NACINOVICH FRANCISCO
Transcription
NACINOVICH FRANCISCO
INVASIVE PNEUMOCCOCAL DISEASES (IPD) IN PEOPLE WITHOUT CO MORBIDITIES. Nacinovich FM, Marin M, Bonvehí PE, Gentile J, Stamboulian D. Nº 452 (on behalf of IPD Study Group - Fundación Centro de Estudios Infectológicos) [email protected] BACKGROUND IPD remains a major cause of morbidity and mortality worldwide and developing countries bear the major burden of this challenging disease. Occurs principally in the extremes of age (children <2 yo and adults >65 yo) and people with cardiovascular and respiratory diseases, diabetes, immunosuppression, etc. are wellknown associated with an increased susceptibility to pneumococcal disease and are further associated with higher mortality. RESULTS From 25 centers in 11 provinces of Argentina (January 2000 to January 2002) (Figure 1): • 202 S. pneumoniae strains were isolated. • 75 (37.13%) from people without evident co morbidities. FIGURE 1: PARTICIPATING CENTERS PARTICIPATING CENTERS Bariloche Buenos Aires Capital Federal Catamarca Comodoro Rivadavia Mar del Plata Mendoza Neuquén Rosario Santa Fé Tandil Tucumán METHODS • Subanalisys of the first prospective, multicenter and observational study of IPD in adults ≥18 yo performed in Argentina. • Only cases with S. pneumoniae strains isolated from sterile sites were considered (blood cultures, CSF, pleural, pericardial and peritoneal fluid, bone and joints). • Demographic data, high-risk conditions for IPD (age, cardiovascular diseases – CVD-, chronic pulmonary diseases – CPD -, diabetes, esplenectomy, smoking, among others) and previous pneumococcal vaccination status of each eligible subject was obtained through interview and/or from clinical records. All data were collected in a data collecting form. • Minimal inhibitory concentrations tests (MICs) to penicillin were determined by broth microdilution method according to CLSI guidelines, 2008. • Serotyping was carried out by the Quellung reaction using antiserum from the Statens Seruminstitute (Copenhagen, Denmark). • Financial support: this study was partially supported by Sanofi Pasteur, GlaxoSmithKline and Fundación Alberto Roemmers (Argentina). • Characteristics of patients without evident co morbidities: -Age: 64±DS 22. -Male sex 28.6%. -30/75 patients (40%) were <65 yo. -Source of isolation (table 1): TABLE 1: SOURCE OF ISOLATION OF S. PNEUMONIAE (n= 75 EPISODES) Blood cultures Pleural fluid CSF Peritoneal fluid TABLE 2: SEROTYPES OF STRAINS WITH AVAILABLE IPD CLINICAL DATA Serotype There is limited data regarding IPD in adults in Latin America and particularly in Argentina, not only in people with predisposing conditions but also IPD affecting those people without co morbidities. The aim of this study was to analyze the clinical presentation, mortality and serotypes involved in IPD in people without evident co morbidities (NC) and compare NC group with the people with co morbidities (C). • More frequent clinical presentation: pneumonia (76%) and meningitis (14.7%) (table 2): 59 (78.7%) 9 (12%) 11 (14.7%) 3 (4 %) Soft tissue infection 2 (2.6 %) Sinovial fluid 1 (1.3%) All IPD n (%) No evident co morbidities (NC) n=75 With evident co morbidities (C) n=127 Pneumonia Meningitis Bacteremia Pneumonia Meningitis • Serotypes in people who died (n): -14 (2) -1 (1) -18 (1) -3 (3) -19 A (2) -4 (1) -NT (2) -12 F (1) • Comparing between ages (<65 yo vs. >65 yo) people >65 yo died almost 6 times more frequently (2/30 vs 11/45) than younger people, but it was a non-significant tendency to mortality (6.67% vs 24.44%; p= 0.063) between both groups. Bacteremia 14 25 (14.8) 7 2 1 12 1 21 5 20 (11.9) 11 1 3 7 - 15 1 17 (10.7) 6 1 3 10 - 14 3 14 (8.3) 4 2 4 4 1 8 19A 12 (7.1) 4 - - 8 - 9 7F 11 (6.5) 2 - - - - 10 23F 10 (6) 2 - 1 5 - 8 18 9 (5.4) 3 1 - 2 3 7 8 7 (4.2) 2 - - 4 1 6 9V 7 (4.2) 1 - - 6 - 7 12F 6 (3.6) 3 - - 2 - 6 19F 5 (3) - - - 4 - 4 20 4 (2.4) 1 - - 1 - 3 4 4 (2.4) 3 - 1 1 - 1 6A 4 (2.4) - 1 - 2 - 4 6B 3 (1.8) - - - 3 - 1 9N 3 (1.8) 1 - 1 1 - 2 23B 3 (1.8) - - - 2 - 2 22 2 (1.2) - - - 1 - 1 7A 1 (0.6) - - - 1 - 1 NT § 34 (17) 7 3 1 17 - 5 Total 202 (100) 57 11 15 93 6 135 §NT not serotyped Serotypes in PCV13: 1, 3, 4, 5, 6A, 6B, 7F, 9V, 14, 18C, 19A, 19F, 23F. Serotypes in PPV23: 1, 2, 3, 4, 5, 6B, 7F, 8, 9N, 9V, 10A, 11A, 12F, 14, 15B, 17F, 18C, 19A, 19F, 20, 22F, 23F, 33F. • Available vaccine coverage of the identified serotypes: - PCV 13: 76.5%. - PPV23: 100%. • There were no significant differences between NC and C group regarding clinical presentation of IPD (although NC group had more meningitis episodes) and serotypes involved. CONCLUSION • IPD may affect people of any ages and also those without any evident co morbidities. • Age >65 yo seems to be a risk factor per se to IPD, with or without associated co morbid diseases. • Of note, patients with a previous IPD are not in the list of candidates to receive the current available pneumococcal vaccines. • Due to almost 40% of the people with IPD had no evident risk factors for it, population studies are needed in order to confirm these findings that could have implications for prevention with vaccines. • To assess pneumococcal disease burden, estimate the potential impact of new vaccines, and identify gaps in vaccine recommendations, regional monitoring of S. pneumoniae serotype prevalence and antibiotic susceptibility is an outstanding task in the Latinoamerican region. • All the strains were sensitive to penicillin. • No people had previous pneumococcal vaccination. IPD STUDY GROUP Dr. Lazovsky J, Dra. De Wouters L, Dr. Costilla Campero G, Dr. Casellas JM*, Dra. Gutson K, Dr. Gómez R, Dra. Mónica Grazziutti, Dr. Oscar Caberlotto, Dra. Gabriela Vidal, Dra. Marisa Fernández, Dr. Diego Maurizi, Dr. Carlos • Hospital mortality (global): 13/75 (17.3%); 2/13 <65 yo. -10 pneumonias -2 meningitis -1 peritonitis Barclay, Dra. María Ester Lázaro, Dr. Jorge Brugna, Dr. Ernesto Jakob, Dr. José Luis Corrales, Dr. Luis Leiva, Dra. María Gonzalez Arzac, Dr. Jorge Mera, Dra. Liliana Calanni, Dr. Carlos Bantar, Dr. José Luis De Michelis, Dr. Joaquín Bermejo, Dra. Adriana Falco, Dra. Graciela Ortega, Dra. Deborah Stepanek. (*) In memoriam.