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2.
Rev Med Interne ; 43(10): 622-625, 2022 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-36089427

RESUMO

Hemophagocytic syndrome is a rare life-threatening disorder that can be triggered by various conditions such as HIV infection and opportunistic agents. We report a case of disseminated toxoplasmosis complicated with severe hemophagocytic syndrome and revealing an unknown acquired immunodeficiency syndrome. The patient presented with multiple organ failure in intensive care unit. Once diagnosed, he benefitted from etoposide infusion, administration of specific anti-toxoplasmosis treatments and secondary antiretroviral therapy. He was alive at intensive care unit discharge and returned home with little sequalae. This case illustrates both the importance of rapid investigations of hemophagocytic syndrome etiologies in HIV positive patients and the necessity to prompt etoposide and specific treatments in order to improve potentially dramatic outcomes.


Assuntos
Síndrome da Imunodeficiência Adquirida , Infecções por HIV , Linfo-Histiocitose Hemofagocítica , Toxoplasmose , Síndrome da Imunodeficiência Adquirida/complicações , Síndrome da Imunodeficiência Adquirida/diagnóstico , Etoposídeo/uso terapêutico , Infecções por HIV/complicações , Infecções por HIV/diagnóstico , Humanos , Linfo-Histiocitose Hemofagocítica/complicações , Linfo-Histiocitose Hemofagocítica/diagnóstico , Masculino , Toxoplasmose/complicações , Toxoplasmose/diagnóstico
4.
Rev Med Interne ; 41(6): 368-374, 2020 Jun.
Artigo em Francês | MEDLINE | ID: mdl-32008801

RESUMO

INTRODUCTION: Blended-learning methods could be a response to student nonattendance. Non-compulsory teaching combining e-learning/interactive face-to-face sessions has been implemented at Paris-Diderot Medical School for the teaching of intensive care and emergency medicine during the 2018/2019 university period. The aim of the study was to assess this newly-implemented blended teaching. METHODS: Questionnaire submitted to the 388 DFASM3 medical students present at the faculty exam of intensive care/emergency medicine. Attendance at a teaching modality was defined by the follow-up of more than half of this teaching modality. Correlations between attendance at e-learning and/or interactive face-to-face sessions, and grade were performed. RESULTS: A total of 358/388 (92%) students participated in this survey. A quarter of the students (88/321 - 25%) reported they usually attended at traditional lectures. Regarding blended-learning, 210/317 (67%) students reported having attended at e-learning courses and 84/321 (27%) attended at interactive face-to-face sessions. The distribution of students according to their attendance at e-learning and/or interactive face-to-face sessions was significantly different (P<0.01). There was a significant correlation (P<0.001) between attendance at e-learning and grade obtained at the faculty exam. Nevertheless, this correlation was also found for these students in another course taught traditionally. Overall, 309/315 (98%) students were satisfied with the blended teaching, 297/318 (93%) wanted its extent to the whole medical school's curriculum. CONCLUSION: The use of combined learning methods reached more students than traditional teachings and allowed the University to focus on its role of knowledge transfer.


Assuntos
Cuidados Críticos , Educação Médica/métodos , Avaliação Educacional , Medicina de Emergência/educação , Práticas Interdisciplinares/métodos , Absenteísmo , Cuidados Críticos/métodos , Cuidados Críticos/organização & administração , Currículo , Educação a Distância/métodos , Educação a Distância/organização & administração , Educação Médica/organização & administração , Medicina de Emergência/métodos , Medicina de Emergência/organização & administração , Hospitais Universitários/organização & administração , Humanos , Ciência da Implementação , Práticas Interdisciplinares/organização & administração , Paris , Satisfação Pessoal , Faculdades de Medicina/organização & administração , Estudantes de Medicina/psicologia , Inquéritos e Questionários , Visitas de Preceptoria/métodos , Visitas de Preceptoria/organização & administração
6.
Rev Mal Respir ; 35(4): 430-440, 2018 Apr.
Artigo em Francês | MEDLINE | ID: mdl-29754841

RESUMO

INTRODUCTION: Outpatient treatment of community-acquired pneumonia (CAP) patients with non-steroidal anti-inflammatory drugs (NSAIDs) is frequent, although this is not based on clinical recommendations and there is no scientific evidence supporting better symptom relief in comparison to acetaminophen. STATE OF THE ART: Experimental data suggest that NSAIDs alter the intrinsic functions of neutrophils, limit their locoregional recruitment, alter bacterial clearance and delay the resolution of inflammatory processes during acute bacterial pulmonary challenge. In hospitalized children and adults with CAP, observational data suggest a strong and independent association between the outpatient exposure to NSAIDs and the occurrence of pleuropulmonary complications (pleural empyema, excavation, and abscess). In the only study taking into account possible protopathic bias, the association still persists. Other markers of morbidity have been described, including delay in hospital management, prolonged antibiotic therapy, and higher transfer rate to an intensive care unit. PERSPECTIVES: Data describing the role of self-medication and the biological mechanisms involved are needed. CONCLUSIONS: Intake of NSAIDs during outpatient treatment of CAP is probably the second modifiable factor of morbidity after inadequate antibiotic therapy. In light of existing data in children and adults, health authorities should urgently reassess the risk-benefit ratio of NSAIDS in CAP.


Assuntos
Anti-Inflamatórios não Esteroides/uso terapêutico , Infecções Comunitárias Adquiridas/tratamento farmacológico , Pneumonia/tratamento farmacológico , Adulto , Antibacterianos/uso terapêutico , Anti-Inflamatórios não Esteroides/efeitos adversos , Criança , Infecções Comunitárias Adquiridas/epidemiologia , Comorbidade , Humanos , Pneumonia/epidemiologia , Fatores de Risco , Automedicação/efeitos adversos
8.
Rev Med Interne ; 37(3): 166-72, 2016 Mar.
Artigo em Francês | MEDLINE | ID: mdl-26827272

RESUMO

BACKGROUND: The year 2016 will be pivotal for the evaluation of French medical students with the introduction of the first computerized National Ranking Test (ECNi). The SIDES, online electronic system for medical student evaluation, was created for this purpose. All the universities have already organized faculty exams but few a joint computerized ranking test at several universities simultaneously. We report our experience on the organization of a mock ECNi by universities Paris Descartes, Paris Diderot and Paris 13. METHODS: Docimological, administrative and technical working groups were created to organize this ECNi. Students in their fifth year of medical studies, who will be the first students to sit for the official ECNi in 2016, were invited to attend this mock exam that represented more than 50% of what will be proposed in 2016. A final electronic questionnaire allowed a docimological and organizational evaluation by students. An analysis of ratings and rankings and their distribution on a 1000-point scale were performed. RESULTS: Sixty-four percent of enrolled students (i.e., 654) attended the three half-day exams. No difference in total score and ranking between the three universities was observed. Students' feedback was extremely positive. Normalized over 1000 points, 99% of students were scored on 300 points only. Progressive clinical cases were the most discriminating test. CONCLUSION: The organization of a mock ECNi involving multiple universities was a docimological and technical success but required an important administrative, technical and teaching investment.


Assuntos
Computadores , Avaliação Educacional/métodos , Docentes de Medicina , Retroalimentação , Estudantes de Medicina , Inquéritos e Questionários , Universidades , Atitude do Pessoal de Saúde , Comportamento do Consumidor , Docentes de Medicina/psicologia , Humanos , Paris , Satisfação Pessoal , Universidades/organização & administração , Universidades/normas
9.
Intensive Care Med ; 40(2): 211-219, 2014 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-24275900

RESUMO

PURPOSE: The use of heat and moisture exchangers (HME) during noninvasive ventilation (NIV) can increase the work of breathing, decrease alveolar ventilation, and deliver less humidity in comparison with heated humidifiers (HH). We tested the hypothesis that the use of HH during NIV with ICU ventilators for patients with acute respiratory failure would decrease the rate of intubation (primary endpoint) as compared with HME. METHODS: We conducted a multicenter randomized controlled study in 15 centers. After stratification by center and type of respiratory failure (hypoxemic or hypercapnic), eligible patients were randomized to receive NIV with HH or HME. RESULTS: Of the 247 patients included, 128 patients were allocated to the HME group and 119 to the HH group. Patients were comparable at baseline. The intubation rate was not significantly different: 29.7% in the HME group and 36.9% in the HH group (p = 0.28). PaCO2 did not significantly differ between the two arms, even in the subgroup of hypercapnic patients. No significant difference was observed for NIV duration, ICU and hospital LOS, or ICU mortality (HME 14.1 vs. HH 21.5%, p = 0.18). CONCLUSIONS: In this study, the short-term physiological benefits of HH in comparison with HME during NIV with ICU ventilators were not observed, and no difference in intubation rate was found. The physiologic effects may have been obscured by leaks or other important factors in the clinical settings. This study does not support the recent recommendation favoring the use of HH during NIV with ICU ventilators.


Assuntos
Umidade , Intubação/estatística & dados numéricos , Ventilação não Invasiva/instrumentação , Insuficiência Respiratória/terapia , Ventiladores Mecânicos , Idoso , Feminino , Temperatura Alta , Humanos , Unidades de Terapia Intensiva , Masculino , Pessoa de Meia-Idade , Estudos Prospectivos
10.
Reanimation ; 22(Suppl 2): 336-342, 2013.
Artigo em Francês | MEDLINE | ID: mdl-32288733

RESUMO

Treatment of acute respiratory distress syndrome (ARDS) has been subject to many researches, sometimes leading to intense controversy. New findings in this field are varied. Effects on prognosis of commonly used treatments for ARDS have recently been investigated. Consistently, prone position, previously known to improve oxygenation without effect on mortality, has been shown to improve survival of the most severely hypoxemic patients. Administration of neuromuscular blocking agents in the acute phase of ARDS has been also shown to be beneficial on survival. In contrast, the exact place of extracorporeal membrane oxygenation (ECMO) in ARDS management remains to be defined despite data suggesting its possible efficiency. In addition, a new era of research has emerged with the advent of cell therapy. Mesenchymal stem cells are able to both promote alveolar epithelium repair and prevent infections. Their efficacy in animal models of ARDS still needs to be confirmed by clinical trials. Finally, other promising therapies including beta-2 adrenergic agonists and omega-3 fatty acids have shown significant limitations in large clinical studies on ARDS.

11.
Ann Fr Anesth Reanim ; 31(10): 802-5, 2012 Oct.
Artigo em Francês | MEDLINE | ID: mdl-22925937

RESUMO

Amniotic fluid embolism is a relatively rare clinical entity and with difficult medical recognition. However, it is the second leading cause of maternal mortality. We report here the case of a 32-year-old patient who underwent elective caesarean section complicated by an amniotic fluid embolism with cardiac arrest. The presence of a major disseminated intravascular coagulation favored the occurrence of a retroperitoneal hematoma of iatrogenic origin on attempt of femoral venous catheterization and that of hemoperitoneum on bleeding of an hepatic adenoma. The diagnostic of amniotic fluid embolism was confirmed by the presence of amniotic cells in the bronchoalveolar lavage. The patient survived without sequelae.


Assuntos
Adenoma/terapia , Coagulação Intravascular Disseminada/complicações , Embolia Amniótica/etiologia , Parada Cardíaca/etiologia , Hemoperitônio/terapia , Complicações Intraoperatórias/terapia , Neoplasias Hepáticas/terapia , Adulto , Líquido da Lavagem Broncoalveolar/citologia , Cateterismo Periférico , Cesárea , Coagulação Intravascular Disseminada/terapia , Embolia Amniótica/terapia , Feminino , Veia Femoral , Parada Cardíaca/terapia , Hemoperitônio/complicações , Humanos , Doença Iatrogênica , Recém-Nascido , Gravidez , Gravidez de Gêmeos , Espaço Retroperitoneal , Resultado do Tratamento
12.
Minerva Anestesiol ; 78(7): 836-41, 2012 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-22531566

RESUMO

Use of high flow nasal cannula oxygen (HFNC) is increasingly popular in adult ICUs for patients with acute hypoxemic respiratory failure. This is the result of the successful long-term use of HFNC in the neonatal field and recent clinical data in adults indicating beneficial effects of HFNC over conventional facemask oxygen therapy. HFNC rapidly alleviates symptoms of respiratory distress and improves oxygenation by several mechanisms, including deadspace washout, reduction in oxygen dilution and in inspiratory nasopharyngeal resistance, a moderate positive airway pressure effect that may generate alveolar recruitment and an overall greater tolerance and comfort with the interface and the heated and humidified inspired gases. Indications of HFNC are broad, encompassing most if not all causes of acute hypoxemic respiratory failure. HFNC can also provide oxygen during invasive procedures, and be used to prevent or treat post-extubation respiratory failure. HFNC may also alleviate respiratory distress in patients at a palliative stage. Although observational studies suggest that HFNC might reduce the need for intubation in acute hypoxemic respiratory failure; such a reduction has not yet been demonstrated. Beyond this potential additional effect on outcome, the evidence already published argues in favor of the large use of HFNC as first line therapy for acute respiratory failure.


Assuntos
Oxigenoterapia/métodos , Insuficiência Respiratória/terapia , Administração Intranasal , Extubação , Resistência das Vias Respiratórias/efeitos dos fármacos , Humanos , Hipóxia/terapia , Medidas de Volume Pulmonar , Oxigênio/administração & dosagem , Oxigênio/farmacologia , Oxigenoterapia/efeitos adversos , Cuidados Paliativos , Respiração com Pressão Positiva , Resultado do Tratamento
13.
Circulation ; 124(8): 901-11, 1-7, 2011 Aug 23.
Artigo em Inglês | MEDLINE | ID: mdl-21810660

RESUMO

BACKGROUND: In animal models of cardiac arrest, the benefit afforded by hypothermia is closely linked to the rapidity of the decrease in body temperature after resuscitation. Because total liquid ventilation (TLV) with temperature-controlled perfluorocarbons induces a very rapid and generalized cooling, we aimed to determine whether this could limit the post-cardiac arrest syndrome in a rabbit model. We especially focused on neurological, cardiac, pulmonary, liver and kidney dysfunctions. METHODS AND RESULTS: Anesthetized rabbits were submitted to either 5 or 10 minutes of untreated ventricular fibrillation. After cardiopulmonary resuscitation and resumption of a spontaneous circulation, the animals underwent either normothermic life support (control) or therapeutic hypothermia induced by TLV. The latter procedure decreased esophageal and tympanic temperatures to 32°C to 33°C within only 10 minutes. After rewarming, the animals submitted to TLV exhibited an attenuated neurological dysfunction and decreased mortality 7 days later compared with control. The neuroprotective effect of TLV was confirmed by a significant reduction in brain histological damages. We also observed limitation of myocardial necrosis, along with a decrease in troponin I release and a reduced myocardial caspase 3 activity, with TLV. The beneficial effects of TLV were directly related to the rapidity of hypothermia induction because neither conventional cooling (cold saline infusion plus external cooling) nor normothermic TLV elicited a similar protection. CONCLUSIONS: Ultrafast cooling instituted by TLV exerts potent neurological and cardiac protection in an experimental model of cardiac arrest in rabbits. This could be a relevant approach to provide a global and protective hypothermia against the post-cardiac arrest syndrome.


Assuntos
Reanimação Cardiopulmonar , Fluorocarbonos , Parada Cardíaca/terapia , Hipotermia Induzida/métodos , Traumatismo por Reperfusão/prevenção & controle , Animais , Modelos Animais de Doenças , Coração/fisiologia , Parada Cardíaca/mortalidade , Parada Cardíaca/fisiopatologia , Rim/fisiologia , Ventilação Líquida , Fígado/fisiologia , Pulmão/fisiologia , Fenômenos Fisiológicos do Sistema Nervoso , Coelhos , Traumatismo por Reperfusão/mortalidade , Traumatismo por Reperfusão/fisiopatologia , Fatores de Tempo , Fibrilação Ventricular/mortalidade , Fibrilação Ventricular/fisiopatologia , Fibrilação Ventricular/terapia
15.
Eur Respir J ; 35(4): 795-804, 2010 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-19741030

RESUMO

The aim of the present study was to examine whether prone positioning (PP) affects ventilator associated-pneumonia (VAP) and mortality in patients with acute lung injury/adult respiratory distress syndrome. 2,409 prospectively included patients were admitted over 9 yrs (2000-2008) to 12 French intensive care units (ICUs) (OUTCOMEREA). The patients required invasive mechanical ventilation (MV) and had arterial oxygen tension/inspiratory oxygen fraction ratios <300 during the first 48 h. Controls were matched to PP patients on the PP propensity score (+/-10%), MV duration longer than that in PP patients before the first turn prone, and centre. VAP incidence was similar in the PP and control groups (24 versus 13 episodes.1,000 patient-days MV(-1) respectively, p = 0.14). After adjustment, PP did not decrease VAP occurrence (HR 1.64 (95% CI 0.70-3.84); p = 0.25) but significantly delayed hospital mortality (HR 0.56 (95% CI 0.39-0.79); p = 0.001), without decreasing 28-day mortality (37% in both groups). Post hoc analyses indicated that PP did not protect against VAP but, when used for >1 day, might decrease mortality and benefit the sickest patients (Simplified Acute Physiology Score >50). In ICU patients with hypoxaemic acute respiratory failure, PP had no effect on the risk of VAP. PP delayed mortality without decreasing 28-day mortality. PP >1 day might decrease mortality, particularly in the sickest patients.


Assuntos
Hipóxia/mortalidade , Hipóxia/terapia , Pneumonia , Decúbito Ventral , Respiração Artificial/efeitos adversos , Respiração Artificial/mortalidade , Doença Aguda , Idoso , Estudos de Casos e Controles , Bases de Dados Factuais/estatística & dados numéricos , Feminino , Mortalidade Hospitalar , Humanos , Incidência , Unidades de Terapia Intensiva/estatística & dados numéricos , Estimativa de Kaplan-Meier , Masculino , Pessoa de Meia-Idade , Pneumonia/etiologia , Pneumonia/mortalidade , Pneumonia/prevenção & controle , Valor Preditivo dos Testes , Modelos de Riscos Proporcionais , Insuficiência Respiratória/mortalidade , Insuficiência Respiratória/terapia , Fatores de Risco
17.
Ann Fr Anesth Reanim ; 27(3): 237-9, 2008 Mar.
Artigo em Francês | MEDLINE | ID: mdl-18281185

RESUMO

Idiopathic chronic eosinophilic pneumonia (ICEP) is one of the idiopathic hypereosinophilic lung diseases. ICEP differs from idiopathic acute eosinophilic pneumonia (IAEP) by its progressive onset, and the absence of severe hypoxemia. We report a case of acute respiratory distress syndrome revealing an ICEP, which needed a 48h of mechanical ventilation. ICEP is an exceptional cause of acute respiratory failure. Symptoms always improve with corticosteroids. But relapses are frequent after stopping corticosteroid treatment, as well as the occurrence of severe asthma. Distinction between ICEP and IAEP is essential because of its impact on treatment duration and on prognosis.


Assuntos
Eosinofilia Pulmonar/diagnóstico , Síndrome do Desconforto Respiratório/etiologia , Doença Aguda , Adulto , Doença Crônica , Diagnóstico Diferencial , Dispneia/etiologia , Humanos , Masculino , Prognóstico
18.
Eur Respir J Suppl ; 42: 2s-9s, 2003 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-12945994

RESUMO

During mechanical ventilation, high end-inspiratory lung volume (whether it be because of large tidal volume (VT) and/or high levels of positive end-expiratory pressure) results in a permeability type pulmonary oedema, called ventilator-induced lung injury (VILI). Previous injury sensitises lung to mechanical ventilation. This experimental concept has recently received a resounding clinical illustration after a 22% reduction of mortality was observed in acute respiratory distress syndrome patients whose VT had been reduced. In addition, it has been suggested that repetitive opening and closing of distal units at low lung volume could induce lung injury but this notion has been challenged both conceptually and clinically after the negative results of the Acute Respiratory Distress Syndrome clinical Network Assessment of Low tidal Volume and Elevated end-expiratory volume to Obviate Lung Injury (ARDSNet ALVEOLI) study. Experimentally and clinically, involvement of inflammatory cytokines in VILI has not been unequivocally demonstrated. Cellular response to mechanical stretch has been increasingly investigated, both on the epithelial and the endothelial side. Lipid membrane trafficking has been thought to be a means by which cells respond to stress failure. Alterations in the respiratory system pressure/volume curve during ventilator-induced lung injury that include decrease in compliance and position of the upper inflection point are due to distal obstruction of airways that reduce aerated lung volume. Information from this curve could help avoid potentially harmful excessive tidal volume reduction.


Assuntos
Lesão Pulmonar , Pulmão/fisiopatologia , Respiração Artificial/efeitos adversos , Humanos , Respiração com Pressão Positiva , Síndrome do Desconforto Respiratório/fisiopatologia , Síndrome do Desconforto Respiratório/terapia , Volume de Ventilação Pulmonar
20.
Am J Respir Crit Care Med ; 164(4): 627-32, 2001 Aug 15.
Artigo em Inglês | MEDLINE | ID: mdl-11520727

RESUMO

UNLABELLED: The hypothesis that the changes in the respiratory system pressure- volume (PV) curve during pulmonary edema mainly reflect distal airway obstruction was investigated in rats. Normal rats had a well-defined upper inflection point (UIP) at low airway pressure. Airway occlusion by liquid instillation decreased compliance (Crs) and the volume (Vuip) of the UIP, and increased end-inspiratory pressure. The same changes were observed during the progression of edema produced by high volume ventilation (HV). Changes in Vuip and in Crs produced by HV were correlated with edema severity in normal rats or rats with lungs preinjured with alpha-naphthylthiourea. Vuip and Crs changes were proportional, reflecting compression of the PV curve on the volume axis and suggesting reduction of the amount of ventilatable lung at low airway pressure. In keeping with this explanation, the lower Vuip and Crs were before HV, the more severe HV-induced edema was in alpha-naphthylthiourea-injected rats. When edema was profuse, PV curves displayed a marked lower inflection point (LIP), the UIP at low pressure disappeared but another was seen at high volume above the LIP, and the correlation between Vuip changes and edema severity was lost. These observations may have clinical relevance in the context of the "open lung" strategy. KEYWORDS: ventilator-induced lung injury; respiratory mechanics; acute respiratory distress syndrome


Assuntos
Resistência das Vias Respiratórias , Modelos Animais de Doenças , Complacência Pulmonar , Medidas de Volume Pulmonar , Edema Pulmonar/fisiopatologia , Síndrome do Desconforto Respiratório/fisiopatologia , Animais , Capacidade Inspiratória , Masculino , Valor Preditivo dos Testes , Edema Pulmonar/induzido quimicamente , Edema Pulmonar/classificação , Edema Pulmonar/etiologia , Ratos , Ratos Wistar , Análise de Regressão , Respiração Artificial/efeitos adversos , Síndrome do Desconforto Respiratório/induzido quimicamente , Síndrome do Desconforto Respiratório/classificação , Síndrome do Desconforto Respiratório/etiologia , Índice de Gravidade de Doença , Tioureia/análogos & derivados
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