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1.
Transpl Infect Dis ; 20(2): e12855, 2018 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-29427356

RESUMEN

BACKGROUND: Clostridium difficile infection (CDI) is a common complication of lung and allogeneic hematopoietic cell (HCT) transplant, but the epidemiology and outcomes of CDI after transplant are poorly described. METHODS: We performed a prospective, multicenter study of CDI within 365 days post-allogeneic HCT or lung transplantation. Data were collected via patient interviews and medical chart review. Participants were followed weekly in the 12 weeks post-transplant and while hospitalized and contacted monthly up to 18 months post-transplantation. RESULTS: Six sites participated in the study with 614 total participants; 4 enrolled allogeneic HCT (385 participants) and 5 enrolled lung transplant recipients (229 participants). One hundred and fifty CDI cases occurred within 1 year of transplantation; the incidence among lung transplant recipients was 13.1% and among allogeneic HCTs was 31.2%. Median time to CDI was significantly shorter among allogeneic HCT than lung transplant recipients (27 days vs 90 days; P = .037). CDI was associated with significantly higher mortality from 31 to 180 days post-index date among the allogeneic HCT recipients (Hazard ratio [HR] = 1.80; P = .007). There was a trend towards increased mortality among lung transplant recipients from 120 to 180 days post-index date (HR = 4.7, P = .09). CONCLUSIONS: The epidemiology and outcomes of CDI vary by transplant population; surveillance for CDI should continue beyond the immediate post-transplant period.


Asunto(s)
Infecciones por Clostridium/tratamiento farmacológico , Infecciones por Clostridium/epidemiología , Trasplante de Células Madre Hematopoyéticas/efectos adversos , Trasplante de Pulmón/efectos adversos , Receptores de Trasplantes , Femenino , Humanos , Masculino , Estudios Prospectivos , Factores de Riesgo
2.
Am J Transplant ; 17(1): 296-299, 2017 01.
Artículo en Inglés | MEDLINE | ID: mdl-28029734

RESUMEN

November 11, 2016/65(44);1234-1237. What is already known about this topic? Candida auris is an emerging pathogenic fungus that has been reported from at least a dozen countries on four continents during 2009-2015. The organism is difficult to identify using traditional biochemical methods, some isolates have been found to be resistant to all three major classes of antifungal medications, and C. auris has caused health care-associated outbreaks. What is added by this report? This is the first description of C. auris cases in the United States. C. auris appears to have emerged in the United States only in the last few years, and U.S. isolates are related to isolates from South America and South Asia. Evidence from U.S. case investigations suggests likely transmission of the organism occurred in health care settings. What are the implications for public health practice? It is important that U.S. laboratories accurately identify C. auris and for health care facilities to implement recommended infection control practices to prevent the spread of C. auris. Local and state health departments and CDC should be notified of possible cases of C. auris and of isolates of C. haemulonii and Candida spp. that cannot be identified after routine testing.


Asunto(s)
Candida/aislamiento & purificación , Candidiasis/diagnóstico , Candidiasis/microbiología , Farmacorresistencia Fúngica Múltiple , Antifúngicos/uso terapéutico , Candida/efectos de los fármacos , Candidiasis/tratamiento farmacológico , Enfermedades Transmisibles Emergentes , Salud Global , Humanos , Pronóstico , Factores de Riesgo , Factores de Tiempo , Estados Unidos
3.
HIV Med ; 16(8): 468-76, 2015 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-25689352

RESUMEN

OBJECTIVES: We retrospectively evaluated clinic-based screening to determine the prevalence of cryptococcal antigenaemia and management and outcome of patients with antigenaemia. METHODS: Cryptococcal antigen (CrAg) screening of HIV-infected adults who attended the HIV clinic at Chris Hani Baragwanath Hospital was conducted over 19 months. Data collected from CrAg-positive patients included CD4 T-lymphocyte count at screening, prior or subsequent cryptococcal meningitis (CM), antifungal and antiretroviral treatment and outcome after at least 8 months. RESULTS: Of 1460 patients with no prior CM, 30 (2.1%) had a positive CrAg test. The prevalence of antigenaemia among patients with a CD4 count < 100 cells/µl and no prior CM was 2.8% (20 of 708). Of 29 evaluable CrAg-positive patients with no prior CM, 14 (48%) did not return for post-screening follow-up. Of these 14, five developed CM and one (7%) was known to be alive at follow-up. Of 15 patients who returned for follow-up, two already had evidence of nonmeningeal cryptococcosis. Overall, 11 received fluconazole, one did not and fluconazole treatment was unknown for three. Among these 15, one developed CM and 10 (67%) were known to be alive at follow-up. Overall, 18 (62%) of 29 CrAg-positive patients died or were lost to follow-up. Seven (0.5%) of 1430 CrAg-negative patients developed CM a median of 83 days post-screening (range 34 to 219 days). CONCLUSIONS: Loss to follow-up is the major operational issue relevant to scale-up of screen-and-treat. Patient outcomes may be improved by rapid access to CrAg results and focus on linkage to and retention in HIV care.


Asunto(s)
Infecciones Oportunistas Relacionadas con el SIDA/epidemiología , Infecciones por VIH/complicaciones , Meningitis Criptocócica/epidemiología , Infecciones Oportunistas Relacionadas con el SIDA/diagnóstico , Infecciones Oportunistas Relacionadas con el SIDA/tratamiento farmacológico , Adulto , Antifúngicos/uso terapéutico , Antígenos Fúngicos/análisis , Antígenos Fúngicos/sangre , Recuento de Linfocito CD4 , Cryptococcus neoformans/inmunología , Cryptococcus neoformans/aislamiento & purificación , Femenino , Humanos , Masculino , Meningitis Criptocócica/diagnóstico , Meningitis Criptocócica/tratamiento farmacológico , Persona de Mediana Edad , Prevalencia , Estudios Retrospectivos , Sudáfrica/epidemiología
4.
Transpl Infect Dis ; 16(2): 213-24, 2014 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-24589027

RESUMEN

BACKGROUND: Invasive fungal infections are a major cause of morbidity and mortality among solid organ transplant (SOT) and hematopoietic cell transplant (HCT) recipients, but few data have been reported on the epidemiology of endemic fungal infections in these populations. METHODS: Fifteen institutions belonging to the Transplant-Associated Infection Surveillance Network prospectively enrolled SOT and HCT recipients with histoplasmosis, blastomycosis, or coccidioidomycosis occurring between March 2001 and March 2006. RESULTS: A total of 70 patients (64 SOT recipients and 6 HCT recipients) had infection with an endemic mycosis, including 52 with histoplasmosis, 9 with blastomycosis, and 9 with coccidioidomycosis. The 12-month cumulative incidence rate among SOT recipients for histoplasmosis was 0.102%. Occurrence of infection was bimodal; 28 (40%) infections occurred in the first 6 months post transplantation, and 24 (34%) occurred between 2 and 11 years post transplantation. Three patients were documented to have acquired infection from the donor organ. Seven SOT recipients with histoplasmosis and 3 with coccidioidomycosis died (16%); no HCT recipient died. CONCLUSIONS: This 5-year multicenter prospective surveillance study found that endemic mycoses occur uncommonly in SOT and HCT recipients, and that the period at risk extends for years after transplantation.


Asunto(s)
Blastomicosis/epidemiología , Coccidioidomicosis/epidemiología , Enfermedades Endémicas , Trasplante de Células Madre Hematopoyéticas/efectos adversos , Histoplasmosis/epidemiología , Trasplante de Órganos/efectos adversos , Adolescente , Adulto , Anciano , Anfotericina B/uso terapéutico , Antifúngicos/uso terapéutico , Blastomicosis/tratamiento farmacológico , Niño , Coccidioidomicosis/tratamiento farmacológico , Coinfección/tratamiento farmacológico , Coinfección/epidemiología , Comorbilidad , Femenino , Histoplasmosis/tratamiento farmacológico , Humanos , Incidencia , Itraconazol/uso terapéutico , Masculino , Persona de Mediana Edad , Estudios Prospectivos , Infecciones del Sistema Respiratorio/epidemiología , Infecciones del Sistema Respiratorio/microbiología , Factores de Tiempo , Estados Unidos/epidemiología , Adulto Joven
5.
Artículo en Inglés | MEDLINE | ID: mdl-19357424

RESUMEN

BACKGROUND: Trimethoprim-sulfamethoxazole (TMP-SMZ) has been recommended by World Health Organization (WHO) as daily prophylaxis for Africans with AIDS to prevent opportunistic infections. Daily TMP-SMZ may reduce its susceptibility to commensal intestinal Escherichia coli (E coli), increasing the burden of TMP-SMZ-resistant pathogens. METHODS: Participants received either daily TMP-SMZ (CD4 <350 cells/mm(3)) or daily multivitamins (MVIs; CD4 > or =350 cells/mm(3)) for 6 months. Stool was collected at baseline, 2 weeks, 2 months, and 6 months. A random E coli was tested for susceptibility. RESULTS: Baseline prevalence of TMP-SMZ resistance ranged from 71% to 81% and was not different across CD4 strata. At 2 weeks, prevalence of TMP-SMZ-resistant E coli increased significantly from 78% to 98% (P < .001) among persons taking daily TMP-SMZ and did not change among persons taking MVIs. CONCLUSIONS: Daily prophylaxis with TMP-SMZ induced in vivo resistance to the drug after 2 weeks. Empiric therapy for diarrhea with agents other than TMP-SMZ should be considered for HIV-infected persons receiving daily TMP-SMZ prophylaxis.


Asunto(s)
Infecciones Oportunistas Relacionadas con el SIDA/prevención & control , Antiinfecciosos/farmacología , Farmacorresistencia Bacteriana , Escherichia coli/efectos de los fármacos , Infecciones por VIH/tratamiento farmacológico , Combinación Trimetoprim y Sulfametoxazol/farmacología , Adolescente , Adulto , Antiinfecciosos/uso terapéutico , Recuento de Linfocito CD4 , Estudios de Cohortes , Escherichia coli/aislamiento & purificación , Heces/microbiología , Femenino , Infecciones por VIH/sangre , Humanos , Kenia , Masculino , Persona de Mediana Edad , Combinación Trimetoprim y Sulfametoxazol/uso terapéutico , Vitaminas/administración & dosificación , Adulto Joven
6.
Foodborne Pathog Dis ; 3(1): 106-17, 2006.
Artículo en Inglés | MEDLINE | ID: mdl-16602986

RESUMEN

Salmonella isolates were recovered from a monthly sampling of chicken breasts, ground turkey, ground beef, and pork chops purchased from selected grocery stores in six participating FoodNet sites (Connecticut, Georgia, Maryland, Minnesota, Oregon, and Tennessee) in 2002 and an additional two sites in 2003 (California and New York). In 2002 and 2003, a total of 6,046 retail meats were examined, including 1,513 chicken breasts, 1,499 ground turkey samples, 1,522 ground beef samples, and 1,502 pork chops. Retail meat samples tested increased to 3,533 in 2003 as compared to 2,513 in 2002. Overall, six percent of 6,046 retail meat samples (n = 365) were contaminated with Salmonella, the bulk recovered from either ground turkey (52%) or chicken breast (39%). Salmonella isolates were serotyped and susceptibility tested using a panel of 16 antimicrobial agents. S. Heidelberg was the predominant serotype identified (23%), followed by S. Saintpaul (12%), S. Typhimurium (11%), and S. Kentucky (10%). Overall, resistance was most often observed to tetracycline (40%), streptomycin (37%), ampicillin (26%), and sulfamethoxazole (25%). Twelve percent of isolates were resistant to cefoxitin and ceftiofur, though only one isolate was resistant to ceftriaxone. All isolates were susceptible to amikacin and ciprofloxacin; however, 3% of isolates were resistant to nalidixic acid and were almost exclusive to ground turkey samples (n = 11/12). All Salmonella isolates were analyzed for genetic relatedness using pulsed-field gel electrophoresis (PFGE) patterns generated by digestion with Xba1 or Xba1 plus Bln1. PFGE fingerprinting profiles showed that Salmonella, in general, were genetically diverse with a total of 175 Xba1 PFGE profiles generated from the 365 isolates. PFGE profiles showed good correlation with serotypes and in some instances, antimicrobial resistance profiles. Results demonstrated a varied spectrum of antimicrobial resistance and PFGE patterns, including several multidrug resistant clonal groups among Salmonella isolates, and signify the importance of sustained surveillance of foodborne pathogens in retail meats.


Asunto(s)
Antibacterianos/farmacología , Farmacorresistencia Bacteriana/genética , Contaminación de Alimentos/análisis , Carne/microbiología , Salmonella/efectos de los fármacos , Salmonella/genética , Animales , Seguridad de Productos para el Consumidor , Farmacorresistencia Bacteriana Múltiple , Electroforesis en Gel de Campo Pulsado/métodos , Microbiología de Alimentos , Variación Genética , Humanos , Productos de la Carne/microbiología , Pruebas de Sensibilidad Microbiana , Filogenia , Salmonella/clasificación , Estados Unidos
7.
Infect Dis Clin North Am ; 9(2): 439-43, 1995 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-7673680

RESUMEN

At the heart of imminent healthcare reform are the future physicians of this decade. Medical educators will want to stimulate a desire within students to practice humanitarian, cost-effective, community-oriented primary care. Further studies to examine the effects of medical student experiences in international electives should be encouraged.


Asunto(s)
Educación Médica , Salud Global , Cooperación Internacional , Louisiana , Desarrollo de Programa , Facultades de Medicina
8.
Am J Trop Med Hyg ; 43(6): 650-6, 1990 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-2125177

RESUMEN

Sera from 38 Paraguayans with positive skin tests to Leishmania braziliensis panamensis and 51 sera from Paraguayan patients in different stages of Chagas' disease were analyzed by Western blotting using antigen from Trypanosoma cruzi Y strain epimastigotes and from L. b. panamensis promastigotes. Using a single serum sample, distinctive patterns of IgG antibody response to both antigens were identified allowing the differentiation between T. cruzi infection, Leishmania infection, and probable double infection. Sera from patients with T. cruzi infections consistently recognized bands of approximately 25 kDa, 38 kDa, and greater than 97 kDa in T. cruzi antigen lysates and recognized a band of 38 kDa of 66 kDa in Leishmania antigen lysates but did not consistently recognize any bands using T. cruzi antigen. Sera from patients with probable double infections recognized all bands normally detected by individual sera from patients infected with either T. cruzi or Leishmania. In our study population, T. cruzi infection among leishmaniasis patients was as frequent as among individuals free of leishmaniasis.


Asunto(s)
Anticuerpos Antiprotozoarios/inmunología , Antígenos de Protozoos/inmunología , Enfermedad de Chagas/diagnóstico , Leishmaniasis/diagnóstico , Animales , Antígenos de Protozoos/sangre , Western Blotting , Enfermedad de Chagas/sangre , Enfermedad de Chagas/inmunología , Reacciones Cruzadas , Diagnóstico Diferencial , Electroforesis en Gel de Poliacrilamida , Ensayo de Inmunoadsorción Enzimática , Humanos , Inmunoglobulina G/inmunología , Leishmania braziliensis/inmunología , Leishmaniasis/sangre , Leishmaniasis/inmunología , Paraguay , Sobreinfección , Trypanosoma cruzi/inmunología
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