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1.
PLoS One ; 14(10): e0224563, 2019.
Artigo em Inglês | MEDLINE | ID: mdl-31665179

RESUMO

INTRODUCTION: Acute respiratory distress syndrome (ARDS) is characterized by acute, diffuse, inflammatory lung injury leading to increased pulmonary vascular permeability, pulmonary oedema and loss of aerated tissue. Previous literature showed that restrictive fluid therapy in ARDS shortens time on mechanical ventilation and length of ICU-stay. However, the effect of intravenous fluid use on mortality remains uncertain. We investigated the relationship between cumulative fluid balance (FB), time on mechanical ventilation and mortality in ARDS patients. MATERIALS AND METHODS: Retrospective observational study. Patients were divided in four cohorts based on cumulative FB on day 7 of ICU-admission: ≤0 L (Group I); 0-3.5 L (Group II); 3.5-8 L (Group III) and ≥8 L (Group IV). In addition, we used cumulative FB on day 7 as continuum as a predictor of mortality. Primary outcomes were 28-day mortality and ventilator-free days. Secondary outcomes were 90-day mortality and ICU length of stay. RESULTS: Six hundred ARDS patients were included, of whom 156 (26%) died within 28 days. Patients with a higher cumulative FB on day 7 had a longer length of ICU-stay and fewer ventilator-free days on day 28. Furthermore, after adjusting for severity of illness, a higher cumulative FB was associated with 28-day mortality (Group II, adjusted OR (aOR) 2.1 [1.0-4.6], p = 0.045; Group III, aOR 3.3 [1.7-7.2], p = 0.001; Group IV, aOR 7.9 [4.0-16.8], p<0.001). Using restricted cubic splines, a non-linear dose-response relationship between cumulative FB and probability of death at day 28 was found; where a more positive FB predicted mortality and a negative FB showed a trend towards survival. CONCLUSIONS: A higher cumulative fluid balance is independently associated with increased risk of death, longer time on mechanical ventilation and longer length of ICU-stay in patients with ARDS. This underlines the importance of implementing restrictive fluid therapy in ARDS patients.


Assuntos
Respiração Artificial , Síndrome do Desconforto Respiratório/mortalidade , Equilíbrio Hidroeletrolítico , Idoso , Estudos de Coortes , Cuidados Críticos , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Respiração Artificial/estatística & dados numéricos , Síndrome do Desconforto Respiratório/fisiopatologia , Síndrome do Desconforto Respiratório/terapia , Estudos Retrospectivos , Tempo
2.
Crit Care Med ; 40(2): 651-3, 2012 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-21946654

RESUMO

OBJECTIVE: The management of patients with sickle-cell disease and cardiac arrest presents special challenges. Mild therapeutic hypothermia may improve survival and neurologic outcome after cardiac arrest, however, it may also precipitate sickling in patients with sickle-cell disease. Rigorous exchange transfusion may enable mild therapeutic hypothermia after cardiac arrest in patients with sickle-cell disease. DESIGN: Case report. SETTING: A 28-bed closed format intensive care unit in a university hospital. PATIENT: A 41-yr-old man with a double-heterozygous sickle-cell ß-0 thalassemia was admitted to the internal ward for acute chest syndrome. On the third day he developed cardiac arrest. Return of spontaneous circulation was achieved after 45 mins of full cardiopulmonary resuscitation. INTERVENTIONS: Postcardiac arrest rigorous exchange transfusion and mild therapeutic hypothermia were applied. MEASUREMENT AND MAIN RESULT: Erythrocytapheresis lowered the content of hemoglobin S to 5.6%, and therapeutic hypothermia was successfully maintained for 24 hrs without adverse events. After 2 critical weeks, the patient regained full consciousness. CONCLUSION: Therapeutic hypothermia after cardiac arrest is feasible following rigorous exchange transfusion in patients with sickle-cell disease.


Assuntos
Parada Cardíaca/etiologia , Parada Cardíaca/terapia , Hipotermia Induzida/métodos , Talassemia beta/complicações , Adulto , Reanimação Cardiopulmonar/métodos , Terapia Combinada , Progressão da Doença , Transfusão Total/métodos , Seguimentos , Hospitais Universitários , Humanos , Unidades de Terapia Intensiva , Masculino , Medição de Risco , Resultado do Tratamento , Talassemia beta/diagnóstico
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