Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 8 de 8
Filter
1.
J Gynecol Obstet Biol Reprod (Paris) ; 40(2): 169-73, 2011 Apr.
Article in French | MEDLINE | ID: mdl-21115305

ABSTRACT

We report a case of placenta percreta with bladder invasion in a multiparous woman with five previous cesarean sections. At 25 weeks of gestation, because of severe hematuria, antenatal diagnosis was easy. A multidisciplinary management was carried out with conservative treatment. Three repeated artery embolizations were necessary because of placenta volume and collateral vessels. None surgical treatment was realized to avoid hemorrhage and morbidity secondary to hysterectomy and partial cystectomy.


Subject(s)
Placenta Accreta/pathology , Placenta Accreta/therapy , Urinary Bladder/pathology , Adult , Embolization, Therapeutic , Female , Gestational Age , Hematuria , Humans , Magnetic Resonance Imaging , Placenta Accreta/diagnosis , Pregnancy
2.
Ann Fr Anesth Reanim ; 28(3): 206-10, 2009 Mar.
Article in French | MEDLINE | ID: mdl-19304443

ABSTRACT

OBJECTIVE: To determine the epidemiology and risk factors for gastric aspiration in a French university hospital. METHODS: Files were prospectively selected from a computer database of rare and severe complications between January 2002 et April 2007. Medical files were then analyzed according to a predetermined list of specific items. RESULTS: Forty patients suffered from gastric aspiration among 117 033 anaesthesias (4 medical files lost) (31/100,000 global incidence). All occurred during general anaesthesia, 83% at induction, 8% in the recovery room, half of the cases for emergent cases (15% of emergency). In emergency, the incidence of gastric aspiration increased by 4.5. Only 14 patients (39%) had a "full stomach", 17 (47%) other risk factors and five (14%) none. A rapid induction-intubation sequence with a Sellick manoeuvre was performed in only 50% of patients with a full stomach and in 23.6% of those with other risk factors. Gastric aspiration occurred in three patients with a laryngeal mask. Aspiration was associated with clinical symptoms in 21 patients. Eleven patients developed an ARDS (5 deaths). DISCUSSION: The incidence of gastric aspiration was slightly higher in this series than in other published series. Rapid induction-intubation sequence with Sellick manoeuvre is not always used in patients with a full stomach. Restraining this technique only to these latter patients does not guarantee practitioners to avoid the risk of gastric aspiration. There is a large need to define which patients are at higher risk of gastric aspiration by national recommendations of clinical practice.


Subject(s)
Anesthesia, General , Intraoperative Complications/epidemiology , Pneumonia, Aspiration/epidemiology , Respiratory Aspiration/epidemiology , Adult , Aged , Emergencies , Female , France/epidemiology , Hospitals, University/statistics & numerical data , Humans , Incidence , Intraoperative Complications/etiology , Intraoperative Complications/prevention & control , Laryngeal Masks/adverse effects , Male , Middle Aged , Organ Size , Pneumonia, Aspiration/etiology , Pneumonia, Aspiration/prevention & control , Postoperative Complications/etiology , Postoperative Complications/mortality , Preoperative Care , Prospective Studies , Respiratory Aspiration/etiology , Respiratory Aspiration/prevention & control , Respiratory Distress Syndrome/etiology , Respiratory Distress Syndrome/mortality , Risk Factors , Stomach
3.
Ann Fr Anesth Reanim ; 28(1): 86-90, 2009 Jan.
Article in French | MEDLINE | ID: mdl-19101109

ABSTRACT

Inherited bleeding disorders contraindicate epidural analgesia because of the risk of epidural haematoma. However, there is no consensus about a minimal rate of factor XI required for its performance. We report here a case of epidural analgesia in a pregnant woman with a moderate and symptomatic factor XI deficiency, despite this theoretical contraindication. Indeed, the factor XI deficiency results in a haemorrhagic risk which is variable and not easily foreseeable. Nevertheless, no neurological after-effect or excessive bleeding occurred although no specific prophylaxis had been performed.


Subject(s)
Analgesia, Epidural/adverse effects , Analgesia, Obstetrical/adverse effects , Factor XI Deficiency/complications , Factor XI/physiology , Adult , Factor XI/therapeutic use , Female , Hemoglobins/metabolism , Hemorrhage/drug therapy , Hemorrhage/epidemiology , Humans , Platelet Count , Pregnancy , Risk Assessment
4.
Ann Fr Anesth Reanim ; 25(4): 417-23, 2006 Apr.
Article in French | MEDLINE | ID: mdl-16310339

ABSTRACT

Because of specific paediatric respiratory physiology (mainly decreased compliance and functional residual capacity, increased O2 demand and CO2 production), ventilators for paediatric anaesthesia need to be powerful and able to deliver small volumes at a high rate without compression volume loss. The compensation of compliance now available on every anaesthesia machine, compensates for the volume of gas lost by compression in the circuit tubing allowing the tidal volume to reach preset commands, even for bellow in box respirators. Preset tidal volume is then totally delivered to the lung by volume-controlled ventilation because it becomes independent of total pulmonary compliance and fresh gas flow. Increased precision of electronic flowmeters and better air-tightness of circuits allow reducing with precision fresh gas flow to values approaching children's O2 consumption and N2O diffusion. New modes of ventilation are now available on anaesthesia machine. Pressure controlled mode, by increasing and maintaining mean airway pressures, ameliorates intrapulmonary gas distribution and compensates for the gas leak from uncuffed tracheal tubes. Unsteady tidal volume resulting from variation of total compliance, is the main drawback of pressure-controlled ventilation that may be overcome by using the "autoflow" mode (better described as a pressure controlled mode ensuring tidal volume) available with one of the last generation of ventilators. Increased accuracy and security of the mode "pressure assist" might increase the use of spontaneous ventilation in paediatric anaesthesia even for low weight children. However tidal volume remains variable with compliance and depth of anaesthesia, which may require several adjustments of ventilator's settings. The clinical conditions (mainly airway control) of pressure assist use for children less than 10 kg should be elucidated before recommending its use.


Subject(s)
Anesthesiology/trends , Pediatrics/trends , Respiration, Artificial/instrumentation , Anesthetics, Inhalation/administration & dosage , Child , Child, Preschool , Compliance , Equipment Design , Humans , Infant , Monitoring, Intraoperative , Nitrous Oxide/administration & dosage , Oxygen/administration & dosage , Pressure , Respiration, Artificial/trends , Tidal Volume
5.
Best Pract Res Clin Anaesthesiol ; 19(3): 399-413, 2005 Sep.
Article in English | MEDLINE | ID: mdl-16013690

ABSTRACT

Even when anaesthesia does not represent a major part of the expense of a given surgical operation, reducing costs is not negligible because the large number of patients passing through a department of anaesthesia accounts for a huge annual budget. Volatile anaesthetics contribute 20% of the drug expenses in anaesthesia, coming just behind the myorelaxants; however, the cost of halogenated agents has potential for savings because a significant part of the delivered amount is wasted when a non- or partial-rebreathing system is used. The cost of inhaled agents is related to more than the amount taken up; it also depends on their market prices, their relative potencies, the amount of vapour released per millilitre of liquid, and last but not least the fresh-gas flow rate (FGF) delivered to the vaporizer--the most important factor determining the cost of anaesthesia. Poorly soluble agents like desflurane and sevoflurane facilitate the control of low-flow anaesthesia and reduce the duration of temporary high-flow phases to rapidly wash in or adjust the circuit gas concentrations. Modelling low-flow or minimal-flow anaesthesia will help anaesthetists to understand the kinetics of inhaled agents in those circumstances and to design their own clinical protocols. The monitoring facilities present on modern anaesthesia machines should convince clinicians that low- or even minimal-flow anaesthesia would not jeopardize the safety of their patients. Cost containment requires primarily a decrease in FGFs, but it may also be influenced by a rational use of the available halogenated agents. Isoflurane, the cheapest generic agent, might be advantageous for maintenance of anaesthesia of less than 3 hours. Sevoflurane is the agent of choice for inhalational induction and might also be used for maintenance. Desflurane might be preferred for long anaesthetics where rapid recovery will generate savings in the PACU.


Subject(s)
Anesthesia, Inhalation/economics , Anesthesia, Inhalation/instrumentation , Anesthesiology/economics , Anesthesiology/instrumentation , Animals , Drug Costs , Drug Utilization , Humans
6.
Ann Fr Anesth Reanim ; 24(1): 13-8, 2005 Jan.
Article in French | MEDLINE | ID: mdl-15661459

ABSTRACT

OBJECTIVES: To evaluate the efficacy of continuous infusion of nefopam. Indeed this analgesic is commonly used by continuous infusion by many anaesthetists to reduce its adverse effects. However whether the analgesic effect of an intermittent administration of nefopam has been proven, the efficacy of continuous infusion has not been established. STUDY DESIGN: Double-blind placebo controlled prospective randomised study. PATIENTS AND METHODS: Sixty patients ASA 1 to 3 undergoing planned urological surgery with laparotomy were included. At the end of surgery, bolus doses of placebo (Group 3) or nefopam 20 mg (Group 1 and 2) were administered to all the patients. Placebo (Group 3), nefopam 80 mg (Group 1) or 120 mg (Group 2) was thereafter continuously infused over 24 hours. All patients received additional analgesia with PCA morphine. We measured pain at rest and on cough with VAS. Adverse side effects such as nausea and vomiting, sedation and respiratory depression were evaluated. Mental performance was measured with mini mental status tests. RESULTS: Patients were older in the placebo group by approximately six years but anesthetic and surgical variables were not different between groups. Pain at rest and on cough was not statistically different between groups. In the placebo group, the median (interquartile range) morphine consumption reached 29 mg (13-53) whereas in patients receiving 80 and 120 mg nefopam, it levelled to 44 mg (11-54) and 35 mg (9-82) respectively (p > 0.05). Patients needed morphine during the same time period whether they received nefopam or not. Patients suffering from adverse effects were similar between groups. CONCLUSION: In this study, continuous administration of nefopam did not reduce morphine consumption nor ameliorate analgesia and thus may not be recommended in urological surgery. Nefopam pharmacokinetics when used with continuous infusion as well as surgery types and differences in age between groups may explain these results.


Subject(s)
Analgesics, Non-Narcotic/therapeutic use , Nefopam/therapeutic use , Pain, Postoperative/drug therapy , Urologic Surgical Procedures, Male , Aged , Analgesia, Patient-Controlled , Analgesics, Non-Narcotic/administration & dosage , Analgesics, Non-Narcotic/adverse effects , Analgesics, Opioid/administration & dosage , Analgesics, Opioid/therapeutic use , Double-Blind Method , Humans , Infusions, Intravenous , Laparotomy , Male , Middle Aged , Morphine/administration & dosage , Morphine/therapeutic use , Nefopam/administration & dosage , Nefopam/adverse effects , Neuropsychological Tests , Postoperative Nausea and Vomiting/epidemiology , Prospective Studies
7.
Ann Fr Anesth Reanim ; 23(6): 581-8, 2004 Jun.
Article in French | MEDLINE | ID: mdl-15234723

ABSTRACT

OBJECTIVES: To evaluate in high-risk patients and in usual clinical conditions, the efficiency of treatments based on an algorithm on late (24 h) postoperative nausea and vomiting (PONV). STUDY DESIGN: Prospective and descriptive. METHODS: The nature and efficiency of prophylactic and curative PONV treatments was evaluated 24 h after surgery under general anesthesia in patients at high risk of PONV, one and 15 month after the introduction of a clinical and therapeutic algorithm. A risk score based on the type of surgery and patients characteristics determined the prophylactic treatment: high risk = droperidol 1.25 mg + ondansetron 4 mg; moderate risk = droperidol 1.25 mg. Cost of prophylactic and curative treatment was calculated according to the exact number of vials of antiemetics used. RESULTS: The use of the therapeutic algorithm leads to a reduction of PONV by a half (47.7% of 109 patients in 1999 vs. 24.5% of 102 patients in 2001) while twice more patients received a prophylactic treatment (32.1% vs. 75.5%). The number of patients needed to be treated (NNT) according to the algorithm to avoid PONV was 1.8 in this high-risk population. However, the relative risk to have PONV was only reduced by 66% with the combination of two antiemetics in 2001 and 22.5% patients still suffered from PONV despite the double prophylactic treatments. The relative risk of PONV without prophylactic treatment was spontaneously reduced by 25% between the two study periods (54% vs. 40%). After 15 months, the recommendations were followed in 43.1% of patients. A curative treatment was given in the same percentage of patients in 2001 and 1999 (63.4% vs. 68%), but followed the recommendations in fivefold more patients (47% vs. 9.1%). The cost of PONV treatment (prophylactic and curative) was increased by 3.5-fold between the two periods ( 55 for 109 patients vs. 190 for 102 patients). CONCLUSION: The use of a PONV therapeutic algorithm based on a scored risk was associated to a lower reduction of late PONV than already published in the literature while the cost was increased as expected. This suggests the efficacy of antiemetic prophylactic treatment might have been overestimated by large multicenter trials and is less in usual clinical conditions. Thus local evaluation of practice is required by performing quality insurance programs.


Subject(s)
Algorithms , Postoperative Nausea and Vomiting/economics , Postoperative Nausea and Vomiting/epidemiology , Adult , Aged , Antiemetics/economics , Antiemetics/therapeutic use , Costs and Cost Analysis , Droperidol/therapeutic use , Drug Therapy, Combination , Female , Humans , Male , Middle Aged , Ondansetron/therapeutic use , Postoperative Nausea and Vomiting/prevention & control , Prospective Studies , Risk Assessment
8.
Ann Fr Anesth Reanim ; 22(8): 697-703, 2003 Oct.
Article in French | MEDLINE | ID: mdl-14522388

ABSTRACT

OBJECTIVES: To report the efficiency and direct cost induced by a quality insurance programme (QIP) aimed to reduce the incidence of post-operative nausea and vomiting (PONV) in the post-anaesthesia care unit. TYPE OF STUDY: Prospective and descriptive study. METHODS: The occurrence and treatment of PONV were prospectively recorded in the post-anaesthesia care unit in a standardised file before and following therapeutic recommendations made by volunteers component of a QIP. Prophylaxis was administered to patients according to a score of risks based on the type of surgery and patient characteristics. The real cost induced by this change of practice was evaluated according to pharmacists' accounts over 1 year. RESULTS: The QIP was associated to a 33.5% reduction of PONV relative risk and a 50% increase in prophylactic treatments. When this reduction of PONV was extrapolated to the total number of anaesthesia over 1 year, this QIP avoided PONV in 770 patients each year. The increase of cost reached 3572 as the cost by patient receiving a prophylactic treatment increased from 0.66 to 1. CONCLUSION: Despite an increase in the individual cost of PONV prophylaxis, the selection of patients by a "home" score of risk limits the indications of prophylactic treatment. Thus the increase in cost remains in acceptable ranges.


Subject(s)
Postoperative Nausea and Vomiting/economics , Quality Assurance, Health Care , Adult , Anesthesia Recovery Period , Antiemetics/economics , Antiemetics/therapeutic use , Cost-Benefit Analysis , Drug Costs , Female , Humans , Male , Middle Aged , Pharmacy Service, Hospital/economics , Postoperative Nausea and Vomiting/prevention & control , Prospective Studies
SELECTION OF CITATIONS
SEARCH DETAIL
...