Subject(s)
Diabetes Mellitus, Type 1/prevention & control , Adolescent , Child , Child Development , Diabetes Mellitus, Type 1/drug therapy , Diabetes Mellitus, Type 1/nursing , Diabetes Mellitus, Type 1/psychology , Humans , Hypoglycemic Agents/therapeutic use , Insulin/therapeutic use , Pediatric Nursing/methods , Psychology, Adolescent , Psychology, ChildABSTRACT
The aim of this study was to audit the organization of services and management at diagnosis of Type 1 diabetes mellitus (IDDM) in children in the eight districts of East Anglia. Representatives of each district met and agreed indicators of good practice. Service organization was assessed by questionnaire. Provision of care was audited using a proforma completed prospectively for every newly diagnosed child. Outcomes were audited by an anonymous questionnaire to families at the first outpatient appointment to assess satisfaction with care, the education received, and confidence in basic skills needed for home care of diabetes. All districts had a designated paediatric diabetic clinic, all but one led by a paediatrician. All had nurse specialists, but the posts varied widely. Only three units had joint clinics for adolescents. In total, 75% of the families returned the questionnaire. Satisfaction with support by health professionals was high. Education was good for injection technique, blood testing and diet management. Home visits by nurses were variable. Contact with schools and introduction to support groups was poor. Confidence in management was best when there was a dedicated paediatric specialist nurse with adequate cover within the team to allow home and school visits. Following peer review and implementation of an action plan, reaudit was undertaken one year later. Modest improvements were achieved in problem areas; solutions varied in different districts. Collaborative, multi-district audit allows comparison between demographically similar districts. Audit encourages improved practice within existing teams and allows an informed bid for scarce resources.
Subject(s)
Child Health Services/standards , Diabetes Mellitus, Type 1/therapy , Medical Audit , Outcome and Process Assessment, Health Care , Adolescent , Child , Child, Preschool , Diabetes Mellitus, Type 1/epidemiology , Humans , Incidence , Surveys and Questionnaires , United Kingdom/epidemiologyABSTRACT
A simple method for collecting capillary blood for measurement of glycosylated haemoglobin (HbA1c) was developed that allows samples to be obtained at home and then mailed to the laboratory 2 weeks before a hospital visit. A single drop of blood is collected into a 2 ml plastic tube and sent for HbA1c assay on the Diamat HPLC system which has inter- and intra-assay coefficients of variation < 2.6 and < 1.2%, respectively. Results of simultaneously obtained venous and capillary samples in 32 diabetic children agreed well with each other. A separate study of 25 patients was performed to determine whether transport conditions affected the samples. Posted samples were compared with venous samples; again the values were in good agreement. This method is now used routinely in the diabetic clinic. Its value was determined by questionnaire in 40 children with age range 4-17 years. No family experienced difficulty collecting samples and all samples received were suitable for analysis. Children preferred this method to blood collection in the clinic as they felt it was less traumatic and more convenient. Seventy-nine percent of them understood its value in the long-term control of diabetes. In 40.5% of visits changes to management were made at the clinic due to the availability of the results.
Subject(s)
Blood Specimen Collection/methods , Diabetes Mellitus, Type 1/blood , Glycated Hemoglobin/analysis , Adolescent , Analysis of Variance , Capillaries , Child , Child, Preschool , Chromatography, High Pressure Liquid , Female , Humans , Male , Surveys and QuestionnairesABSTRACT
A questionnaire was designed to assess teenagers' knowledge, habits and beliefs in a variety of health education topics. 1,418 (74%) fourth year secondary school pupils participated. The results on smoking, alcohol, drugs, diet and exercise are presented, together with teenagers' own suggestions for improvements in the methods of acquisition of health education messages. A change of emphasis is necessary and an advisory role for the school health service is suggested.
Subject(s)
Health Education/standards , Health Knowledge, Attitudes, Practice , Adolescent , England , Female , Humans , Male , Program Evaluation , Surveys and QuestionnairesABSTRACT
Four unrelated patients are reported with short stature, stiffness of the joints, short fingers, inability to make a fist, and thickened skin on the forearms. Investigations have failed to show a lysosomal storage disorder and radiographs show non-specific changes with a delayed carpal bone age. The clinical features in the four children are very similar to the recently described acromicric dysplasia. There are also similarities to Moore-Federman syndrome which has only been described in one family. The case is made that acromicric dysplasia and Moore-Federman syndrome are the same entity.
Subject(s)
Abnormalities, Multiple/diagnosis , Dwarfism/diagnosis , Face/abnormalities , Hand Deformities, Congenital/diagnosis , Hyperopia/diagnosis , Child , Child, Preschool , Diagnosis, Differential , Female , Genes, Dominant , Humans , Male , SyndromeABSTRACT
A psychotherapist joined the medical team of the paediatric diabetic clinic three years ago. After some initial difficulties all agreed there had been appreciable benefits, not only to individual patients but also to the team in their handling of the psychological aspects of diabetes.
Subject(s)
Diabetes Mellitus, Type 1/psychology , Patient Care Team , Psychotherapy , Adolescent , Child , Diabetes Mellitus, Type 1/genetics , Diabetes Mellitus, Type 1/therapy , England , Family Therapy , Female , Humans , Male , Outpatient Clinics, Hospital , PedigreeABSTRACT
Twenty patients with acute myeloid leukaemia (AML) were treated with a combination of chemotherapy which included daunorubicin, cytosine arabino-side and 6-thioguanine (DAT). The complete remission rate was 85% and was achieved, in responsive cases, after an average of 2 courses of therapy. Patients remained in hospital for an average of 37.5 days during remission-induction therapy and 3.7 days per month thereafter. The median remission period was 48 weeks and median survival was 70 weeks. A disappointing feature was the high relapse rate. This feature of the results re-affirms the need for a more effective form of remission therapy.