Overview of the influenza sentinel surveillance system during 2011-2017
In Zambia, an ISSS was first established in 2008 in Lusaka Province (the most populated province of the country where the capital city is located) [3] and subsequently expanded to the Copperbelt Province (the second most populated province). The objectives of the Zambia-ISSS were to: (i) monitor the temporal trends of influenza virus circulation; (ii) monitor the circulating influenza virus types and subtypes annually, including pandemic strains; (iii) assess the proportion of patients meeting the ILI and SARI case definition attributable to influenza virus infection; (iv) assess risk factors for influenza-associated severe illness; (v) assess the burden of influenza-associated illness; and (vi) obtain and share clinical samples for annual selection of influenza virus strains for influenza vaccine formulation under the WHO-Global Influenza Surveillance and Response Network. During 2011-2017, ILI influenza sentinel surveillance was conducted in three urban outpatient clinics targeting outpatients with ILI and three large referral hospitals targeting inpatients with SARI (Figure 1, panel A). Both pediatric and adult cases were investigated.
A case of ILI was defined as an outpatient of any age presenting with a recorded temperature ≥38°C and cough or sore throat of duration of ≤7 days [6]. A case of SARI was defined as a hospitalized person who had illness onset within 7 days of admission and who met age-specific clinical inclusion criteria. A case in children aged 2 days to <5 years included any hospitalized patient with cough or difficulty breathing and at least one of the following danger signs: unable to drink or breastfeed, lethargic, vomits everything, convulsion, chest in-drawing or stridor in a calm child. A case in persons aged ≥5 years included any hospitalized patient with fever (≥38°C), cough and shortness of breath or difficulty breathing [6]. All patients with SARI were eligible for enrollment; whereas 5 patients with ILI (the first patient every day from Monday to Friday) were targeted for enrollment per week and per facility.
Activities at the sentinel sites situated in Lusaka were coordinated by a dedicated surveillance officer from the National Influenza Center (NIC). For sites situated in the Copperbelt Province, supervision was conducted by a focal point at the Provincial Medical Office. Due to high staff turnover, training was conducted once a year while supervisory visits to sites were done at least quarterly. Clinical staff at sentinel sites tasked with surveillance implementation were remunerated according to time spent on surveillance activities. The Zambia ISSS is co-funded by the Zambia-MoH, the U.S. Centers for Disease Control and Prevention (U.S. CDC) and WHO.
Data and sample collection procedures
Data were collected from eligible cases using WHO adapted and standardized case investigation forms (CIF) by trained nurses in each sentinel site. For patients meeting the SARI case definition the number of patients eligible for enrollment was also collected. A combination of nasopharyngeal and oropharyngeal swabs were collected from consenting patients, placed in universal transport medium (Copan, Murrieta, California, USA) and transported to the University Teaching Hospital Virology Laboratory, the WHO-recognized NIC in Lusaka, via a cold chain for testing. Samples with respective CIF forms collected from sites situated in Lusaka were sent to the laboratory within 48 hours, while those from the Copperbelt Province were refrigerated and sent within two weeks of collection [[22]]. Verbal informed consent was obtained from all patients prior to data and specimen collection. For children aged <15 years, verbal consent was obtained from a parent or legal guardian.
Sample processing
At the NIC, samples and accompanying CIFs were logged by recording key data in the laboratory log book. Specimens were tested for the presence of influenza viruses using the U.S. CDC real-time reverse-transcription polymerase chain reaction (RT-PCR) protocol for characterization of influenza viruses [3]. During 2011-2012, all specimens from children aged <5 years with SARI were tested for other respiratory viruses including parainfluenza virus (PIV) types 1, 2 and 3, respiratory syncytial virus (RSV), adenovirus, rhinovirus, human metapneumovirus (hMPV), coronavirus (OC43, NL63, 229E, HKU1) and bocavirus using an FTD multiplex real-time RT-PCR assay [24]. Since 2012, RT-PCR influenza-positive samples with a cycle threshold value <28 were cultured at the NIC, after which further viral identification of the samples was done using Haemagglutination (HA) and Haemagglutination Inhibition (HAI) testing. Confirmed virus isolates were shared with WHO Collaborating Centers for further characterization; both viral isolates and clinical specimens were shared twice a year.
Data management and reporting
Data from the CIF including demographics and clinical information, exposure risk and past medical history were captured in a customized influenza sentinel surveillance MS Access® database with inbuilt data validation checks. Data entry was done daily as forms were received. Monthly reports of the total number of samples received and processed (including positive specimens by subtype) were reported to the Ministry of Health public health units. A separate patient line-list was also sent monthly to the sentinel sites; the results report included total samples processed by sentinel site and total confirmed influenza infections. Weekly influenza surveillance data and influenza-positive specimens were reported to WHO AFRO using an excel template. Virological and epidemiological data were reported to WHO FLUNET / FLUID.
Evaluation of the influenza sentinel surveillance system
The evaluation of the ISSS was based on CDC guidelines [5] and focused on the performance of the system from January 2011 to December 2017. The objective of the evaluation was to determine: (i) whether the surveillance system was designed and operated in such a way as to be capable of detecting and monitoring seasonal influenza viruses, including pandemic strains; (ii) the usefulness of the collected data to assess influenza disease burden in the general population; (iii) the impact of the system in informing public health intervention and policies; and (iv) the ability of the system to contribute to the annual selection of influenza strains for vaccine development. The performance of the system was assessed using nine surveillance attributes, namely: (i) data quality and completeness for selected key variables, (ii) timeliness, (iii) representativeness, (iv) flexibility, (v) simplicity (vi) acceptability, (vii) stability; (viii) utility; and (ix) sustainability.
For consistency and comparability of findings we used the evaluation method and scoring system utilized for influenza surveillance evaluations conducted in other African countries [17,18,19,20,21]. Each of the above mentioned attribute was evaluated using pre-defined quantitative or qualitative indicators. A total of 38 indicators were developed for the evaluation. The number of indicators evaluated for each attribute is provided in Table 1; whereas the individual indicators and the calculations and data sources used to evaluate each indicator are provided in Tables 2-5.
Data for calculation of the indicators for data quality and completeness, timeliness, stability and utility were obtained from various sources including the main influenza sentinel surveillance database, the laboratory database, annual reports and other documents and records. In order to assess simplicity, acceptability, stability and utility, a self-administered questionnaire was designed targeting staff involved in surveillance at the sentinel sites. The questionnaire was designed to capture data based on staff perceptions of the program. Data collected from the surveillance system were also compared with WHO minimum data collection standards for ILI and SARI surveillance [6].
For each quantitative indicator we first obtained the proportion (expressed as percentage) of the outcome of interest over the total [18,19,20,21]. For instance, for the indicator on completeness of laboratory testing (one of the indicators used to evaluate the data quality and completeness attribute) we divided the number of samples with available influenza results by the total number of samples collected and received by the laboratory. Subsequently, similar to other influenza surveillance evaluations conducted in Africa, we used a scale from 1 to 3 to provide a score for each quantitative indicator as follows: <60% (as obtained in the example above) scored 1 (weak performance); 60-79% scored 2 (moderate performance); ≥80% scored 3 (good performance) [18,19,20,21]. For indicators for which a proportion over a total could not be obtained (qualitative indicators) a score was assigned based on the same scale using expert consensus.
Thereafter, the scores assigned to each indicator were averaged for all indicators evaluated within each attribute to provide an overall score for each surveillance attribute assessed in this study. An overall score for the surveillance system was obtained by averaging the scores of all evaluated indicators as previously described [18,19,20,21]. All data generated by the surveillance system during the review period were included in the evaluation. The analysis was implemented using Stata version 14.2 (StataCorp, College Station, Texas, USA).
Ethical approval
This surveillance evaluation was deemed non-research by the Zambia-MoH and the US CDC.