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S116

Abstracts / Journal of Clinical Virology 82S (2016) S1–S142

Methods:

In this retrospective study we examined a total of

2637 samples (nasopharyngeal, nose and throat swabs). They were

taken from patients with symptoms of respiratory infection admit-

ted to University Medical Centre Maribor during the years of 2014

and 2015. HPIV RNAs were detected with a commercial automated

multiplex PCR system (FilmArray, Biofire).

Results:

Out of 2637 samples, 173 (6.56%) tested positive for

HPIVs. Nearly half of the HPIV-positive patients were infected

with HPIV-3 (49.71%, 86), followed by HPIV-4 (21.39%, 37), HPIV-1

(16.76%, 29) and HPIV-2 (15.03%, 26), respectively. Most frequently

identified type was HPIV-3, with regular activity throughout 2014

and 2015, including a substantial increase in both autumn-winter

seasons with peaks in November of 2014 and 2015. It was also the

predominant HPIV type represented in summer months of both

years alongside minute occurrences of type 2 and 4. An apparent

outbreak of HPIV-4 infections starting in summer, and progressing

in autumn of 2015 with a peak in September, was observed. At

the same time, HPIV-3 and HPIV-2 were in decline. Also, type 1

and 3 started to increase as HPIV-4 decreased. Type 2 was com-

pletely absent in spring 2014 but had a slight peak in October 2014

and was subsequently present in smaller numbers for the rest of

2015. The median age of HPIV-tested patients was 5, and ranged

from less than a year to 96 years old. The majority (82.08%, 142)

of infected patients were children under the age of 5. Among the

elderly (>65 years old) 12.75% (13/102) tested positive for one of

HPIVs, the oldest being 87 years old. The male to female ratio of

patients infected with HPIV was 1:1. HPIV was detected as the

only cause of infection in 60.11% (107) of cases and 5 of them

tested positive for two types of HPIV. In forty-eight (26.97%) HPIV-

positive samples one co-infection with other respiratory pathogen

was detected, 18 (10.11%) had two co-infections and 5 (2.81%)

had three or more co-infections. The prevalent (50.00%) pathogen

of co-infection was rhinovirus, followed by adenovirus in 18.00%,

enterovirus in 12.00% and respiratory syncytial virus in 10.00% of

samples. Coronavirus (HKU1 and OC43),

Mycoplasma pneumoniae

,

humanmetapneumovirus and

Bordetella pertussis

accounted for the

remaining 10.00%.

Conclusions:

Overall, the analysed data suggests HPIV-3 as the

most prevalent type of HPIV infections in NE Slovenia. Both HPIV-2

andHPIV-3 showed continual presence in the studied 2-year period

with the latter greatly outnumbered the former. A similar bien-

nial distribution pattern for HPIV-1 and HPIV-4 was noted, which

couldmean that they tend to occur in odd-numbered years. We also

observed an epidemic of HPIV-4 which is rarely reported in liter-

ature. From previously published reports it appears that seasonal

trends vary in different parts of the world and that the distribu-

tion of HPIV types is also affected by environmental conditions.

Additional data from following years is needed for a more clear

understanding of HPIV seasonal trends and interactions between

all four types in NE Slovenia.

http://dx.doi.org/10.1016/j.jcv.2016.08.233

Abstract no: 252

Presentation at ESCV 2016: Poster 194

Seasonality of respiratory syncytial virus

infection in the EU/EEA, 2010–2016

Eeva Broberg

1 ,

, Kari Johansen

1

,

Cornelia Adlhoch

1

, René Snacken

1

,

Pasi Penttinen

1

, on behalf of the European

Influenza Surveillance Networ

k 2

1

European Centre for Disease Prevention and

Control (ECDC), Sweden

2

The European Influenza Surveillance Network,

Sweden

Background:

Respiratory syncytial virus (RSV) is considered

the most common pathogen causing severe lower respiratory tract

infections among infants and children. RSV vaccine candidates are

in development and the World Health Organization is prepar-

ing global RSV surveillance to estimate the impact of future RSV

vaccines. One of the surveillance objectives is to monitor RSV

seasonality and intensity. A subset of EU/EEA Member States (MS)

are already testing clinical specimens for influenza and RSV as part

of their routine influenza surveillance. In this study, we are describ-

ing the seasonality of RSV infection in these countries.

Methods:

We performed a retrospective descriptive study of

laboratory-confirmed RSV detections reported weekly through the

European Influenza Surveillance Network based on influenza-like

illness (ILI) or acute respiratory infection case definitions between

weeks 40/2010 and 14/2016. We compared findings between sys-

tematically sampled primary-care-based sentinel specimens tested

according to a standard protocol and convenience sampled primary

and hospital-care-based non-sentinel specimens. We also studied

the correlation between the median week of peak RSV detections

and the latitude of each reporting country’s capital by Pearson’s cor-

relation. RSV seasons were defined as the number of weeks when

detections exceeded 5% of total detections per season per country.

Results:

SeventeenMS reportedRSVdetections during the study

period: seven MS reported 4399 sentinel detections and fifteen

MS reported 156,698 non-sentinel detections. Two MS contributed

60% of sentinel and 61% of non-sentinel detections. Seasonality was

observed within both surveillance systems. The median length of

RSV season estimated based on sentinel and non-sentinel surveil-

lance was 11 (with country range 6–28) and 10 (range 6–18)

weeks, respectively. The median peak week for sentinel detec-

tions was week 6 (range 48–18), and for non-sentinel detections

week 5 (range 49–17). RSV was detected by non-sentinel surveil-

lance throughout the year but in sentinel systemonly during weeks

45–13 with consistent reporting. RSV detections peaked later with

increasing latitude (

r

= 0.41 for sentinel and 0.46 for non-sentinel).

Conclusions:

RSV detections in 17EU/EEA MS followed a sea-

sonal pattern, peaking regularly early February and lasting around

10 weeks. Our data confirm the moderate correlation between

the timing of the epidemic peak and increasing latitude that has

been shown earlier. Our study suggests that RSV seasonality can be

assessed through both sentinel and non-sentinel influenza surveil-

lance systems but more sensitively in the latter one. Overall, the

number of sentinel RSV detections were vastly lower compared to

non-sentinel specimens which is a reflection of different surveil-

lance systems and number of participating countries. We do not

have RSV-specific denominator data and can therefore not calculate

proportions. Further limitations of the data include that large detec-

tion volumes originate from only two MS. Despite the limitations,

this study supports the use of influenza surveillance systems for

monitoring RSV seasonalitywith consideration to adjust the ILI case

definition to establish an RSV-specific surveillance system. Further-