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1.
Respir Care ; 57(3): 363-9, 2012 Mar.
Article in English | MEDLINE | ID: mdl-21968296

ABSTRACT

BACKGROUND: The application of CPAP has been used to minimize postoperative pulmonary complications after lung resection surgery. The aim of this study was to quantify both the CPAP effects upon lung function and functional capacity in early postoperative lung resection, as well as to evaluate if CPAP prolongs air leak through the chest drain. METHODS: Thirty patients in the postoperative period of lung resection were allocated into 2 groups: an experimental group, consisting of 15 patients who underwent a 10 cm H(2)O CPAP, and a 15 patient control group, who performed breathing exercises. Arterial blood gas analysis, peak expiratory flow (PEF), respiratory muscle strength, spirometry, and 6-min walk test (6MWT) were assessed in the preoperative period, and repeated postoperatively on the first and on the seventh day (6MWT was repeated only on the seventh day). RESULTS: Significant increases in PEF, muscle strength, and FEV(1) between the first and seventh postoperative day were observed, both in the experimental and in the control group, whereas FVC and P(aO(2)) increased significantly between the first and seventh postoperative day only in the experimental group. The average loss in 6-min walk distance (6MWD) from preoperative to postoperative day 7 in the experimental group was significantly lower than in control group. When comparing the 2 groups, only 6MWD was statistically different (P < .001). There was no air leakage increase through the drain with the early use of CPAP. CONCLUSION: When compared to breathing exercises, CPAP increases the 6MWD in postoperative lung resection patients, without prolonging air leak through the chest drain.


Subject(s)
Continuous Positive Airway Pressure , Exercise Test , Pneumonectomy , Adolescent , Adult , Aged , Aged, 80 and over , Female , Humans , Lung Diseases/physiopathology , Lung Diseases/surgery , Male , Middle Aged , Pneumonectomy/rehabilitation , Postoperative Period , Recovery of Function , Respiratory Function Tests , Young Adult
2.
Carcinogenesis ; 23(4): 611-6, 2002 Apr.
Article in English | MEDLINE | ID: mdl-11960914

ABSTRACT

Oesophageal cancer is one of the most common and lethal malignancies in the world. Despite many efforts, treatment is still ineffective for most cases; thus, the development of preventive strategies is crucial for decreasing the burden presented by this disease. Environmental factors, particularly nitrosamines, are thought to be involved in the genesis of oesophageal tumours, and knowledge about the expression of enzymes capable of activating pre-carcinogens in human oesophagus is very important for the development of preventive measures. We analysed the expression of CYP1A1, CYP1A2, CYP2A6/2A7, CYP2E1 and CYP3A4 mRNA in oesophageal mucosa of 50 patients by semi-quantitative RT-PCR. In five patients, who suffered from squamous cell carcinoma, we measured Nnitrosodimethylamine and N-nitrosodiethylamine metabolism in normal and tumorous tissue. CYP2A6/2A7 mRNA was expressed in 61% and CYP2E1 mRNA in 96% of the patients, but in the latter a lower degree of inter-individual variation was observed. These enzymes were expressed either in the distal or middle portions of the oesophagus of 90% of the patients. CYP1A1, CYP1A2 and CYP3A4 mRNA expression was not detected in any portion of the oesophagus. Oesophageal microsomes activated N-nitrosodimethylamine with a low degree of inter-individual variation and microsomes prepared from the tumour of a patient who strongly expressed CYP2A6/2A7 mRNA activated N-nitrosodiethylamine. We conclude that the human oesophagus expresses CYP2A6/2A7 and CYP2E1 and can activate nitrosamines. Notably, the expression of these enzymes is preferentially localized to the most common sites where tumours arise.


Subject(s)
Aryl Hydrocarbon Hydroxylases , Cytochrome P-450 CYP2E1/biosynthesis , Cytochrome P-450 Enzyme System/biosynthesis , Esophagus/enzymology , Mixed Function Oxygenases/biosynthesis , Mouth Mucosa/enzymology , Alkylating Agents/metabolism , Carcinoma, Squamous Cell/enzymology , Cytochrome P-450 CYP2A6 , Cytochrome P450 Family 2 , Diethylnitrosamine/metabolism , Dimethylnitrosamine/metabolism , Humans , Microsomes/enzymology , Mouth Neoplasms/enzymology , RNA, Messenger/metabolism , Reverse Transcriptase Polymerase Chain Reaction , Time Factors
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