HIV-positive patients had a similar outcome to HIV-negative
patients during the 2009/10 swine flu pandemic, Spanish researchers report in
the online edition of AIDS.
Rates of secondary pneumonia, admission to intensive care,
the use of mechanical ventilation and mortality were similarly low in both
groups of patients.
Patients with HIV did not take any longer to recover from
the infection, and did not require a longer stay in hospital.
The investigators describe these findings as “remarkable”.
In June 2009, the World Health Organization (WHO) issued an
alert about a new strain of human influenza A in Mexico. Called H1N1, the virus
originated in pigs, hence its popular name, swine flu.
Unlike seasonal flu outbreaks, it appeared that younger
adults had an increased risk of developing swine flu-related complications.
This was also the case for patients with underlying medical conditions,
including those caused by immunosuppression.
Therefore, patients with HIV were one of the groups
prioritised to receive vaccination against the infection.
Despite this recommendation little is known about the
outcome of HIV-positive patients who contracted swine flu. Only one fatality in
an HIV-positive patient with the infection has so far been reported.
Therefore investigators undertook a prospective study in
order to describe the symptoms, complications and outcomes of swine flu in
HIV-positive patients who were admitted to 13 hospitals in Spain between
June and November 2009. The characteristics of these HIV-positive patients were
compared to HIV-negative swine flu patients to see if outcomes differed between
these two groups.
A total of 585 patients with confirmed H1N1 infection were
included in the investigators’ analysis. Of these patients, 26 were
HIV-positive.
Age (43 vs 40 years), sex (69% vs 50% male) and pregnancy
status (12% vs 35%) were similar between the HIV-positive and HIV-negative
patients.
Those with HIV were more likely to smoke (54% vs 31%, p =
0.013). However, a higher proportion of HIV-infected patients had received the
seasonal flu vaccine (56% vs 11%, p < 0.001), as well as the vaccine against
pneumococcal pneumonia (50% vs 3%, p < 0.001).
Other than liver failure (31% vs 4%, p < 0.001) patients
with HIV were no more likely to have other serious underlying health
conditions.
Most (89%) of the HIV-positive patients were taking
antiretroviral therapy, their median CD4 cell count was 503 cells/mm3,
and 84% had an undetectable viral load.
There was no difference between the two groups of patients
between the types of swine flu symptoms reported and the interval between the
appearance of symptoms and admission to hospital.
With the exception of thrombocytopenia (p = 0.002),
HIV-positive patients did not have a higher rate of laboratory abnormalities
than those who were HIV-negative.
Chest X-ray results were abnormal in 50% of patients with
HIV and 42% of HIV-negative patients. Secondary bacterial pneumonia developed
in 12% vs 8% of patients.
Virtually all the patients received antiviral flu therapy.
However, overall only 36% of patients started this therapy within the
recommended 48 hours of the onset of symptoms.
Antibiotics were provided to 80% of HIV-positive patients
and 72% of HIV-negative individuals. The mean duration of therapy was 9 vs 8
days.
There was no evidence that swine flu was more severe in
patients with HIV. Outcomes were similar, irrespective of HIV status.
Both groups of patients started to improve an average of 2.5
days after their admission to hospital. The duration of the stay in hospital
was similar for the two groups: 6 days for those with HIV compared to 7 days
for non-HIV patients.
Similar proportions of HIV-negative (12%) and HIV-positive
(12%) patients were admitted to intensive care and required mechanical
ventilation (8% vs 9%).
None of the HIV-positive individuals died compared to 2% of
the HIV-negative patients.
“The fact that no differences in clinical outcomes were
observed between HIV-1-infected and seronegative patients is remarkable”,
comment the investigators.
They conclude, “in HIV patients, well controlled
on HAART, the new influenza virus AH1N1 had similar clinical outcomes and
prognosis to non-HIV patients.”