E were included 2007th Admissions were selected for  <a href=”http://www.selleckbio.com/brivanib-S1084.html”>Brivanib VEGFR inhibitor</a> analysis hlt When a malignant hour Dermatological disease as prime Re or secondary Had re reason for the approval or reasons for admission to their medical history. An analysis of the distribution of F Lle and the result was performed on these recordings. A logistic regression analysis was used to analyze the effect of the variable intake on acute hospital mortality. Input variables S were selected a priori Hlt. RESULTS. There were 7689 admissions justified. The mean (SD APACHE II score at admission was 24.4 (7.9. ICU mortality T was 43.1% (3312 deaths and acute hospital mortality 59.2% (4239 Todesf Ll. Hospital mortality T and ICU acute with the number of organ failure during recording.<br> entry features increases with hospital mortality t in patients with a primary Ren or secondary Ren diagnosis of h dermatological malignancies (2980 patients were admitted connected age, previous bone marrow transplantation, Hodgkin’s  <a href=”http://www.selleckbio.com/mln8054-S1100.html”>MLN8054 869363-13-3</a> disease , Lymphoma, length of stay in B Pital before admission, tachycardia, tachypnea, GCS \ 13, sedation, P / F \ 200 mmHg, acidosis, oliguria, Hyponatri chemistry and origin chemistry. factors associated with acute hospital mortality in patients with malignant h dermatological diseases in their medical history (4,361 patients were age, severe sepsis, duration of stay in ‘h Pital prior to admission, hypotension, tachycardia, tachypnea, P / F \ 100 mmHg, low GCS, oliguria , sedation, respiration, blood urea, serum creatinine less than 0.6 l L mol 1, hypo-or Hypernatri anemia, acidosis, An chemistry and alkalaemia.<br> CONCLUSION. acute hospital mortality admissions to intensive care units in England, Wales and Northern Ireland, with h dermatological malignancies almost twice as high ICU admissions others. Mortality increases with the number of failing organs on admission to the ICU, and that the duration of hospital stay increases before admission to the ICU. REFERENCE (. S. 1-Blot F, M Guigeut, Nitenberg G and al.Prognostic factors for neutropenic patients in the intensive care unit. r the respective underlying tumors and organ failure Eur J Cancer 1997, 33:1031 February 7 as Lamia, Hellot. . MF, Girault C, et al Ver changes in the scores of the severity of the St tion and allowed the organ as a prognostic factor in patients with h dermatological malignancies onco to the ICU ICM 2006, 32:.<br> 1560 8 0650 causes risk factors and the Effect of acute renal failure in critically ill patients OBSTETRICS Souissi1 R., N. Baffoun1, W. Trabelsi1, Baccar1 K., H. Souissi2, C. Kaddour1 1Anesthesia. and Critical Care Medicine, National Institute of Neurology, 2Surgery B, H Pital The Rabta The Rabta INTRODUCTION Tunisia. acute renal failure (IRA is a serious complication of pregnancy. It is true independence as a factor Independent mortality tsrisiko in the intensive care unit (ICU and is associated with an increased Hten mortality t. The aim of this study was to determine the causes and identify risk factors and outcome of peripartum ARF. METHODS. A prospective study, open, observational study in a multi-disciplinary Ren ICU. demographic and obstetric management (transfusion, cesarean section, hysterectomy, anesthetic complications, data, etc.<br> were collected and analyzed. ARF as serum creatinine 100 L mol C has been defined / l and / or oliguria \ 150 ml / 8 hours or \ 500 ml / day and / or doubling of serum creatinine at baseline. general scoring systems (SAPS II, APACHE II, APACHE III and organ systems of notation dysfunction were calculated at admission and at t glicher basis. data on SPSS 11.5 for Windows XP compatibility t were calculated. results were taken as mean standard deviation expressed. Statistical analysis was performed based on chi-square and Student t-test corrected by exact test Fisher. RESULTS. Between January 1996 and December 2003, 541 patients at our obstetric intensive care unit were admited. The average age was 31.2 5.9 years, average duration was 34.<br>7 4.5 weeks. Pr eclampsia, eclampsia and peripartum haemorrhage were the main causes associated with ARF. Univariate analysis showed that uterine atony, blood transfusion, multiple pregnancy, vaginal delivery was significantly associated with ARF, w during cesarean section showed an odds ratio ( OR 0.455. multiple regression analysis retained only transfusion before admission to intensive care associated with it as significantly associated with the IRA. oliguria and level of kidney failure are predicting factors of mortality. The overall mortality t was 10.4% (n 57th ARF in 68 patients was found to develop with a mortality t of 33.8% (n 23 The relative risk (RR for mortality t in patients with ARF was 4.7 with an OR of 6.6 means for patients with and without ARF were respectively.<br> 41.1 20.9 21.6 13.7 and for SAPS II, 16 8 7.5 6 63.3 for APACHE II and 31.6 23.8 and 24.4 for APACHE III (P \ 0.01 for all scores was kidney failure usually with at least one other context. organ dysfunction than median SOFA on day 1 (9.3 4.5, demonstrates w while without ARF 3.7 3 (P \ was 0.001. conclusion. ARF is a high mortality t ([assigned to 30%. Aggressive treatment and Pr prevention of renal failure is necessary to improve the prognosis.