Volume 11, Number 1—January 2005
Invasive Group A Streptococcal Infections, Clinical Manifestations and Their Predictors, Montreal, 1995–2002
Highlight and copy the desired format.
|EID||Hollm-Delgado M, Allard R, Pilon PA. Invasive Group A Streptococcal Infections, Clinical Manifestations and Their Predictors, Montreal, 1995–2002. Emerg Infect Dis. 2005;11(1):77-82. https://dx.doi.org/10.3201/eid1101.030651|
|AMA||Hollm-Delgado M, Allard R, Pilon PA. Invasive Group A Streptococcal Infections, Clinical Manifestations and Their Predictors, Montreal, 1995–2002. Emerging Infectious Diseases. 2005;11(1):77-82. doi:10.3201/eid1101.030651.|
|APA||Hollm-Delgado, M., Allard, R., & Pilon, P. A. (2005). Invasive Group A Streptococcal Infections, Clinical Manifestations and Their Predictors, Montreal, 1995–2002. Emerging Infectious Diseases, 11(1), 77-82. https://dx.doi.org/10.3201/eid1101.030651.|
We identified 306 invasive group A streptococcal infections (IGASI) by passive population-based surveillance in Montreal, Canada, from 1995 to 2001. The average yearly reported incidence was 2.4 per 100,000 persons, with a 14% death rate. Among clinical manifestations, incidence of pneumonia increased from 0.06 per 100,000 in 1995 to 0.50 per 100,000 in 2000. Over a span of 7 years, the odds of developing pneumonia increased (odds ratio [OR] = 1.21, 95% confidence interval [CI] 1.0–1.5), while they decreased for soft-tissue infections (OR = 0.86, 95% CI 0.7–1.0). Serotypes M1 and M3 accounted for 30% of IGASI. However, neither serotype was significantly associated with specific clinical manifestations, which suggests that manifestation development among IGASI might be attributable to host or environmental factors rather than the pathogen. In our study, these factors included age, gender, underlying medical conditions, and living environment, yet none explained temporal changes in risk for pneumonia and soft-tissue infections.
Since the mid-1980s, concern has grown that invasive group A streptococcal infections (IGASI) have been increasing in incidence and severity (1–3). In particular, the emergence of streptococcal toxic shock syndrome (STSS) during the 1980s is frequently cited as an example of increasing severity (4).
Person-to-person transmission of Streptococcus pyogenes (the causative agent for IGASI) primarily occurs through respiratory droplets, although it may also spread through body secretions from an infected patient (5,6). Additionally, M serotypes of S. pyogenes that cause severe disease in a patient are more likely to cause severe disease in subsequent patients (6). These serotypes include 3 (M1, M3, and M18) that are strongly associated with pathogenicity (7). Nonetheless, some evidence indicates that persons in whom IGASI from the same strain of S. pyogenes develops may have different clinical manifestations of this disease (8,9). Other risk factors for IGASI include patient’s age and underlying medical conditions (e.g., varicella). However, what factors may be associated with different clinical manifestations of IGASI is unclear (10–22).
Some studies have examined the role of age, varicella, and chronic conditions such as diabetes mellitus and alcoholism as predictors for necrotizing fasciitis, soft-tissue infections, and STSS (21–24), yet little is known regarding other IGASI determinants. In this study, we describe the status of both IGASI and their clinical manifestations on the island of Montreal. We also identify predictors for clinical manifestations and death due to IGASI, which could explain temporal fluctuations in the incidence and severity of this disease.
Surveillance of IGASI
Data used in our study were collected during passive surveillance of IGASI among all residents of the island of Montreal (population = 1.8 million: 21,529 births per year from 1996 to 1999 ). Cases that occurred and were reported from January 1, 1995 (the year IGASI became a notifiable disease in the province of Quebec), through February 28, 2002, were included in our study.
Once the public health department had been notified of a potential case, usually by a hospital laboratory, a 6-part questionnaire was completed by using information from the physician or infection control nurse of the health center where the case-patient was identified or treated. Questions included the patient’s demographic information, general medical information, laboratory results, diagnostic criteria, and medical history before the IGASI. With this information, all IGASI were classified into 1 of 3 groups: confirmed cases (S. pyogenes isolated from a normally sterile site), clinical cases (S. pyogenes isolated from a nonsterile site and toxic shock not attributable to any other cause), or noncases. Data on confirmed and clinical cases were entered into the regional notifiable infections computer database. This database was used for our study.
Laboratory Assessment of IGASI Isolates
Initial laboratory confirmation of S. pyogenes was made by using standard methods (26). Isolates were then collected and sent to the Canadian National Center for Streptococcus in Edmonton for further testing of the opacity factor, as well as M, T, and R surface proteins. The methods have been described in detail elsewhere (27). Briefly, antiopacity factor (AOF) typing was performed on any positive opacity factor sample. Although AOF testing does not possess the same type specificity as M typing, it is frequently used because of difficulties in producing antisera for certain M serotypes. Its use has been validated for most strains identified in industrialized countries. However, since 2000, the national center has supplemented AOF testing with emm gene sequencing for some nontypeable M serotype samples. Data on these results were not available for this study.
Classification of Outcomes
For our study, we looked at 5 dichotomous outcomes: STSS, soft-tissue infections, bacteremia, pneumonia, and death attributable to IGASI. All were invasive and defined in accordance with the classification of group A streptococcal infections (28).
STSS was defined according to the 1993 Working Group on Severe Streptococcal Infections consensus definition for a probable or confirmed case (28). Soft-tissue outcomes included fasciitis, myositis, cellulitis, or erysipelas. Bacteremia was characterized by a positive hemoculture, without any source of infection. Pneumonia attributable to IGASI was based on a clinical diagnosis made by the treating physician and could include STSS with respiratory distress.
Classification of Independent Variables
Age, calendar month, and year in which the IGASI case occurred were included in our study as continuous variables. Gender (male or female); underlying medical conditions (drug use, alcohol abuse, varicella, prior trauma or wound, cancer, and immunosuppression); type of living environment (hospital, daycare or preschool, school, work, other, and not available); as well as M, T, and R surface protein serotypes (presence or absence of a specific serotype) were all included as dichotomous variables. For those serotypes with identical strength of association with a given outcome, a single new dichotomous variable was created to represent the presence of one or the other (e.g., presence of either serotype M12 or M28 versus absence of both serotypes). Finally, since predominant site of infection (bacteremia, fasciitis, cellulitis or erysipelas, myositis, peritonitis, respiratory manifestations, septic arthritis, and other) was partially used in distinguishing between bacteremia, pneumonia, and soft-tissue infections, this variable was only considered a covariate of interest in models with STSS and death as their outcomes.
The incidence (per 100,000), death rate attributable to IGASI, and proportion of IGASI cases due to a specific clinical manifestation were estimated by using data collected from 1995 through 2001. Incidence and proportion estimates were not calculated for 2002, given that only 2 months of data were available. Projected annual population estimates for Montreal were used when calculating the reported annual incidence of IGASI (25). Incidence and proportion of IGASI cases stratified by gender, calendar year, and age group were then calculated. Finally, temporal trends were assessed by using the chi-square test for trend.
For the inferential component of our study, we conducted unconditional logistic regression with SAS version 8.0 (SAS Institute, Cary, NC, USA). This test was initially performed by including in the model variables with a univariate likelihood ratio p value < 0.20. Among these factors, those with the highest multivariate Wald chi-square p value were then individually dropped, until the lowest Akaike Information Criterion value was attained. The McGill University Faculty of Medicine Institutional Review Board approved the study.
From 1995 through 2001, a total of 306 cases of IGASI were reported on the island of Montreal. The incidence of IGASI rose from 1.05 per 100,000 (19 cases) in 1995 to 1.71 (31 cases) in 1996 and 3.32 (60 cases) in 1997. After 1997, the incidence appeared to stabilize: 2.77 (50 cases) in 1998, 2.50 (45 cases) in 1999, 3.21 (58 cases) in 2000, and 2.37 (43 cases) in 2001. The average annual incidence of IGASI was 2.4 per 100,000. Most IGASI cases occurred in persons >40 years of age (172 [56%] of 306 cases) (Figure 1). The median age of patients was 46 years (range 1.5 months to 92 years).
Of the 306 reported IGASI cases, 112 (37%) were soft-tissue infections, 84 (28%) bacteremia, 32 (10%) pneumonia, and 29 (10%) STSS. Among patients with soft-tissue infections, 6 (5%) of 112 cases had myositis, 31 (28%) had cellulitis, and 76 (68%) had necrotizing fasciitis; 1 patient had both cellulitis and necrotizing fasciitis. We did not identify any significant trend over time with regard to the proportion of different clinical manifestations. As for specific clinical manifestations of IGASI, we estimated that bacteremia occurred, on average, in 0.66 per 100,000 persons each year, STSS in 0.23 per 100,000, soft-tissue infections in 0.89 per 100,000, and pneumonia in 0.25 per 100,000.
The predominant M serotypes included M1 (22%), M3 (12%), M28 (9%), M12 (8%), M4 (6%), and M6 (4%). Remaining serotypes accounted for <3% of isolates. Twenty percent of samples were nontypeable.
The incidence of pneumonia appeared to significantly increase over time (χ2 = 5.65, p = 0.018), with an annual incidence of 0.06 per 100,000 in 1995 and 1996, 0.28 in 1997 and 1998, 0.39 in 1999, 0.50 in 2000, and 0.22 in 2001. This finding was confirmed by the odds of having pneumonia significantly increasing with each successive calendar year (adjusted odds ratio [aOR] = 1.21, 95% confidence interval [CI] 1.0–1.5). The proportion of women and girls with pneumonia (Figure 2) also significantly increased (χ2 = 5.03, p = 0.025), with women more likely to have pneumonia as compared to men (aOR 2.20, 95% CI 1.0–4.9). Gender was not associated with year in which the case occurred.
We did not detect a significant secular trend in the occurrence of STSS (χ2 = 0.54, p = 0.46). Persons who abused alcohol (aOR 7.66, 95% CI 1.9–30.3]), were infected with serotype M9 (aOR 39.98, 95% CI 1.9–836]), or who had fasciitis (aOR 10.21, 95% CI 4.1–25.7]) were at a significantly greater risk of having STSS.
No significant secular trend was apparent in the incidence of soft-tissue infections (χ2 = 0.48, p = 0.49). However, the odds of developing this manifestation as opposed to another significantly decreased with each successive calendar year (aOR 0.86, 95% CI 0.7–1.0). Drug use was weakly associated with soft-tissue infections (unadjusted OR 1.86, 95% CI 0.8–4.4). Given that trauma was a significant univariate risk marker for soft-tissue infections (OR 2.78, 95% CI 1.6–4.8), this association might have been attributable to injection drug use resulting in a trauma or wound. However, in our study, no correlation was seen between drug use and trauma (r = 0.002, p = 0.97). Furthermore, the association between drug use and soft-tissue infections became significant after adjusting for trauma or wound (OR 2.83, 95% CI 1.0–8.0).
Varicella and serotypes M6, M12, or M22 were significant predictors for developing soft-tissue infections with aORs of 5.69 (95% CI 1.4–23.1), 4.3 (95% CI 1.1–16.7), 9.1 (95% CI 1.3–64.5), and 27.9 (95% CI 2.7–289), respectively. None of these factors were correlated with calendar year.
The incidence of bacteremia did not appear to change over time (χ2 = 0.56, p = 0.45). Only protective factors against bacteremia were identified: attending a school (aOR 0.15, 95% CI 0.0–0.7) and trauma or wound (aOR 0.4, 95% CI 0.2–0.9).
Death Due to IGASI
The death ratio from IGASI was 15% (42 deaths among 306 cases). The highest proportion of known deaths was among patients with pneumonia (38%, 12 deaths among 32 pneumonia cases), followed by STSS (35%, 10 among 29), bacteremia (17%, 14 among 84), and soft-tissue infections (10%, 11 among 112). Within soft-tissue infections, necrotizing fasciitis had the highest risk for death among all age groups (16%, 5 deaths among 31 cases) followed by cellulitis and erysipelas (8%, 6 among 76). For myositis, among the 6 cases identified during a 7-year period, no deaths were recorded. No secular trends for death ratios were seen for any of the clinical manifestations of IGASI. Among those who died of IGASI, the most common serotypes were M1 (34%) and T1 (30%); however, neither was significantly associated with death (unadjusted OR for M1: 1.86, 95% CI 0.9–4.0; T1: 1.91, 95% CI 0.9–4.1). Predictors for death, after adjustment, are presented in the Table.
When the results of our study are examined, several methodologic considerations must be taken into account. First, given that the administration of questionnaires for this study was not standardized, nondifferential misclassification could explain why certain factors in this study were not identified as potential markers for clinical manifestation outcomes.
An additional limitation of our study was the low statistical power. For some measures of association, the probability of detecting a true association was estimated to be as low as 3%. As a result, while this study can identify potential predictors, it cannot exclude them.
Additionally, given that this study was to a certain extent hypothesis-generating, some of the predictors found in this study (particularly those with weak associations) may have occurred by chance. Considering that an α level of 0.05 was used when testing ≈200 associations, at least 10 significant factors would be expected to be identified by chance. In our study, we identified 25 factors to be significantly associated with specific IGASI manifestations.
IGASI and STSS may be increasing in both incidence and severity (4). In particular, increasing trends in the IGASI incidence in the United States have been recorded in several hospital-based studies (29). Furthermore, past European studies noted a general increase in the incidence, although little evidence shows a trend occurring in the United States (14,30–32). While we documented a trend in the annual incidence of IGASI in Montreal during the first 3 years of our study, the incidence stabilized from 1997 onwards, which suggests that an initial rise in incidence might be attributable to underreporting immediately after IGASI became a notifiable disease. During the 7 years of our study, mortality did not appear to significantly change. Additionally, we could not identify any significant trends in the incidence and mortality of STSS. We did, however, ascertain that pneumonia attributable to IGASI significantly increased during 6 of the 7 years of our study. This finding was particularly evident among women. Our findings agree with those of a study in Ontario, which identified an increasing trend for pneumonia attributable to GAS from 1992 to 1999 (33).
To the best of our knowledge, no research has been published on transmission rates for the different clinical manifestations of IGASI. However, the primary mode of person-to-person transmission of S. pyogenes is through respiratory droplets (5,6). Additionally, S. pyogenes that causes severe disease in one patient is more likely to cause severe disease in subsequent patients (6). Considering these previous study findings, one could hypothesize that secondary contacts of patients with respiratory manifestations might be more likely to acquire an infection leading to severe disease, compared to contacts of patients with other IGASI manifestations.
Even though IGASI is a reportable disease, our results for pneumonia may be an underestimate of the true values. Given that <1% of community-acquired pneumonia is attributed to S. pyogenes (34), pneumonia caused by this bacterium may have been ascribed to other causes and hence not reported. Our findings are further complicated by difficulties in defining pneumonia (33). No standard clinical definition distinguishes IGAS pneumonia from respiratory distress caused by STSS. Although both clinical manifestations might differ with regard to pathophysiology, given that prophylaxis is required for secondary contacts of either manifestation in Quebec, difficulties in distinguishing between these manifestations will probably not affect the public health implications of our findings.
With regard to the generalizability of our results, when comparing our findings with previously published studies, we did not detect any geographic differences in the incidence of IGASI (17). Our data showed that the yearly incidence of IGASI in Montreal (1.0–3.3 per 100,000) was similar to the incidence of IGASI in British Columbia (20), Ontario (16), Israel (35), Sweden (19,22), and the United States (14,18). Furthermore, death rates from IGASI in Montreal were comparable to death rates calculated for British Colombia (20) and Sweden (19,22). Only Arizona appeared to have a higher death rate due to IGASI, at 20% (3). This difference might be attributable to the elevated prevalence of diabetes (a risk factor for IGASI) in the Arizona community studied (3).
Along with these descriptive findings, we identified several factors associated with clinical manifestations of IGAS and associated death. Having varicella before IGASI increased the risk of developing a soft-tissue infection 6 times and the risk of dying 5 times. Although we could not identify any literature linking varicella infection with soft-tissue infections, given that soft-tissue infections are the predominant clinical manifestation of IGASI, our findings support previous research that suggests that varicella might be an important risk factor for developing IGASI (16,36).
Soft-tissue infections were almost twice as likely to develop in persons using drugs. This association could be attributable to injection drug use; however, it remains even after controlling for trauma. One explanation for this unexpected finding could be nondifferential misclassification. A subanalysis of drug use showed that 23% of patients indicated a trauma or wound. However, we were unable to determine the reliability of reporting. While a patient could have affirmatively answered to drug use, a wound inflicted by intravenous drug use may not have been considered sufficiently severe to indicate a trauma or wound.
Our descriptive analysis appears to support previous research findings that those <1 year of age and those >60 years of age have the highest incidence of IGASI (3,21–23). However, previous studies also suggest that children might have a lower incidence of STSS and be at a decreased risk of dying of IGASI (21). This research includes a study that identified a nonsignificant 5-fold rise in risk for death per year increase in age. In contrast, our study showed a 2%–4% increase.
Our study finding that M1 and M3 accounted for >30% of all isolates tested for M surface proteins was consistent with previous studies that reported these 2 M serotypes as the most common for IGASI (3,15,16,23,24). This finding is also consistent with the choice of serotypes to include in streptococcal vaccines being evaluated at the moment. The hexavalent vaccine (37) is composed of serotypes 1, 3, 5, 6, 19, and 24; these types represent 38% of isolates in our study. The types in the 26-valent vaccine (38) represent 70% of our isolates. This number includes M1 with 22%; M3 with 12%; M28 with 9%; M12 with 8%; M6 with 4%; M22 and M11 each with 3%; M89 with 2%; and M75, M2, M77, M43, M5, M76, and M33 each with 1%.
Furthermore, our study confirmed univariate model findings from a study by O’Brien et al. that found M3 to be significantly associated with STSS (14). However, this association did not remain in our multivariate analysis. Our findings would thus appear to concur with those of a another (case-control) study that found while M1 and M3 may be significant risk factors for IGASI, once a person is infected, environmental and host factors might have a role in determining the type of invasive disease manifestations (8,9). This finding could explain why IGASI may develop in patients infected with the same strain of GAS but have different clinical manifestations of the disease (e.g., STSS versus pneumonia) (9). Future epidemiologic studies of risk factors for clinical manifestations of IGASI might be designed to look at risk factors separately in patients identified with M1 and M3 serotypes. By doing so, nondifferential misclassification might be minimized and risk factors with weaker associations might be more easily identified.
Ms. Hollm-Delgado is a doctoral student in public health at the Université de Montréal. This paper originates from research she completed at the Direction de Santé Publique (Montreal, Canada) while earning her Masters degree in epidemiology from McGill University. Her current research interests include respiratory infections and antimicrobial resistance.
We thank Lucie Bédard for providing permission to use the database to conduct this study and for her helpful comments on an initial draft of the protocol, Louise Marcotte for preparing the dataset, Gilles Paradis for his helpful comments on an initial draft of this paper, Paul Rivest for being available for questions regarding the surveillance procedure, and Agnès Beaume for her administrative assistance.
- Stevens DL, Tanner MH, Winship J, Swarts R, Ries KM, Schlievert PM, Severe group A streptococcal infections associated with a toxic shock-like syndrome. N Engl J Med. 1989;321:1–7.
- Stevens DL. Invasive group A streptococcus infections. Clin Infect Dis. 1992;14:2–11.
- Hoge CW, Schwartz B, Talkington DF, Breiman RF, MacNeil EM, Englender SJ. The changing epidemiology of invasive group A streptococcal infections and the emergence of streptococcal toxic shock-like syndrome. JAMA. 1993;269:384–9.
- Stevens DL. Streptococcal toxic-shock syndrome: spectrum of disease, pathogenesis, and new concepts in treatment. Emerg Infect Dis. 1995;1:69–78.
- Weiss K, Laverdière M, Lovgren M, Delorme J, Poirier J, Béliveau C. Group A streptococcus carriage among close contacts of patients with invasive infections. Am J Epidemiol. 1999;149:863–8.
- Weiss K, Roger M, Maziade PJ, Frenette C, LeCorre I, Delorme J, A household cluster of fulminant group A streptococcus pneumonia associated with toxic shock syndrome—Quebec. Can Commun Dis Rep. 1996;22:36–43.
- Schwartz B, Facklam RR, Breiman RF. Changing epidemiology of group A streptococcal infection in the USA. Lancet. 1990;336:1167–71.
- Kotb M, Norrby-Teglund A, McGeer A, El-Sherbini H, Dorak MT, Khurshid A, An immunogenetic and molecular basis for differences in outcomes of invasive group A streptococcal infections. Nat Med. 2002;8:1398–404.
- Chatellier S, Ihenyane N, Kansal RG, Khambaty F, Basma H, Norrby-Teglund A, Genetic relatedness and superantigen expression in group A streptococcus serotype M1 isolates from patients with severe and nonsevere invasive diseases. Infect Immun. 2000;68:3523–34.
- Davies HD, Schwartz B. Invasive group A streptococcal infections in children. Adv Pediatr Infect Dis. 1999;14:129–45.
- Factor SH, Levine OS, Schwartz B, Harrison LH, Farley MM, McGeer A, Invasive group A streptococcal disease: risk factors for adults. Emerg Infect Dis. 2003;9:970–7.
- Mulla ZD, Leaverton PE, Wiersma ST. Invasive group A streptococcal infections in Florida. South Med J. 2003;96:968–73.
- Passaro DJ, Smitht DS, Hett EC, Reingold AL, Daily P, van Beneden CA, Invasive group A streptococcal infections in the San Francisco Bay area, 1989–99. Epidemiol Infect. 2002;129:471–8.
- O’Brien KL, Beall B, Barrett NL, 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.
- Von Hunolstein C, Suligoi B, Patarachia M, Scopetti F, Reccha S, Greco D, Clinical and microbiological characteristics of severe group A streptococcal infections in Italy. Adv Exp Med Biol. 1997;418:79–81.
- Davies HD, McGeer A, Schwartz B, Green K, Cann D, Simor AE, Invasive group A streptococcal infections in Ontario, Canada. N Engl J Med. 1996;335:547–54.
- Hsueh PR, Wu JJ, Tsai PJ, Liu JW, Chuang YC, Luh KT. Invasive group A streptococcal disease in Taiwan is not associated with the presence of streptococcal pyogenic exotoxin genes. Clin Infect Dis. 1998;26:584–9.
- 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.
- Svensson N, Öberg B, Henriques B, Holm S, Kallenius G, Romanus V, Invasive group A streptococcal infections in Sweden in 1994 and 1995: epidemiology and clinical spectrum. Scand J Infect Dis. 2000;32:609–14.
- Bjornson GL, Scheifele DW, Bell A, King A. Population-based surveillance of invasive group A streptococcal disease in British Colombia: 1996 to 1998. Can J Infect Dis. 2001;12:232–6.
- Davies HD, Matlow A, Scriver SR, Schlievert P, Lovgren M, Talbot JA, Apparent lower rates of streptococcal toxic shock syndrome and lower mortality in children with invasive group A streptococcal infections compared with adults. Pediatr Infect Dis J. 1994;13:49–56.
- 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.
- Sharkawy A, Low DE, Saginur R, Gregson D, Schwartz B, Jessamine P, Severe group A streptococcal soft-tissue infections in Ontario: 1992-1996. Clin Infect Dis. 2002;34:454–60.
- Kaul R, McGeer A, Low DE, Green K, Schwartz B, Ontario Group A Streptococcal Study Group, et al. Population-based surveillance for group A streptococcal necrotizing fasciitis: clinical features, prognostic indicators, and microbiologic analysis of seventy—seven cases. Am J Med. 1997;103:18–24.
- Direction de Santé Publique de Montréal. Région de Montréal: charactéristiques de la population. [cited 2002 May 20]. Available from http://www.santepub-mtl.qc.ca/Portrait/Montreal/mtl.html
- Wu WG. Medical microbiology: a laboratory study. 3rd ed. Belmont (CA): Star Publishing Company; 1995.
- Tyrrell GJ, Lovgren M, Forwick B, Hoe NP, Musser JM, Talbot JA. M types of group A streptococcal isolates submitted to the National Centre for Streptococcus (Canada) from 1993 to 1999. J Clin Microbiol. 2002;40:4466–71.
- The Working Group on Severe Streptococcal Infections. Defining the group A streptococcal toxic shock syndrome: rationale and consensus definition. JAMA. 1993;269:390–1.
- Rotta J, Tikhomirov E. Streptococcal diseases worldwide: present status and future prospects. Bull World Health Organ. 1987;65:769–82.
- Gaworzewska E, Colman G. Changes in the pattern of infection caused by Streptococcus pyogenes. Epidemiol Infect. 1988;100:257–69.
- Centers for Disease Control and Prevention. Invasive group A streptococcal infections—United Kingdom, 1994. MMWR Morb Mortal Wkly Rep. 1994;43:401–2.
- Colman G, Tanna A, Efstratiou A, Gaworzewska ET. The serotypes of Streptococcus pyogenes present in Britain during 1980–1990 and their association with disease. J Med Microbiol. 1993;39:165–78.
- Muller MP, Low DE, Green KA, Simor AE, Loeb M, Gregson D, Clinical and epidemiological features of group A streptococcal pneumonia in Ontario, Canada. Arch Intern Med. 2003;163:467–72.
- Birch C, Gowardman J. Streptococcus pyogenes: a forgotten cause of severe community-acquired pneumonia. Anaesth Intensive Care. 2000;28:87–90.
- Moses AE, Goldberg S, Korenman Z, Ravins M, Hanski E, Shapiro M, Invasive group A streptococcal infections, Israel. Emerg Infect Dis. 2002;8:421–6.
- Centers for Disease Control and Prevention. Outbreak of invasive group A Streptococcus associated with varicella in a childcare center—Boston, Massachusetts, 1997. MMWR Morb Mortal Wkly Rep. 1997;46:944–8.
- 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. JAMA. 2004;292:709–15.
- Hu MC, Walls MA, Stroop SD, Reddish MA, Beall B, Dale JB. Immunogenicity of a 26-valent group A streptococcal vaccine. Infect Immun. 2002;70:2171–7.
- Figure 1. Annual incidence and death rate of invasive group A streptococcal infections, by age, in Montreal, Canada, 1995–2001.
- Figure 2. Pneumonia as a proportion of invasive group A streptococcal infections (IGASI) by gender, Montreal, Canada, 1995–2001.
- Table. Adjusted odds ratio (OR) for factors associated with death attributable to invasive group A streptococcal infections, Montreal, Canada, 1995–2002
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: April 14, 2011
- Page last updated: April 14, 2011
- Page last reviewed: April 14, 2011
- Centers for Disease Control and Prevention,
National Center for Emerging and Zoonotic Infectious Diseases (NCEZID)
Office of the Director (OD)