Influenza epidemiology and influenza vaccine effectiveness during the 2015–2016 season: results from the Global Influenza Hospital Surveillance Network
verfasst von:
Joan Puig-Barberà, Ainara Mira-Iglesias, Elena Burtseva, Benjamin J. Cowling, Unal Serhat, Guillermo Miguel Ruiz-Palacios, Odile Launay, Jan Kyncl, Parvaiz Koul, Marilda M. Siqueira, Anna Sominina, on behalf of the Global Influenza Hospital Surveillance Network
The Global Influenza Hospital Surveillance Network is an international platform whose primary objective is to study severe cases of influenza requiring hospitalization.
Methods
During the 2015–2016 influenza season, 11 sites in the Global Influenza Hospital Surveillance Network in nine countries (Russian Federation, Czech Republic, Turkey, France, China, Spain, Mexico, India, and Brazil) participated in a prospective, active-surveillance, hospital-based epidemiological study. Influenza infection was confirmed by reverse transcription-polymerase chain reaction. Influenza vaccine effectiveness (IVE) against laboratory-confirmed influenza was estimated using a test-negative approach.
Results
9882 patients with laboratory results were included of which 2415 (24.4%) were positive for influenza, including 1415 (14.3%) for A(H1N1)pdm09, 235 (2.4%) for A(H3N2), 180 (1.8%) for A not subtyped, 45 (0.5%) for B/Yamagata-lineage, 532 (5.4%) for B/Victoria-lineage, and 33 (0.3%) for B not subtyped. Of included admissions, 39% were < 5 years of age and 67% had no underlying conditions. The odds of being admitted with influenza were higher among pregnant than non-pregnant women (odds ratio, 2.82 [95% confidence interval (CI), 1.90 to 4.19]). Adjusted IVE against influenza-related hospitalization was 16.3% (95% CI, 0.4 to 29.7). Among patients targeted for influenza vaccination, adjusted IVE against hospital admission with influenza was 16.2% (95% CI, − 3.6 to 32.2) overall, 23.0% (95% CI, − 3.3 to 42.6) against A(H1N1)pdm09, and − 25.6% (95% CI, − 86.3 to 15.4) against B/Victoria lineage.
Conclusions
The 2015–2016 influenza season was dominated by A(H1N1)pdm09 and B/Victoria-lineage. Hospitalization with influenza often occurred in healthy and young individuals, and pregnant women were at increased risk of influenza-related hospitalization. Influenza vaccines provided low to moderate protection against hospitalization with influenza and no protection against the predominant circulating B lineage, highlighting the need for more effective and broader influenza vaccines.
Influenza surveillance is essential for tracking and controlling influenza infections and for assessing influenza vaccine effectiveness (IVE). Since 2012, the Global Influenza Hospital Surveillance Network (GIHSN) has run an annual prospective, active-surveillance, hospital-based study to collect epidemiological and virological data on influenza [1]. The aim of the GIHSN is to improve understanding of influenza epidemiology to better inform public health policy decisions.
During the 2015–2016 influenza season, the GIHSN included 11 coordinating sites and 27 hospitals in nine countries (St. Petersburg and Moscow, Russian Federation; Prague, Czech Republic; Ankara, Turkey; Paris, France; Beijing, China; Valencia, Spain; Tlalpan, Mexico; Jammu and Kashmir, India; and Fortaleza and Curitiba, Brazil). All sites in the GIHSN share a common core protocol, follow standard operating procedures, use a shared questionnaire to collect patient information, and perform reverse transcription-polymerase chain reaction to confirm influenza infection [1]. Thus, the GIHSN can attain large sample sizes and relevant data on severe influenza and IVE among hospitalized individuals from geographically disperse regions. In addition, several limitations of other surveillance systems are avoided or adjusted for, such as non-systematic sampling and incomplete case ascertainment, as well as a lack of comparison groups, adjustment for confounders, and consensus about case definitions [2‐4]. Results have been published for the GIHSN’s first three seasons (2012–2013 [5, 6], 2013–2014 [7], and 2014–2015 [8]). Here, we present the influenza epidemiology and IVE results by age and influenza strain for the 2015–2016 influenza season.
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Methods
Study design
The GIHSN was initiated by Sanofi Pasteur in 2011 to fill the gap in influenza epidemiology and public health knowledge. The GIHSN is a public-private partnership between Sanofi Pasteur and several institutions that are affiliated with national health authorities (including the WHO National Influenza Centers, national ministries of health, and China’s Centers for Diseases Control and Prevention). Each of these institutions acts as a coordinating site and supervises a local network of hospitals. Not-for-profit institutions with proposals aligned with the GIHSN scope and study design are eligible to apply for grants from the Foundation for Influenza Epidemiology. Sanofi Pasteur participated in the design of the study but did not participate in the collection, management, or analysis of data.
The methodology for the GIHSN study has previously been described in detail [1, 5, 6]. Briefly, the study included patients who had been admitted to one of the participating hospitals for acute illness possibly related to influenza within the last 48 h. The patients had to be residents in the predefined hospital’s catchment area for at least 6 months, not institutionalized, and not discharged from a hospital within 30 days of the current admission. Onset of symptoms had to be within 7 days prior to admission. Acute illness in patients aged ≥5 years had to meet the European Centre for Disease Prevention and Control clinical case definition of influenza-like illness (ILI) [9]; include one of the following general symptoms: fever or feverishness, malaise, myalgia or headache; and include one of the following respiratory complaints: shortness of breath, sore throat, or cough. Patients aged < 5 years were recruited if they presented with any of the signs and symptoms described in Additional file 1: Table S1. Patient eligibility was assessed by research staff using admission rolls, clinical records, and information obtained from the patient after consent. Each site defined the sample collection period according to previous experience in local influenza epidemics (see Additional file 2: Table S2). For each patient, a common standardized questionnaire was completed by face-to-face interview or by searching clinical records. Collected information included age, sex, number of chronic underlying conditions, previous admissions to hospital in the last 12 months, number of visits to a general practitioner in the last 3 months, smoking habits, socioeconomic class (according to occupation), days from onset of symptoms to swabbing, and epidemiological week at admission. The influenza vaccination status of each patient was also collected by face-to face interview, patient records, clinical records, or registries, including the name of the vaccine received and the date of vaccination. Two respiratory swabs were taken from each patient (nasal and nasopharyngeal swabs from patients < 14 years, pharyngeal and nasopharyngeal swabs from patients ≥14 years) and combined to detect the presence of influenza A (H1N1pdm09 and H3N2 subtypes) and B (Yamagata and Victoria lineages) by real-time reverse-transcription polymerase chain reaction. All included patients, or their parents or legal guardians, provided written informed consent.
Statistical analysis
Statistical analyses were performed using Stata version 14.2 (College Station, TX, USA). Differences between categories were estimated by the Pearson Chi-square or Fisher exact test as appropriate. When comparing nested models, P-values for interactions were obtained by likelihood ratio test. P-values below 0.05 were considered statistically significant. Conditional plots were used to describe complex relationships between age, chronic conditions and influenza infection [10].
IVE was estimated using the test-negative approach as (1 − odds ratio [OR]) × 100, where the OR was calculated by mixed effects logistic regression comparing the vaccine coverage rates between influenza-positive and influenza-negative cases, after adjusting for potential confounders. Appropriate variables were included depending on the model. For the IVE model, age was divided into deciles and modelled using restricted cubic splines; sex was a categorical variable; social class was a categorical variable with four levels (qualified, skilled, low or unskilled, and unknown); number of comorbidities was a categorical variable with three levels (none, one, more than one); vaccination status had two levels (yes/no); time from onset to swab was a categorical variable with three levels (0 to 4, 5 to 7, 8 to 9); epidemiological week at admission was modelled using restricted cubic splines. The number of knots for age and epidemiological week was chosen using the Akaike information criterion [11]. IVE was not estimated for individual influenza vaccines. Heterogeneity between sites was controlled by including the site as a random effect in the models. All included patients were considered in the descriptive analysis, but records with missing values for outcome, exposure, or with potential confounders, and individuals with contraindications for vaccination or with previous influenza infections, were excluded from the IVE analysis. IVE values were considered heterogeneous if the I2 statistic was > 50%.
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Results
Patients included in the epidemiological analysis and identified viruses
A total of 18,360 eligible admissions were identified by the 11 coordinating sites during the 2015–2016 influenza season. Of these, 9882 admissions (53.8%) met the inclusion criteria and were included in the study (Table 1). The main reasons for exclusion were the absence of ILI symptoms for subjects ≥5 years of age (n = 3886, 21.2%) and recruitment during weeks without influenza circulation (n = 1524, 8.3%). No cases at the Fortaleza site met the inclusion criteria.
Table 1
Exclusions, inclusions, and RT-PCR results for included admissions
Category
n (%)
St. Petersburg
Moscow
Czech Republic
Turkey
France
Beijing
Valencia
Mexico
India
Fortaleza
Curitiba
Total
N = 2247
N = 2457
N = 248
N = 1351
N = 169
N = 2947
N = 6795
N = 1034
N = 371
N = 157
N = 584
N = 18,360
Excluded from the analysis
Non-resident
10 (0.4)
84 (3.4)
1 (0.4)
10 (0.7)
0 (0.0)
1 (< 0.1)
25 (0.4)
249 (24.1)
5 (1.3)
3 (1.9)
0 (0.0)
388 (2.1)
Institutionalized
0 (0.0)
32 (1.3)
6 (2.4)
25 (1.9)
0 (0.0)
2 (0.1)
0 (0.0)
5 (0.5)
0 (0.0)
1 (0.6)
3 (0.5)
74 (0.4)
Unable to communicate
20 (0.9)
112 (4.6)
14 (5.6)
96 (7.1)
0 (0.0)
0 (0.0)
59 (0.9)
56 (5.4)
0 (0.0)
0 (0.0)
65 (11.1)
422 (2.3)
Did not provide consent
80 (3.6)
26 (1.1)
21 (8.5)
11 (0.8)
0 (0.0)
0 (0.0)
16 (0.2)
40 (3.9)
1 (0.3)
0 (0.0)
3 (0.5)
198 (1.1)
Previous discharge from hospital < 30 d
11 (0.5)
80 (3.3)
6 (2.4)
266 (19.7)
25 (14.8)
24 (0.8)
66 (1.0)
208 (20.1)
9 (2.4)
47 (29.9)
89 (15.2)
831 (4.5)
No ILI symptoms, ≥ 5 y of agea
0 (0.0)
34 (1.4)
60 (24.2)
3 (0.2)
2 (1.2)
0 (0.0)
3708 (54.6)
60 (5.8)
0 (0.0)
19 (12.1)
0 (0.0)
3886 (21.2)
Swabbed > 7 d after onset of symptoms (all ages)b
55 (2.4)
134 (5.5)
16 (6.5)
72 (5.3)
0 (0.0)
28 (1.0)
226 (3.3)
237 (22.9)
17 (4.6)
18 (11.5)
218 (37.3)
1021 (5.6)
Sample inadequatec
0 (0.0)
0 (0.0)
0 (0.0)
0 (0.0)
0 (0.0)
0 (0.0)
2 (< 0.1)
0 (0.0)
0 (0.0)
0 (0.0)
0 (0.0)
2 (< 0.1)
Previous influenza infectiond
3 (0.1)
1 (< 0.1)
1 (0.4)
2 (0.1)
0 (0.0)
0 (0.0)
2 (< 0.1)
0 (0.0)
2 (0.5)
0 (0.0)
0 (0.0)
11 (0.1)
Recruited in weeks without laboratory-confirmed influenza cases
0 (0.0)
0 (0.0)
0 (0.0)
57 (4.2)
1 (0.6)
735 (24.9)
547 (8.1)
83 (8.0)
7 (1.9)
69 (43.9)
25 (4.3)
1524 (8.3)
Included in the analysis
2071 (92.2)
1934 (78.7)
124 (50.0)
704 (52.1)
141 (83.4)
2157 (73.2)
2145 (31.6)
96 (9.3)
331 (89.2)
0 (0.0)
179 (30.7)
9882 (53.8)
RT-PCR result
Negative for influenza
1331 (64.3)
1256 (64.9)
82 (66.1)
561 (79.7)
97 (68.8)
1804 (83.6)
1828 (85.2)
51 (53.1)
294 (88.8)
0 (0.0)
163 (27.9)
7467 (75.6)
Positive for influenza
740 (35.7)
678 (35.1)
42 (33.9)
143 (20.3)
44 (31.2)
353 (16.4)
317 (14.8)
45 (46.9)
37 (11.2)
0 (0.0)
16 (2.7)
2415 (24.4)
Influenza A(H1N1)pdm09
527 (25.4)
462 (23.9)
23 (18.5)
68 (9.7)
25 (17.7)
108 (5.0)
163 (7.6)
21 (21.9)
5 (1.5)
0 (0.0)
13 (2.2)
1415 (14.3)
Influenza A(H3N2)
16 (0.8)
44 (2.3)
2 (1.6)
56 (8.0)
1 (0.7)
82 (3.8)
3 (0.1)
13 (13.5)
18 (5.4)
0 (0.0)
0 (0.0)
235 (2.4)
Influenza A/not subtyped
104 (5.0)
11 (0.6)
1 (0.8)
10 (1.4)
0 (0.0)
0 (0.0)
50 (2.3)
4 (4.2)
0 (0.0)
0 (0.0)
0 (0.0)
180 (1.8)
Influenza B/Yamagata
2 (0.1)
1 (0.1)
8 (6.5)
11 (1.6)
0 (0.0)
12 (0.6)
0 (0.0)
2 (2.1)
9 (2.7)
0 (0.0)
0 (0.0)
45 (0.5)
Influenza B/Victoria
96 (4.6)
153 (7.9)
8 (6.5)
0 (0.0)
16 (11.3)
155 (7.2)
92 (4.3)
4 (4.2)
5 (1.5)
0 (0.0)
3 (0.5)
532 (5.4)
Influenza B/not subtyped
8 (0.4)
7 (0.4)
1 (0.8)
1 (0.1)
2 (1.4)
0 (0.0)
12 (0.6)
2 (2.1)
0 (0.0)
0 (0.0)
0 (0.0)
33 (0.3)
Abbreviations: ILI influenza-like illness, RT-PCR reverse transcriptase-polymerase chain reaction
a9 missing for Turkey
b98 missing for Turkey
c21 missing for Moscow, 1 for India, and 2 for Curitiba
d21 missing for Moscow
Approximately 24% of the included patients were positive for influenza. The most common strain detected was A(H1N1)pdm09 (58.6% of influenza positives), followed by B/Victoria-lineage (22.0%) and A(H3N2) (9.7%). Approximately 9% of influenza-positive samples could not be subtyped.
Description of the 2015–2016 influenza season across sites
Influenza infections were detected over 38 weeks, with the peak at week 4 of 2016 (Fig. 1). The earliest start of the influenza season was in Moscow (week 48 of 2015), where influenza-positive admissions occurred over a span of 27 weeks in two waves, the first due to A(H1N1)pdm09 and the second due to B/Victoria-lineage. The latest influenza-positive admission (week 33 of 2016) was in Curitiba, Brazil, although few cases of confirmed influenza were detected at that site.
Fig. 1
Admissions with influenza by epidemiological week and virus type, subtype, or lineage overall and by site
×
The proportion of samples positive for influenza differed between sites from 2.7% in Curitiba to 46.9% in Mexico (Table 1; P < 0.0001 by test of homogeneity, equal odds). A(H1N1)pdm09 was the most frequently detected influenza virus in St. Petersburg (71.2% of positives), Moscow (68.1%), Czech Republic (54.8%), Turkey (47.6%), France (56.8%), Valencia (51.4%), Mexico (46.7%), and Curitiba (81.3%) (Table 1). B/Victoria-lineage was the second-most frequently detected influenza virus in Moscow (22.6%), St. Petersburg (13.0%), France (36.4%), Valencia (29.0%) and Curitiba (18.8%) and was the most common influenza virus in Beijing (43.9%). Influenza A(H3N2) was the predominant strain in India (48.6%) (Fig. 1 and Table 1).
Main characteristics of included patients
Of the 9882 included admissions, 39.0% were < 5 years of age, 38.0% were 5–64 years of age, and 23.0% were ≥ 65 years of age (Table 2). Just over half of the included patients were male (n = 5380; 54.4%) and more than half (615/1051; 58.5%) of the admitted women 15–45 years of age were pregnant (6.2% of all included patients).
Table 2
Characteristics of included admissions overall and by site
Category
n (%)
St. Petersburg
Moscow
Czech Republic
Turkey
France
Beijing
Valencia
Mexico
India
Curitiba
Total
N = 2071
N = 1934
N = 124
N = 704
N = 141
N = 2157
N = 2145
N = 96
N = 331
N = 179
N = 9882
Age (y), median [IQR]
2 [0–12]
20 [3–29]
48 [31–69]
6 [0–65]
66 [51–79]
9 [3–66]
70 [39–82]
42 [20–58]
37 [0–65]
1 [0–6]
20 [2–61]
Age groupa
0–1 y
813 (39.3)
239 (12.4)
0 (0.0)
247 (35.1)
0 (0.0)
309 (14.3)
317 (14.8)
7 (7.3)
111 (33.5)
102 (57.0)
2145 (21.7)
2–4 y
550 (26.6)
365 (18.9)
0 (0.0)
96 (13.7)
0 (0.0)
572 (26.5)
82 (3.8)
6 (6.3)
13 (3.9)
27 (15.1)
1711 (17.3)
5–17 y
261 (12.6)
228 (11.8)
0 (0.0)
69 (9.8)
0 (0.0)
258 (12.0)
53 (2.5)
10 (10.4)
6 (1.8)
23 (12.8)
908 (9.2)
18–49 y
356 (17.2)
1000 (51.7)
66 (53.2)
41 (5.8)
32 (22.7)
216 (10.0)
190 (8.9)
33 (34.4)
59 (17.8)
8 (4.5)
2001 (20.2)
50–64 y
69 (3.3)
67 (3.5)
18 (14.5)
70 (10.0)
32 (22.7)
239 (11.1)
275 (12.8)
23 (24.0)
41 (12.4)
13 (7.3)
847 (8.6)
65–74 y
6 (0.3)
15 (0.8)
16 (12.9)
59 (8.4)
27 (19.1)
244 (11.3)
352 (16.4)
4 (4.2)
64 (19.3)
5 (2.8)
792 (8.0)
75–84 y
15 (0.7)
17 (0.9)
18 (14.5)
85 (12.1)
29 (20.6)
260 (12.1)
489 (22.8)
11 (11.5)
31 (9.4)
1 (0.6)
956 (9.7)
≥ 85 y
1 (< 0.1)
3 (0.2)
6 (4.8)
36 (5.1)
21 (14.9)
59 (2.7)
387 (18.0)
2 (2.1)
6 (1.8)
0 (0.0)
521 (5.3)
Sex
Male
1180 (57.0)
1002 (51.8)
67 (54.0)
378 (53.7)
63 (44.7)
1223 (56.7)
1151 (53.7)
42 (43.8)
180 (54.4)
94 (52.5)
5380 (54.4)
Female
891 (43.0)
932 (48.2)
57 (46.0)
326 (46.3)
78 (55.3)
934 (43.3)
994 (46.3)
54 (56.3)
151 (45.6)
85 (47.5)
4502 (45.6)
Chronic conditions
0
1872 (90.4)
1718 (88.8)
60 (48.4)
337 (47.9)
42 (29.8)
1529 (70.9)
742 (34.6)
32 (33.3)
156 (47.1)
118 (65.9)
6606 (66.8)
1
164 (7.9)
172 (8.9)
37 (29.8)
177 (25.1)
47 (33.3)
406 (18.8)
611 (28.5)
29 (30.2)
84 (25.4)
40 (22.3)
1767 (17.9)
> 1
35 (1.7)
44 (2.3)
27 (21.8)
190 (27.0)
52 (36.9)
222 (10.3)
792 (36.9)
35 (36.5)
91 (27.5)
21 (11.7)
1509 (15.3)
Hospitalized within ≤12 mo
No
1408 (68.0)
1577 (81.5)
99 (79.8)
385 (54.7)
76 (53.9)
1774 (82.2)
1448 (67.5)
62 (64.6)
202 (61.0)
137 (76.5)
7168 (72.5)
Yes
663 (32.0)
357 (18.5)
25 (20.2)
319 (45.3)
65 (46.1)
383 (17.8)
697 (32.5)
34 (35.4)
129 (39.0)
42 (23.5)
2714 (27.5)
Underlying conditions
Cardiovascular disease
59 (2.8)
100 (5.2)
38 (30.6)
219 (31.1)
60 (42.6)
427 (19.8)
842 (39.3)
30 (31.3)
94 (28.4)
19 (10.6)
1888 (19.1)
Chronic obstructive pulmonary disease
21 (1.0)
18 (0.9)
4 (3.2)
98 (13.9)
30 (21.3)
252 (11.7)
510 (23.8)
7 (7.3)
85 (25.7)
14 (7.8)
1039 (10.5)
Asthma
44 (2.1)
19 (1.0)
10 (8.1)
60 (8.5)
8 (5.7)
52 (2.4)
170 (7.9)
14 (14.6)
18 (5.4)
29 (16.2)
424 (4.3)
Immunodeficiency/organ transplant
11 (0.5)
0 (0.0)
6 (4.8)
33 (4.7)
8 (5.7)
1 (< 0.1)
19 (0.9)
10 (10.4)
3 (0.9)
1 (0.6)
92 (0.9)
Diabetes
14 (0.7)
19 (1.0)
16 (12.9)
88 (12.5)
28 (19.9)
98 (4.5)
515 (24.0)
12 (12.5)
37 (11.2)
13 (7.3)
840 (8.5)
Chronic renal impairment
14 (0.7)
54 (2.8)
6 (4.8)
54 (7.7)
22 (15.6)
15 (0.7)
247 (11.5)
16 (16.7)
26 (7.9)
0 (0.0)
454 (4.6)
Chronic neuromuscular disease
47 (2.3)
19 (1.0)
3 (2.4)
59 (8.4)
4 (2.8)
22 (1.0)
38 (1.8)
7 (7.3)
5 (1.5)
8 (4.5)
212 (2.1)
Active neoplasm
6 (0.3)
8 (0.4)
12 (9.7)
57 (8.1)
18 (12.8)
28 (1.3)
148 (6.9)
4 (4.2)
22 (6.6)
1 (0.6)
304 (3.1)
Chronic liver disease
15 (0.7)
21 (1.1)
3 (2.4)
8 (1.1)
4 (2.8)
9 (0.4)
73 (3.4)
3 (3.1)
1 (0.3)
0 (0.0)
137 (1.4)
Autoimmune disease
13 (0.6)
15 (0.8)
4 (3.2)
10 (1.4)
0 (0.0)
8 (0.4)
27 (1.3)
11 (11.5)
14 (4.2)
2 (1.1)
104 (1.1)
Pregnant (women 15–45 y)
0 (0.0)
596 (30.8)
2 (1.6)
2 (0.3)
4 (2.8)
0 (0.0)
3 (0.1)
0 (0.0)
4 (1.2)
4 (2.2)
615 (6.2)
Obeseb,c
202 (9.8)
200 (10.3)
36 (29.0)
116 (19.5)
23 (16.3)
238 (11.0)
529 (24.7)
25 (26.3)
31 (9.4)
25 (14.0)
1425 (14.4)
Outpatient consultations within ≤3 mod
0
927 (44.8)
655 (33.9)
43 (34.7)
164 (23.3)
17 (12.1)
1039 (48.2)
214 (10.0)
38 (39.6)
46 (13.9)
47 (26.3)
2151 (21.8)
1
660 (31.9)
447 (23.1)
34 (27.4)
186 (26.4)
54 (38.6)
1022 (47.4)
246 (11.5)
18 (18.8)
54 (16.3)
74 (41.3)
2812 (28.5)
≥ 2
484 (23.4)
832 (43.0)
47 (37.9)
354 (50.3)
69 (49.3)
96 (4.45)
1685 (78.6)
40 (41.7)
231 (69.8)
58 (32.4)
4918 (49.8)
Smoking habits (≥ 18 y)e
Never smoked
221 (49.4)
571 (51.8)
70 (56.5)
153 (58.0)
64 (45.4)
570 (56.0)
749 (44.2)
39 (53.4)
103 (51.2)
8 (29.6)
2548 (50.1)
Past smoker
57 (12.8)
249 (22.6)
15 (12.1)
87 (33.0)
41 (29.1)
270 (26.5)
569 (33.6)
29 (39.7)
74 (36.8)
13 (48.1)
1404 (27.6)
Current smoker
169 (37.8)
282 (25.6)
39 (31.5)
24 (9.1)
36 (25.5)
178 (17.5)
375 (22.2)
5 (6.8)
24 (11.9)
6 (22.2)
1138 (22.4)
Functional impairment status (Barthel index, patients ≥65 y)f
Total (0–15)
0 (0.0)
0 (0.0)
1 (2.5)
21 (11.7)
0 (0.0)
37 (11.8)
116 (9.5)
0 (0.0)
5 (5.1)
0 (0.0)
180 (8.9)
Severe (20–35)
0 (0.0)
0 (0.0)
0 (0.0)
12 (6.7)
1 (1.3)
10 (3.2)
45 (3.7)
1 (5.9)
8 (8.2)
0 (0.0)
77 (3.8)
Moderate (40–55)
0 (0.0)
0 (0.0)
1 (2.5)
14 (7.8)
4 (5.2)
38 (12.1)
72 (5.9)
2 (11.8)
23 (23.5)
0 (0.0)
154 (7.7)
Mild (60–90)
4 (18.2)
7 (20.0)
5 (12.5)
71 (39.7)
16 (20.8)
172 (55.0)
230 (18.7)
8 (47.1)
41 (41.8)
0 (0.0)
554 (27.5)
Minimal (95–100)
18 (81.8)
28 (80.0)
33 (82.5)
61 (34.1)
56 (72.7)
56 (17.9)
764 (62.3)
6 (35.3)
21 (21.4)
5 (100.0)
1048 (52.1)
Time from onset of symptoms to swabbing
0–2 d
1102 (53.2)
1025 (53.1)
41 (33.1)
133 (19.1)
63 (44.7)
503 (23.3)
446 (20.8)
17 (17.9)
34 (10.3)
37 (20.7)
3401 (34.5)
3–4 d
656 (31.7)
619 (32.1)
46 (37.1)
251 (36.1)
41 (29.1)
628 (29.1)
820 (38.3)
22 (23.2)
130 (39.3)
98 (54.7)
3311 (33.6)
5–7 d
313 (15.1)
281 (14.6)
36 (29.0)
301 (43.2)
37 (26.2)
899 (41.7)
681 (31.8)
48 (50.5)
164 (49.5)
43 (24.0)
2803 (28.4)
8–9 d
0 (0.0)
4 (0.2)
1 (0.8)
11 (1.6)
0 (0.0)
126 (5.8)
196 (9.1)
8 (8.4)
3 (0.9)
1 (0.6)
350 (3.5)
> 10 or missing
–
5
–
8
–
1
2
1
–
–
17
Vaccinated for influenza during 2015–2016g
45 (2.2)
87 (4.5)
7 (5.6)
49 (7.0)
60 (42.6)
262 (12.1)
923 (43.0)
19 (19.8)
15 (4.5)
58 (32.4)
1525 (15.4)
≥ 14 d from ILI onseth
45 (100.0)
87 (100.0)
7 (100.0)
41 (83.7)
60 (100.0)
260 (99.2)
912 (98.8)
5 (26.3)
15 (100.0)
46 (79.3)
1478 (96.9)
Abbreviations: ILI influenza-like illness
a1 missing for Turkey
b29 missing for Turkey
cDetermined from the body mass index according to age and sex following the World Health Organization guidelines [12]
d1 missing for France; Beijing categories were 0, 1–3, and ≥ 4
e28 missing in Turkey
f2 missing for Turkey, 250 for Beijing, 1 for Valencia, 3 for India, 1 for Curitiba
g2 missing for St. Petersburg
hPercentages are calculated relative to vaccinated patients
Approximately one-third (n = 3276; 33.2%) of the admissions had chronic conditions, most of which were cardiovascular disease (n = 1888; 19.1%), chronic obstructive pulmonary disease (n = 1039; 10.5%), diabetes (n = 840; 8.5%), renal impairment (n = 454; 4.6%), and asthma (n = 424; 4.3%). Immunodeficiency, neuromuscular disease, active neoplasm, liver disease, and autoimmune disease accounted for < 4% of patients with chronic conditions.
Most patients (n = 7168; 72.5%) had not been hospitalized in the 12 months before the current admission. Half of the hospitalized adults (≥ 18 years old) had never smoked (n = 2548; 50.1%), 27.6% (n = 1404) were past smokers, and 22.4% (n = 1138) were current smokers. According to World Health Organization criteria [12], 14.4% (n = 1425) of patients were obese. Approximately 20% of older adults (≥ 65 years of age) had a functional impairment status between moderate and total on the Barthel Index.
Swabs were obtained within 4 days after the onset of symptoms in 67.9% of patients (n = 6712). The seasonal influenza vaccine had been administered to 1525 patients (15.4%), most of whom (96.9%) had been vaccinated at least 14 days before the onset of ILI symptoms.
Anzeige
Characteristics of included patients across sites
Proportions of younger patients were highest in Curitiba (median age = 1 years) and St. Petersburg (median age = 2 years) (Table 2). Children < 5 years of age accounted for 72.1% of included admissions in Curitiba and 65.8% in St. Petersburg. The Czech Republic and France did not recruit subjects < 18 years of age. Patients were mostly young adults (18–49 years of age) in the Czech Republic (53.2%) and Moscow (51.7%). By contrast, in Valencia (57.2%) and France (54.6%), most included admissions were ≥ 65 years of age.
Admissions were more frequently males than females at all sites (51.8 to 57.0%) except France (44.7%) and Mexico (43.8%). Proportions of patients without comorbidities were highest in St. Petersburg (90.4%) and Moscow (88.8%), followed by Beijing (70.9%), Curitiba (65.9%), Czech Republic (48.4%), Turkey (47.9%), India (47.1%), Valencia (34.6%), Mexico (33.3%), and France (29.8%). Cardiovascular disease was the most common chronic condition at all sites except Curitiba, where asthma was the most common (Table 2).
In Moscow, 30.8% of the included patients were pregnant women. By contrast, at the rest of the sites, pregnant women accounted for < 3% of the included patients.
The proportion of obese patients was highest in the Czech Republic (n = 36; 29.0%), Mexico (n = 25; 26.3%), and Valencia (n = 529; 24.7%) and lowest in India (n = 31; 9.4%), St. Petersburg (n = 202; 9.8%), and Moscow (n = 200; 10.3%).
Anzeige
Visits to general practitioners during the 3 months before hospitalization were the least common in Beijing (n = 1118; 51.8%), St. Petersburg (1144; 55.3%), and Mexico (n = 58; 60.5%) and the most common in Valencia (n = 1931; 90.0%), France (n = 123; 87.9%) and India (n = 285; 86.1%).
The proportion of adult patients who had never smoked ranged from 29.6% (n = 8) in Curitiba to 58.0% (n = 153) in Turkey. The proportion of adult patients that currently smoked ranged from 6.8% (n = 5) in Mexico to 37.8% (n = 169) in St. Petersburg.
Moderate to total functional impairment in older adults (≥ 65 years of age) was least common in St. Petersburg, Moscow, and Curitiba (0.0%) and highest in India (36.7%). Vaccination coverage varied substantially between sites (Table 2). Vaccination coverage rates were (in decreasing order) 43.0% (n = 923) in Valencia, 42.6% (n = 60) in France, 32.4% (n = 58) in Curitiba, 19.8% (n = 19) in Mexico, 12.1% (n = 262) in Beijing, 7.0% (n = 49) in Turkey, 5.6% (n = 7) in the Czech Republic, 4.5% in India (n = 15) and Moscow (n = 87), and 2.2% (n = 45) in St. Petersburg. Among vaccinated individuals, the vaccine had been administered ≥14 days before the onset of symptoms to 26.3% (n = 5) of admissions in Mexico, 79.3% (n = 46) in Curitiba, 83.7% (n = 41) in Turkey, and nearly all admissions (99 to 100%) at other sites. From the information available, 87% of vaccinated individuals had received a trivalent inactivated influenza vaccine (data not shown). Almost all of the remaining 13% also received a trivalent vaccine, based on the vaccines available at each study site (Additional file 3: Table S3).
Admission with influenza according to age and variability by influenza virus
Influenza positivity appeared to be related to age. Admissions positive for influenza were younger than admissions negative for influenza, regardless of having underlying conditions (Fig. 2). More than three-quarters (76.1%) of influenza-positive admissions were < 50 years of age (Table 3, Fig. 2). Admissions positive for A(H1N1)pdm09 were generally younger than admissions negative for influenza, positive for A(H3N2), or positive for B/Yamagata-lineage but older than admissions positive for B/Victoria-lineage (Table 3).
Fig. 2
Admissions with influenza by age and underlying conditions. Adjusted by the interaction of age with chronic conditions, influenza immunization, and site clustering effects
Table 3
Characteristics of included admissions according to RT-PCR result
Characteristic
n (%)
Influenza negative
Any influenza
A(H1N1)pdm09
A(H3N2)
A not subtyped
B/Yamagata
B/Victoria
B not subtyped
N = 7467
N = 2415
N = 1415
N = 235
N = 180
N = 45
N = 532
N = 33
Age (y), median (IQR)
20 (2–65)
18 (3–46)
19 (2–43)
30 (3–71)
4 (1–42)
37 (4–57)
10 (4–31)
25 (5–56)
P vs. influenza negative
–
0.136
0.794
< 0.001
0.001
0.231
< 0.001
0.595
Age groupa
< 1 y
1138 (15.2)
232 (9.6)
135 (9.5)
16 (6.8)
45 (25.0)
7 (15.6)
32 (6.0)
4 (12.1)
1–4 y
1823 (24.4)
663 (27.5)
423 (29.9)
49 (20.9)
47 (26.1)
5 (11.1)
141 (26.5)
3 (9.1)
5–17 y
613 (8.2)
295 (12.2)
135 (9.5)
12 (5.1)
15 (8.3)
6 (13.3)
123 (23.1)
8 (24.2)
18–49 y
1352 (18.1)
649 (26.9)
409 (28.9)
57 (24.3)
33 (18.3)
10 (22.2)
134 (25.2)
7 (21.2)
50–64 y
645 (8.6)
202 (8.4)
137 (9.7)
25 (10.6)
13 (7.2)
9 (20.0)
17 (3.2)
4 (12.1)
65–74 y
640 (8.6)
152 (6.3)
71 (5.0)
27 (11.5)
9 (5.0)
5 (11.1)
38 (7.1)
4 (12.1)
75–84 y
796 (10.7)
160 (6.6)
76 (5.4)
36 (15.3)
12 (6.7)
3 (6.7)
35 (6.6)
1 (3.0)
≥ 85 y
459 (6.1)
62 (2.6)
29 (2.0)
13 (5.5)
6 (3.3)
0 (0.0)
12 (2.3)
2 (6.1)
P vs. influenza negative
–
< 0.001
< 0.001
< 0.001
0.008
0.03
< 0.001
0.010
Sex
Male
4112 (55.1)
1268 (52.5)
738 (52.2)
125 (53.2)
101 (56.1)
24 (53.3)
278 (52.3)
19 (57.6)
Female
3355 (44.9)
1147 (47.5)
677 (47.8)
110 (46.8)
79 (43.9)
21 (46.7)
254 (47.7)
14 (42.4)
P vs. influenza negative
–
0.028
0.041
0.569
0.832
0.815
0.208
0.893
Underlying chronic conditions
No
4869 (65.2)
1737 (71.9)
1038 (73.4)
132 (56.2)
125 (69.4)
22 (48.9)
414 (77.8)
20 (60.6)
Yes
2598 (34.8)
678 (28.1)
377 (26.6)
103 (43.8)
55 (30.6)
23 (51.1)
118 (22.2)
13 (39.4)
P vs. influenza negative
–
< 0.001
< 0.001
0.004
0.259
0.022
< 0.001
0.490
Hospitalized within ≤12 mo
No
5390 (72.2)
1778 (73.6)
1066 (75.3)
160 (68.1)
113 (62.8)
33 (73.3)
405 (76.1)
19 (57.6)
Yes
2077 (27.8)
637 (26.4)
349 (24.7)
75 (31.9)
67 (37.2)
12 (26.7)
127 (23.9)
14 (42.4)
P vs. influenza negative
–
0.168
0.015
0.168
0.005
0.864
0.049
0.107
Underlying chronic conditions
Cardiovascular disease
1543 (20.7)
345 (14.3)
188 (13.3)
57 (24.3)
27 (15.0)
12 (26.7)
59 (11.1)
6 (18.2)
P vs. influenza negative
–
< 0.001
< 0.001
0.182
0.068
0.322
< 0.001
0.79
Chronic obstructive pulmonary disease
860 (11.5)
179 (7.4)
88 (6.2)
37 (15.7)
13 (7.2)
5 (11.1)
35 (6.6)
5 (15.2)
P vs. influenza negative
–
< 0.001
< 0.001
0.047
0.077
1.0
< 0.001
0.409
Asthma
339 (4.5)
85 (3.5)
46 (3.3)
12 (5.1)
13 (7.2)
2 (4.4)
12 (2.3)
2 (6.1)
P vs. influenza negative
–
0.031
0.029
0.682
0.086
1.0
0.013
0.656
Immunodeficiency/organ transplant
66 (0.9)
26 (1.1)
14 (1.0)
6 (2.6)
2 (1.1)
1 (2.2)
2 (0.4)
1 (3.0)
P vs. influenza negative
–
0.391
0.698
0.009
0.674
0.333
0.325
0.250
Diabetes
704 (9.4)
136 (5.6)
72 (5.1)
21 (8.9)
12 (6.7)
7 (15.6)
23 (4.3)
4 (12.1)
P vs. influenza negative
–
< 0.001
< 0.001
0.799
0.216
0.162
< 0.001
0.538
Chronic renal impairment
336 (4.5)
118 (4.9)
63 (4.5)
17 (7.2)
12 (6.7)
3 (6.7)
22 (4.1)
4 (12.1)
P vs. influenza negative
–
0.431
0.941
0.048
0.162
0.456
0.694
0.055
Chronic neuromuscular disease
151 (2.0)
61 (2.5)
33 (2.3)
11 (4.7)
7 (3.9)
1 (2.2)
9 (1.7)
1 (3.0)
P vs. influenza negative
–
0.138
0.451
0.005
0.079
0.603
0.599
0.481
Active neoplasm
245 (3.3)
59 (2.4)
33 (2.3)
12 (5.1)
3 (1.7)
0 (0.0)
11 (2.1)
0 (0.0)
P vs. influenza negative
–
0.038
0.061
0.125
0.289
0.404
0.124
0.626
Chronic liver disease
103 (1.4)
34 (1.4)
28 (2.0)
3 (1.3)
1 (0.6)
1 (2.2)
1 (0.2)
0 (0.0)
P vs. influenza negative
–
0.917
0.086
1.0
0.522
0.467
0.015
1.0
Autoimmune disease
75 (1.0)
29 (1.2)
19 (1.3)
6 (2.6)
1 (0.6)
0 (0.0)
3 (0.6)
0 (0.0)
P vs. influenza negative
–
0.411
0.253
0.022
1.0
1.0
0.489
1.0
Pregnant (women 15–45 y)
337 (4.5)
278 (11.5)
188 (13.3)
22 (9.4)
2 (1.1)
0 (0.0)
62 (11.7)
4 (12.1)
P vs. influenza negative
–
< 0.001
< 0.001
0.014
0.107
0.062
< 0.001
0.373
Obeseb,c
1089 (14.6)
336 (13.9)
208 (14.7)
25 (10.6)
31 (17.2)
11 (24.4)
59 (11.1)
4 (12.1)
P vs. influenza negative
–
0.47
0.84
0.124
0.311
0.063
0.025
1.0
Outpatient consultations within ≤3 mod
0
1478 (19.8)
673 (27.9)
447 (31.6)
44 (18.7)
56 (31.1)
8 (17.8)
120 (22.6)
7 (21.2)
1
1305 (17.5)
468 (19.4)
303 (21.4)
27 (11.5)
43 (23.9)
7 (15.6)
86 (16.2)
4 (12.1)
≥ 2
2880 (38.6)
920 (38.1)
556 (39.3)
82 (34.9)
81 (45.0)
18 (40.0)
171 (32.1)
22 (66.7)
P vs. influenza negative
–
< 0.001
< 0.001
0.284
0.207
0.914
0.039
0.238
Smoking (≥ 18 y)e
Never smoked
1881 (25.2)
667 (27.6)
391 (27.6)
96 (40.9)
35 (19.4)
17 (37.8)
121 (22.7)
9 (27.3)
Past smoker
1104 (14.8)
300 (12.4)
180 (12.7)
41 (17.4)
14 (7.8)
5 (11.1)
60 (11.3)
5 (15.2)
Current smoker
897 (12.0)
241 (10.0)
141 (10.0)
14 (6.0)
24 (13.3)
5 (11.1)
55 (10.3)
4 (12.1)
P vs. influenza negative
–
< 0.001
0.006
< 0.001
0.111
0.371
0.582
1.0
Functional impairment status (Barthel index, ≥ 65 y)f
Total (0–15)
160 (2.1)
20 (0.8)
7 (0.5)
5 (2.1)
4 (2.2)
1 (2.2)
4 (0.8)
0 (0.0)
Severe (20–35)
69 (0.9)
8 (0.3)
2 (0.1)
2 (0.9)
0 (0.0)
1 (2.2)
3 (0.6)
0 (0.0)
Moderate (40–55)
129 (1.7)
25 (1.0)
14 (1.0)
6 (2.6)
2 (1.1)
0 (0.0)
4 (0.8)
0 (0.0)
Mild (60–90)
469 (6.3)
85 (3.5)
35 (2.5)
25 (10.6)
10 (5.6)
0 (0.0)
13 (2.4)
3 (9.1)
Minimal (95–100)
847 (11.3)
201 (8.3)
107 (7.6)
24 (10.2)
11 (6.1)
5 (11.1)
52 (9.8)
4 (12.1)
P vs. influenza negative
–
0.021
0.002
0.244
0.55
0.17
0.053
0.893
Time from onset of symptoms to swabbingg
0–2 d
2384 (31.9)
1017 (42.1)
663 (46.9)
89 (37.9)
68 (37.8)
10 (22.2)
188 (35.3)
11 (33.3)
3–4 d
2514 (33.7)
797 (33.0)
446 (31.5)
68 (28.9)
70 (38.9)
15 (33.3)
189 (35.5)
15 (45.5)
5–7 d
2260 (30.3)
543 (22.5)
277 (19.6)
68 (28.9)
33 (18.3)
20 (44.4)
144 (27.1)
5 (15.2)
8–9 d
300 (4.0)
50 (2.1)
24 (1.7)
8 (3.4)
7 (3.9)
0 (0.0)
11 (2.1)
1 (3.0)
P vs. influenza negative
–
< 0.001
< 0.001
0.222
0.009
0.107
0.031
0.229
Influenza vaccination ≥14 d from ILI onseth,i
1235 (16.5)
243 (10.1)
108 (7.6)
22 (9.4)
17 (9.4)
6 (13.3)
81 (15.2)
11 (33.3)
P vs. influenza negative
–
0.207
0.559
0.007
0.41
1.0
1.0
1.0
Abbreviations: ILI influenza-like illness, IQR interquartile range
a1 missing for influenza negative
bDetermined from the body mass index according to age and sex following the World Health Organization guidelines [12]
c12 missing for influenza negative, 10 for A(H1N1)pdm09 and 7 for A(H3N2)
d1 missing for any influenza and 1 for A(H1N1)pdm09; Beijing not included
e11 missing for influenza negative, 17 for any influenza, 10 for A(H1N1)pdm09, and 7 for A(H3N2)
f222 missing for influenza negative, 35 for any influenza, 11 for A(H1N1)pdm09, 14 for A(H3N2), 1 for B/Yamagata, and 9 for B/Victoria
g9 missing or > 10 d for influenza negative, 8 for any influenza, 5 for A(H1N1)pdm09, 2 for A(H3N2), 2 for A not subtyped, and 1 for B not subtyped
hOnly vaccinated patients
i2 missing for any influenza, 1 for A(H3N2), and 1 for B/Victoria
×
Anzeige
Heterogeneity due to strain was assessed considering A(H1N1)pdm09, A(H3N2), and B/Victoria-lineage using the I2 statistic with adjustment for sex, social class according to occupation, comorbidity, influenza vaccination, time to swab, and site. By age, I2 was 0.0% for admissions 1–4, 18–49, and 65–74 years, 80.5% for 5–17 years, 88.8% for 50–64 years; 44.1% for 75–84 years; and 53.2% for ≥85 years (Fig. 3).
Fig. 3
Adjusted odds ratio (aOR) by age group and strain. Adjusted by age, sex, socioeconomic class, number of chronic conditions, vaccination status, time from onset of symptoms to swabbing, and site. Abbreviation: CI, confidence interval
×
Admission with influenza according to sex and variability by influenza virus
In general, the sex distribution differed significantly between influenza-positive and influenza-negative admissions (Table 3). The risk of admission with influenza was not heterogeneous by strain after adjusting by age, social class according to occupation, comorbidity, influenza vaccination, time to swab, and site, there was no heterogeneity by strain (I2 = 0.0%; data not shown). This was also found when pregnant women were excluded (I2 = 0.0%; data not shown).
Admission with influenza according to presence of comorbidity
Older adults positive for influenza were more likely to have underlying chronic conditions (Fig. 2). However, chronic conditions were reported significantly less frequently for influenza-positive (28.1%) than influenza-negative admissions (34.8%) (P < 0.001; Table 3). This was also found after excluding pregnant women (29.6% for influenza-positive vs. 35.9% for influenza-negative; P < 0.001) (data not shown).
The adjusted OR for admission with influenza was 1.03 (95% confidence interval [CI], 0.86 to 1.19) for patients with comorbidities. No significant heterogeneity by strain was detected (I2 = 37.8%) (Fig. 4).
Fig. 4
Adjusted odds ratio (aOR) by strain in admissions with underlying conditions. Adjusted by age, sex, socioeconomic class, obesity status, vaccination status, time from onset of symptoms to swabbing, and site. Abbreviation: CI, confidence interval
×
Admission with influenza according to pregnancy
A total of 1051 women 15–45 years old were included in the study, of whom 615 were pregnant (596 in Moscow, 2 in the Czech Republic, 2 in Turkey, 4 in France, 3 in Valencia, 4 in India, and 4 in Curitiba; Table 2) and 436 were not (156 in St. Petersburg, 5 in Moscow, 25 in the Czech Republic, 20 in Turkey, 15 in France, 95 in Beijing, 69 in Valencia, 17 in Mexico, 31 in India, and 3 in Curitiba; data not shown). The probability of laboratory-confirmed influenza was significantly higher (P < 0.001) in included pregnant women (45.2%) than non-pregnant women in this age range (23.8%) (data not shown).
After considering site as a random effect and excluding data from St. Petersburg, Beijing, and Mexico (where no pregnant women were enrolled), the crude OR of admission with influenza was 2.82 (95% CI, 1.90 to 4.19) for pregnant women (data not shown). When considering pregnant women with no comorbidities, the crude OR was 2.64 (95% CI, 1.55 to 4.47). For pregnant women with comorbidities, the crude OR was 3.84 (95% CI, 1.96 to 7.53). There was no evidence of an interaction between comorbidity and pregnancy (P = 0.39), but there was evidence of confounding (P < 0.001).
The heterogeneity among strains detected in admitted pregnant women was low to moderate (I2 = 45.7%). This was due to a higher adjusted OR for admission with A(H1N1)pdm09 when adjusted for the presence of comorbidities (Fig. 5).
Fig. 5
Adjusted odds ratio (aOR) by strain in pregnant admissions 15 to 45 years of age. Adjusted by presence of comorbidities. Only in women aged 15–45 years. Abbreviation: CI, confidence interval
×
Patients included in the IVE analysis
Patients with vaccine contraindications (egg allergy or < 6 months of age) or previous laboratory-confirmed influenza in the same season were excluded from the IVE analysis. After applying these exclusions, 8971 samples obtained from patients hospitalized from December, 2015 to May, 2016 were included. Of these, 2269 (25.3%) were positive for influenza. By strain, this included 1327 (58.5%) positive for A(H1N1)pdm09, 511 (22.5%) for B/Victoria-lineage, 224 (9.9%) for A(H3N2), and 41 (1.81%) for B/Yamagata-lineage (Table 4). Overall, 10.8% (n = 246) of influenza-positive admissions and 18.7% (n = 1250) of influenza-negative admissions were vaccinated (P < 0.001) (Table 5).
Table 4
IVE by age and strain overall and for admissions targeted for influenza vaccination
Population
Strain
Age
Influenza-positive
Influenza-negative
Crude IVE
Adjusted IVEa
Total
Vaccinated
Total
Vaccinated
Percent (95% CI)
P interaction
Percent (95% CI)
P interaction
Overall
Any
Any
2269
246
6702
1250
47.0 (38.6, 54.2)
16.3 (0.4, 29.7)
< 65 y
1897
100
4814
354
29.9 (11.9, 44.2)
0.90
11.9 (−12.9, 31.3)
0.70
≥ 65 y
372
146
1888
896
28.5 (10.2, 43.0)
13.4 (−12.7, 33.5)
A(H1N1)pdm09
Any
1327
110
6702
1250
60.6 (51.6, 67.9)
36.0 (18.0, 50.1)
< 65 y
1153
37
4814
354
58.2 (41.0, 70.4)
0.0054
44.8 (19.2, 62.3)
0.69
≥ 65 y
174
73
1888
896
20.0 (−9.6, 41.6)
5.7 (−36.4, 34.8)
A(H3N2)
Any
224
22
6702
1250
52.5 (25.9, 69.6)
16.1 (− 35.9, 48.2)
< 65 y
148
6
4814
354
46.8 (−21.4, 76.7)
0.26
40.2 (−39.5, 74.4)
0.44
≥ 65 y
76
16
1888
896
70.5 (48.2, 83.2)
6.8 (−73.3, 49.9)
A not subtyped
Any
153
16
6702
1250
49.1 (14.2, 69.8)
49.5 (5.5, 73.0)
< 65 y
128
8
4814
354
16.0 (− 73.2, 59.3)
0.40
−3.7 (− 127.9, 52.8)
0.12
≥ 65 y
25
8
1888
896
47.9 (−21.4, 77.6)
67.6 (19.4, 87.0)
B/Yamagata
Any
41
6
6702
1250
25.2 (−78.2, 68.6)
−96.9 (− 406.0, 23.4)
< 65 y
33
4
4814
354
−73.8 (− 397.2, 39.3)
0.11
–
0.59
≥ 65 y
8
2
1888
896
63.1 (−83.5, 92.6)
–
B/Victoria
Any
511
83
6702
1250
15.4 (−7.9, 33.7)
−49.3 (−99.5, −11.7)
< 65 y
426
39
4814
354
−27.0 (−79.6, 10.2)
0.82
−32.9 (−94.0, 9.0)
0.29
≥ 65 y
85
44
1888
896
−18.8 (−83.6, 23.1)
−1.8 (−67.2, 38.0)
B not subtyped
Any
29
11
6702
1250
− 166.5 (− 466.0, −25.5)
−322.2 (− 948.5, −70.0)
< 65 y
22
7
4814
354
− 488.0 (− 1354.1, − 137.7)
0.14
–
0.65
≥ 65 y
7
4
1888
896
−47.6 (− 561.7, 67.1)
–
Individuals targeted for influenza vaccination
Any
Any
1106
189
3554
1065
51.8 (42.7, 59.5)
16.2 (−3.6, 32.2)
< 65 y
734
43
1666
169
44.9 (22.0, 61.1)
0.21
5.3 (−39.4, 35.6)
0.30
≥ 65 y
372
146
1888
896
28.5 (10.2, 43.0)
13.4 (−12.7, 33.5)
A(H1N1)pdm09
Any
646
93
3554
1065
60.7 (50.4, 68.9)
23.0 (−3.3, 42.6)
< 65 y
472
20
1666
169
60.8 (36.8, 75.7)
0.011
20.9 (−36.0, 54.0)
0.54
≥ 65 y
174
73
1888
896
20.0 (−9.6, 41.6)
5.7 (−36.4, 34.8)
A(H3N2)
Any
137
19
3554
1065
62.4 (38.5, 77.0)
−9.1 (−88.4, 36.8)
< 65 y
61
3
1666
169
54.2 (−48.0, 85.8)
0.52
−2.5 (− 263.0, 71.1)
0.10
≥ 65 y
76
16
1888
896
70.5 (48.2, 83.2)
6.8 (−73.3, 49.9)
A not subtyped
Any
71
12
3554
1065
52.5 (11.2, 74.6)
61.7 (21.6, 81.3)
< 65 y
46
4
1666
169
15.6 (−138.2, 70.1)
0.49
25.7 (− 129.6, 76.0)
0.50
≥ 65 y
25
8
1888
896
47.9 (−21.4, 77.6)
67.6 (19.4, 87.0)
B/Yamagata
Any
26
5
3554
1065
44.4 (−48.0, 79.1)
−104.3 (− 508.0, 31.4)
< 65 y
18
3
1666
169
−77.2 (− 518.6, 49.3)
0.13
− 115.4 (− 747.1, 45.2)
0.94
≥ 65 y
8
2
1888
896
63.1 (−83.5, 92.6)
–
B/Victoria
Any
215
55
3554
1065
19.7 (−10.1, 41.4)
−25.6 (−86.3, 15.4)
< 65 y
130
11
1666
169
18.1 (−55.0, 56.7)
0.33
−17.3 (−144.8, 43.8)
0.71
≥ 65 y
85
44
1888
896
−18.8 (− 83.6, 23.1)
−1.8 (−67.2, 38.0)
B not subtyped
Any
17
7
3554
1065
−63.6 (−331.1, 37.9)
–
< 65 y
10
3
1666
169
− 279.6 (− 1385.0, 3.0)
0.37
–
–
≥ 65 y
7
4
1888
896
−47.6 (−561.7, 67.1)
–
Abbreviations: CI 95% CI, IVE influenza vaccine effectiveness
aAdjust for age, sex, number of chronic conditions, time from onset of symptoms to swab, epidemiological week at admission, and site
Table 5
Characteristics of patients included in the IVE analysis by vaccination status
Risk variable
Category
Unvaccinated
Vaccinated
P value
Number of patients, n (%)
Controls
5452 (72.9)
1250 (83.6)
< 0.001
Cases
2023 (27.1)
246 (16.4)
Age (y)
Median (IQR)
19.3 (3.0–51.9)
74.8 (56.3–83.3)
< 0.001
Age group, n (%)
6–11 months
524 (7.0)
14 (0.9)
< 0.001
1–4 y
2370 (31.7)
76 (5.1)
5–17 y
758 (10.1)
136 (9.1)
18–49 y
1879 (25.1)
114 (7.6)
50–64 y
726 (9.7)
114 (7.6)
65–74 y
487 (6.5)
302 (20.2)
75–84 y
513 (6.9)
438 (29.3)
≥ 85 y
218 (2.9)
302 (20.2)
Female, n (%)
–
3480 (46.6)
637 (42.6)
0.005
Comorbidities, n (%)
No
5350 (71.6)
415 (27.7)
< 0.001
Yes
2125 (28.4)
1081 (72.3)
Pregnant (women 15–45 y), n (%)
–
606 (59.4)
8 (29.6)
0.002
Obesea, n (%)
–
1038 (13.9)
321 (21.5)
< 0.001
Hospitalization within ≤12 mo, n (%)
–
1954 (26.1)
549 (36.7)
< 0.001
Outpatient consultations within ≤3 mo, n (%)
No
2624 (35.11)
304 (20.32)
< 0.001
Yes
4850 (64.89)
1192 (79.68)
Smoking (≥ 18 y), n (%)
Current
949 (25.0)
186 (14.7)
< 0.001
Past
924 (24.3)
475 (37.5)
Never
1926 (50.7)
605 (47.8)
Functional impairment (≥ 65 y), n (%)
None or minimal
471 (46.0)
572 (58.3)
< 0.001
Mild
321 (31.4)
232 (23.7)
Moderate
98 (9.6)
54 (5.5)
Severe
38 (3.7)
39 (4.0)
Total
95 (9.3)
84 (8.6)
Sampling interval (d)
Median (IQR)
3 (2–5)
4 (2–5)
< 0.001
Sampling interval, n (%)
≤ 4 d
5139 (68.8)
920 (61.5)
5–7 d
2104 (28.2)
475 (31.8)
8–9 d
232 (3.1)
101 (6.8)
Site, n (%)
St. Petersburg
1645 (22.0)
45 (3.0)
< 0.001
Moscow
1808 (24.2)
87 (5.8)
Czech Republic
115 (1.5)
7 (0.5)
France
81 (1.1)
60 (4.0)
Turkey
522 (7.0)
43 (2.9)
Beijing
1854 (24.8)
258 (17.3)
Valencia
1018 (13.6)
931 (62.2)
India
259 (3.5)
15 (1.0)
Mexico
87 (1.2)
5 (0.3)
Curitiba
86 (1.2)
45 (3.0)
Vaccinated, n (%)
In 2013–2014
526 (7.1)
1073 (72.8)
< 0.001
In 2014–2015
545 (7.4)
1200 (81.2)
< 0.001
aDetermined from the body mass index according to age and sex following the World Health Organization guidelines [12]
The proportion of patients vaccinated with the seasonal influenza vaccine ≥14 days before symptom onset was 2.7% (n = 45) in St. Petersburg, 4.6% (n = 87) in Moscow, 5.7% (n = 7) in the Czech Republic, 7.6% (n = 43) in Turkey, 42.6% (n = 60) in France, 12.2% (n = 258) in Beijing, 47.8% (n = 931) in Valencia, 5.4% (n = 5) in Mexico, 5.5% (n = 15) in India, and 34.4% (n = 45) in Curitiba (data not shown).
Vaccinated admissions were older (median age = 74.8 years) than unvaccinated admissions (median age = 19.3 years) (P < 0.001) (Table 5). The proportion of participants with underlying conditions was significantly higher in vaccinated admissions (72.3%) than in unvaccinated admissions (28.4%) (P < 0.001). Also, the proportion of individuals considered obese was higher for vaccinated (21.5%) than for unvaccinated (13.9%) admissions (P < 0.001). Vaccination was more common in individuals hospitalized in the previous 12 months than in those who had not been (P < 0.001) and more common in individuals who visited a general practitioner within the last 3 months than those who did not (P < 0.001). Only 8 of the 614 pregnant patients (1.3%) were vaccinated. Most patients vaccinated in the 2015–2016 influenza season reported prior influenza vaccination: 72.8% were also vaccinated in 2013–2014, and 81.2% were also vaccinated in 2014–2015.
IVE in overall admissions and in patients targeted for influenza vaccination
Against all-age influenza-related hospitalization, the crude IVE was 47.0% (95% CI, 38.6 to 54.2%) overall (Table 4). After adjusting for age, sex, number of chronic conditions, time from onset of symptoms to swabbing, epidemiological week at admission, and site, IVE was 16.3% (95% CI, 0.4 to 29.7%) overall. By strain, the adjusted IVE was 36.0% (95% CI, 18.0 to 50.1%) against A(H1N1)pdm09, 16.1% (95% CI, − 35.9 to 48.2%) against A(H3N2) and − 49.3% (95% CI,− 99.5 to − 11.7%) against the B/Victoria-lineage. Considering these three predominant strains, IVE heterogeneity between strains was substantial (I2 for adjusted IVE = 84.6%; data not shown). Reliable IVE estimates could not be made by age group for B/Yamagata or B not subtyped because these strains were not frequently detected (Table 4). IVE differed little between younger and older patients in the overall population: the adjusted IVE was 11.9% (95% CI, − 12.9 to 31.3%) for patients < 65 years of age and 13.4% (95% CI, − 12.7 to 33.5%) for patients ≥65 years of age (Table 4). Differences in adjusted IVE between the two age groups for individual strains were not statistically significant.
Results were similar when restricting the analysis to patients targeted for influenza vaccination: the crude IVE for all ages was 51.8% (95% CI, 42.7 to 59.5%) and the adjusted IVE was 16.2% (95% CI, − 3.6 to 32.2%) (Table 4). By strain, the adjusted IVE was 23.0% (95% CI, − 3.3 to 42.6%) against A(H1N1)pdm09, − 9.1% (95% CI, − 88.4 to 36.8%) against A(H3N2), and − 25.6% (95% CI, − 86.3 to 15.4%) against B/Victoria lineage.
IVE across sites
The highest overall IVE among all hospitalizations was detected in Moscow, followed by France, St. Petersburg, Turkey, and India (Fig. 6). The lowest IVE was detected in Curitiba, followed by Mexico, Beijing, Czech Republic, and Valencia. IVE was only significant in Moscow. Between sites, heterogeneity in the estimates of IVE against influenza-related hospitalization was low (I2 for adjusted IVE = 12.1%).
Fig. 6
Adjusted influenza vaccine effectiveness (IVE) by site. Adjusted by age, sex, number of chronic conditions, time from onset of symptoms to swabbing and epidemiological week at admission. Abbreviation: CI, confidence interval
×
The influenza vaccines available and target populations in each represented country are provided in Additional file 3: Table S3.
Discussion
Data collected by active surveillance within the GIHSN sites indicated that during the 2015–2016 influenza season (week 48 of 2015 to week 33 of 2016), the predominant circulating strain in hospitalized individuals was A(H1N1)pdm09 followed by B/Victoria-lineage and A(H3N2) strains. B/Yamagata-lineage strains were relatively rare. This agrees with overall patterns of influenza circulation reported by the World Health Organization and others [13‐17]. The predominance of influenza A(H1N1)pdm09 in Saint Petersburg (Russia), Moscow (Russia), Czech Republic, Turkey, France, Valencia (Spain), Mexico and Curitiba (Brazil), and B/Victoria-lineage in Beijing (China), agree with data reported for these countries [18‐24]. Regional activity for A(H3N2) was reported in India, coinciding with our data obtained in the country’s Jammu and Kashmir state [24].
During the 2015–2016 season, admissions with laboratory-confirmed influenza were younger than those who were negative for influenza, and about three-quarters (76%) of influenza-positive admissions were < 50 years of age. As found by the GIHSN in 2014–2015 season [8], among patients with laboratory-confirmed influenza, those positive for A(H1N1)pdm09 were younger than those positive for A(H3N2) or B/Yamagata-lineage, although patients positive for B/Victoria-lineage were the youngest. Patients with underlying conditions were more prone to be infected by A(H1N1)pdm09 or A(H3N2) than by B/Victoria-lineage. However, most (72%) of the influenza-positive patients did not have chronic conditions (Fig. 2). These results confirm that healthy and young individuals are susceptible to severe influenza, in agreement with our previous reports [5‐8].
As reported previously in the GIHSN [7, 8] and in a recent meta-analysis [25], hospitalized women were more likely to be positive for influenza if they were pregnant. However, only 8 out of 614 (1.3%) pregnant women were vaccinated against influenza. The vaccination coverage rate was also low for the overall study population (15.4%).
According to the current study, IVE in 2015–2016 was low to moderate against hospitalization with laboratory-confirmed influenza (adjusted IVE = 16.3% [95% CI, 0.4 to 29.7%]) and did not differ significantly between younger and older patients. By comparison, the GIHSN reported overall adjusted IVEs against hospitalization with laboratory-confirmed influenza of 33% (95% CI, 11 to 49%) in 2012–2013 [5] and 22% (95% CI, 8 to 33%) in 2014–2015 [8]. Other reports from Hong Kong, the US, and Finland have shown a higher IVE for the 2015–2016 season (IVEs ~ 50%–70%) than that reported in the current study [26‐29]. We speculate that the differences in IVE estimates are related to a combination of different circumstances; among them, the variable genetic and antigenic characteristics of the A(H1N1)pdm09 and A(H3N2) emerging clades circulating in different parts of the world [30‐32], the potential inadequacy of the response to egg-derived vaccines [33], the mismatch between the vaccine and circulating B viruses [34], and the age composition compounded with low levels of vaccination in our population [35].
The highest IVE was against A(H1N1)pdm09 (adjusted IVE = 36.0% [95% CI, 18.0 to 50.1%), in agreement with reports that the circulating A(H1N1)pdm09 virus was antigenically similar to the vaccine strain [15]. Despite a new emerging A(H1N1)pdm09 6B.1 subclade detected in Spain, Canada, and Denmark [30, 31, 36], several other studies have similarly reported moderate effectiveness against A(H1N1)pdm09 in different age groups and healthcare settings [26, 28, 31, 36‐38].
We were unable to obtain reliable IVE estimates for B/Yamagata-lineage or B not subtyped by age group because these strains were not frequently detected. The vaccine had no effect on illness caused by B/Victoria-lineage viruses, which could be due to the absence of a B/Victoria-lineage strain from the WHO-recommended trivalent inactivated vaccine for the northern hemisphere 2015–2016 season [39]. This also suggests that any cross-lineage antibody response from the trivalent vaccine B/Yamagata-lineage strain was insufficient to protect against illness caused by circulating B/Victoria-lineage strains. Although we obtained one isolated negative IVE in preventing admissions with B/Victoria-lineage, all other IVE estimates for the B/Victoria-lineage consistently showed no effect, and so emphasizing this isolated negative IVE would incorrectly reject the null hypothesis [40]. A multi-comparison adjustment could have been used to solve this, though we choose to follow the reasoning of other authors that endorse the reporting of all results, not adjusting for multiple comparisons [41, 42]. These findings are consistent with several other reports for the 2015–2016 season [27, 36, 43] and highlight the need for quadrivalent vaccines containing both B lineages [44‐46].
We observed substantial differences between crude and adjusted IVE estimates. This is likely because young adults have a lower probability of vaccination and underlying conditions compared to older subjects, whereas older adults are more often vaccinated and experience an increased risk of adverse health effects due to age and underlying comorbidities (as shown in Fig. 2). Therefore, when no age distinction is made in the analysis (i.e., no adjustment or stratification by age) this bias leads to a higher vaccination efficacy and, accordingly, the estimate adjusted by age and stratified by age group (i.e., < 65 and ≥ 65 years) is lower than the crude (unadjusted, not stratified) estimate. Indeed, some authors consider it improper to report crude estimates at all [47].
Limitations and considerations
As described previously [7], results from the GIHSN should be interpreted with caution due to the heterogeneity and bias of multi-centric observational studies. The GIHSN takes heterogeneity into account by using a test-negative design that compares laboratory-confirmed influenza admissions with influenza-negative admissions, and by restricting the analysis to periods with influenza circulation, adjusting modeling, and accepting only data from patients admitted within 7 days of the onset of ILI symptoms. In addition, all participating sites follow a standardized protocol that is regularly reviewed and reinforced during the GIHSN annual general meeting and on-site visits at each participating hospital. Through this common core protocol, the ILI case definition used in our study was the same between different study sites, and selection bias was minimized by enrolling consecutive admissions without knowing their vaccination status or the laboratory results for influenza infection.
In addition, different sources of data were used to ensure complete case ascertainment, including data from clinical records, health registries, and information provided by the patient and attending nurses and doctors. Influenza vaccination status was obtained by asking the patient (or representative) if they had received the current season’s influenza vaccine, the date of vaccination, and if the vaccine had been administered at least 2 weeks before the onset of symptoms. Additionally, when records existed, this information was validated by existing registers, vaccination cards, or through contacting the clinic where the vaccine was administered. To describe heterogeneity we reported the I2 parameter. Finally, we used random effects to account for variability by site.
From 2014-2015 to 2015–2016, the GIHSN expanded from seven coordinating sites in six countries to 11 coordinating sites in nine countries. Even though the GIHSN has expanded, the total number of included admissions decreased slightly from the previous year: in 2015–2016, 18,360 eligible admissions were identified of which 9882 (53.8%) met the inclusion criteria, whereas in 2014–2015, 23,551 eligible admissions of which 9614 (40.8%) met the inclusion criteria. Therefore, for some analyses, small numbers continue to be a limitation. The ability to pool data across the GIHSN sites helps, although further improvement will depend on the continued expansion of the network and the growing experience of the participating sites.
Conclusions
The 2015–2016 influenza season was dominated by A(H1N1)pdm09, followed by B/Victoria-lineage and A(H3N2), with few cases of B/Yamagata-lineage. Many of the influenza hospitalizations were for young, otherwise healthy individuals, and as in previous years, hospitalized women were more likely to be positive for influenza if they were pregnant. During the 2015–2016 season, influenza vaccines provided low to moderate protection against hospitalization with influenza and no protection against the predominant circulating B lineage, highlighting the need for more effective and broader influenza vaccines.
Acknowledgements
Medical editing was provided by Drs. Phillip Leventhal and Jonathan Pitt (4Clinics, Paris, France) and paid for by Sanofi Pasteur.
The GIHSN members include: O. Afanasieva, Research Institute of Influenza, St. Petersburg, Russian Federation; M. Akcay Ciblak, Sanofi Pasteur, Istanbul, Turkey; A. Bagci Bosi, Hacettepe University, Faculty of Medicine, Ankara, Turkey; V. Baselga-Moreno, FISABIO-Public Health, Valencia, Spain; E. Burtseva, D.I. Ivanovsky Institute of Virology FSBI “N.F. Gamaleya NRCEM”, Moscow, Russian Federation; M. Carballido-Fernández, Hospital General de Castellón, Castellón, Spain; P. Cervantes, Sanofi Pasteur, France; B. Costa-Caetano, Foundation Oswaldo Cruz Foundation (FIOCRUZ), Rio de Janeiro, Brazil; B. Cowling, School of Public Health, Li Ka Shing Faculty of Medicine, University of Hong Kong, Hong Kong Special Administrative Region, China; M. de los Ángeles-Gutiérrez, Sanofi Pasteur, Mexico; J. Díez-Domingo, FISABIO-Public Health, Valencia, Spain; M. Durusu Tanriover, Turkish Society of Internal Medicine, Ankara, Turkey; C. El Guerche-Seblain, Sanofi Pasteur, Lyon, France; A. Goldstein, Sanofi Pasteur, Moscow, Russia Federation; M.L. Guerrero-Almeida, Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán, Departamento de Infectología, México; B. Guglieri-López, FISABIO-Public Health, Valencia, Spain; J. Gurlichova, Sanofi Pasteur, Lyon, France; Y. Hongjie, Key Laboratory of Surveillance and Early-warning on Infectious Disease, Division of Infectious Disease, Chinese Center for Disease Control and Prevention, Beijing, China; L. Kisteneva, D.I. Ivanovsky Institute of Virology FSBI “N.F. Gamaleya NRCEM”, Moscow, Russian Federation; L. Kolobukhina, D.I. Ivanovsky Institute of Virology FSBI “N.F. Gamaleya NRCEM”, Moscow, Russian Federation; P. Koul, Department of Internal and Pulmonary Medicine, Sher-i-Kashmir Institute of Medical Sciences (SKIMS), Soura, Srinagar, Jammu & Kashmir, India; J. Kyncl, National Institute of Public Health, Prague, Czech Republic; O. Launay, INSERM, Réseau National d’Investigation Clinique en Vaccinologie (I-REIVAC), Université Paris Descartes, Sorbonne Paris Cité, and Assistance Publique Hôpitaux de Paris, Hôpital Cochin, Paris, France; Z. Lesieur, INSERM, Réseau National d’Investigation Clinique en Vaccinologie (I-REIVAC), Paris, France; F.X. López-Labrador, FISABIO-Public Health, Valencia, Spain; P. Loulergue, Hôpital Cochin, Paris, France; F. Luzhao, Key Laboratory of Surveillance and Early-warning on Infectious Disease, Division of Infectious Disease, Chinese Center for Disease Control and Prevention, Beijing, China; C. Mahé, Sanofi Pasteur, Lyon, France; Z. Mandakova, National Institute of Public Health, Prague, Czech Republic; A. Mira-Iglesias, FISABIO-Public Health, Valencia, Spain; J. Mollar-Maseres, Hospital Universitario y Politécnico La Fe, Valencia, Spain; F.E. Moura, Universidade Federal do Ceará, Fortaleza, Brazil; K. Mubashir, Department of Internal and Pulmonary Medicine, Sher-i-Kashmir Institute of Medical Sciences (SKIMS), Soura, Srinagar, Jammu & Kashmir, India; W. Peng, School of Public Health, Li Ka Shing Faculty of Medicine, University of Hong Kong, Hong Kong Special Administrative Region, China; V. Picot, Fondation Mérieux, Lyon, France; M. Pisareva, Research Institute of Influenza, St. Petersburg, Russian Federation; F. Pradel, Fondation Mérieux, Lyon, France; J. Puig-Barberà, FISABIO-Public Health, Valencia, Spain; Y Qin, Key Laboratory of Surveillance and Early-warning on Infectious Disease, Division of Infectious Disease, Chinese Center for Disease Control and Prevention, Beijing, China; S. Raboni, Hospital de Clínicas / Universidade Federal do Paraná, Curitiba, Brazil; G.M. Ruiz-Palacios, FIDSA, Director, Comisión Coordinadora de los Institutos Nacionales de Salud y Hospitales de Alta Especialidad, Secretaría de Salud, México; H. Schwarz-Chávarri, Hospital General de Alicante, Alicante, Spain; M. Siqueira, Oswaldo Cruz Foundation (FIOCRUZ), Rio de Janeiro, Brazil; A. Sominina, Research Institute of Influenza, St. Petersburg, Russian Federation; K. Stolyarov, Research Institute of Influenza, St. Petersburg, Russian Federation; M. Tortajada-Girbés, Hospital Universitario Doctor Peset, Valencia, Spain; S. Trushakova, D.I. Ivanovsky Institute of Virology FSBI “N.F. Gamaleya NRCEM”, Moscow, Russian Federation; S. Unal, Turkish Society of Internal Medicine, Ankara, Turkey; and C. Vlasich, Sanofi Pasteur, France
Funding
This study was funded by the local coordinating institutions at each site with additional catalytic funding support provided from the Fondation pour l’Epidemiologie de la Grippe. FISABIO received additional funding from the Fondation pour l’Epidemiologie de la Grippe to coordinate the study. The Fondation pour l’Epidemiologie de la Grippe did not participate in the design, conduct of the research, analysis, or decision to publish the study.
Availability of data and materials
The datasets used and/or analyzed during the current study available from the corresponding author on reasonable request.
Ethics approval and consent to participate
The GIHSN study protocol was approved by the institutional review board of each participating site: in India, the Institutional Ethics Committee of the Sher-i-Kashmir Institute of Medical Sciences, Srinagar; in Beijing, China, “The Institutional Review Board of the University of Hong Kong/Hospital Authority Hong Kong West Cluster”; in France, “CPP Ile de France IV, Saint-Louis hospital in Paris”; in the Czech Republic, the “Ethics Committee of the Hospital Na Bulovce”; in Turkey, the “Hacettepe University Non-interventional Clinical Research Ethics Board”; in Moscow, Russia, “The local Ethic Committee of Hospital #1 for Infectious Diseases of Moscow Health Department”; in Brazil (Fortaleza & Curitiba), the “Ethical Committee of the Evandro Chagas National Institute of Infectology (INI-Fiocruz)”; in Mexico, the “Research Ethics Committee of the National Institute of Medical Science and Nutrition Salvador Zubirán” & “Research Committee of the National Institute of Medical Science and Nutrition Salvador Zubirán”; in St Petersburg, Russia, “Local Ethical Committee under the FGBU ‘Research Institute of Influenza’ of the Ministry of Health of the Russian Federation”; and in Spain, the “Research Ethics Committee of the General Directorate of Public Health and High Center for Public Health Research (CEI DGSP-CSISP)”. All subjects or legal representatives provided written or (if approved by the associated institutional review board) oral informed consent; consent to participate was collected from the parents/guardians of any participants under 16 years of age.
Consent for publication
Not applicable.
Competing interests
BJC received grants from Sanofi Pasteur unrelated to the submitted work. PK has served as a consultant to Sanofi, Zydus, and Cadila. All other authors declare no competing interests.
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Influenza epidemiology and influenza vaccine effectiveness during the 2015–2016 season: results from the Global Influenza Hospital Surveillance Network
verfasst von
Joan Puig-Barberà Ainara Mira-Iglesias Elena Burtseva Benjamin J. Cowling Unal Serhat Guillermo Miguel Ruiz-Palacios Odile Launay Jan Kyncl Parvaiz Koul Marilda M. Siqueira Anna Sominina on behalf of the Global Influenza Hospital Surveillance Network
