Volume 15, Number 2—February 2009
Prospective Surveillance of Invasive Group A Streptococcal Disease, Fiji, 2005–2007
We undertook a prospective active surveillance study of invasive group A streptococcal (GAS) disease in Fiji over a 23-month period, 2005–2007. We identified 64 cases of invasive GAS disease, which represents an average annualized all-ages incidence of 9.9 cases/100,000 population per year (95% confidence interval [CI] 7.6–12.6). Rates were highest in those >65 years of age and in those <5 years, particularly in infants, for whom the incidence was 44.9/100,000 (95% CI 18.1–92.5). The case-fatality rate was 32% and was associated with increasing age and underlying coexisting disease, including diabetes and renal disease. Fifty-five of the GAS isolates underwent emm sequence typing; the types were highly diverse, with 38 different emm subtypes and no particular dominant type. Our data support the view that invasive GAS disease is common in developing countries and deserves increased public health attention.
Invasive disease caused by group A streptococci (GAS) occurs when the bacteria infect a normally sterile site. Invasive GAS disease is often life threatening; mortality rate is ≈10%–15% in industrialized countries, increasing to up to 50% in the presence of streptococcal toxic shock syndrome (1,2).
A review of the global effects of invasive GAS disease in 2005 estimated that at least 663,000 new cases and 163,000 deaths occur each year (3). Although >95% of these cases and deaths occur in developing countries, few data exist about the epidemiology of these infections in developing countries. In addition, few data describe the clinical signs and symptoms, case-fatality rate, and risk factors associated with invasive GAS disease or the molecular epidemiology of invasive GAS disease in developing countries because most published reports originate from industrialized countries (4–8).
We recently reported incidence of invasive GAS infection in Fiji from a retrospective study in the years 2000–2005 (9). This study indicated that potentially substantial effects of invasive GAS disease occur in Fiji. We therefore designed a prospective study with active surveillance to ensure good case ascertainment and the acquisition of more detailed clinical information.
This prospective study was performed at the Colonial War Memorial Hospital in Suva, Fiji, during the 23-month period from December 5, 2005, through November 5, 2007. During the first year of the study, we noticed that a considerable number of invasive group C streptococcal (GCS) and group G streptococcal (GGS) infections occurred. We therefore amended the protocol midway through the study (December 5, 2006) to include cases of invasive GCS and GGS infection (year 2). We analyzed 2 datasets: the first was the data available for 23 months of invasive GAS infections, and the second was the data available in year 2 for the 11 months of surveillance of all invasive β-hemolytic streptococcal infections (GAS, GCS, and GGS).
Fiji is a nation of ≈330 islands located in the Western Pacific. It has a population of 827,900 persons consisting of 2 major racial groups, indigenous Fijians (57.3%) and Indo-Fijians (37.6%) (10). Approximately 49% of the population lives in rural areas (10). Of 177 nations on the United Nations Development Programme Human Development Index, Fiji is number 90. Fiji has a gross domestic product per capita of US$6,066, and indexes of wealth are similar for the 2 major racial groups; Indo-Fijians are at a slight disadvantage. The 2002–2003 Household Income and Expenditure Survey estimated that 35.6% of the Indo-Fijian population live in poverty compared with 34.2% of the indigenous Fijian population (11,12). Life expectancy at birth is 63.8 years for men and 66.8 years for women and is similar for both major racial groups (11,12). Fiji has an infant mortality rate of 17.2/1,000 population, slightly higher for Indo-Fijians at 19.1/1,000 than for indigenous Fijians at 16.8/1,000 (11,12). The major hospital, the Colonial War Memorial Hospital (CWMH), is located in the capital, Suva, on the main island of Viti Levu, and primarily serves the Central Division, the largest of the 4 administrative divisions in Fiji. Five subdivisional hospitals are located in the Central Division of Fiji, but most seriously ill patients are admitted to CWMH. This circumstance is due to the 568-bed capacity of CWMH compared with the 81-bed capacity of all 5 subdivisional hospitals combined. CWMH has ≈20,500 admissions per year; the number of indigenous Fijians and Indo-Fijians admitted is proportionate to the population of the Central Division. The total population of the Central Division in 2007 was 340,843: 65% indigenous Fijians and 30.2% Indo-Fijians (10). The remainder of the population includes a substantial Chinese population as well as Europeans and Pacific Islanders, including persons from Rotuma, a volcanic island >400 km north of Fiji (it is politically part of Fiji, but its people are ethnically distinct from indigenous Fijians) (13).
Surveillance and Case Definitions
Admission registers at CWMH were checked, and treating physicians were consulted daily for any admitted patient that may have had invasive GAS disease, including those admitted with necrotizing fasciitis, sepsis, and soft tissue infections. The diagnostic microbiology laboratory at CWMH was also contacted daily for any new β-hemolytic streptococcal isolates obtained from sterile and nonsterile sites. We used a consensus case definition of invasive GAS disease developed in 2005 by a World Health Organization/US National Institutes of Health working group; the definition is currently being prepared for publication (F. Rubin, pers. comm.) (Table 1). Cases of streptococcal toxic shock syndrome were defined according to published criteria (14). Clinical data were collected from review of the medical records and from information provided by the treating physicians when necessary.
All blood cultures collected at CWMH were processed in an automated blood culture machine in the diagnostic microbiology laboratory. Isolates that were suspected of being GAS, GCS, or GGS were subcultured onto sheep blood agar and regrown for Lancefield grouping (Oxoid; Cambridge, UK). Susceptibility testing was performed on sheep blood Mueller-Hinton agar by the disk-diffusion method by using Clnical Laboratory Standards Institute guidelines against a panel of 4 antimicrobial drugs: penicillin (10 µg), erythromycin (15 µg), clindamycin (2 µg), and chloramphenicol (30 µg) (Oxoid). Isolates were transported to the Queensland Institute of Medical Research for emm sequence typing according to the standard methods developed by the Centers for Disease Control and Prevention (Atlanta, Georgia, USA) (15).
We used the population of the Central Division from the 2007 national census as the basis for denominator calculations. Because surveillance occurred during 2005 (1 month), 2006 (12 months), and 2007 (10 months), we extrapolated a total population figure for 2005 and 2006 using the pro rata difference between the last official census in 1996 and the latest census in 2007. In calculating average annualized rates, the denominator of person-months was calculated by multiplying each year’s population by the number of months of surveillance for each year (i.e., 2005 population by 1 month, 2006 by 12 months, and 2007 population by 10 months) and adding these totals. The total number of cases over the 23 months was then divided by the total person-months and multiplied by 12 to give average annualized incidence rates with binomial exact 95% confidence intervals (CI). Incidence rate ratios were used to compare rates between ethnic groups. We used χ2 calculations of odds ratios (ORs) for univariate analysis of categorical data. Data were analyzed by using Stata version 10.0 (StataCorp, College Station, TX, USA).
Ethical approval was obtained from the Fiji National Research Ethics Review Committee, the Fiji National Health Research Committee, the University of Melbourne Human Research Ethics Committee, and the Queensland Institute of Medical Research Human Research Ethics Committee. We asked all patients for their consent for the collection of more detailed clinical and outcome data as well as for the transport and testing of the clinical isolates. Information sheets in Fijian and English were provided to potential participants before enrollment. We required that all patients provide written informed consent before information was collected. Children were only enrolled if a parent or guardian provided written consent, and we also required written assent from children >10 years of age. When patients did not consent, the case was noted for incidence calculations, but more detailed clinical and outcome data were not collected.
Invasive Group A Streptococcal Infections
Sixty-four cases of invasive GAS disease occurred during the 23 months of surveillance. Sixty-two cases met the criteria for a definite case, and 2 cases met the criteria for a probable case. The average annualized all-ages incidence of invasive GAS disease (both definite and probable) in the Central Division was 9.9 cases/100,000 population/year (95% CI 7.6–2.6). There were an equal number of male and female case-patients. The median age of patients with invasive GAS disease was 51.6 years (interquartile range [IQR] 27.6–66.4 years). The youngest patient was aged 1 month, and 7 patients were <1 year of age, representing an incidence of 44.9/100,000 population (95% CI 18.1–92.5) in this age group (Figure). The peak incidence occurred in patients >65 years (incidence 80.6/100,000, 95% CI 46.1–130.8). Fifty-three cases occurred in indigenous Fijians (incidence 13.1/100,000, 95% CI 9.8–17.1), 5 cases in Indo-Fijians (incidence 2.5/100,000, 95% CI 0.8–5.9), and 6 cases in persons of other races (incidence 12.8/100,000, 95% CI 4.7–27.8). Of the 6 cases in persons of other races, 4 patients were Rotuman (incidence 47.4/100,000, 95% CI 12.9–121.4). When adjusted for the population of the Central Division, the incidence rate ratio for invasive GAS disease in indigenous Fijians versus other races was 2.9 (95% CI 1.5–6.1).
Of the 64 case-patients with invasive GAS disease, informed consent to collect clinical and outcome information was obtained from 60. Soft tissue infection (with associated bacteremia) was the most common clinical infection (23 cases [38%]; Table 2); followed by bacteremia with no clinical focus of infection (17 cases [28%]), and necrotizing fasciitis (4 cases [7%]). Three cases (5%) fulfilled the criteria for streptococcal toxic shock syndrome; the clinical focus for these infections was soft tissue infection in 2 case-patients and pneumonia in the third case-patient. Group A streptococci were isolated from blood cultures of 55 (92%) of the 60 case-patients, from both blood culture and other sterile fluid of 4 case-patients, from sterile fluid alone of 3 case-patients, and from nonsterile sites (breast abscess fluid and leg cellulitis swab) of the 2 patients with probable cases. GAS was isolated from blood culture for all 4 case-patients from whom consent to obtain further clinical information was not obtained.
Thirty-eight case-patients (63%) had at least 1 known coexisting chronic medical condition (Table 3). Diabetes was the most common coexisting condition (25 patients [42%]), and was found in 7 of the 12 patients with soft tissue infection who were >50 years of age. No significant difference was found in the rates of underlying disease for indigenous Fijians (62%) compared with rates for persons of other races (70%; p = 0.6). Eighteen patients (30%) had current or recent impetigo. Impetigo was more common in younger patients and was present in 7 of the 10 patients with invasive GAS disease who were <5 years of age and in 4 of the 7 patients <1 year of age. No cases of varicella-zoster virus infection were found in this study, and only 1 patient reported the recent use of a nonsteroidal antiinflammatory drug.
Outcome and Case-Fatality Rate Data
Of the 60 case-patients for whom outcome data were available, 19 died, representing a case-fatality rate of 32%. The case-fatality rate increased with patient age; peak fatality rate was 44% in those >65 years of age. The odds of death for patients >50 years compared with those of the rest of the patient group was 3.1 (95% CI 0.9–11.7). The youngest patient to die from invasive GAS disease was 1 year and 2 months of age; this was the only death in patients <25 years. No significant difference was found in case-fatality rate for indigenous Fijians (32%) compared with that for persons of other races (30%; p = 0.9). All deaths occurred within 6 days of admission; 5 deaths (26%) occurred within the first 24 hours, 12 deaths (63%) within the first 48 hours, and 15 deaths (79%) within the first 72 hours. The clinical sites of infection in the group of patients that died were similar to the pattern seen overall: 7 patients had a soft tissue infection, 9 patients had bacteremia alone, 2 patients had pneumonia, and 1 had necrotizing fasciitis. All 3 patients with streptococcal toxic shock syndrome died. A coexisting chronic medical condition was associated with an increased risk for death from invasive GAS disease (OR 4.6, 95% CI 1.0–27.7). Twelve patients with diabetes died (OR 3.7, 95% CI 1–13.7), and 8 patients with renal disease died (OR 5.2, 95% CI 1.2–24.2).
Fourteen patients (23%) required surgery as part of their treatment regimen, and 2 of these patients had a leg amputated below the knee. Five patients (8%) were admitted to the intensive care unit, and 1 patient required mechanical ventilation. Twenty-nine patients (48%) were admitted to the hospital for >10 days. Of the 41 survivors of invasive GAS infection, 16 had a residual disability (39%). Overall, 35 patients (58%) died or had a disability as a result of an invasive GAS infection.
Susceptibility testing was performed on 57 of the 60 isolates, and all 57 isolates were susceptible to all 4 antimicrobial drugs tested. Fifty-five of the 60 isolates were able to be emm sequence typed (Table 4); 37 different emm types and 38 different emm subtypes with no particular dominant types emerged from this series. The most common subtypes were emm100 and emm76.4 (4 cases each), followed by emm11, emm33, and emm106 (3 cases each). No emm type 1 isolates were found. Eight of the 55 isolates emm typed were in nonindigenous Fijian patients, and of these, only 1 emm subtype was also observed among indigenous Fijian patients.
Invasive β-hemolytic Streptococcal Infections after December 5, 2006
In addition to the GAS infections, 4 cases of invasive GCS infection and 14 cases of invasive GGS infection were found in year 2, making a total of 44 cases of invasive β-hemolytic streptococcal infection during the 11 months of surveillance in year 2. This represents an annualized all-ages incidence of 14.1 cases/100,000 population/year (95% CI 10.2–18.9), an incidence rate of invasive GCS disease of 1.3/100,000 (95% CI 0.3–3.3), and an incidence rate of invasive GGS disease of 4.5/100,000 (95% CI 2.5–7.5). Overall, 24 male patients and 20 female patients were infected. The peak incidence was in those >65 years of age (incidence 104.7/100,000, 95% CI 50.2–192.4), and 3 cases occurred in infants. Thirty-four cases occurred in indigenous Fijians (incidence 17.4/100,000, 95% CI 12–24.3), and 10 cases occurred in persons of other races (incidence 8.6/100,000, 95% CI 4.1–15.8); incidence rate ratio for indigenous Fijians was 2 (95% CI 1–4.6).
Clinical, Outcome, and Laboratory Data Relating to GCS and GGS Disease
Of the 18 cases of invasive GCS and GGS disease, informed consent to collect clinical and outcome information was obtained for 12 of 14 case-patients with invasive GGS infection and for all 4 case-patients with invasive GCS infection. The clinical spectrum of GCS and GGS infection was similar to that for invasive GAS infection, although the number of patients with bacteremia with no clinical focus was higher, and a case of meningitis in a neonate caused by GCS was added (Table 5). Similar to the experience of patients with invasive GAS disease, a high proportion of patients with invasive GCS and GGS disease had a coexisting chronic medical condition (69%); 44% of patients had cardiac disease, 31% of patients had diabetes, and 6% had renal disease. Six deaths occurred (38%). emm sequence typing was performed on 12 isolates (2 GCS and 10 GGS), and 9 different emm types were found (Table 4). One was emm12, which is normally associated with GAS.
This study confirms the extensive effects that invasive GAS infections have in Fiji and adds to the small amount of existing data indicating that the incidence and case-fatality rates of these infections are ≈3–4 times higher in developing countries than in industrialized countries. A study in Kenya found that the incidence of GAS bacteremia in children <15 years of age was 13/100 000 population and that mortality rate was 25% (16), similar to the results in our study. In indigenous populations in wealthy countries, such as Aboriginal Australians and Native Americans, the all-ages incidence of invasive GAS disease is as high as 82.5/100,000 and 46/100,000, respectively (2,17,18).
We observed a nearly 3-fold higher risk for invasive GAS disease in indigenous Fijians. The reasons are not entirely clear and do not appear to be related to socioeconomic status or to coexisting conditions, including diabetes; detailed studies of diabetes in Fiji have shown that the prevalence of diabetes is higher in Indo-Fijians (19,20) than in indigenous Fijians. One possible explanation is that GAS skin disease is more extensive in indigenous Fijian communities and that this leads to a higher risk for invasive GAS disease. We have observed a higher prevalence in Fiji of bacterial skin disease in indigenous Fijian children (A. Steer, unpub. data), and high rates of GAS skin disease have been found in Pacific Islanders in other parts of the world, including in Maoris and other Polynesians in New Zealand (21,22).
In most industrialized countries, the annual incidence of invasive GAS disease is 2.5–3.5/100,000 population (8,23), and the case-fatality rate is 7%–15% (6,8,23–26). Although some epidemiologic similarities were found between invasive GAS disease in these countries and in Fiji, such as the high rates for elderly persons with coexisting medical conditions, as well as in the clinical spectrum of disease, major differences stand out. Not only was the all-ages incidence rate higher, but we also found that the incidence rate for children in Fiji was disproportionately high when compared with rates in industrialized countries. For example, the average annualized incidence rate for infants in the United States in 2000–2004 was 5.3/100,000, whereas in Fiji it was 44.9/100,000 (8).
The high case-fatality rate in our study (32%) may reflect the late appearance of clinical signs and symptoms, particularly because such a high proportion of deaths occurred in the first 24–48 hours after admission. It may also reflect inadequate treatment of invasive GAS infection, particularly of early sepsis, possibly because of reduced access to intensive care facilities and advanced therapies. The rate of diabetes was also higher in our study than in other studies, potentially further increasing the case-fatality rate.
The emm typing profile of invasive GAS isolates was different than that in industrialized countries. In most epidemiologic studies in wealthy countries, a high proportion of disease is caused by a small number of emm types that include emm1 (22% of emm types in the United States), emm3 (9%), and emm28 (9%) (8). None of these emm types were found in our study, and we observed a lack of dominant emm types. The diversity in emm types may reflect the high diversity of GAS in impetigo lesions, as can be seen in tropical settings other than Fiji (27).
We observed a substantial number of non-GAS invasive cases in the second year of the study after we expanded our surveillance to include these cases. Individual cases of GCS and GGS invasive disease have been described before (28,29), but prospective surveillance has not been performed. Our data suggest that surveillance of invasive GAS disease in developing countries should also include surveillance of invasive GCS and GGS disease because the disease profile of these organisms is similar and because control strategies, including vaccines that can offer cross-protection between Lancefield groups, may also be similar.
Identification of factors associated with invasive GAS disease, in particular deaths from invasive GAS disease, can guide disease prevention and disease management efforts. In adults, diabetes was an important risk factor that was associated with death. In children, impetigo appeared to be associated with invasive GAS disease. Control of diabetes in the elderly and control of impetigo in the young may be important disease prevention public health goals. With so many deaths occurring shortly after hospital admission, improved recognition and case management of early sepsis may be important disease management goals. The findings of this study also have implications for GAS vaccine development. Several GAS antigens have been identified as potential vaccine candidates. However, only 1 GAS vaccine, a 26-valent M protein vaccine, has reached phase I and II clinical trials (30). Serotypes included in this vaccine were chosen if they were common emm types in the United States (31,32). Although clinical development of the 26-valent vaccine is in its early stages, our results raise concerns about the applicability of this vaccine to developing country settings, because only 10 of 37 emm types in our study are types included in the vaccine, accounting for 33% of GAS isolates.
Our study confirms that invasive disease caused by GAS and other β-hemolytic streptococci has substantial effects in Fiji. This study provides the detailed epidemiologic and clinical data on invasive GAS infections from a developing country.
Dr Steer is a pediatrician with the Centre for International Child Health at the University of Melbourne and the Royal Children’s Hospital in Melbourne. His work in the Fiji Islands is focused on investigating the epidemiology of group A streptococcal infections as part of a project aimed at development of a novel group A streptococcal vaccine.
We acknowledge the assistance of the Fiji Group A Streptococcal research team including Roselyn Ritika, Laisiana Matatolu, Frances Matanatabu, Jyotishna Mani, Maureen Ah-Kee, and Loraine Kelpie. We also to thank Graham Magor and Jon Hartas who undertook the emm sequencing.
This study was funded by a grant from the National Institutes of Allergy and Infectious Diseases grant number U01AI60579. A.C.S. is funded by the National Health and Medical Research Council of Australia.
- Steer AC, Curtis N, Carapetis JR. Diagnosis and treatment of invasive group A streptococcal infections. Expert Opinion in Medical Diagnostics. 2007;2:289–302.
- Hoge CW, Schwartz B, Talkington DF, Breiman RF, MacNeill EM, Englender SJ. The changing epidemiology of invasive group A streptococcal infections and the emergence of streptococcal toxic shock-like syndrome. A retrospective population-based study. JAMA. 1993;269:384–9.
- Carapetis JR, Steer AC, Mulholland EK, Weber M. The global burden of group A streptococcal diseases. Lancet Infect Dis. 2005;5:685–94.
- Lamagni TL, Duckworth G, Emery M, Tanna A, George RC, Efstratiou A. The changing epidemiology of invasive Streptococcus pyogenes infections in England and Wales: 1991–2001. 15th Lancefield International Symposium on Streptococci and Streptococcal Diseases; 2002; Goa, India. p. O1.4.
- Lamagni TL, Efstratiou A, Vuopio-Varkila J, Jasir A, Schalen C. Strep-EURO. The epidemiology of severe Streptococcus pyogenes associated disease in Europe. Euro Surveill. 2005;10:179–84.
- O'Brien KL, Beall B, Barrett L, Cieslak PR, Reingold A, Farley MM, Epidemiology of invasive group A streptococcus disease in the United States, 1995–1999. Clin Infect Dis. 2002;35:268–76.
- Li Z, Sakota V, Jackson D, Franklin AR, Beall B. Array of protein gene subtypes in 1064 recent invasive group A streptococcus isolates recovered from the Active Bacterial Core Surveillance. J Infect Dis. 2003;188:1587–92.
- O’Loughlin RE, Roberson A, Cieslak PR, Lynfield R, Gershman K, Craig A, The epidemiology of invasive group A streptococcal infection and potential vaccine implications: United States, 2000–2004. Clin Infect Dis. 2007;45:853–62.
- Steer AC, Jenney AJ, Oppedisano F, Batzloff MR, Hartas J, Passmore J, High burden of invasive beta-haemolytic streptococcal infections in Fiji. Epidemiol Infect. 2008;136:621–7.
- Statistical News Press Release No. 52. Suva (Fiji): Fiji Islands Bureau of Statistics; October 31, 2007.
- Human Development Report 2006: United Nations Development Programme. New York: Palgrave Macmillan; 2006.
- Fiji facts and figures as of July 2007. Suva (Fiji): Fiji Islands Bureau of Statistics; 2007.
- Howard A, Rensel J. Island legacy: a history of the Rotuman people, 1st ed. Victoria (Canada): Trafford Publishing; 2007.
- Defining the group A streptococcal toxic shock syndrome. Rationale and consensus definition. The Working Group on Severe Streptococcal Infections. JAMA. 1993;269:390–1.
- Beall B, Facklam R, Thompson T. Sequencing emm-specific PCR products for routine and accurate typing of group A streptococci. J Clin Microbiol. 1996;34:953–8.
- Berkley JA, Lowe BS, Mwangi I, Williams T, Bauni E, Mwarumba S, Bacteremia among children admitted to a rural hospital in Kenya. N Engl J Med. 2005;352:39–47.
- Norton R, Smith HV, Wood N, Siegbrecht E, Ross A, Ketheesan N. Invasive group A streptococcal disease in North Queensland (1996–2001). Indian J Med Res. 2004;119(Suppl):148–51.
- Carapetis JR, Walker AM, Hibble M, Sriprakash KS, Currie BJ. Clinical and epidemiological features of group A streptococcal bacteraemia in a region with hyperendemic superficial streptococcal infection. Epidemiol Infect. 1999;122:59–65.
- Zimmet P, Taylor R, Ram P, King H, Sloman G, Raper LR, Prevalence of diabetes and impaired glucose tolerance in the biracial (Melanesian and Indian) population of Fiji: a rural-urban comparison. Am J Epidemiol. 1983;118:673–88.
- Collins VR, Dowse GK, Cabealawa S, Ram P, Zimmet P. High mortality from cardiovascular disease and analysis of risk factors in Indian and Melanesian Fijians. Int J Epidemiol. 1996;25:59–69.
- Finger F, Rossaak M, Umstaetter R, Reulbach U, Pitto R. Skin infections of the limbs of Polynesian children. N Z Med J. 2004;117:U847.
- Tiu A, Martin R, Vanniasingham P, MacCormick AD, Hill AG. Necrotizing fasciitis: analysis of 48 cases in South Auckland, New Zealand. ANZ J Surg. 2005;75:32–4.
- O'Grady K-A, Kelpie L, Andrews RA, Curtis N, Nolan TM, Selvaraj G, The epidemiology of invasive group A streptococcal disease in Victoria, Australia. Med J Aust. 2007;186:565–9.
- Zurawski CA, Bardsley M, Beall B, Elliott JA, Facklam R, Schwartz B, Invasive group A streptococcal disease in metropolitan Atlanta: a population-based assessment. Clin Infect Dis. 1998;27:150–7.
- Tyrrell GJ, Lovgren M, Kress B, Grimsrud K. Invasive group A streptococcal disease in Alberta, Canada (2000–2002). J Clin Microbiol. 2005;43:1678–83.
- Eriksson BK, Andersson J, Holm SE, Norgren M. Epidemiological and clinical aspects of invasive group A streptococcal infections and the streptococcal toxic shock syndrome. Clin Infect Dis. 1998;27:1428–36.
- Bessen DE, Carapetis JR, Beall B, Katz R, Hibble M, Currie BJ, Contrasting molecular epidemiology of group A streptococci causing tropical and nontropical infections of the skin and throat. J Infect Dis. 2000;182:1109–16.
- Wagner JG, Schlievert PM, Assimacopoulos AP, Stoehr JA, Carson PJ, Komadina K. Acute group G streptococcal myositis associated with streptococcal toxic shock syndrome: case report and review. Clin Infect Dis. 1996;23:1159–61.
- Sharma M, Khatib R, Fakih M. Clinical characteristics of necrotizing fasciitis caused by group G Streptococcus: case report and review of the literature. Scand J Infect Dis. 2002;34:468–71.
- Bisno AL, Rubin FA, Cleary PP, Dale JB. Prospects for a group A streptococcal vaccine: rationale, feasibility, and obstacles—report of a National Institute of Allergy and Infectious Diseases workshop. Clin Infect Dis. 2005;41:1150–6.
- Kotloff KL, Corretti M, Palmer K, Campbell JD, Reddish MA, Hu MC, Safety and immunogenicity of a recombinant multivalent group a streptococcal vaccine in healthy adults: phase 1 trial. JAMA. 2004;292:709–15.
- McNeil SA, Halperin SA, Langley JM, Smith B, Warren A, Sharratt GP, Safety and immunogenicity of 26-valent group A streptococcus vaccine in healthy adult volunteers. Clin Infect Dis. 2005;41:1114–22.
- Figure. Invasive group A streptococcal disease in the Central Division of Fiji, December 5, 2005–November 5, 2007
- Table 1. Case definitions for invasive GAS disease, Fiji, 2005–2007
- Table 2. Clinical signs and symptoms in patients with invasive GAS infection, by age, Fiji, 2005–2007
- Table 3. Underlying coexisting medical conditions in patients with invasive GAS disease, Fiji, 2005–2007
- Table 4. emm sequence subtypes of 55 invasive GAS isolates and 12 invasive GCS and GGS isolates from hospital surveillance, Fiji, 2005–2007
- Table 5. Clinical signs and symptoms of invasive GCS and GGS infection, Fiji, 2005–2007
Suggested citation for this article: Steer AC, Jenney A, Kado J, Good MR, Batzloff M, Waqatakirewa L, et al. Prospective surveillance of invasive group A streptococcal disease, Fiji, 2005–2007. Emerg Infect Dis [serial on the Internet]. 2009 Feb [date cited]. Available from http://wwwnc.cdc.gov/eid/article/15/2/08-0558
Please use the form below to submit correspondence to the authors or contact them at the following address:
Andrew C. Steer, Centre for International Child Health, University of Melbourne, Department of Paediatrics, Royal Children’s Hospital, Melbourne, Victoria, Australia
Comment submitted successfully, thank you for your feedback.
The conclusions, findings, and opinions expressed by authors contributing to this journal do not necessarily reflect the official position of the U.S. Department of Health and Human Services, the Public Health Service, the Centers for Disease Control and Prevention, or the authors' affiliated institutions. Use of trade names is for identification only and does not imply endorsement by any of the groups named above.
- Page created: December 08, 2010
- Page last updated: December 08, 2010
- Page last reviewed: December 08, 2010
- Centers for Disease Control and Prevention,
National Center for Emerging and Zoonotic Infectious Diseases (NCEZID)
Office of the Director (OD)