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101.
Between January 1980 and July 1983, percutaneous transluminal angioplasty was attempted on 137 stenotic renal arteries in 100 patients. At termination of follow-up studies (3-39 months, mean of 16 months), 70% of those treated for hypertension had benefited from the procedure. Stenosis secondary to fibromuscular dysplasia responded better than stenosis from arteriosclerosis (85% and 65% of the patients, respectively). Benefit was minimal for those with stenosis of the renal artery ostium or renal insufficiency. Determining levels of renal vein renin before angioplasty is helpful in selecting patients; following angioplasty, this has considerable significance in predicting the success of the procedure.  相似文献   
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Lufkin  RB; Hanafee  WN; Wortham  D; Hoover  L 《Radiology》1986,158(3):747-754
Forty patients with disorders of the larynx or hypopharynx were studied with magnetic resonance (MR) imaging. Axial, coronal, and sagittal sections, 4 mm thick, were obtained. Twenty-eight of the patients underwent computed tomography (CT) scanning; 17 underwent surgery, and specimens were obtained for organ sectioning. Correlation was made between these three studies as well as with clinical history, physical examination, and endoscopic photography. In 13 patients who underwent all three studies, the depiction of cartilage invasion, adenopathy, and intraorgan and extraorgan spread of disease was compared. MR consistently showed superior soft-tissue definition and extent of disease compared with CT. Neither CT nor MR was able to depict histologic detail or microscopic spread of disease. Both studies were also less effective in the postoperative or postirradiated neck. The use of direct coronal and sagittal imaging planes on MR allowed the visualization of intrinsic laryngeal musculature, which was important in the recognition of subtle tumor extension. For these reasons, surface coil MR imaging is currently the imaging study of choice at our institution for disorders of the larynx and hypopharynx.  相似文献   
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Incidence rates and death rates for acute myocardial infarction (AMI) were compared in New South Wales and Queensland to investigate whether changes in death rates were correlated with changes in incidence rates. The incidence of AMI was 1.9 per cent higher for males and 14.9 per cent lower for females in Queensland than in New South Wales. Differences in age-specific incidence rates paralleled differences in age-specific death rates, suggesting that observed changes in death rates may reflect changes in incidence, rather than case-fatality. Risk factor patterns are broadly similar between the two states, apart from the prevalence of cigarette smoking which, like the incidence of AMI, is higher in males and lower in females in Queensland.  相似文献   
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RB Parad 《Pediatrics》1998,101(5):851-855
OBJECTIVES: To assess the application of DNA-based cystic fibrosis transmembrane conductance regulator (CFTR) gene mutation analysis as a primary cystic fibrosis (CF) diagnostic test in preterm and term newborns and infants for whom the quantitative pilocarpine iontophoresis test (QPIT) cannot be used. DESIGN: Retrospective survey. SETTING: DNA Diagnostic Laboratory, Children's Hospital, Boston, Massachusetts. Buccal cell DNA samples were received from inpatients, outpatients, and three neonatal intensive care units. OUTCOME MEASURE: Detection of at least 1 of 12 CFTR mutations. PATIENTS: Between November 1, 1992, and April 30, 1994, 28 newborns and infants under 12 months of age at risk for CF had CFTR DNA mutation analysis performed because a sweat chloride (SC) value could not be obtained. QPIT was either not performed (infant weight <2 kg, QPIT not available at site of hospitalization, or infant not accessible to QPIT laboratory) or was inconclusive (sweat volume <75 mg or indeterminate SC [>/=40, <60 mEq/L]). The postnatal age at time of testing ranged from 1 day to 11 months, and gestational age at birth from 25 to 40 weeks. RESULTS: Six (21%) of 28 infants with unobtainable or indeterminate QPIT had 1 or 2 CFTR mutations detected. Immediate CF diagnosis by direct detection of 2 CFTR mutations was made in 5 of these 6 patients. Definitive CF diagnosis in the infant with 1 CFTR mutation was delayed until an elevation in SC could be documented. The patients with no CFTR mutations detected had a low likelihood of CF. CONCLUSIONS: For infants in whom CF is suspected but QPIT cannot be obtained, buccal cell DNA-based CFTR mutation analysis can be used as a rapid, noninvasive primary diagnostic test. This simple mode of DNA collection may aid in the diagnosis of other inherited disorders in newborns.  相似文献   
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OBJECTIVES: Estimate pregnancy, abortion, and birth rates for 1990 to 1995 for all teens, sexually experienced teens, and sexually active teens. DESISN: Retrospective analysis of national data on pregnancies, abortions, and births. Participants. US women aged 15 to 19 years. OUTCOME MEASURES: Annual pregnancy, abortion, and birth rates for 1990 to 1995 for women aged 15 to 19 years, with and without adjustments for sexual experience (ever had intercourse), and sexual activity (had intercourse within last 3 months). RESULTS: Approximately 40% of women aged 15 to 19 years were sexually active in 1995. Teen pregnancy rates were constant from 1990 to 1991. From 1991 to 1995, the annual pregnancy rate for women aged 15 to 19 years decreased by 13% to 83.6 per 1000. The percentage of teen pregnancies that ended in induced abortions decreased yearly; thus, the abortion rate decreased more than the birth rate (21% vs 9%). From 1988 to 1995, the proportion of sexually experienced teens decreased nonsignificantly. CONCLUSIONS: After a 9% rise from 1985 to 1990, teen pregnancy rates reached a turning point in 1991 and are now declining. Physicians should counsel their adolescent patients about responsible sexual behavior, including abstinence and proper use of regular and emergency contraception.  相似文献   
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