0.001
CRP ≥100 mg/l†	46 (16)	4.41 (2.14 to 9.10)	0.001
Spo2 <94% on air†	107 (31)	3.60 (2.17 to 6.27)	0.001

Reflects a 1% increase in risk of severe outcome for each additional year of age.

Information about smoking history was documented for 216 cases; ethnicity was recorded for 537 cases; heart rate, with corrections for temperature, was available for 512 cases; respiratory rate was recorded for 470 cases; chest radiography findings were recorded for 349 cases; CRP levels were recorded for 306 cases; Spo data were recorded for 252 cases.

45 severe outcomes among 335 non-white patients.

COPD, chronic obstructive pulmonary disease; CRP, C-reactive protein; Spo2, peripheral oxygen saturation.

Table 5

Results of logistic regression analyses of (A) demography, comorbidities and clinical characteristics and (B) selected investigations and other possible prognostic indicators for critical care requirement or death in hospital

	Odds ratio (95% CI)	p Value
(A) Clinical conditions*
Obesity recorded on admission	6.08 (1.45 to 25.37)	0.013
Chronic respiratory disease other than asthma or COPD	3.17 (1.22 to 8.24)	0.018
(B) Other clinical parameters†
Radiologically-confirmed pneumonia	4.97 (2.09 to 11.81)	0.001
C-reactive protein >100 mg/l	3.06 (1.20 to 7.81)	0.019

Multivariable analysis of demography, comorbidities and clinical characteristics was constructed based on observations from 631 cases.

A separate multivariable analysis was constructed for selected investigations and other possible prognostic indicators based on observations from 193 cases.

COPD, chronic obstructive pulmonary disease.

Discussion

The strengths of this study include confirmation by standardised PCR criteria, relatively few missing data and a setting in which hospitalisation and management of cases is driven by national guidelines.19 Reported cases were followed up without selection. Except in Scotland, the acquisition of cases closely mirrored the national epidemic curve geographically and temporally, with most occurring in Greater London, the English Midlands and Northern Ireland (see figures 1 and 2 in the online supplement). Overall, 12% of patients required high dependency or intensive care and 4.6% died; the mortality among those requiring enhanced care was 31%.

The median age of cases was 23 years and 46% had risk factors for seasonal influenza complications. In relation to the source population, hospitalisations were highest in those aged <5 years and lowest in those aged ≥55 years, consistent with the age-specific prevalence of cross-reacting antibodies.20 Similar to other reports,13 mortality was significantly higher above 44 years of age.

Over one-half of all admissions and 59% of all in-hospital deaths occurred in previously healthy people. In contrast, Donaldson et al found that 36% of patients who died had no (19%) or only mild (17%) underlying illnesses.21 The principal comorbidity was asthma (in adults and children). About 45% of hospitalised patients with asthma with pandemic H1N1 infection did not routinely use inhaled or oral steroids, suggesting that pandemic influenza vaccine (H1N1) might be beneficial for all patients with asthma rather than just those with more severe disease.

Pregnancy substantially increases the risks for severe respiratory illness and excess deaths during pandemics and seasonal influenza,22 and in our series pregnant women comprised 18% of admissions among women aged 16–44 years compared with an expected prevalence of 6% in the source population. These findings suggest that pregnant women are about three times more likely to be admitted to hospital with H1N1 infection than non-pregnant women of similar age and confirm the importance of vaccinating pregnant women, which may also protect their newborn infant.23

Obesity has been previously identified as a risk factor for severe pandemic H1N1 infection.13 24 25 Obesity recorded on admission was identified as an independent risk factor for a severe outcome. This observation possibly reflects that gross (as opposed to mild) obesity is more likely to be recorded by physicians in case notes and the lack of reserve respiratory capacity in such individuals.

Univariate analyses showed that patients with a severe outcome were more likely to be recorded as obese and to have pulmonary disease other than asthma or COPD (eg, cystic fibrosis, fibrosing alveolitis and congenital lung defects), altered consciousness level, shortness of breath, radiologically-confirmed pneumonia, CRP level ≥100 mg/l, peripheral oxygen saturation of <94% on air or to have required supplemental oxygen or intravenous fluids on admission than those managed on standard wards. These findings are similar to those of previous studies7 13 and highlight the importance of regular monitoring for dyspnoea and peripheral oxygen saturation. Multivariable analysis of clinical features revealed that obesity recorded on admission and pulmonary conditions other than asthma or COPD remained significant clinical risk factors for a severe outcome. In addition, radiologically-confirmed pneumonia and CRP levels ≥100 mg/l were independently associated with a severe outcome. In general, CRP levels are higher in patients with bacterial infections than in those with non-bacterial infections, and high levels are associated with mortality.26 Our findings should alert physicians to the possibility of very high CRP levels in patients with pandemic H1N1 infection and its potential seriousness. In our study, 29% of patients with chest x-rays had findings consistent with pneumonia. The median duration of stay of these patients was twice as long as those without pneumonia, and mortality in cases with radiographic pneumonia was several fold higher than for the whole case series (12% vs 4.6%). Bacterial co-infections were less commonly reported than in other case series,27 28 although we did not access autopsy data.29

Higher rates of severe pandemic H1N1 infection have been reported in indigenous or disadvantaged populations,24 30 31 as also occurred during 1918–19.32 In our study, the number of Asian and black people who were admitted exceeded population estimates of ethnic profile 3–4-fold. The reasons for this excess are unclear, but could include language barriers affecting consulting behaviour or treatment access, overcrowding, household size and genetic susceptibility.

Fewer than one-sixth of all children and adults in this case series, including those with underlying medical risk factors for complications, received antiviral drugs before admission; this requires further investigation. In this case series, 25% were not prescribed antiviral drugs during the admission for reasons that are unclear; in most cases (93%) they did not receive an antiviral drug before hospital admission either. While the median interval between illness onset and hospital admission was just 1 day in children and 2 days in adults, 28% of children and 23% of adults in our study were apyrexial on admission, while just over half had a fever of ≥38°C. Such findings question the appropriateness of specifying fever of at least 38°C as part of the clinical case definition in current diagnostic, treatment and infection control algorithms.

The median length of stay in hospital was 3 days in children and 4 days in adults, which was unaffected by comorbidity or the use of antiviral drugs before admission. While cases that received antiviral drugs before admission were less likely to require high dependency or intensive care and were 50% less likely to die in hospital, neither trend was significant. A number of other studies now suggest that early treatment with oseltamivir may reduce the likelihood of hospitalisation and death due to pandemic H1N1 influenza.33–35

Conclusions

While most patients with pandemic H1N1 influenza experience mild disease, 12% of those admitted to hospital require high dependency or intensive care, about 30% have radiographic pneumonia and 5% die. Pandemic H1N1 influenza should be considered in the differential diagnosis of any respiratory illness while the pandemic virus is circulating in the community; fever ≥38°C is a poor discriminator. Patients admitted to hospital with illness compatible with influenza should have a chest x-ray on admission and should be actively monitored for altered level of consciousness, dyspnoea and low peripheral oxygen saturation. An abnormal chest x-ray or raised CRP level—especially in patients who are observed to be obese, have pulmonary conditions other than asthma or COPD or are pregnant—may suggest a potentially serious outcome. Our findings support the use of H1N1 pandemic vaccine in pregnant women, children aged <5 years and those with chronic lung disease as a priority, including patients with asthma, regardless of severity.