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1.
J Infect Dis ; 224(12 Suppl 2): S228-S236, 2021 09 01.
Artículo en Inglés | MEDLINE | ID: mdl-34469563

RESUMEN

BACKGROUND: In 2013, the Dominican Republic introduced 13-valent pneumococcal conjugate vaccine (PCV13) using a 3-dose schedule (at 2, 4 and 12 months of age). We evaluated the impact of PCV13 on serotypes causing pneumococcal pneumonia with pleural effusion. METHODS: Surveillance data after PCV13 introduction (July 2014 to June 2016) were compared with data before PCV13 introduction (July 2009 to June 2011). Cases were defined as radiologic evidence of pneumonia with pleural effusion in a child aged <15 years. Pneumococcus was detected in pleural fluid by either culture or polymerase chain reaction, and serotyping was performed. The Ministry of Health's PCV13 uptake data for 2014-2016 were obtained. RESULTS: The prevalence of pneumococcus among cases was similar before and after PCV13 introduction (56.4% and 52.8%, respectively). The proportion of pneumococcal cases caused by vaccine serotypes was 86% for children <2 years old both before and PCV13 introduction. Compared with before PCV13, serotype 14 accounted for a smaller (28% vs 13%, respectively; P = .02) and serotype 1 for a larger (23% vs 37%; P = .09) proportion of pneumococcal cases after PCV13 introduction. National uptake for the first, second, and third PCV13 doses was 94%, 81%, and 28%, respectively, in 2014 and 75%, 61%, and 26% in 2015. DISCUSSION: While the decrease in pneumococcal pneumonia with pleural effusion caused by serotype 14 may reflect an early effect of PCV13 implementation, other vaccine serotypes, including serotype 1, are not well controlled. Better PCV13 coverage for all 3 doses is needed.


Asunto(s)
Infecciones Neumocócicas/epidemiología , Vacunas Neumococicas/administración & dosificación , Vacunas Neumococicas/efectos adversos , Neumonía Neumocócica/epidemiología , Vacunas Conjugadas/efectos adversos , Niño , Preescolar , República Dominicana/epidemiología , Femenino , Humanos , Lactante , Masculino , Derrame Pleural/epidemiología , Derrame Pleural/etiología , Infecciones Neumocócicas/complicaciones , Infecciones Neumocócicas/prevención & control , Vacunas Neumococicas/inmunología , Neumonía Neumocócica/complicaciones , Neumonía Neumocócica/prevención & control , Complicaciones Posoperatorias , Prevalencia , Serogrupo , Streptococcus pneumoniae/inmunología , Streptococcus pneumoniae/aislamiento & purificación , Vacunación , Vacunas Conjugadas/administración & dosificación , Vacunas Conjugadas/inmunología
2.
BMC Infect Dis ; 18(1): 152, 2018 04 02.
Artículo en Inglés | MEDLINE | ID: mdl-29609548

RESUMEN

BACKGROUND: Limited data are available on the effectiveness of 13-valent pneumococcal conjugate vaccine (PCV13) in resource-poor settings and PCV naïve populations. The Dominican Republic introduced PCV13 in September 2013 using a 2 + 1 schedule (2, 4, and 12 months) without a catch-up campaign. We evaluated PCV13 effectiveness against vaccine-type (VT) invasive pneumococcal disease (IPD) among children in the Dominican Republic. METHODS: We conducted a matched case-control study. A case-patient was defined as VT-IPD identified by culture or polymerase chain reaction (PCR) from a normally sterile-site in a hospitalized child who was age-eligible to have received ≥1 PCV13 dose. Four age- and neighborhood-matched controls were enrolled for each case-patient. We collected demographic, vaccination history, and risk factor data. Conditional logistic regression was performed. Vaccine effectiveness was calculated as (1- adjusted matched odds ratio for vaccination) X 100%. RESULTS: We enrolled 39 case-patients and 149 matched-controls. Most case-patients had pneumonia with pleural effusion (64%), followed by meningitis (28%) and septicemia (13%). The most common pneumococcal serotypes identified included 14 (18%), 3 (13%), 19A (10%), and 1 (8%). Fewer case-patients had ≥1 PCV13 dose as compared to controls (61.5% vs. 80.0%; p = 0.006). Adjusting for malnutrition and socioeconomic status, VE of ≥1 PCV13 dose compared to no doses was 67.2% (95% CI: 2.3% to 90.0%). Only 44% of controls were up-to-date for PCV13, suggesting low vaccine coverage in the population. CONCLUSIONS: We found that PCV13 provided individual protection against VT-IPD in this resource-poor setting with a PCV-naïve population, despite low PCV13 coverage. Expanding vaccination coverage might increase PCV13 impact.


Asunto(s)
Infecciones Neumocócicas/prevención & control , Vacunas Neumococicas/uso terapéutico , Vacunas Conjugadas/uso terapéutico , Estudios de Casos y Controles , Niño Hospitalizado , República Dominicana/epidemiología , Femenino , Humanos , Lactante , Masculino , Infecciones Neumocócicas/epidemiología , Infecciones Neumocócicas/patología , Sepsis/epidemiología , Sepsis/prevención & control , Clase Social , Resultado del Tratamiento , Vacunación/estadística & datos numéricos
3.
Pneumonia (Nathan) ; 4: 8-15, 2014.
Artículo en Inglés | MEDLINE | ID: mdl-29725575

RESUMEN

Pleural effusion is a serious complication of pneumonia, and Streptococcus pneumoniae is a leading cause. We describe the aetiology of pneumonia with effusion among children in the Dominican Republic before the introduction of the 13-valent pneumococcal conjugate vaccine (PCV) in 2013 and the performance characteristics of a rapid immunochromatographic test (ICT) for detecting S. pneumoniae in pleural fluid. From July 2009 to June 2011, we enrolled children <15 years old admitted with pneumonia and pleural effusion to Robert Reid Cabral Children's Hospital, Dominican Republic. Pleural fluid was tested by culture, polymerase chain reaction (PCR) for bacterial (S. pyogenes, S. pneumoniae) and viral (respiratory syncytial virus and human rhinovirus) pathogens, and by ICT for S. pneumoniae. We calculated the performance of ICT and culture compared with PCR. Among 121 cases, the median age was 31 months (range 1 week to 14 years). Pleural fluid culture (n = 121) and PCR testing (n = 112) identified an aetiology in 85 (70.2%) cases, including 62 S. pneumoniae (51.2%) and 19 Staphylococcus aureus (15.7%). The viruses tested were not detected. The most prevalent pneumococcal serotypes were 14 (n = 20), 1 (n = 13), and 3 (n = 12). Serotype coverage of the 10- and 13-valent PCVs would be 70.5% and 95.1%, respectively. The sensitivity of point-of-care ICT was 100% (95% confidence interval [CI] 94.1%-100%), while specificity was 86.3% (95% CI 73.7%-94.3%). S. pneumoniae caused more than half of paediatric pneumonia with effusion cases; introduction of PCV in the Dominican Republic could reduce the burden by 36-49%. ICT is a practical, valid diagnostic tool for clinical care and surveillance in settings with limited laboratory capacity.

4.
Rev. panam. salud pública ; 25(4): 305-313, abr. 2009. graf, tab
Artículo en Español | LILACS | ID: lil-515969
5.
Rev Panam Salud Publica ; 25(4),abr. 2009 graf, tab
Artículo | PAHO-IRIS | ID: phr-9863
6.
Arch. domin. pediatr ; 33(1): 14-7, ene.-abr. 1997. tab, graf
Artículo en Español | LILACS | ID: lil-269156

RESUMEN

Con el propósito de conocer las características clínicas y epidemiológicas de la estafilococcemia, realizamos un estudio observacional en la Clínica Infantil Dr. Robert Read Cabral durante el período abril 1994 a marzo 1995. En total se incluyeron 30 pacientes con estafilococcemia, de los cuales, la mayor frecuencia correspondió al grupo etáreo comprendido entre 2 a 5 años con 13.43//; el sexo más afectado fue el masculino con 18 casos, 60//. El 80// vivía en hacinamiento. El Staphylococcus aureus (coagulasa positivo) se encontró en el 96.6// de los cultivos de sangre. Todos los estafilococos fueron sensibles a la oxacilina y resistentes a la penicilina; la letalidad fue de 23.3//


Asunto(s)
Humanos , Masculino , Femenino , Preescolar , Coagulasa/aislamiento & purificación , Staphylococcus aureus/aislamiento & purificación , Staphylococcus aureus/patogenicidad
7.
Arch. domin. pediatr ; 32(1): 21-5, ene.-abr. 1996.
Artículo en Español | LILACS | ID: lil-170310

RESUMEN

El presente trabajo es una revisión resumida de los elementos fundamentales que debe cumplir un nuevo medicamento para que pueda ir desde el laboratorio de investigación al mostrador del farmacéutico y ser expendido al público. Identifica las fases que debe cumplir la investigación de una nueva droga (preclínica, registro de investigación de nueva droga, ensayo clínico en sus diferentes fases), así como los elementos técnicos y éticos que deben respetar los protocolos de investigación de nuevos medicamentos


Asunto(s)
Preparaciones Farmacéuticas/economía , Preparaciones Farmacéuticas/normas
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