Response to a large rotavirus outbreak on South Tarawa, Kiribati, 2013

Outbreak Investigation Report

Teanibuaka Tabunga,a Maryanne Utiera,a Rosemary Tekoaua,a Tebikau Tibwe,a Teatao Tira,a Tebuka Toatu,b Sala Elbourne Duituturaga,b Eric Nillesc and Adam Craigc

a Ministry of Health and Medical Services, Public Health Division, Kiribati.
b Secretariat of the Pacific Community, Public Health Division.
c World Health Organization Division of Pacific Technical Support, Emerging Disease Surveillance and Response Unit, Suva, Fiji.

Correspondence to Teanibuaka Tabunga (e-mail: teanibuaka.tebunga@gmail.com).


To cite this article:

Tabunga T et al. Response to a large rotavirus outbreak on South Tarawa, Kiribati, 2013. Western Pacific Surveillance and Response Journal, 2014, 5(2). doi:10.5365/wpsar.2013.4.4.006


Abstract

Introduction: In July 2013, during annual independence celebrations in Kiribati, staff at Tungaru Central Hospital on South Tarawa reported an increase in children presenting with severe diarrhoea. This report describes the outbreak investigation, findings and response.

Method: After notification of the outbreak, all health facilities on South Tarawa began reporting cases of acute diarrhoea and/or vomiting through the early warning syndromic surveillance system on a daily basis. Community awareness was raised and the public was encouraged to present to a health facility if ill with acute gastroenteritis. Specimens were collected and sent for laboratory testing.

Results: Between 10 and 24 July 2013, 1118 cases of gastroenteritis were reported; 103 were hospitalized and six died. The median age of cases was one year (range: 0–68 years); 93.4% were aged less than five years. Rotavirus was identified in 81% of specimens tested. The outbreak response included enhanced surveillance, community education, clinical training and changes to in-hospital patient management for infection control.

Discussion: This outbreak was the largest diarrhoea outbreak in Kiribati in five years. Factors that may have contributed to the magnitude and severity of the outbreak included high household density, inadequate sanitation infrastructure and a mass gathering – all increasing the chance of transmission – as well as limited clinical response capacity. The current outbreak highlights the importance of clinical management to minimize severe dehydration and death. Rotavirus vaccination should be considered as an adjunct to other comprehensive enteric disease control measures as recommended by the World Health Organization.


Kiribati is located in the Pacific Ocean and consists of one volcanic island and 32 low-lying atolls. Despite being spread over 3.5 million km2 of ocean, the total land area is only 811 km2.1 The population of Kiribati in 2010 was 103 058 people, with an average population density of 128 per km2. Almost half (48.7%) of the population live on the capital islands – the islets that make up South Tarawa and the atoll of Betio.

South Tarawa (including Betio) is a string of low lying islets that stretches 23 km from Betio to Tanaea (Figure 1). South Tarawa is less than 3 m above the sea level, with an average width of 450 m, has a total of 16 km2, of which 10 km2 is usable.2 The population density on South Tarawa is 3184 persons per km2 with a household density of seven to eight people per household, making South Tarawa among the most densely populated areas of the world.2,3 Residents of South Tarawa (and especially the islet of Betio) experience high rates of respiratory infections, diarrhoea and dysentery. High incidence of these illnesses have been linked to overcrowding.1,2 Kiribati’s routine childhood vaccination programme does not include rotavirus vaccine.


Figure 1. Map of South Tarawa, Kiribati

In mid-July each year Kiribati celebrates its independence with a weeklong national holiday. Celebrants visiting South Tarawa result in further overcrowding and increased pressure on water, environmental and food hygiene infrastructures.

On 10 July 2013, mid-way through the 2013 independence celebrations, staff from the Tungaru Central Hospital (TCH) on South Tarawa reported to the Ministry of Health and Medical Services (MHMS) Public Health Division through the established syndromic surveillance system that 20 children had presented with severe acute diarrhoea. This potential outbreak was subsequently investigated, and this report describes the outbreak investigation, findings and response.

Methods

The Kiribati Syndromic Surveillance System, which is part of the regional Pacific Syndromic Surveillance System, was enhanced for this investigation by adding a specific outbreak case definition. All health facilities (two hospitals and 14 community clinics) on South Tarawa reported cases that met the case definition through the existing reporting mechanisms. The outbreak case definition was: “any person presenting to a health facility on South Tarawa with acute diarrhoea and/or vomiting after 10 July 2013”. Health facility staff applied the outbreak case definition along with their routine syndromic surveillance activities for the duration of the outbreak. Health facilities reported the number of presentations, as well as any unusual events (e.g. particularly severe cases or deaths) to the National Health Information Systems Unit (HIS) for collation, analysis and dissemination of information.

Rotavirus enzyme-linked immunosorbent assay testing was performed at the Fiji Centre for Disease Control Laboratory on suspect-case stool samples. Genotyping of rotavirus-positive samples was conducted at the WHO Collaborating Centre, Murdoch Childrens Research Institute, Melbourne, Australia.

Clinical and public health control measures were implemented at the health facilities and in the community. Control measures included health promotion and enhancement of clinical care capacity.

Results

Epidemiological investigation

From 10 to 24 July 2013, 1118 cases met the outbreak case definition on South Tarawa (attack rate: 2.3%), of which 103/1118 (9.2%) required hospitalization and 6/1118 died (case fatality rate: 0.54%). Males constituted 566 cases (50.6%), and the median age was one year (mean: 2.9 years; range: zero to 68 years). Most cases (1044/1118, 93.4%) and all deaths were less than five years old; the attack rate among this group was 13% (Table 1).


Table 1. Number of suspected cases and incidence proportion by sex, age and village of residence

NA – not applicable; ND – not determined.
Note: Some columns may not add up to 100% due to the rounding off of decimal places.


The first reported case presented to the emergency department of TCH on 10 July 2013. The number of new presentations peaked on 18 July 2013 and returned to pre-outbreak levels by 24 July 2013 (Figure 2). Most cases (n = 988; 88.5%) reported suffering acute diarrhoea, and 759 cases (67.9%) reported acute vomiting. Fever was reported in 21 (1.9%) cases.


Figure 2. Outbreak epidemic curve of the number of suspected cases, by reported date of illness onset, South Tarawa, Kiribati, July 2013

The majority of cases resided in the villages of Betio and Bairiki at the western end of South Tarawa and Tangintebu and Eita on central South Tarawa. The other 45.4% of cases resided in villages geographically dispersed along South Tarawa (Figure 1; Table 1).

Laboratory investigation

Of the 20 specimens collected, 16 returned a result with 13 (81%) positive for rotavirus. Eight rotavirus-positive specimens were forwarded for genotyping and were all identified as G3P. Tests for other infectious agents returned negative results.

Control measures

The clinical response to the outbreak included:

Community clinics extended their hours of operation (with four open 24 hours a day) to enhance health care accessibility. Pharmacy supplies were distributed to all health facilities on South Tarawa.

A health promotion campaign for hand hygiene, environmental sanitation and food safety was conducted through local radio village talks, announcements during church services and in locations where risk of transmission is high (i.e. kava bars, child care centres, primary schools). This campaign continued for approximately three weeks after the number of cases had returned to pre-outbreak levels and was extended to reach outlining islands.

Surveillance was enhanced on atolls neighbouring South Tarawa, with atoll health facilities notified and requested to report patients that met the outbreak case definition. A short-lived slight increase in the number of presentations with acute diarrhoea increased in the period immediately after the South Tarawa outbreak was reported.

During the outbreak the MHMS issued situation updates once a day to relevant government and non-government stakeholders. The updates also formed the basis of public communication messages released by MHMS.

Discussion

This outbreak was the largest diarrhoeal outbreak experienced in Kiribati in five years, with 1118 cases and an incidence proportion of 13%. Rotavirus G3P, a common genotype of rotavirus circulating globally, was implicated in the majority of suspected cases tested. Rotavirus is the most common cause of severe diarrhoeal disease among infants and young children globally and is estimated to be responsible for over two million hospitalizations (mainly for severe dehydration) and 527 000 deaths annually with 85% of deaths occurring in low-income countries, usually due to late presentation to hospital or inadequate capacity to provide appropriate clinical care.4 Rotavirus is primarily transmitted by the faecal-oral route and may be present in contaminated water.5

The outbreak response caused significant strain on both the clinical and public health systems of Kiribati and raised anxiety among the population; however, it was considered effective. The outbreak demonstrated the importance of having strong management structures for public health events, including a designated event commander to oversee response activities and preparedness plans. Having pre-approved and protocol-driven surveillance and response arrangements in place before the outbreak occurred made the response easier to manage. Such arrangements must be easily activated, understood by all involved and adaptable to account for ever-changing situations. The MHMS has invested much effort to develop the national health system’s preparedness for public health emergencies. These capacities have been developed to help meet Kiribati’s obligations to the International Health Regulations (2005).6 Reference laboratory testing was facilitated by the laboratory network of the Pacific Public Health Surveillance Network.7

Communication between the event commander and relevant response managers was critical for coordination. The early detection of this outbreak highlighted the role played by early warning syndromic surveillance in Kiribati. Further, the reach of the Kiribati Syndromic Surveillance System (all health facilities on South Tarawa) and the ability to use the system’s well-established reporting mechanisms meant that enhanced surveillance was implemented quickly across all sites and data were reported to the HIS in a streamlined manner. This greatly enhanced the speed at which data were shared and lessened the burden of data capture and management placed upon staff at the national level. It is noted that as the outbreak case definition was based on presentations to a health facility, the number of cases identified is likely to be less than the true number of people affected.

Mortality from childhood diarrhoea is overwhelmingly secondary to severe dehydration. This outbreak highlights the importance of a systematic and rapid assessment for dehydration followed by either oral or intravenous rehydration, or resuscitation based upon findings. Most cases of childhood diarrhoea can be managed with zinc and low-osmolality oral rehydration solution (ORS), but a small proportion of severely dehydrated children – or children with persistent vomiting – will require intravenous rehydration or occasionally urgent intravenous resuscitation. Breast milk is an excellent rehydration fluid and should be encouraged, together with ORS, for children still breastfeeding. In addition to fluid replacement, children with diarrhoea should continue to be fed during their illness as food intake supports fluid absorption, and helps maintain nutritional status and the body’s ability to fight infection. Zinc treatment may be used to help reduce the duration and severity of diarrhoea and hence fluid loss.5,8 Severely ill children requiring hospitalization should remain under medical supervision until recovered or risk of relapse has passed.

This outbreak highlights the importance of rotavirus as an epidemic pathogen and a potentially important role for rotavirus vaccination as one element in a comprehensive programme to control causes of diarrhoeal disease. In 2009, WHO recommended that rotavirus vaccine be included in all national immunization programmes and considered a priority, particularly in countries with high rotavirus gastroenteric-associated mortality rates;8 to date, rotavirus vaccine has not been implemented in Kiribati. Given the high rate of infection in low-income countries and reported high level of protection offered by the rotavirus vaccination, consideration of vaccine use is recommended. Rotavirus vaccination is reported to offer 40–90% protection against rotavirus gastroenteritis after one and/or two years of follow up.8 WHO provides guidelines for the implementation of population-wide rotavirus vaccination.

This outbreak coincided with a mass gathering on South Tarawa, an event that likely affected the spread and severity of the outbreak. The gathering likely changed the outbreak transmission dynamics by increasing the density of the population on the atolls and increasing the chance of poorly handled, cooked or stored food. Health facility staff vacations for the gathering reduced response capacity. In the future, risk assessment to identify and determine the impact mass gatherings may have on health and health systems capacity as well as pre-emptive public health planning is advised.


Conflicts of interest

None declared.


Funding

None.


Acknowledgements

We acknowledge the Fiji Centre for Disease Control Laboratories (Mataika House) and the WHO Collaborating Centre at Murdoch Childrens Research Institute in Melbourne for their support with the testing and genotyping of specimen samples. We also acknowledge the work of clinical and public health staff of MHMS.


References