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1.
Am J Cardiol ; 220: 84-91, 2024 Jun 01.
Artigo em Inglês | MEDLINE | ID: mdl-38604492

RESUMO

Development of functional tricuspid regurgitation (TR) because of chronic mitral disease and subsequent heart failure is common. However, the effect of TR on clinical outcomes after transcatheter mitral valve replacement (TMVR) remains unclear. We aimed to evaluate the impact of baseline TR on outcomes after TMVR. This was a single-center, retrospective analysis of patients who received valve-in-valve or valve-in-ring TMVR between 2012 and 2022. Patients were categorized into none/mild TR and moderate/severe TR based on baseline echocardiography. The primary outcome was 3 years all-cause death and the secondary outcomes were in-hospital events. Of the 135 patients who underwent TMVR, 64 (47%) exhibited none/mild TR at baseline, whereas 71 (53%) demonstrated moderate/severe TR. There were no significant differences in in-hospital events between the groups. At 3 years, the moderate/severe TR group exhibited a significantly increased risk of all-cause death (adjusted hazard ratio 3.37, 95% confidence interval 1.35 to 8.41, p = 0.009). When patients with baseline moderate/severe TR were stratified by echocardiography at 30 days into improved (36%) and nonimproved (64%) TR groups, although limited by small sample size, there was no significant difference in 3-year all-cause mortality (p = 0.48). In conclusion, this study investigating the impact of baseline TR on clinical outcomes revealed that moderate/severe TR is prevalent in those who underwent TMVR and is an independent predictor of 3-year all-cause mortality. Earlier mitral valve intervention before the development of significant TR may play a pivotal role in improving outcomes after TMVR.


Assuntos
Ecocardiografia , Implante de Prótese de Valva Cardíaca , Insuficiência da Valva Mitral , Insuficiência da Valva Tricúspide , Humanos , Masculino , Insuficiência da Valva Tricúspide/cirurgia , Feminino , Estudos Retrospectivos , Idoso , Implante de Prótese de Valva Cardíaca/métodos , Insuficiência da Valva Mitral/cirurgia , Cateterismo Cardíaco/métodos , Índice de Gravidade de Doença , Resultado do Tratamento , Causas de Morte/tendências , Complicações Pós-Operatórias/epidemiologia , Idoso de 80 Anos ou mais , Valva Mitral/cirurgia , Valva Mitral/diagnóstico por imagem
2.
Catheter Cardiovasc Interv ; 101(1): 140-146, 2023 01.
Artigo em Inglês | MEDLINE | ID: mdl-36448401

RESUMO

OBJECTIVES: Compare in-hospital outcomes of patients treated with either mechanical thrombectomy (MT) or catheter directed lysis (CDL) in treatment of acute pulmonary embolism (PE). METHODS: This is a multicenter, retrospective cohort study of patients undergoing MT or CDL for acute PE between 2014 and 2021. The primary outcome was the composite of in-hospital death, significant bleed, vascular complication, or need for mechanical support post-procedure. Secondary outcomes included the individual components of the composite outcome in addition to blood transfusions, invasive hemodynamics, echocardiographic data, and intensive care unit (ICU) utilization. RESULTS: 458 patients were treated for PE with 266 patients in the CDL arm and 192 patients in the MT arm. The primary composite endpoint was not significantly different between the two groups with CDL 12% versus MT 11% (p = 0.5). There was a significant difference in total length of ICU time required with more in the CDL group versus MT (3.8 ± 2.0 vs. 2.8 ± 3.0 days, p = 0.009). All other secondary end points showed no significant difference between the groups. CONCLUSIONS: In patients undergoing catheter directed treatment of PE, there was no difference between MT and CDL in terms of in-hospital mortality, bleeds, catheter-related complications, and hemodynamics.


Assuntos
Embolia Pulmonar , Terapia Trombolítica , Humanos , Terapia Trombolítica/métodos , Estudos Retrospectivos , Mortalidade Hospitalar , Resultado do Tratamento , Embolia Pulmonar/terapia , Embolia Pulmonar/tratamento farmacológico , Trombectomia/efeitos adversos , Trombectomia/métodos , Catéteres , Hemorragia/induzido quimicamente , Fibrinolíticos/efeitos adversos
3.
Infect Control Hosp Epidemiol ; 40(8): 839-846, 2019 08.
Artigo em Inglês | MEDLINE | ID: mdl-31133088

RESUMO

OBJECTIVE: To determine the best nursing home facility characteristics for aggregating antibiotic susceptibility testing results across nursing homes to produce a useful annual antibiogram that nursing homes can use in their antimicrobial stewardship programs. DESIGN: Derivation cohort study. SETTING: Center for Medicare and Medicaid Services (CMS) certified skilled nursing facilities in Georgia (N = 231). PARTICIPANTS: All residents of eligible facilities submitting urine culture specimens for microbiologic testing at a regional referral laboratory. METHODS: Crude and adjusted metrics of antibiotic resistance prevalence (percent of isolates testing susceptible) for 5 bacterial species commonly recovered from urine specimens were calculated using mixed linear models to determine which facility characteristics were predictive of testing antibiotic susceptibility. RESULTS: In a single year, most facilities had an insufficient number of isolates tested to create facility-specific antibiograms: 49% of facilities had sufficient Escherichia coli isolates tested, but only about 1 in 10 had sufficient isolates of Klebsiella pneumoniae, Proteus mirabilis, Enterococcus faecalis, or Pseudomonas aeruginosa. After accounting for antibiotic tested and age of the patient, facility characteristics predictive of susceptibility were: E. coli, region, year, average length of stay; K. pneumoniae, region, bed size; P. mirabilis, region; and for E. faecalis or P. aerginosa no facility parameter remained in the model. CONCLUSIONS: Nursing homes often have insufficient data to create facility-specific antibiograms; aggregating data across nursing homes in a region is a statistically sound approach to overcoming data shortages in nursing home stewardship programs.


Assuntos
Gestão de Antimicrobianos , Resistência Microbiana a Medicamentos/efeitos dos fármacos , Testes de Sensibilidade Microbiana , Casas de Saúde , Instituições de Cuidados Especializados de Enfermagem , Estudos de Coortes , Escherichia coli/efeitos dos fármacos , Georgia , Klebsiella pneumoniae/efeitos dos fármacos , Estados Unidos
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