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1.
BJU Int ; 85(9): 1014-8, 2000 Jun.
Article in English | MEDLINE | ID: mdl-10848686

ABSTRACT

OBJECTIVE: To assess the sensitivity of serum creatinine level in detecting clinically important and early deterioration of renal function in patients with spinal cord injury (SCI), and to evaluate the optimal method of determining creatinine clearance in these patients. PATIENTS AND METHODS: The serum creatinine level of 36 patients (25 paraplegics and 11 quadriplegics) was evaluated and compared with the corresponding measured creatinine clearance rate. Correlations were also assessed between the creatinine clearance measured by 24-h endogenous clearance, single-shot 99mTc-labelled diethylenetriamine pentaacetic acid (99mTc-DTPA) clearance technique, and the Cockcroft-Gault formula, to test their validity. RESULTS: Of the 36 patients 11 (31%) had a measured creatinine clearance of < 100 mL/min (mean 84.8) and a corresponding normal serum creatinine level. Creatinine clearance calculated by the Cockcroft-Gault formula did not correlate well with that measured by the 24-h endogenous clearance (r = 0.426) and 99mTc-DTPA clearance (r = 0. 366), overestimating creatinine clearance in all but three patients. The mean (SD) difference between the creatinine clearance measured by the 24-h and DTPA clearance technique was 17.7 (16.5)% and the correlation between these techniques was good (r = 0.71). CONCLUSION: Serum creatinine level is not sensitive in detecting early deterioration of renal function in patients with SCI. The Cockcroft-Gault formula generally significantly overestimates the true creatinine clearance and is not recommended. The 24-h endogenous creatinine clearance measured on appropriately collected urine samples is an acceptable accurate and practical method of determining glomerular filtration rate in patients with SCI.


Subject(s)
Creatinine/blood , Renal Insufficiency/diagnosis , Spinal Cord Injuries/complications , Adult , Aged , Biomarkers/blood , Biomarkers/urine , Creatinine/urine , Female , Glomerular Filtration Rate/physiology , Humans , Male , Middle Aged , Paraplegia/complications , Quadriplegia/complications , Renal Insufficiency/etiology , Renal Insufficiency/physiopathology , Sensitivity and Specificity , Urinary Bladder, Neurogenic/etiology , Urinary Bladder, Neurogenic/physiopathology
2.
Urology ; 55(3): 408-13, 2000 Mar.
Article in English | MEDLINE | ID: mdl-10699622

ABSTRACT

OBJECTIVES: To assess a newly designed balloon dilation catheter for the treatment of urethral stricture disease. The dilating capability of the catheter, the tolerability and safety of the procedure, and its short-term efficacy were evaluated. METHODS: Fifty-one patients with urethral strictures underwent dilation with the UrethraMax or a coude tip balloon dilation catheter. Efficacy parameters included measurement of the American Urological Association symptom score and maximum urinary flow rate 3, 6, and 12 months after treatment. The adequacy of dilation and the degree of mucosal trauma and hematuria were assessed endoscopically, and patient pain was measured using a visual analog scale. RESULTS: Forty-three patients (84.3%) were successfully dilated, achieving a urethral caliber of 20F or greater. Dilation resulted in statistically significant improvements in both the mean American Urological Association symptom score and mean maximum urinary flow rate at 3 and 6 months. Mucosal trauma was mild in all but 4 cases, and no patient developed significant hematuria. The mean visual analog pain score was 3.9 (range 0.1 to 9.4). CONCLUSIONS: Balloon dilation is a safe, well-tolerated, office-based procedure that theoretically offers several advantages over sequential rigid dilation and internal urethrotomy. It is associated with minimal complications, and its short-term efficacy is acceptable. We regard this as the dilation procedure of choice and first-line therapy for most strictures.


Subject(s)
Catheterization/instrumentation , Urethral Stricture/therapy , Adult , Aged , Aged, 80 and over , Evaluation Studies as Topic , Humans , Male , Middle Aged
3.
J Urol ; 162(5): 1629-32, 1999 Nov.
Article in English | MEDLINE | ID: mdl-10524884

ABSTRACT

PURPOSE: We compare the efficacy of 4 versus 8 mg. doxazosin for benign prostatic hyperplasia. MATERIALS AND METHODS: A total of 82 patients with benign prostatic hyperplasia successfully treated with 4 mg. doxazosin were randomized in a double-blind fashion to take 4 or 8 mg. Patients were evaluated with American Urological Association (AUA) symptom score, Boyarsky score, uroflowmetry and side effect profile before, and 1 and 3 months following randomization. RESULTS: Of the patients 42 and 40 were randomized to receive 4 and 8 mg. doxazosin, respectively. Both groups were similar with respect to patient age, baseline Boyarsky and AUA symptom scores, and baseline maximum urinary flow rate. At 3 months mean improvement from baseline plus or minus standard deviation in Boyarsky score was 0.6 +/- 6.5 and 4.9 +/- 6.6 in the 4 and 8 mg. groups (p <0.05), respectively, mean improvement in AUA symptom score was 1.6 +/- 5.3 and 5.3 +/- 8.0 (p <0.05), and mean maximum flow rate difference was -0.6 +/- 6.4 and +1.4 +/- 7.9 (p >0.05). Of the patients 7 and 8 in the 4 and 8 mg. groups dropped out of the study, and there were no statistical differences in side effects between dosages. CONCLUSIONS: A dose of 8 mg. doxazosin was more efficacious than 4 mg. and the side effects associated with both dosages appeared to be similar. The 8 mg. dose should be tried in patients who have not achieved an adequate therapeutic response to 4 mg. and are tolerating the medication. Consideration should be given to increasing the dosage to 8 mg. in patients who are clinically improved at lower dosages.


Subject(s)
Adrenergic alpha-Antagonists/administration & dosage , Doxazosin/administration & dosage , Prostatic Hyperplasia/drug therapy , Aged , Double-Blind Method , Drug Prescriptions/statistics & numerical data , Humans , Male , Middle Aged
5.
Pharmacotherapy ; 12(2 Pt 2): 2S-10S, 1992.
Article in English | MEDLINE | ID: mdl-1598310

ABSTRACT

The immune system is a complex network of components functioning to provide host defense. This network consists of immunologic cells and their products (e.g., interleukins and colony-stimulating factors), organs, tissues, complement, and major histocompatibility complex antigens. These components are organized into specific and nonspecific immune systems, the major functional activities of which include antigen presentation and cell-mediated cytotoxicity.


Subject(s)
Immune System , Complement System Proteins/physiology , Cytokines/physiology , Cytotoxicity, Immunologic , Humans , Hypersensitivity/immunology , Immune System/cytology , Immune System/immunology , Leukocytes/immunology , Lymphoid Tissue/cytology , Lymphoid Tissue/immunology
7.
Am J Hosp Pharm ; 46(7): 1389-92, 1989 Jul.
Article in English | MEDLINE | ID: mdl-2757046

ABSTRACT

The justification, establishment, and evaluation of a full-service cancer center pharmacy satellite for a university hospital are described. Providing efficient and effective pharmaceutical services was difficult because (1) the cancer center is housed in a freestanding building adjacent to the hospital and (2) there are special considerations inherent in the ordering and preparation of antineoplastic medications. Data collected and presented by the pharmacy, along with letters of support from nursing and medical staff, provided justification of the need to establish an oncology satellite pharmacy. The satellite, open 8.0 hours per day Monday through Friday, is primarily responsible for preparing antineoplastic agents and dispensing first doses of other intravenous and oral medications for the cancer center. Satellite staffing consists of 1.2 full-time-equivalent (FTE) pharmacists and 2.0 FTE technicians. A technician works in the satellite the same number of hours as the pharmacist but is also available to prepare antineoplastic drugs in the central pharmacy on weekends. Pharmacist activities also include providing drug and dosing information to the medical and nursing staff, as well as handling investigational drugs. The satellite pharmacy has decreased medication turnaround time by one-half and has improved pharmaceutical services to the nursing staff.


Subject(s)
Hospital Units/organization & administration , Pharmacy Service, Hospital/organization & administration , Antineoplastic Agents/therapeutic use , Kentucky , Pharmacists
9.
Radiology ; 134(1): 149-54, 1980 Jan.
Article in English | MEDLINE | ID: mdl-7350595

ABSTRACT

Observer accuracy in the identification of low-contrast objects in computed tomography (CT) was studied. Thresholds were established for detection of lesions of various sizes and attenuation differences in CT images produced at different radiation doses. Noise reduction was important in identifying certain types of lesions. Detection was not accurate when the standard deviation of the mean of an organ exceeded the difference in the means of the lesion and the surround region.


Subject(s)
Technology, Radiologic , Tomography, X-Ray Computed/standards , Humans
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