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2.
J Med Screen ; 3(4): 211-5, 1996.
Article in English | MEDLINE | ID: mdl-9041488

ABSTRACT

OBJECTIVES: To study two different procedures for inviting subjects to screening for malignant melanoma, and to study the role of specially trained nurses as primary examiners. METHODS: The study was carried out in Stockholm county and comprised 5000 randomly selected men and women aged 40 to 60, of whom 2,500 were invited with a personal invitation letter and with a set time of appointment and 2,500 were sent a questionnaire and instructions for self examination of the skin. To test the nurses' competence, a survey was made, comparing the judgments of skin examination between nurses and doctors. RESULTS: 1654 (66%) of those invited for a skin examination took part. 1507 (60%) replied in the questionnaire group, of whom 1024 (41%) requested and attended a subsequent skin examination. Of the subjects attending from both groups, the nurses judged 9% v 11% as having skin lesions suggesting malignant melanoma, whereas the two doctors referred 4% v 3% of the subjects for surgical biopsy. Two malignant melanomas were detected, both of them in the questionnaire group. In the study of nurses' screening competence, both nurses and doctors equally judged one case out of 19 as having a lesion suspicious for malignant melanoma. CONCLUSIONS: When the questionnaire method was used the results were achieved with one third fewer skin examinations, but it is difficult to conclude whether one of the procedures is better than the other. The results also indicate that nurses can be trained to be the primary examiners in a melanoma screening programme.


Subject(s)
Mass Screening , Melanoma/epidemiology , Skin Neoplasms/epidemiology , Adult , Clinical Competence , Feasibility Studies , Female , Humans , Male , Middle Aged , Nurses , Physical Examination , Physicians , Program Evaluation , Self-Examination , Surveys and Questionnaires , Sweden/epidemiology
4.
Acta Derm Venereol ; 66(2): 144-8, 1986.
Article in English | MEDLINE | ID: mdl-2424238

ABSTRACT

During a trial of isotretinoin (0.5 mg/kg body weight/day for 3 months) in 90 patients with severe acne, the leucocyte (WBC) count, and particularly the number of neutrophils, decreased significantly. In patients with a good response the mean WBC count fell by 24% and the neutrophils by 33%, whereas in those with a poor response these variables decreased by 8% and 14%, respectively. The serum ALAT, ASAT, cholesterol and triglyceride levels increased significantly. Patients with a poor response (n = 35) received a higher dosage (0.75 mg/kg) for an additional 3 months, and during this period there was a further decrease in the WBC and neutrophil counts and an increase in the triglyceride level. In the other patients, who initially responded well, the dosage was decreased to 0.1 or 0 mg/kg during the second 3-month period, which resulted in reversion of the laboratory variables to the pre-treatment levels. The observed changes were clearly both dose-dependent and reversible.


Subject(s)
Acne Vulgaris/drug therapy , Tretinoin/therapeutic use , Adolescent , Adult , Alanine Transaminase/blood , Aspartate Aminotransferases/blood , Cholesterol/blood , Clinical Trials as Topic , Dose-Response Relationship, Drug , Female , Humans , Isotretinoin , Leukocyte Count/drug effects , Male , Tretinoin/administration & dosage , Tretinoin/adverse effects , Triglycerides/blood
5.
Acta Derm Venereol ; 59(3): 274-6, 1979.
Article in English | MEDLINE | ID: mdl-87094

ABSTRACT

In a double-blind study, 38 adults with scabies were treated with the scabicide Tenutex (a proprietary aqueous emulsion containing 0.5% DDT, 2% disulfiram and 22.5% benzyl benzoate) and 42 patients were treated with a similar emulsion lacking DDT. The treatment consisted of a single whole-body (except for the head) application which was washed off after 24 hours. When examined 3 weeks later, both groups were completely cured. Thereafter, a further 35 patients took part in an open trial with the DDT-free Tenutex emulsion and all patients were cured, irrespective of whether the treatments were administered by skilled personnel or by themselves at home. It is concluded that for the treatment of scabies in Sweden, the most commonly used preparation, Tenutex, can be replaced, without risk of loss of efficacy, by an emulsion containing 2% disulfiram and 22.5% benzyl benzoate, i.e. Tenutex without DDT.


Subject(s)
Benzoates/therapeutic use , Benzyl Compounds/therapeutic use , Disulfiram/therapeutic use , Scabies/drug therapy , Administration, Topical , Adolescent , Adult , Benzoates/administration & dosage , Benzyl Compounds/administration & dosage , Clinical Trials as Topic , DDT/administration & dosage , DDT/therapeutic use , Disulfiram/administration & dosage , Double-Blind Method , Drug Combinations , Drug Evaluation , Emulsions , Humans , Middle Aged
6.
Acta Med Scand ; 198(1-2): 95-9, 1975.
Article in English | MEDLINE | ID: mdl-1166830

ABSTRACT

The iron metabolism has been studied in 11 patients with porphyria cutanea tarda. Despite significantly increased amounts of iron in the serum and liver, the porphyria patients absorb not less but significantly more radioiron than normal controls. Whereas phlebotomy-induced iron deficiency stimulates the absorption in controls, no further stimulation is found in the porphyria patients. The plasma iron turnover is high in the porphyria patients, and some of this iron is probably deposited in the liver. The relationship between the high iron absorption, high plasma iron turnover, high liver iron, liver damage and uroporphyrin production in the liver is discussed. It is suggested that two concurrent genetic defects may cause porphyria cutanea tarda, one in iron absorption and one in porphyrin synthesis by damaged liver cells. The absorption of inorganic iron was higher than that of hemaglobin iron. The possible damage which fortification with inorganic iron could cause to the very small group of porphyria patients is discussed.


Subject(s)
Iron/metabolism , Porphyrias/metabolism , Adult , Aged , Alcohol Drinking , Biopsy, Needle , Bloodletting , Coproporphyrins/urine , Female , Humans , Intestinal Absorption , Liver/metabolism , Liver/pathology , Male , Middle Aged , Porphyrias/therapy , Uroporphyrins/urine
7.
Scand J Soc Med ; 3(1): 13-7, 1975.
Article in English | MEDLINE | ID: mdl-1138350

ABSTRACT

The results of a combined dermatological and surgical treatment of varicose ulcers was studied in 100 patients. This chronic disease, often persisting for decades, was halted in 90 percent of leg operated upon. Even when the general outcome of the treatment was favourable, it was found that, for 5 out of the 12 ulcers which were the same or larger in size at follow-up than before operation, the patient assessed the result as good or even excellent. This finding deserves further study. It indicates that patients and physicians sometimes use different standards by which to measure therapeutic success.


Subject(s)
Varicose Ulcer/therapy , Aged , Consumer Behavior , Evaluation Studies as Topic , Female , Follow-Up Studies , Humans , Male , Middle Aged , Varicose Ulcer/surgery
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