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1.
Pharmacopsychiatry ; 44(5): 165-8, 2011 Jul.
Article in English | MEDLINE | ID: mdl-21751125

ABSTRACT

INTRODUCTION: Although several adverse effects of antidepressants on the gastrointestinal tract have been described (bleeding, constipation, dolichocolon), their influence on gallbladder motility was not investigated.The aim of our study was to investigate the effects of selected antidepressants on gallbladder emptying in patients with major depression. METHODS: The study was set up as an open clinical trial, with the same intervention (ingestion of test meal provoking gallbladder emptying) undertaken in 112 patients with major depression. There were 30 patients not taking antidepressants (the control group), 25 patients taking amitriptyline, 30 patients taking maprotiline, and 27 patients taking fluoxetine. The volume of gallbladder in the study patients was measured by ultrasonography before the test meal, and 15, 30, 45 and 60 min after the meal. RESULTS: 1 h after ingestion of the study meal, the amitriptyline group showed incomplete gallbladder emptying (F=10.829, df=3, p=0.000; mean residual volume 11.0±6.1 mL), while in the control, maprotiline and fluoxetine groups emptying of gallbladder was complete (mean residual volumes 5.0±3.3 mL, 5.6±3.7 mL and 5.7±2.3 mL, respectively). DISCUSSION: In patients with cholecystitis, it would be wise to use antidepressants which do not impair gallbladder emptying, like maprotiline or fluoxetine, and to avoid amitriptyline.


Subject(s)
Amitriptyline/adverse effects , Depressive Disorder, Major/drug therapy , Fluoxetine/adverse effects , Gallbladder Emptying/drug effects , Gallbladder/pathology , Maprotiline/adverse effects , Adolescent , Adult , Aged , Antidepressive Agents/adverse effects , Case-Control Studies , Depressive Disorder, Major/complications , Female , Gallbladder/diagnostic imaging , Gallbladder/drug effects , Humans , Male , Middle Aged , Organ Size/drug effects , Ultrasonography
2.
Int J Artif Organs ; 27(10): 848-54, 2004 Oct.
Article in English | MEDLINE | ID: mdl-15560679

ABSTRACT

BACKGROUND: Temporary hemodialysis catheters are necessary in patients with uremia, but complications associated with these catheters represent one of the most important sources of morbidity among ESRD patients. There is no general agreement about the optimal venous access for insertion of a central venous catheter, while risk factors of catheter related complications have not been entirely elucidated. METHODS: One hundred and seven consecutive patients who required a temporary hemodialysis catheter were prospectively examined. RESULTS: Catheters were placed in 107 consecutive patients (66 right jugular (JC), 41 right femoral (FC)) and maintained in situ for a cumulative total of 2101 days. Early complications (puncture site hemorrhage, hematoma formation, artery puncture) were infrequent, without clinical sequelae. The main late complication was catheter related bacteremia (CRB). There were 16 episodes of CRB (JC-10; FC-6) and Staphylococcus aureus was the most frequently isolated cause of CRB. The mean catheter duration before the onset of CRB was 19.9 and 18.2 days for JC and FC, respectively. Duration of catheter use, and the number of hemodialyses significantly increased the risk for CRB. Actuarial survival for FC was significantly worse than for JC, while Cox proportional hazard models revealed that the femoral site, chronic renal failure and kidney transplantation increased the risk of catheter failure significantly. CONCLUSION: CRB was the most common late complication. Its frequency was similar in JC and FC. The main risk factors for development of CRB were duration of catheter use and the number of performed dialyses. Cumulative hazard of CRB was significantly magnified 3 weeks after insertion for both JC and FC, but actuarial survival with JC was significantly longer.


Subject(s)
Catheterization, Central Venous , Catheters, Indwelling , Renal Dialysis/instrumentation , Renal Insufficiency/therapy , Bacteremia/etiology , Bacterial Infections/etiology , Catheterization, Central Venous/adverse effects , Catheters, Indwelling/adverse effects , Equipment Design , Equipment Failure , Female , Femoral Vein , Hematoma/etiology , Hemorrhage/etiology , Humans , Iliac Vein , Jugular Veins , Male , Middle Aged , Multivariate Analysis , Proportional Hazards Models , Prospective Studies , Punctures/adverse effects , Risk Factors , Time Factors , Venous Thrombosis/etiology
4.
Ren Fail ; 21(2): 177-87, 1999 Mar.
Article in English | MEDLINE | ID: mdl-10088178

ABSTRACT

One of the most important characteristics of chronic renal failure (CRF) is its progression to end stage renal disease. CRF progression depends of many factors indicated in numerous experimental and clinical studies. The present study was undertaken with the aim to examine the role of sex, etiology of CRF, renal function at the beginning of the study, hypertension and protein intake on CRF progression. Ninety-two patients (47 female and 45 male) aged between 17 and 70, with various underlying kidney diseases and various degrees of CRF were followed for 8 years. CRF progression was expressed as Creatinine clearance (CCr) and reciprocal values of serum Creatinine (SCr) against time. CRF progression was slower in women than in men, but not significantly. Patients with diabetic nephropathy (b = 0.00006) and glomerulonephritis (b = 0.00005) had faster progression of CRF than patients with nephrosclerosis (b = 0.00002), tubulointerstitial nephritis (b = 0.00003) and polycystic kidney disease (b = 0.00003). The fastest progression of CRF was in patients with the lowest SCr values at the beginning of the study. Proper regulation of blood pressure was the most important factor in slowing down CRF progression, independently of kind of antihypertensive drugs. Neither angiotensin converting enzyme inhibitors (b = -0.00001) nor calcium channel blockers (b = -0.00002) showed better effects on CRF progression slowing down in comparison with other antihypertensive drugs (b = -0.00001). Low protein diet slowed down CRF progression, but not significantly. In conclusion, our retrospective study confirms that CRF progression depends on sex, underlying renal diseases and serum Creatinine levels at the beginning of the study. Good regulation of blood pressure and low protein diet can slow down CRF progression.


Subject(s)
Kidney Failure, Chronic/etiology , Adolescent , Adult , Aged , Antihypertensive Agents/therapeutic use , Blood Pressure/drug effects , Creatinine/blood , Diet, Protein-Restricted , Disease Progression , Female , Follow-Up Studies , Humans , Kidney Failure, Chronic/physiopathology , Kidney Failure, Chronic/prevention & control , Male , Middle Aged , Retrospective Studies , Risk Factors , Sex Factors
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