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1.
J Clin Endocrinol Metab ; 99(8): E1459-65, 2014 Aug.
Article in English | MEDLINE | ID: mdl-24840812

ABSTRACT

CONTEXT: Viral/bacterial infection is proposed as a trigger for the autoimmune thyroid diseases (AITD): Graves' disease (GD) and Hashimoto's thyroiditis (HT). Previous studies in European Caucasian AITD subjects found higher birth rates in the autumn/winter, suggesting those born in the autumn/winter experience increased viral/bacterial exposure after birth, impacting upon immune system development and predisposing to AITD later in life. OBJECTIVE: Month of birth effects were investigated in three independent European Caucasian AITD datasets. DESIGN: Variation in GD and HT onset was compared across months and seasons, with fluctuations across all 12 months analyzed using a Walter-Elwood test. SETTING: The study was conducted at a research laboratory. PATIENTS: National UK Caucasian AITD Case Control Collection (2746 GD and 502 HT compared with 1 423 716 UK births), National UK Caucasian GD Family Collection (239 GD and 227 unaffected siblings), and OXAGEN AITD Caucasian Family Collection (885 GD, 717 HT, and 794 unaffected siblings of European Caucasian decent). MAIN OUTCOME MEASURES: Case-control and family-based association studies were measured. RESULTS: No consistent month of birth effects were detected in GD females or males across all three collections. In HT females from the OXAGEN AITD Caucasian Family Collection, slightly higher birth rates were detected in autumn (Walter's test statistic = 7.47, P = .024) however, this was not seen in the HT females from the case-control cohort. CONCLUSION: Our results suggest in UK/Northern European Caucasian GD subjects, month of birth does not impact on AITD development. Although some month of birth effects for HT females in one collection cannot be excluded, only further work in larger European Caucasian AITD collections can confirm these effects.


Subject(s)
Parturition/immunology , Seasons , Thyroiditis, Autoimmune/epidemiology , Case-Control Studies , Disease Susceptibility/epidemiology , Europe/epidemiology , Female , Humans , Male , Risk Factors , Siblings , Time Factors , United Kingdom/epidemiology , White People
2.
Med Teach ; 33(2): e75-83, 2011.
Article in English | MEDLINE | ID: mdl-21275537

ABSTRACT

BACKGROUND: The UK Department of Health is considering a single, generic multi-source feedback (MSF) questionnaire to inform revalidation. METHOD: Evaluation of an implementation pilot, reporting: response rates, assessor mix, question redundancy and participants' perceptions. Reliability was estimated using Generalisability theory. RESULTS: A total of 12,540 responses were received on 977 doctors. The mean time taken to complete an MSF exercise was 68.2 days. The mean number of responses received per doctor was 12.0 (range 1-17) with no significant difference between specialties. Individual question response rates and participants' comments about questions indicate that some questions are less appropriate for some specialities. There was a significant difference in the mean score between specialities. Despite guidance, there were significant differences in the mix of assessors across specialties. More favourable scores were given by progressively more junior doctors. Nurses gave the most reliable scores. CONCLUSIONS: It is feasible to electronically administer a generic questionnaire to a large population of doctors. Generic content is appropriate for most but not all specialties. The differences in mean scores and the reliability of the MSF between specialties may be in part due to the specialty differences in assessor mix. Therefore the number and assessor mix should be standardised at specialty level and scores should not be compared across specialties.


Subject(s)
Employee Performance Appraisal/methods , Feedback , Licensure/legislation & jurisprudence , Peer Group , Physicians , Clinical Competence , Humans , Medicine , United Kingdom
4.
Am J Med ; 123(2): 183.e1-9, 2010 Feb.
Article in English | MEDLINE | ID: mdl-20103030

ABSTRACT

BACKGROUND: Common autoimmune disorders tend to coexist in the same subjects and to cluster in families. METHODS: We performed a cross-sectional multicenter study of 3286 Caucasian subjects (2791 with Graves' disease; 495 with Hashimoto's thyroiditis) attending UK hospital thyroid clinics to quantify the prevalence of coexisting autoimmune disorders. All subjects completed a structured questionnaire seeking a personal and parental history of common autoimmune disorders, as well as a history of hyperthyroidism or hypothyroidism among parents. RESULTS: The frequency of another autoimmune disorder was 9.67% in Graves' disease and 14.3% in Hashimoto's thyroiditis index cases (P=.005). Rheumatoid arthritis was the most common coexisting autoimmune disorder (found in 3.15% of Graves' disease and 4.24% of Hashimoto's thyroiditis cases). Relative risks of almost all other autoimmune diseases in Graves' disease or Hashimoto's thyroiditis were significantly increased (>10 for pernicious anemia, systemic lupus erythematosus, Addison's disease, celiac disease, and vitiligo). There was relative "clustering" of Graves' disease in the index case with parental hyperthyroidism and of Hashimoto's thyroiditis in the index case with parental hypothyroidism. Relative risks for most other coexisting autoimmune disorders were markedly increased among parents of index cases. CONCLUSION: This is one of the largest studies to date to quantify the risk of diagnosis of coexisting autoimmune diseases in more than 3000 index cases with well-characterized Graves' disease or Hashimoto's thyroiditis. These risks highlight the importance of screening for other autoimmune diagnoses if subjects with autoimmune thyroid disease present with new or nonspecific symptoms.


Subject(s)
Graves Disease/complications , Graves Disease/epidemiology , Hashimoto Disease/complications , Hashimoto Disease/epidemiology , Adult , Age Distribution , Aged , Cluster Analysis , Cohort Studies , Cross-Sectional Studies , Female , Genetic Predisposition to Disease , Graves Disease/genetics , Hashimoto Disease/genetics , Humans , Male , Middle Aged , Prevalence , Risk , Sex Distribution , United Kingdom/epidemiology
5.
Arch Ophthalmol ; 126(7): 891-5, 2008 Jul.
Article in English | MEDLINE | ID: mdl-18625933

ABSTRACT

OBJECTIVE: To investigate the feasibility, acceptability, efficacy, and cost of a newly developed translucent shield that can be fixed by sutures to the orbital rim for a month of amblyopia therapy. METHODS: In an institutional review board-approved protocol for patients with amblyopia who do not adhere to the use of conventional patching, shield occluders were fashioned from heat-moldable sturdy black or translucent (20/4000) plastic with holes drilled for attachment. Under brief general anesthesia, patients aged 5 to 10 years had a thorough examination before the shield occluder was sewn to the brow and cheek of the nonamblyopic eye with 3-0 monofilament polypropylene sutures. RESULTS: Ten children completed this protocol from December 1999 through January 2002. All tolerated the occluder for 12 to 36 days. The resultant skin scars were acceptable to parents, patients, and investigators. The amblyopic eyes improved from a mean (SD) of 0.77 (0.30) logMAR (Snellen equivalent, 20/119) to 0.45 (0.29) logMAR (Snellen equivalent, 20/57), a change of 0.32 (0.16) logMAR lines. There was no damage to the sound (occluded) eye. CONCLUSION: Sew-on occluder shields are an alternative when adherence to the use of other types of patching (often referred to as compliance with patching) is not satisfactory.


Subject(s)
Amblyopia/therapy , Biocompatible Materials , Ophthalmology/instrumentation , Polymers , Sensory Deprivation , Suture Techniques , Child , Child, Preschool , Feasibility Studies , Female , Health Care Costs , Humans , Male , Ophthalmologic Surgical Procedures , Ophthalmology/economics , Polypropylenes , Sutures , Treatment Outcome , Visual Acuity
6.
Clin Med (Lond) ; 8(2): 144-8, 2008 Apr.
Article in English | MEDLINE | ID: mdl-18478855

ABSTRACT

Clinical responsibility is an area that requires extensive consideration and development to align with other changes in healthcare in the NHS. Increasing levels of litigation and investigation into the practice of medical practitioners have highlighted the need for clearer guidance for doctors. Using hypothetical case studies, this project explored the understandings and experiences of physicians and potential solutions in areas where there was ambiguity in clinical responsibility. In addition, existing policy and practice within trusts throughout the UK was analysed. The output from the focus group discussion and policy analysis led to the recommendations and guidance for doctors outlined in this paper, with the aim of illustrating the central themes that both doctors and trusts need to address in the future.


Subject(s)
Clinical Medicine/standards , Continuity of Patient Care/standards , Physician's Role , Quality Assurance, Health Care , Humans , Organizational Policy , Patient Transfer/standards , Social Responsibility , United Kingdom
7.
Clin Med (Lond) ; 8(2): 155-6, 2008 Apr.
Article in English | MEDLINE | ID: mdl-18478858

ABSTRACT

The Royal College of Physicians has completed a survey of Members and Fellows to ascertain opinions about the development of specialist standards and the applicability of potential methods/evidence for specialist recertification. Of 985 respondents, 68.6% felt that 11 of the suggested methods would be appropriate for specialist practice and most of these would also be applicable to sub-specialist practice. More than two thirds agreed that it was appropriate to include evidence related to the performance of the clinical team for individual recertification. Respondents expressed concern about the current appraisal process but many felt that it could be effective if it was strengthened and consistently applied.


Subject(s)
Certification , Medicine/standards , Physicians/standards , Specialization , Clinical Competence/standards , Humans , Surveys and Questionnaires , United Kingdom
15.
Clin Med (Lond) ; 5(5): 460-4, 2005.
Article in English | MEDLINE | ID: mdl-16268327

ABSTRACT

The aim of revalidation is to reassure the public that doctors are up to date and fit to practise. The Royal College of Physicians has developed various programmes of work, both ongoing and under development, in support of revalidation. The purpose of this work is to provide guidance for doctors about the standards of practice expected and the types of evidence required for revalidation. A range of methods and tools are outlined that could be used by doctors to demonstrate their commitment to evaluating and reflecting on the way they practise medicine. These methods include ways of assessing both professional standards and clinical competence. Although the conclusions of the Chief Medical Officer in terms of the absolute requirements for revalidation are still unknown, the College is committed to supporting its Members and Fellows to prepare for revalidation through setting educational, professional and clinical standards in medicine.


Subject(s)
Clinical Competence/standards , Quality Assurance, Health Care/methods , Societies, Medical , United Kingdom
19.
Clin Endocrinol (Oxf) ; 59(2): 145-55, 2003 Aug.
Article in English | MEDLINE | ID: mdl-12864790

ABSTRACT

Millions of women are treated with hormone replacement therapy (HRT) for relief of menopausal symptoms, including vasomotor flushes and sweats for which oestrogen is uniquely and highly effective. Others may continue longer-term treatment in the hope that HRT will help to prevent chronic disease. The preservation of bone mass with continuing oestrogen therapy and reduction of subsequent risk of fracture is well established. Observational studies of the metabolic and vascular effects of oestrogens have suggested a potential benefit in reducing the risk of vascular disease, but recently published randomized controlled trials demonstrate no evidence of benefit in women with established vascular disease or in apparently healthy women. The increased risks of breast cancer and thromboembolic disease have been confirmed in these trials, with evidence of increased risk of stroke. Observational data suggest there may be a small increased risk of ovarian cancer associated with longer-term use of HRT. The premature termination of one arm of the Women's Health Initiative randomized controlled trial caused concern among patients, doctors and pharmaceutical companies. There are difficulties in extrapolating the results from trials using a specific HRT product to advise women on the wide range of other hormone products, doses, combinations and routes of administration. However, in the absence of evidence that other products are safer, the data suggest that for many women the risks associated with long-term use of HRT outweigh the benefits. There are nonhormonal strategies for the prevention and treatment of osteoporosis. HRT is not, and has never been, licensed in the UK for the prevention or treatment of vascular disease, and the data suggesting potential benefit should now be regarded as biased. The absolute incidence of an adverse event is low, and the risk in an individual woman in a single year is very small, but the risks are cumulative over time with long-term use. The risk-benefit balance of each woman needs regular reappraisal with continued use.


Subject(s)
Estrogen Replacement Therapy/adverse effects , Neoplasms/chemically induced , Progestins/adverse effects , Alzheimer Disease/prevention & control , Breast Neoplasms/chemically induced , Colonic Neoplasms/prevention & control , Coronary Disease/prevention & control , Endometrial Neoplasms/chemically induced , Female , Hot Flashes/prevention & control , Humans , Middle Aged , Osteoporosis, Postmenopausal/prevention & control , Ovarian Neoplasms/chemically induced , Progestins/therapeutic use , Pulmonary Embolism/chemically induced , Randomized Controlled Trials as Topic , Risk Assessment , Stroke/chemically induced , Treatment Failure , Venous Thrombosis/chemically induced
20.
Clin Med (Lond) ; 2(4): 331-3, 2002.
Article in English | MEDLINE | ID: mdl-12195861

ABSTRACT

Consultant-led medical admission units have been developed as one method of managing the increasing number of acute medical emergencies. The need to document such innovations and to evaluate and analyse the role of an acute care physician in meeting the problems of acute care has been emphasised. We therefore report our experience of an acute admissions unit led by a consultant physician in acute medicine in a district general hospital.


Subject(s)
Admitting Department, Hospital/organization & administration , Consultants , Critical Care/organization & administration , Emergency Service, Hospital/organization & administration , Patient Admission , Physician's Role , Efficiency, Organizational , Hospitals, General/organization & administration , Humans , Personnel Staffing and Scheduling , United Kingdom , Workforce
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