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2.
J Eur Acad Dermatol Venereol ; 29(8): 1636-40, 2015 Aug.
Article in English | MEDLINE | ID: mdl-25175822

ABSTRACT

BACKGROUND: Clinical practice guideline (CPG) development starts with selecting appropriate topics, as resources to develop a guideline are limited. However, a standardized method for topic selection is commonly missing and the way different criteria are used to prioritize is not clear. OBJECTIVES: To select and prioritize dermatological topics for CPG development and elucidate criteria dermatologists find important in selecting guideline topics. METHODS: All 410 dermatologists in the Netherlands were asked to create a top 20 of dermatological topics for which a guideline would be desirable, regardless of existing guidelines. They also rated, on a 5-point Likert scale, 10 determinative criteria derived from a combined search in literature and across (inter)national guideline developers. Top 20 topics received scores ranging from 0.01 to 0.2 and combined scores yielded a total score. RESULTS: The 118 surveys (response 29%) identified 157 different topics. Melanoma, squamous cell carcinoma, basal cell carcinoma, psoriasis and atopic dermatitis are top priority guideline topics. Venous leg ulcer, vasculitis, varicose veins, urticaria, acne, Lyme borreliosis, cutaneous lupus erythematosus, pruritus, syphilis, lymphoedema, decubitus ulcer, hidradenitis suppurativa, androgenic alopecia and bullous pemphigoïd complete the top 20. A further 15 topics have overlapping confidence intervals. Mortality and healthcare costs are regarded as less important criteria in topic selection (P < 0.04), than other criteria like the potential to reduce unwanted variation in practice. CONCLUSION: Dermatological professional organizations worldwide succeeded in developing guidelines for all top 20 topics. Respondents mostly agree with (inter)national guideline programmes and literature concerning the criteria important to selecting guideline topics.


Subject(s)
Dermatology , Practice Guidelines as Topic , Skin Diseases , Humans , Netherlands , Research , Skin Diseases/classification
3.
Br J Dermatol ; 172(4): 1008-13, 2015 Apr.
Article in English | MEDLINE | ID: mdl-25123410

ABSTRACT

BACKGROUND: Clinical practice guideline implementation may be at variance with actual daily practice, as guideline adherence is a complex process depending on many actors and factors. Feedback regarding adherence is essential to monitor the effect that a guideline has in clinical practice and whether or not the quality of care is raised by implementation. OBJECTIVES: Developing a tool for obtaining and giving nationwide feedback regarding adherence. METHODS: From February 2010 to June 2013, a 32-item questionnaire was used as an audit tool during committee visits to assess adherence across 37 dermatological centres in The Netherlands. The questions were derived from the recommendations by the Dutch Dermatological and Venereological Society (NVDV) in the Dutch Basal Cell Carcinoma (BCC) guideline. Five selected medical records per dermatologist were audited and the results were discussed with the audited centre. Data were pooled to calculate the compliance with each recommendation across all participating centres. RESULTS: Adherence to recommended actions varied considerably (20·2-100%) across the domains of prevention, diagnostics, treatments and aftercare. Using and reporting surgical margins, giving patient advice, restricting the use of cryosurgery for certain BCCs and reporting on prognostic factors all failed to reach a threshold of 80%. Nonadherence to recommended actions proved to be related to whether or not a dermatologist was directly involved. CONCLUSIONS: The findings emphasize the importance of direct feedback to practitioners regarding adherence. Furthermore, together with existing frameworks, the method described could be used by developers in a guideline update to identify and anticipate barriers to successful implementation.


Subject(s)
Carcinoma, Basal Cell/therapy , Guideline Adherence , Practice Guidelines as Topic , Skin Neoplasms/therapy , Female , Humans , Male , Netherlands
4.
Dermatol Online J ; 20(3)2014 Mar 17.
Article in English | MEDLINE | ID: mdl-24656281

ABSTRACT

This document provides a summary of the Dutch S3-guidelines on the treatment of psoriasis. These guidelines were finalized in December 2011 and contain unique chapters on the treatment of psoriasis of the face and flexures, childhood psoriasis as well as the patient's perspective on treatment. They also cover the topical treatment of psoriasis, photo(chemo)therapy, conventional systemic therapy and biological therapy.


Subject(s)
Psoriasis/therapy , Adult , Anti-Inflammatory Agents/therapeutic use , Antibodies, Monoclonal/therapeutic use , Biological Products/therapeutic use , Child , Combined Modality Therapy , Contraindications , Drug Administration Routes , Drug Administration Schedule , Drug Interactions , Drug Therapy, Combination , Humans , Immunosuppressive Agents/therapeutic use , Netherlands , Patient Acceptance of Health Care , Psoriasis/drug therapy , Psoriasis/radiotherapy , Retinoids/therapeutic use , Ultraviolet Therapy/adverse effects , Ultraviolet Therapy/economics
5.
Ned Tijdschr Geneeskd ; 152(35): 1914-7, 2008 Aug 30.
Article in Dutch | MEDLINE | ID: mdl-18808080

ABSTRACT

Psychiatric consultation in primary care as well as in the hospital is both effective and cost-effective if certain procedures are followed. With the professional guideline 'Consultation psychiatry', the Dutch Psychiatric Association aims at setting a standard for psychiatric consultations in non-psychiatric settings. In general practice, the psychiatric consultation is preferably embedded in 'collaborative care', an integrated care model including the general practitioner and a case manager (usually a nurse), with the consultant psychiatrist being regularly available for clearly defined indications. The psychiatrist should see the patient himself or herself, establish a diagnosis and treatment plan, and provide the general practitioner and the patient with a so-called 'consultation letter', which is then discussed with both. In a general hospital, systematic screening of patients at risk of psychiatric comorbidity can be organised. Early detection of complex patients can further improve the effectiveness of psychiatric consultation. Follow-up contacts and investing in liaison contacts improve adherence to the advice provided.


Subject(s)
Practice Guidelines as Topic , Primary Health Care/standards , Psychiatry/standards , Hospitalization , Humans , Netherlands , Practice Patterns, Physicians' , Referral and Consultation , Societies, Medical
7.
Tijdschr Psychiatr ; 50(6): 317-22, 2008.
Article in Dutch | MEDLINE | ID: mdl-18548408

ABSTRACT

Evidence-based medicine, evidence-based psychiatry and evidence-based development of clinical guidelines are all flourishing today because of developments that have taken place in both science and society. These concepts will be explained and placed in their context. Medical treatment is based on the one hand on scientific knowledge and experience, on the other hand on compassion and consideration for others. Non-specific and relational factors play an important role, particularly in psychiatry and mental health care, but the scientific way of thinking remains as important as ever.


Subject(s)
Evidence-Based Medicine , Practice Guidelines as Topic , Psychiatry/methods , Psychiatry/standards , Humans , Netherlands , Treatment Outcome
8.
Ned Tijdschr Geneeskd ; 152(13): 742-6, 2008 Mar 29.
Article in Dutch | MEDLINE | ID: mdl-18461890

ABSTRACT

Annually, 0.5-1 million injections of contrast media containing iodine are administered in the Netherlands. Almost all contrast media nowadays are low-osmolar and nonionic. Nevertheless, the development ofcontrast-induced nephropathy is still a relevant clinical problem. Through an initiative by the Radiological Society of the Netherlands and with aid of the Dutch Institute for Healthcare Improvement (CBO), a guideline was conceived for the intravascular use of iodine-containing contrast media, based on recent scientific literature. The guideline defines the risk factors for contrast-induced nephropathy. One of the major risk factors is an impaired renal function. It is important to measure the glomerular filtration rate (GFR) in patients with a possible impaired kidney function, preferably by using the 'Modification of diet in renal disease' (MDRD)-study formula. The key measures for avoidance of contrast nephropathy are: limiting the amount of contrast agent used and to assure good hydration, by infusion of sodium chloride 0.9% 12-16 ml/kg body weight, both prior to and after contrast infusion. If time is limited, intravenous administration of sodium bicarbonate is an option. The guideline recommends discontinuation of metformin use from the day of contrast injection, if the GFR < 60 ml/min/1.73 m2, and to restart metformin 2 days following contrast infusion providing the GFR has not significantly deteriorated. Only in the case of previous moderate or severe adverse reactions to contrast media, prophylaxis with corticosteroids and antihistamines is recommended. Iodine allergy or an atopic condition is not a contraindication for the use of iodine-containing contrast media, and no prophylaxis is required. No specific measures are indicated in case of hyperthyroidism, acute pancreatitis, or phaeochromocytoma. Injection of contrast media is not contraindicated in case of pregnancy or lactation.


Subject(s)
Contrast Media/adverse effects , Iodine/adverse effects , Kidney Diseases/chemically induced , Practice Guidelines as Topic , Contrast Media/administration & dosage , Contrast Media/metabolism , Glomerular Filtration Rate/physiology , Humans , Iodine/administration & dosage , Iodine/metabolism , Kidney Diseases/pathology , Kidney Diseases/prevention & control , Rehydration Solutions , Risk Assessment
9.
Ned Tijdschr Geneeskd ; 151(38): 2105-10, 2007 Sep 22.
Article in Dutch | MEDLINE | ID: mdl-17948827

ABSTRACT

OBJECTIVE: To examine the relationship between the number of procedures performed per hospital or per surgeon and health care outcomes. DESIGN: Literature review. METHOD: Relevant literature was identified using recent systematic reviews from Germany, England, France and the United States. The Cochrane Library, Medline and Embase were also searched for recent studies (2000-2005) published in German, English, French, or Dutch using the combined search terms 'surgery' and 'volume'; included studies reported mortality or morbidity as measures of health care quality. RESULTS: 5 systematic reviews were found, which described the results of a total of 41 relevant articles. 8 original articles of sufficient quality published since 2000 were also identified. Most of these articles were also included in the reviews. Relationships between volume per hospital and per surgeon and case fatality (or survival) and morbidity were found for a number of surgical procedures. The strongest associations between volume and case fatality were found for pancreatic and oesophageal resection and, to a lesser degree, elective repair ofabdominal aortic aneurysm. For other procedures the relationship was relatively weak, absent, or not studied. CONCLUSION: Volume appears to be related to quality for some surgical procedures. The magnitude of the relationship differs depending on the procedure. For technically less complex procedures, organisation within the hospital appears to have a greater influence on the differences between hospitals than the performing surgeon.


Subject(s)
Hospital Mortality , Outcome Assessment, Health Care , Quality of Health Care , Surgical Procedures, Operative/standards , Evidence-Based Medicine , Health Care Rationing , Hospitals/statistics & numerical data , Humans , Netherlands , Quality Assurance, Health Care , Quality Indicators, Health Care , Survival Analysis
10.
J Eur Acad Dermatol Venereol ; 21(9): 1193-8, 2007 Oct.
Article in English | MEDLINE | ID: mdl-17894704

ABSTRACT

BACKGROUND: Clinical practice guidelines are increasingly used. To determine the quality of guidelines the Appraisal of Guidelines and Research and Evaluation (AGREE) instrument was developed and introduced in 2001. The AGREE instrument consists of 23 criteria, grouped in six domains. OBJECTIVE: Assessment of quality of evidence-based guidelines in dermatological oncological care according to the AGREE instrument. METHODS: We searched MEDLINE, PubMed, EMBASE and Cochrane literature and relevant websites of guidelines development programmes and the national dermatological society to identify evidence-based dermatological guidelines especially in the treatment of to basal cell carcinoma, squamous cell carcinoma and melanoma. Twenty guidelines, published between 1990 and 2005, were appraised according to the AGREE instrument by three authors. Standardized domain scores were calculated as advised by AGREE. We compared guidelines published before 2002 with those published later. RESULTS: Domain scores in the domains Scope & Purpose and Clarity were scored best. Applicability and Editorial Independence were scored worst (see Table 1). In time a weak trend towards better guidelines was seen. This trend can be attributed to better scores in the domains Search Strategy and Level of Evidence which are closely related to evidence-based medicine. The increase in score is due to more explicitly mentioning the search strategy, possible conflict of interest and involvement of different specialties in development of the guideline. Using the Mann-Whitney test to compare guidelines published before the AGREE and afterwards only a statistically significant better score was found for the domain Clarity (P < 0.05; Table 2). CONCLUSIONS: Guidelines in dermatological oncological care are of reasonable quality according to the AGREE instrument. The domains in the AGREE instrument concern especially the methods of development of guidelines. The score according to AGREE can be improved by explicitly mentioning the different items. As clinical guidelines are regarded to be an important instrument to improve quality of care, improvements are needed.


Subject(s)
Dermatology/standards , Medical Oncology/standards , Practice Guidelines as Topic/standards , Quality Control , Evidence-Based Medicine , Humans , Statistics, Nonparametric
11.
Ned Tijdschr Geneeskd ; 151(25): 1399-402, 2007 Jun 23.
Article in Dutch | MEDLINE | ID: mdl-17668603

ABSTRACT

Since clear evidence is lacking that avoidance of exposure to inhalation or food allergens will have a favourable effect on the course of atopic dermatitis, allergological screening should be restricted to patients having acute allergic symptoms. Topical corticosteroids are the treatment of choice. The working group recommends starting with a class 2-3 corticosteroid daily followed by intermittent maintenance therapy with a corticosteroid of the same class or daily administration of a class 1 corticosteroid. When used in this way, corticosteroids are safe as far as local and systemic side effects are concerned; patients with severe atopic dermatitis have decreased serum-cortisol levels but this is due to the illness and not the corticosteroid. Serum-cortisol levels will usually return to normal following topical steroid therapy. Topical calcineurin inhibitors are a good second-line alternative for patients in whom corticosteroids are insufficiently effective or produce side effects. During such treatment, the skin should be protected against ultraviolet light. Non-sedating antihistamines have no place in the treatment of atopic dermatitis. Cyclosporin is the agent of choice for the systemic treatment of severe atopic dermatitis. The attending physician should also pay attention to psychosocial factors, since severe eczema in children, their parents and adults has a serious impact on the quality of life. Patients with severe atopic dermatitis should be discouraged from working in a wet environment. Patients with moderately active atopic dermatitis without eczema of the hands should avoid exposure to water and other irritating factors.


Subject(s)
Adrenal Cortex Hormones/therapeutic use , Dermatitis, Atopic/diagnosis , Dermatitis, Atopic/drug therapy , Practice Guidelines as Topic , Practice Patterns, Physicians' , Adrenal Cortex Hormones/administration & dosage , Dermatitis, Atopic/etiology , Food Hypersensitivity/complications , Netherlands , Quality of Life , Societies, Medical
13.
Ned Tijdschr Geneeskd ; 151(5): 319-22, 2007 Feb 03.
Article in Dutch | MEDLINE | ID: mdl-17326478

ABSTRACT

In recent years, increasing attention has been given to the importance of disclosing medical errors. Many physicians are still reluctant to disclose errors and to discuss them with the patient. Recent legislative developments have reduced the existing uncertainty regarding the legal consequences of full disclosure. It is important that physicians are open and honest about the errors they make, that they apologise if necessary, and that measures are taken to prevent the same errors from happening again. Psychological factors hindering the full disclosure of errors require continued attention.


Subject(s)
Disclosure , Medical Errors , Physician-Patient Relations , Physicians/psychology , Disclosure/legislation & jurisprudence , Humans , Medical Errors/legislation & jurisprudence , Netherlands
15.
Ned Tijdschr Geneeskd ; 150(45): 2484, 2006 Nov 11.
Article in Dutch | MEDLINE | ID: mdl-17137094

ABSTRACT

A classification of scientific evidence into 'levels', in which the type of research design is graded according to its strength, is useful because it helps the medical community to sort out a system that is accepted all over the world. It not only makes the highest levels of evidential value explicit for a particular clinical question, but also makes the lack of evidence visible. Selected articles will contain labels identifying the strength of evidence supporting key recommendations.


Subject(s)
Evidence-Based Medicine , Health Knowledge, Attitudes, Practice , Evidence-Based Medicine/standards , Humans , Research
16.
Ned Tijdschr Geneeskd ; 150(36): 1976-81, 2006 Sep 09.
Article in Dutch | MEDLINE | ID: mdl-17002186

ABSTRACT

A working group of the Dutch Society for Dermatology and Venereology (NVDV), in collaboration with the Dutch Institute for Health Care Improvement (CBO), has written an evidence-based guideline for the treatment of vitiligo. A distinction is made between generalised or non-segmental vitiligo and localised, including segmental, vitiligo. In patients with generalised vitiligo phototherapy (especially narrow-band ultraviolet B) is the treatment of first choice while in localised vitiligo, this is surgery, particularly autologous skin transplantation (Thiersch grafting, the use of blister epidermis and cell suspensions). However, on the basis of the results of the treatments proposed in the guideline, the working group cannot advise dermatologists to propose a particular treatment to each vitiligo patient they see. On the other hand, the working group is of the opinion that, based on a proper medical examination and an assessment of the disease burden, well-considered advice--and in some cases therapy--should be given to every vitiligo patient who requests it. The benefit of the guideline is that it provides clarity to dermatologists, general practitioners and patients regarding the therapeutic possibilities and limitations.


Subject(s)
Practice Guidelines as Topic , Vitiligo/therapy , Diagnosis, Differential , Evidence-Based Medicine , Humans , Phototherapy , Skin Transplantation , Vitiligo/surgery
17.
Ned Tijdschr Geneeskd ; 149(33): 1839-43, 2005 Aug 13.
Article in Dutch | MEDLINE | ID: mdl-16128181

ABSTRACT

The guidelines 'Melanoma' (3rd revision) are evidence-based in nature. A number of outcomes are summarised in this article. Dermatoscopy deserves a standard role in the clinical diagnosis of pigmented skin abnormalities. Pathological findings from a diagnostic excision should be recorded meticulously to include anatomical localisation, type of intervention used, excision margin, diagnosis, Breslow thickness, and the completeness of the removal. The sentinel node procedure should be reserved for patients who want to be as informed as possible about their prognosis. The procedure is not considered a part of standard diagnosis. Sentinel node assessment should include stains for specific markers and should be conducted in multiple sections. The following margins of non-affected skin are recommended for therapeutic re-excision of melanoma: in situ melanoma, 0.5 cm; Breslow thickness < or = 2 mm, 1 cm; Breslow thickness > 2 mm, 2 cm. Pathological assessment of a re-excised specimen depends on the completeness of the first excision. Systematic adjuvant treatment of patients with melanoma is not recommended outside the context of a clinical study. Patients with metastatic melanoma are preferably treated within a clinical study. Outside of a clinical study, these patients should be treated with dacarbazine. There is no evidence to suggest that survival is improved by frequent follow-up. However, follow-up can be a useful way to meet the information needs of patients and care requirements for physicians.


Subject(s)
Dermatology/standards , Melanoma/diagnosis , Skin Neoplasms/diagnosis , Dermoscopy , Diagnosis, Differential , Evidence-Based Medicine , Humans , Melanoma/pathology , Melanoma/therapy , Netherlands , Skin Neoplasms/pathology , Skin Neoplasms/therapy , Survival Rate
18.
Ned Tijdschr Geneeskd ; 149(21): 1142-3, 2005 May 21.
Article in Dutch | MEDLINE | ID: mdl-15940916

ABSTRACT

Organizational as well as managerial aspects can influence the outcome of patient care, in the establishment of a stroke service unit for instance. Critics wonder whether organisational aspects should be excluded from evidence-based guidelines as strong evidence is often lacking and managers are not included in the working party. It can be argued that it is neither the outcome nor the strength of the published evidence that determines whether a guideline is evidence-based but the method of guideline development. This includes a systematic search and critical appraisal of the literature as well as a rigorous external review in order to achieve consensus on statements including those pertaining to organization of care, for which evidence is poor or lacking.


Subject(s)
Benchmarking , Delivery of Health Care/organization & administration , Evidence-Based Medicine , Peer Review , Delivery of Health Care/standards , Guidelines as Topic , Humans , Netherlands
19.
Ned Tijdschr Geneeskd ; 149(16): 878-84, 2005 Apr 16.
Article in Dutch | MEDLINE | ID: mdl-15868993

ABSTRACT

OBJECTIVE: To determine the rate of PID in women with genital Chlamydia trachomatis infection. DESIGN: Systematic literature review. METHOD: MEDLINE and EMBASE were searched over the years 1975-2003 using the keywords 'Chlamydia trachomatis', 'complication', 'pelvic (inflammatory disease)', 'PID', 'endometritis', 'adnexitis', and 'salpingitis'. The reference lists ofthe articles retrieved were checked for other relevant publications. The PID complication rate was determined, as were the characteristics of the study populations and the validity of the diagnostic methods and outcome measures used. RESULTS: 9 prospective studies were identified. The rate of PID in women with a genital C. trachomatis infection varied between o and 72%. Asymptomatic women who were diagnosed with C. trachomatis infection in general screening had the lowest rate of PID: 0-4%. PID occurred in 12-30% of symptomatic women or women with a higher risk of having an STD (e.g. visitor of an STD clinic, double-infection with gonorrhoea, high risk assessed by questionnaire, having a partner with symptomatic C. trachomatis infection). Women who underwent legal abortion had the highest rate of PID (27-72%). CONCLUSION: The PID rate in women with C. trachomatis varied considerably. Risk depended on whether the infection was symptomatic and the prior probability of having an STD.


Subject(s)
Chlamydia Infections/epidemiology , Chlamydia trachomatis , Genital Diseases, Female/epidemiology , Pelvic Inflammatory Disease/epidemiology , Adult , Chlamydia Infections/pathology , Female , Genital Diseases, Female/microbiology , Genital Diseases, Female/pathology , Humans , Mass Screening , Meta-Analysis as Topic , Netherlands/epidemiology , Pelvic Inflammatory Disease/pathology , Risk Factors
20.
Ned Tijdschr Geneeskd ; 149(19): 1062-7, 2005 May 07.
Article in Dutch | MEDLINE | ID: mdl-15909397

ABSTRACT

The Hippocratic oath derives its name from the ancient Greek physician Hippocrates. It has been embraced as a code of conduct by the medical profession throughout the ages, and is used by medical faculties as an explicit moment of reflection during graduation ceremonies. Although this oath is primarily of ceremonial value, it was felt that the text needed revision as it no longer reflected the current ethical norms in the Netherlands. The new Dutch oath drawn up in 2003 has a dual function: it is symbolic in that it represents the end of a doctor's training, but it is also intended to trigger the discussion of moral issues during the medical studies.


Subject(s)
Hippocratic Oath , Bioethics , Humans , Netherlands
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