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1.
Chest ; 160(4): 1534-1551, 2021 10.
Artigo em Inglês | MEDLINE | ID: mdl-34023322

RESUMO

BACKGROUND: Comprehensive US epidemiologic data for adult pleural disease are not available. RESEARCH QUESTION: What are the epidemiologic measures related to adult pleural disease in the United States? STUDY DESIGN AND METHODS: Retrospective cohort study using Healthcare Utilization Project databases (2007-2016). Adults (≥ 18 years of age) with malignant pleural mesothelioma, malignant pleural effusion, nonmalignant pleural effusion, empyema, primary and secondary spontaneous pneumothorax, iatrogenic pneumothorax, and pleural TB were studied. RESULTS: In 2016, ED treat-and-discharge (T&D) visits totaled 42,215, accounting for charges of $286.7 million. In 2016, a total of 361,270 hospitalizations occurred, resulting in national costs of $10.1 billion. A total of 64,174 readmissions contributed $1.16 billion in additional national costs. Nonmalignant pleural effusion constituted 85.5% of ED T&D visits, 63.5% of hospitalizations, and 66.3% of 30-day readmissions. Contemporary sex distribution (male to female ratio) in primary spontaneous pneumothorax (2.1:1) differs from older estimates (6.2:1). Decadal analyses of annual hospitalization rates/100,000 adult population (2007 vs 2016) showed a significant (P < .001) decrease for malignant pleural mesothelioma (1.3 vs 1.09, respectively), malignant pleural effusion (33.4 vs 31.9, respectively), iatrogenic pneumothorax (17.9 vs 13.9, respectively), and pleural TB (0.20 vs 0.09, respectively) and an increase for empyema (8.1 vs 11.1, respectively) and nonmalignant pleural effusion (78.1 vs 100.1, respectively). Empyema hospitalizations have high costs per case ($38,591) and length of stay (13.8 days). The mean proportion of readmissions attributed to a pleural cause varied widely: malignant pleural mesothelioma, 49%; malignant pleural effusion, 45%; nonmalignant pleural effusion, 31%; empyema, 27%; primary spontaneous pneumothorax, 27%; secondary spontaneous pneumothorax, 27%; and iatrogenic pneumothorax, 20%. Secondary spontaneous pneumothorax had the shortest time to readmission in 2016 (10.3 days, 95% CI, 8.8-11.8 days). INTERPRETATION: Significant epidemiologic trends and changes in various pleural diseases were observed. The analysis identifies multiple opportunities for improvement in management of pleural diseases.


Assuntos
Doenças Pleurais/epidemiologia , Adolescente , Adulto , Idoso , Empiema/economia , Empiema/epidemiologia , Feminino , Coalizão em Cuidados de Saúde , Gastos em Saúde , Hospitalização/economia , Humanos , Incidência , Masculino , Mesotelioma Maligno/economia , Mesotelioma Maligno/epidemiologia , Pessoa de Meia-Idade , Readmissão do Paciente/economia , Doenças Pleurais/economia , Derrame Pleural/economia , Derrame Pleural/epidemiologia , Derrame Pleural Maligno , Neoplasias Pleurais/economia , Neoplasias Pleurais/epidemiologia , Pneumotórax/economia , Pneumotórax/epidemiologia , Tuberculose Pleural/economia , Tuberculose Pleural/epidemiologia , Estados Unidos/epidemiologia , Adulto Jovem
2.
BMJ Case Rep ; 20172017 Jun 08.
Artigo em Inglês | MEDLINE | ID: mdl-28596204

RESUMO

Malignant hypertension can occasionally be associated with microangiopathic haemolytic anaemia. A 38-year-old male presented with nausea, vomiting, loss of appetite and oliguria for 2 weeks. He was diagnosed with hypertensive emergency with cardiac and renal dysfunction. Interestingly, further workup was diagnostic for the presence of thrombotic microangiopathy (TMA): haemoglobin =12.7 g/dL, indirect bilirubin =2.0 mg/dL, haptoglobin ≤6 mg/dL, platelet count =121 000/µL and schistocytes on peripheral smear. At the outset, the cause of TMA was unclear. Patient denied having diarrhoea, making haemolytic uremic syndrome less likely. A normal ADAMTS13 activity test ruled out thrombotic thrombocytopaenic purpura. Malignant hypertension induced TMA was highest on the differential and plasma exchange was deferred. Renal biopsy revealed features of TMA and malignant nephrosclerosis. Patient eventually became dialysis dependent. Aggressive blood pressure control was obtained with multiple medications.


Assuntos
Hipertensão Maligna/complicações , Rim/patologia , Microangiopatias Trombóticas/complicações , Microangiopatias Trombóticas/etiologia , Injúria Renal Aguda/complicações , Injúria Renal Aguda/patologia , Adulto , Negro ou Afro-Americano/etnologia , Anti-Hipertensivos/uso terapêutico , Diagnóstico Diferencial , Humanos , Hipertensão Maligna/diagnóstico , Hipertensão Maligna/tratamento farmacológico , Hipertrofia Ventricular Esquerda/complicações , Hipertrofia Ventricular Esquerda/patologia , Rim/irrigação sanguínea , Masculino , Nefroesclerose/complicações , Nefroesclerose/patologia , Diálise Renal/métodos , Microangiopatias Trombóticas/diagnóstico , Resultado do Tratamento
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