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1.
Ann Burns Fire Disasters ; 28(1): 5-8, 2015 Mar 31.
Article in English | MEDLINE | ID: mdl-26668555

ABSTRACT

Abdominal compartment syndrome (ACS) occurs when increasing intra abdominal-pressure (IAP) reduces blood flow to abdominal organs. This results in impairment of pulmonary, cardiovascular, renal, hepatic, central nervous system and gastro-intestinal (gi) function, causing multiple organ dysfunction syndrome and death. The significant prognostic value of elevated intra-abdominal pressure has prompted many intensive care units to adopt measurement of this physiologic parameter as a routine vital sign in patients at risk. ACS generally occurs in patients who are critically ill due to any of a wide variety of medical and surgical conditions. it has been recently described as a rare complication of burn injury. it is fundamental to: 1) recognize IAP and ACS; 2) resuscitate effectively; and 3) prevent the development IAP-induced end-organ dysfunction and failure. We present our recent experience with one patient suffering from ACS secondary to burn injury and the physiologic results of abdominal wall escharotomy.


Le syndrome du compartiment abdominal (SCA) se produit lorsque l'augmente de la pression intra-abdominale (PIA) réduit le flux sanguin vers les organes abdominaux. Il en résulte une dépréciation de pulmonaires, cardiovasculaires, rénales, hépatiques, système nerveux central et la fonction (GI) gastro-intestinale, causant le syndrome de défaillance multiviscérale et la mort. La valeur pronostique de la pression intra-abdominale élevée a incité de nombreuses unités de soins intensifs à adopter la mesure de ce paramètre physiologique comme un signe vital de routine chez les patients à risque. Le SCA se produit généralement chez des patients gravement malades en raison d'une grande variété de conditions médicales et chirurgicales. Il a récemment été décrit comme une complication rare associée aux brûlures. Il est fondamental de: 1) reconnaître la PIA et le SCA; 2) ressusciter efficacement; et 3) prévenir le développement de la dysfonction et la défaillance des organes cibles induites par la PIA. Nous présentons notre expérience récente d'un patient souffrant du SCA suite aux brûlures et les résultats physiologiques d'une escarrotomie de la paroi abdominale.

2.
J BUON ; 10(4): 499-504, 2005.
Article in English | MEDLINE | ID: mdl-17357207

ABSTRACT

PURPOSE: To evaluate the effectiveness of 6-month therapy with leucovorin (LV)+5-fluorouracil (5-FU) versus 12-month therapy with levamisole (LVS)+5-FU, as adjuvant chemotherapy in patients with completely resected Aster-Coller stage B(2) or C(1)/C(2) rectal cancer (RC). PATIENTS AND METHODS: One hundred and fifty patients with surgically resected RC were enrolled. Seventy patients with stage B(2) and 80 with stage C were randomly assigned to adjuvant chemotherapy with 5-FU+LXx6 months or 5-FU+LVSx12 months. Patient characteristics were equally balanced between the examined groups. Adjuvant chemotherapy consisted of LV 20 mg/m(2) intravenously (i.v.) plus 5-FU 450 mg/m(2) i.v. bolus every week plus LVS tablets 50 mg t.i.dx3 days every 2 weeks for 1 year. RESULTS: After a median follow up for survivors of 8.7 years (range 1.8-10.5), all of the patients were evaluable. There were no significant differences between the two treatment groups with respect to the recurrence rates (p=0.821). Moreover, there were no significant differences between the two tratment groups in disease-free survival (DFS) (p=0.84) [B(2)(p=0.805) and C (p=0.978)] and overall survival (OS) rates for patients of either stage B(2) or C (p=0.78). Toxicities were more frequent in the 5-FU+LVS versus 5-FU+LV group: myelosuppression (grade 3 leucopenia, 12 versus 4%, p<0.04), diarrhea (grade 0, 60 versus 76%, p<0.02), and liver toxicity (increase of transaminases >3-fold, 12 patients versus 2, p<0.03.). No patient stopped chemotherapy because of toxicity, and there were no treatment-related deaths. CONCLUSION: Adjuvant chemotherapy in RC with LV+5-FU for 6 months is equally effective and less toxic than LVS+5-FU for 12 months.

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