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1.
J Low Genit Tract Dis ; 2(3): 148-50, 1998 Jul.
Article in English | MEDLINE | ID: mdl-25950099

ABSTRACT

OBJECTIVE: Our aim was to test a new cryosurgical wart treatment, dimethylether (Histofreezer), for clinical effi-cacy in newly diagnosed cases of genital warts. METHODS: All patients of the gynecology clinic of a teaching hospital who were at least 12 years of age and who had between one and eight external genital warts were eligible. Treatment occurred at the initial visit and at follow-up visits at 2, 4, 6, and 8 weeks. If all warts were gone at any particular visit, the patient had completed the study and was not required to return. RESULTS: In 14 of 15 patients [93%; 95% confidence interval (Cl), 81-100%], all warts resolved within the 8-week study period. This included 39 of 44 warts (89%; 95% Cl 80-98%). Most warts [35 of 44 (80%)] resolved within 4 weeks. One patient with five warts failed treatment. No known complications were seen. Condusion. Dimethylether (Histofreezer) is an effective cryosurgical treatment for genital warts.

2.
Radiology ; 187(1): 279-83, 1993 Apr.
Article in English | MEDLINE | ID: mdl-8451429

ABSTRACT

Informed consent forms used before intravenous administration of contrast media by both private practice (Pennsylvania Blue Shield) and academic (Association of University Radiologists) physician groups were analyzed to evaluate for readability and content. Most of the 160 consent forms required at least a high school education to be understood; 10 (6%) required a college education. Consent forms from academic institutions tended to be longer and contain more problems with sentence structure than those from private practice. Consent forms from both groups tended to have a weak, wordy writing style. Although most of the consent forms discussed at least some of the potential adverse reactions from intravenous contrast media, 37 (23%) made no mention of any potential adverse reaction. Indeed, 25 (16%) made no mention of contrast media at all. Only 12 (8%) consent forms included a discussion of nonionic contrast media. The authors provide sample consent forms that cover the common risks of ionic and nonionic contrast media and describe the availability of nonionic contrast media; these forms are understandable by an individual reading at only an eighth-grade level.


Subject(s)
Comprehension , Consent Forms , Contrast Media/administration & dosage , Informed Consent , Disclosure , Humans , Injections, Intravenous , Iodine , Risk Assessment
3.
Radiology ; 184(1): 145-8, 1992 Jul.
Article in English | MEDLINE | ID: mdl-1609071

ABSTRACT

The use of informed consent before intravenous administration of contrast material remains a controversial issue. It involves explaining the risks of intravenous contrast material and obtaining the patient's permission for its use. All physician groups who had billed Pennsylvania Blue Shield for at least three intravenous contrast material-enhanced procedures performed in 1989 were surveyed. Informed consent was obtained from at least some patients by about two-thirds of physician groups before using intravenous contrast material, regardless of whether it was ionic or nonionic. Nonradiologists were more likely to obtain informed consent before the use of ionic contrast material than radiologists. Regardless of specialty, practices associated with larger hospitals (greater than 250 beds), larger physician groups (greater than 10), or a university used informed consent less often than smaller physician groups or those associated with a smaller hospital or a private practice. Though results may be affected by regional variation or increased usage since previous surveys, the use of informed consent before the intravenous injection of contrast material is a common practice; it is obtained in the majority of patients.


Subject(s)
Contrast Media , Informed Consent , Attitude of Health Personnel , Consent Forms , Contrast Media/adverse effects , Disclosure , Humans , Informed Consent/legislation & jurisprudence , Medical Staff, Hospital , Pennsylvania , Radiology , Risk Assessment , Risk Factors , Surveys and Questionnaires
4.
Urol Radiol ; 14(3): 218-20, 1992.
Article in English | MEDLINE | ID: mdl-1290217

ABSTRACT

All physicians who had billed Pennsylvania Blue Shield for at least three intravenous contrast studies during 1989 were surveyed on their use of nonionic versus ionic contrast. This surveyed group represents a diversity of hospital sizes, practice types, and group sizes. Of the 383 physician groups surveyed, responses were obtained from 285. The majority of the responding groups were radiologists (94.0%). Nonionic contrast is utilized in 41.3% of all intravenous studies. Radiologists use nonionic contrast in a much greater proportion than nonradiologists (P < 0.0001), with 17.6% of radiologists utilizing nonionic contrast in all of their patients. Conversely, 75% of nonradiologists utilize ionic contrast in all of their patients. For all physician groups surveyed, 40.3% utilize nonionic for at least 50%, while 27.6% use nonionics for more than 75% of their patients. The routine use of steroid premedication prior to the injection of ionic contrast is not a common practice. The increased utilization of nonionic contrast found in this survey may reflect the cross-section of physicians and practice types surveyed or may represent changing practice patterns among physicians utilizing contrast material.


Subject(s)
Contrast Media/administration & dosage , Radiography/statistics & numerical data , Hospital Bed Capacity , Hospitals, University/trends , Humans , Injections, Intravenous , Osmolar Concentration , Physicians' Offices/trends , Private Practice/trends , Radiography/trends , Radiology Department, Hospital/trends , Surveys and Questionnaires , Tomography, X-Ray Computed/statistics & numerical data , Tomography, X-Ray Computed/trends , United States
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