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1.
Ann Fr Anesth Reanim ; 29(9): 621-8, 2010 Sep.
Article in English | MEDLINE | ID: mdl-20634026

ABSTRACT

INTRODUCTION: We determined whether the implementation of a bundle of 10 recommendations leads to the reduction of mortality in ICU patients with severe sepsis or septic shock. METHODS: All patients with severe sepsis or septic shock during two consecutive phases: a 6-month quality control period (observational) and secondly a 6-month intervention period based on the implementation of a bundle of 10 recommendations adapted from the Surviving Sepsis Campaign guidelines (initial bacteriological samples and initiating antibiotics, measurement of arterial lactate, volume expansion > or =20 ml/kg, targeted mean arterial pressure > or =65 mmHg and the assessments of central venous pressure and Scv(O2); glucose control, low doses of corticosteroids, a tidal volume < or =8 ml/kg in mechanically ventilated patients with ALI; adequate use of recombinant human activated protein C) were evaluated in 15 ICUs. The primary endpoint was the 28-day mortality rate and the secondary endpoint was the compliance with the recommendations of the care bundle. MEASUREMENT AND RESULTS: Four hundred and forty-five patients (230 and 215 in the observational and intervention periods, respectively) were included. In the two periods, the patients had similar characteristics. The 28-day mortality rate significantly decreased from 40% in the observational period to 27% in the intervention period (P=0.02). According to each recommendation, compliance with the care bundle was achieved in 9 to 100% of patients. CONCLUSION: The implementation of a care bundle adapted from the Surviving Sepsis Campaign guidelines decreases the 28-day mortality rate in patients with severe sepsis and/or septic shock.


Subject(s)
Sepsis/mortality , Shock, Septic/mortality , Aged , Female , Guideline Adherence , Humans , Male , Middle Aged , Practice Guidelines as Topic , Prospective Studies , Retrospective Studies , Sepsis/prevention & control , Severity of Illness Index , Shock, Septic/prevention & control
2.
Ann Fr Anesth Reanim ; 28(7-8): 658-65, 2009.
Article in French | MEDLINE | ID: mdl-19577408

ABSTRACT

OBJECTIVE: To summarize the benefits and lateral effects of hyaluronidase (H) use in ophthalmologic anaesthesia and to address its unavailability in current practice in France. DATA SOURCES: The Medline data bank and the Cochrane database were consulted. The keywords employed separately or in combination were: H, regional anaesthesia, ophthalmologic surgery, local aneasthetics myotoxicity, diplopia. STUDY SELECTION: Original articles since 1949 were selected. We also selected isolated clinical cases according to their relevance compared with the existing literature. DATA SYNTHESIS: H is a "spreading factor" of animal origin used as an adjuvant in ophthalmic anaesthesia for more than half a century. It allows a moderate better block quality with a slightly quicker onset. It also limits the acute intraocular pressure increase secondary to periocular injection and seems to have a protective effect against local anaesthetics myotoxicity resulting in postoperative strabismus. However, during these last 50 years, numerous studies often ended in divergent results. CONCLUSION: H seems to be a useful adjuvant in ophthalmologic anaesthesia in spite of his current unavailability in France. Recombinant H could be the solution in the near future.


Subject(s)
Adjuvants, Anesthesia , Anesthesia, Conduction , Hyaluronoglucosaminidase/therapeutic use , Ophthalmologic Surgical Procedures , Diplopia/surgery , France , Humans , Hyaluronoglucosaminidase/administration & dosage , Injections , Intraocular Pressure/drug effects , Ophthalmoplegia/chemically induced , Ophthalmoplegia/prevention & control , Postoperative Complications/prevention & control , Protective Agents/therapeutic use , Strabismus/etiology , Strabismus/prevention & control
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