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1.
Intensive Care Med ; 44(7): 1039-1049, 2018 07.
Artigo em Inglês | MEDLINE | ID: mdl-29808345

RESUMO

PURPOSE: Whether the quality of the ethical climate in the intensive care unit (ICU) improves the identification of patients receiving excessive care and affects patient outcomes is unknown. METHODS: In this prospective observational study, perceptions of excessive care (PECs) by clinicians working in 68 ICUs in Europe and the USA were collected daily during a 28-day period. The quality of the ethical climate in the ICUs was assessed via a validated questionnaire. We compared the combined endpoint (death, not at home or poor quality of life at 1 year) of patients with PECs and the time from PECs until written treatment-limitation decisions (TLDs) and death across the four climates defined via cluster analysis. RESULTS: Of the 4747 eligible clinicians, 2992 (63%) evaluated the ethical climate in their ICU. Of the 321 and 623 patients not admitted for monitoring only in ICUs with a good (n = 12, 18%) and poor (n = 24, 35%) climate, 36 (11%) and 74 (12%), respectively were identified with PECs by at least two clinicians. Of the 35 and 71 identified patients with an available combined endpoint, 100% (95% CI 90.0-1.00) and 85.9% (75.4-92.0) (P = 0.02) attained that endpoint. The risk of death (HR 1.88, 95% CI 1.20-2.92) or receiving a written TLD (HR 2.32, CI 1.11-4.85) in patients with PECs by at least two clinicians was higher in ICUs with a good climate than in those with a poor one. The differences between ICUs with an average climate, with (n = 12, 18%) or without (n = 20, 29%) nursing involvement at the end of life, and ICUs with a poor climate were less obvious but still in favour of the former. CONCLUSION: Enhancing the quality of the ethical climate in the ICU may improve both the identification of patients receiving excessive care and the decision-making process at the end of life.


Assuntos
Unidades de Terapia Intensiva , Cultura Organizacional , Qualidade de Vida , Procedimentos Desnecessários , Fatores Etários , Europa (Continente) , Humanos , Unidades de Terapia Intensiva/ética , Estudos Prospectivos
2.
Minerva Pediatr ; 67(6): 457-63, 2015 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-25034218

RESUMO

AIM: It has been speculated that single incision pediatric endoscopic surgery (SIPES) in children could result in more postoperative pain given the device size for a child umbilicus. Herein, we compare the postoperative pain in children who underwent SIPES or standard laparoscopy (SL). METHODS: Patients who underwent SIPES via Olympus TriPort™ Access system between 2010 and 2011 were prospectively compared with SL controls (similar age, sex and type of operation). Primary endpoint was analgesic requirement (number of doses and dose/kg). A systematic review of the literature included all articles (2008-2012) comparing postoperative pain following transumbilical SIPES and SL in children. Data were analyzed using non-parametric tests. RESULTS: Ten patients (8 males, median age 9 years, range 4-15) underwent 11 SIPES procedures: appendicectomy (N.=6), orchidopexy (N.=2), cholecystectomy (N.=2), and total colectomy (N.=1). There was no difference in paracetamol requirement between SIPES (median 74 mg/kg, range 14-149) and SL (median 59 mg/kg, range 13-108, P=0.76) patients. Morphine was required by only two patients per group (no difference in dosage or frequency). Eight studies (2010-2012) comparing 334 SIPES vs. 343 SL patients were analysed. Three studies showed advantage of SIPES, and four no difference between SIPES and SL. One randomized trial reported greater pain in SIPES appendicectomy, but no difference with SL once patients were discharged home. CONCLUSION: SIPES does not seem to be associated with more postoperative pain than SL in children. In appropriate cases, SIPES is a valid alternative to SL for a good range of pediatric procedures.


Assuntos
Analgésicos/administração & dosagem , Endoscopia/métodos , Laparoscopia/métodos , Dor Pós-Operatória/epidemiologia , Acetaminofen/administração & dosagem , Adolescente , Analgésicos Opioides/administração & dosagem , Apendicectomia/métodos , Criança , Pré-Escolar , Colecistectomia/métodos , Colectomia/métodos , Feminino , Humanos , Masculino , Morfina/administração & dosagem , Orquidopexia/métodos , Dor Pós-Operatória/tratamento farmacológico , Estudos Prospectivos , Umbigo
3.
Clin Exp Allergy ; 44(9): 1200-3, 2014 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-25132278

RESUMO

Inhaled cationic airway lining modulator (iCALM) is a cationic aerosol therapy comprised of 1.29% calcium chloride dissolved in 0.9% isotonic saline that enhances the biophysical barrier function of the airway lining fluid and primes the host defense response. It's ability to attenuate bronchitis caused by inhaled particles was investigated using an allergen-inhalation model in a proof-of-concept study. In a randomized, double-blind, placebo-controlled cross-over trial of 6 mild atopic steroid-naïve asthmatic subjects, 3 doses of iCALM were well tolerated and they attenuated allergen-induced increase in sputum eosinophils, and levels of IL-5, MCP-1 and eotaxin. This study provides an opportunity to investigate the role of enhancing epithelial barrier to decrease airway inflammation provoked by inhaled particles in a variety of airway diseases.


Assuntos
Alérgenos/imunologia , Asma/tratamento farmacológico , Asma/imunologia , Cloreto de Cálcio/uso terapêutico , Cloreto de Sódio/uso terapêutico , Adulto , Aerossóis , Asma/metabolismo , Cloreto de Cálcio/administração & dosagem , Citocinas/sangue , Citocinas/metabolismo , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Cloreto de Sódio/administração & dosagem , Resultado do Tratamento , Adulto Jovem
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