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1.
Annals of Thoracic Medicine. 2014; 9 (2): 87-91
in English | IMEMR | ID: emr-141994

ABSTRACT

Patients with obesity hypoventilation syndrome [OHS] have significant morbidity and mortality. Early diagnosis and treatment is important and there are limited data on its prevalence and predictive factors. The objective of this observational study was to determine the frequency and predictors of OHS in hospitalized patients at a tertiary health care institution. All blood gas analyses of hospitalized adult [age over 18 years] patients were prospectively recruited from the biochemistry laboratory at a tertiary health care center between August 2009 and July 2010. Patients who had hypercapnia [PaCO[2] >/= 45 mmHg] while breathing room air were included and clinical and laboratory data were obtained from hospital records. A standard questionnaire was also filled by face-to-face interview with patients and/or relatives. A total of 9480 patients' arterial blood gases were evaluated and 330 patients [3.4%] who met the selection criteria were included in the analysis during the study period. Hypoventilation was associated with acute diseases in 64.2% and chronic diseases in 35.8% of the patients. Of the chronic hypoventilation patients, 24.4% had OHS. Univariate logistic regression analysis showed that, female gender, body mass index [BMI], smoking, PaO[2], SaO[2] and a PaCO[2]/BMI <1.5 were significantly related to OHS. In multivariate logistic regression analysis, BMI >35 kg/m[2], SaO[2] <91.4% and PaCO[2]/BMI <1.5 were significantly related to OHS. A PaCO[2]/BMI <1.5 was an independent variable strongly predictive of OHS [odds ratio: 36.9, 95% of the confidence interval: 2.75-492.95, P = 0.007]. OHS is a common cause of chronic alveolar hypoventilation. A careful examination PaCO[2]/BMI ratio may prevent misdiagnoses among hypercapnic patients.


Subject(s)
Humans , Male , Female , Tertiary Healthcare , Obesity , Hypoventilation , Hypercapnia , Prospective Studies
2.
Saudi Medical Journal. 2012; 33 (2): 146-151
in English | IMEMR | ID: emr-117119

ABSTRACT

To determine predictive fatality criteria based on clinical and laboratory findings on admission to hospital in patients diagnosed with pandemic influenza A [H1N1] virus infection. The study was conducted at the School of Medicine, Karadeniz Technical University, Trabzon, Turkey. Demographic, clinical, and laboratory data for hospitalized cases with a diagnosis of A [H1N1] virus infection between October 2009 and May 2010 were analyzed retrospectively. Patients were divided into 2 groups: fatal [group I] and non-fatal [group II]. The 2 group's demographic, clinical, and laboratory data were compared on admission. Ten [20%] of the 50 patients included in the study died. The average age of group I was significantly higher than that of the group II. No significant difference was observed between the groups in terms of underlying chronic diseases and pregnancy. Fever, phlegm, shortness of breath, tachypnea, cyanosis were observed at significantly higher levels in group I compared to group II. Serum hemoglobin, glucose, albumin levels, arterial oxygen saturation were significantly lower in group I compared to group II; aspartate transaminase, alanine aminotransferase, C-reactive protein, procalcitonin, blood urea nitrogen levels, time between onset of symptoms and commencement of antiviral treatment were all significantly higher in group I. This study shows that in addition to demographic characteristics and clinical findings, prognosis of patients with A [H1N1] virus infection can be determined beforehand with various laboratory tests. But these parameters, which can guide the clinician in the prior identification of potentially fatal A [H1N1] cases will contribute to the provision of supporting treatment and, when necessary, intensive care services for such patients

3.
Medical Principles and Practice. 2011; 20 (2): 181-186
in English | IMEMR | ID: emr-104199

ABSTRACT

The aim of this study was to investigate the effect of early or delayed warfarin administration with unfrac-tionated heparin [UFH] on coagulation parameters in pulmonary thromboembolism [PTE]. This study was performed between November 2006 and July 2007. Thirty-three patients with PTE were sequentially slotted to early [n = 16] and delayed [n = 17] warfarin treatment groups. In the early group, both UFH infusion and warfarin were started simultaneously and in the delayed group, warfarin was added [1-3 days later] based on when partial thromboplastin time reached the therapeutic level with UFH. The proteins C and S, D-dimer, hematocrit levels, and platelet counts for all patients were studied prior to treatment and 6.24, and 48 h after warfarin treatment. In order to determine the overall effect of early and delayed warfarin treatment on clot formation, a thromboelastogram was performed simultaneously. In both groups, a similar chronological decrease in protein C levels reaching maximum at 24 h with warfarin treatment was observed. However, intragroup or intergroup decreases in protein S levels were not different. On thromboelastogram, INTEM and EXTEM clotting times were significantly prolonged chronologically, but this prolongation was not different between groups. The suppressor effect of warfarin on proteins C and S in the early period of double anticoagulant treatment did not appear to aggravate the risk of thrombosis in patients with PTE in whom warfarin was started simultaneously with UFH

4.
Medical Principles and Practice. 2004; 13 (4): 211-214
in English | IMEMR | ID: emr-67713

ABSTRACT

To determine the delay between the onset and the diagnosis and treatment of patients with lung cancer in two cancer centres in the Eastern Black Sea Region of Turkey. Subjects and The records of 226 patients [217 males, 9 females] were evaluated retrospectively for the dates noted for the onset of symptoms, first presentation to a physician, histopathological diagnosis and start of treatment. The median time intervals from the appearance of the first symptom to definitive diagnosis and treatment were calculated. The patients presented to their physicians 30 [range 2-365] days after their complaints began. The time that elapsed between admission and histopathological diagnosis and between the diagnosis and initiation of therapy were 8 [range 1-210] and 17.5 days [range 0-206], respectively. The median time span from presentation to treatment was 30 days [range 1-253]. There were no significant time interval differences between onset of symptoms and first presentation and the subsequent diagnostic and therapeutic processes for histopathology, stage of the tumour and treatment procedures [p > 0.05]. Reasons for the delayed treatment of lung cancer patients were late presentation to the physician and the long time interval between tissue diagnosis and treatment. This delay was mostly associated with a large number of patients and delayed appointments for imaging procedures - the result of organisational problems within the health services of Turkey


Subject(s)
Humans , Male , Time , Retrospective Studies
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