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1.
J Dermatolog Treat ; 35(1): 2369616, 2024 Dec.
Article in English | MEDLINE | ID: mdl-38897615

ABSTRACT

BACKGROUND: During the COVID-19 pandemic, psoriasis care underwent significant changes in consultation methods and treatment management. However, comprehensive data on these changes and patient perceptions are limited. AIMS: To evaluate the pandemic's implications on psoriasis patients, focusing on access to information, consultation methods, patient satisfaction, disease control assessment, and treatment management changes. METHODS: A multicenter cross-sectional survey was performed in psoriasis patients from 4 dutch hospitals during the second wave of the pandemic. RESULTS: Among 551 respondents, approximately 55% received information their treatment in relation to COVID-19 from their treating physician, while 16.3% sought information online. Consultation methods were shifted to remote formats for 43.6% of patients, primarily via phone and the shift was often initiated by physicians. Overall patient satisfaction during the pandemic scored high (8.0), with remote consultations scoring between 8.0-9.0. Patients on biological treatment reported better disease control (8.0), compared to those on topical (6.0) or conventional systemic treatments (7.0). However, within the systemic treatment group and biologics group, a notable percentage interrupted (16.3% resp. 12.9%) or discontinued treatment (14.1 resp. 10.6%) during the pandemic. Disease control was moderate-to-good assessed by 75% of patients receiving face-to-face and 68% receiving remote consultations. CONCLUSION: Remote care appears to be a viable alternative to face-to-face consultations, with potential benefits in enhancing access to information provided by treating physicians.


Subject(s)
COVID-19 , Patient Satisfaction , Psoriasis , Humans , Psoriasis/therapy , COVID-19/epidemiology , Cross-Sectional Studies , Male , Female , Middle Aged , Patient Satisfaction/statistics & numerical data , Netherlands/epidemiology , Adult , Surveys and Questionnaires , SARS-CoV-2 , Telemedicine/statistics & numerical data , Aged , Remote Consultation/statistics & numerical data
2.
Ned Tijdschr Geneeskd ; 161: D1660, 2017.
Article in Dutch | MEDLINE | ID: mdl-29098969

ABSTRACT

OBJECTIVE: To gain insight into the trends in the use of psychostimulants among adults. DESIGN: Retrospective database study. METHODS: We selected data on adults (≥ 18 years) who had had a minimum of 2 prescriptions for a psychostimulant drug within 1 year from IADB.nl, a Netherlands database of filled prescriptions (59 public pharmacies, approximately 600,000 patients). We calculated both the number of new users and the total number of users of psychostimulants per year in the period 2004-2014. We also assessed which agent was the most commonly prescribed psychostimulant drug and who had initiated treatment. RESULTS: The number of adults who were prescribed psychostimulants (methylphenidate, dexamphetamine and amphetamine) increased from 1.5 per 1000 adults in 2004 to 7.8 per 1000 adults in 2014. Users were mainly male (63.0%) and methylphenidate was the most frequently prescribed agent (85.7%). The number of new users of these agents increased from 0.5 to 1.5 per 1000 adults, and the greatest increase was observed among young adults (< 30 years). The increase in new users seems to have stabilized since 2012. Around 40% of new treatments were initiated by the GP. CONCLUSION: The large increase in the number of adults who are prescribed psychostimulants seems mainly to be the result of an increase in the number of new users, especially among young adults. As psychostimulants are only approved for the treatment of ADHD in children from 6 years of age and in adolescents, short- and long-term effects and side effects of these drugs need to be better assessed in the adult population.


Subject(s)
Central Nervous System Stimulants/therapeutic use , Methylphenidate/therapeutic use , Practice Patterns, Physicians'/statistics & numerical data , Adolescent , Adult , Attention Deficit Disorder with Hyperactivity , Humans , Male , Netherlands , Retrospective Studies
3.
Ned Tijdschr Geneeskd ; 150(16): 918-23, 2006 Apr 22.
Article in Dutch | MEDLINE | ID: mdl-16686094

ABSTRACT

An outbreak of scabies in a teaching hospital, two nursing homes and six health-care institutions for the elderly, occurred in the Nijmegen area in the Netherlands, between September 2004 and April 2005. In November 2004 the diagnosis of scabies crustosa (scabies norvegica) was made in the index patient - a 78-year-old woman. An atypical presentation, without much itching, as is not infrequently seen in elderly patients, resulted in there being a considerable delay before the diagnosis was made. This resulted in a total of 51 people, both in and outside the hospital, becoming infected. Based on article 7 of the Dutch Infectious Diseases Act, the Municipal Health Service (GGD) advised institutions on the policy and carried out both source and contact tracing. According to this Act notification and cooperation between hospital, care institutions and the GGD are of importance for the effective handling of epidemics. Systemic treatment with ivermectin is the main alternative to local treatment in outbreaks in institutions.


Subject(s)
Antiparasitic Agents/therapeutic use , Cross Infection/epidemiology , Disease Outbreaks , Ivermectin/therapeutic use , Scabies/epidemiology , Aged , Contact Tracing , Cross Infection/drug therapy , Female , Homes for the Aged , Hospitals , Humans , Male , Netherlands/epidemiology , Nursing Homes , Scabies/drug therapy
4.
Br J Dermatol ; 154(5): 880-4, 2006 May.
Article in English | MEDLINE | ID: mdl-16634890

ABSTRACT

BACKGROUND: Eruptive naevi have been described to potentially arise in immune compromised patients. OBJECTIVES: We describe three patients with eruptive benign melanocytic naevi during a phase of immunosuppressive therapy. METHODS/DIAGNOSIS: Two patients with Crohn disease were treated with either azathioprine monotherapy or a combination of azathioprine and infliximab, when eruptive naevi arose particularly at the palms and soles. Our third patient with plaque psoriasis developed eruptive naevi during two episodes of treatment: during a course with the biological agent alefacept and during etanercept therapy. CONCLUSIONS: We conclude that treatment with the recently available biological agents might be associated with the formation of eruptive naevi. Although positive evidence for the occurrence of malignant pigmented lesions is lacking, alertness to the development of eruptive melanocytic naevi during treatment with biological agents is indicated.


Subject(s)
Drug Eruptions/etiology , Immunologic Factors/adverse effects , Immunosuppressive Agents/adverse effects , Nevus, Pigmented/chemically induced , Skin Neoplasms/chemically induced , Adult , Azathioprine/adverse effects , Drug Eruptions/immunology , Drug Eruptions/pathology , Female , Humans , Immunocompromised Host , Male , Middle Aged , Nevus, Pigmented/immunology , Nevus, Pigmented/pathology , Skin Neoplasms/immunology , Skin Neoplasms/pathology
5.
J Eur Acad Dermatol Venereol ; 19(1): 56-60, 2005 Jan.
Article in English | MEDLINE | ID: mdl-15649192

ABSTRACT

Long-term treatments for chronic diseases such as vitiligo need to be evaluated for their clinical efficacy. Assessment of the quality of life (QOL), however, may provide the most relevant information on the actual benefit for these patients. In this study we evaluated QOL after long-term narrowband ultraviolet (UV) B for the treatment of vitiligo. All patients, with long-term stable vitiligo vulgaris, who were treated at our clinic during the last 4 years received specifically for this study a designed QOL questionnaire, which included questions about general well-being, camouflage and psychosocial aspects; 71.4% of the patients responded. Most patients indicated an improvement on a psychological level, but an increase in camouflaging. The present study shows that, after long-term narrowband UVB phototherapy, skin appearance does not play a major role in the life of vitiligo patients, while well being only improved in a minority of patients.


Subject(s)
Quality of Life , Ultraviolet Therapy , Vitiligo/psychology , Vitiligo/radiotherapy , Humans , Retrospective Studies , Surveys and Questionnaires
6.
Exp Dermatol ; 12(4): 460-5, 2003 Aug.
Article in English | MEDLINE | ID: mdl-12930303

ABSTRACT

TNF-alpha is known to play an important role in UV-induced immunomodulation and photodamage. It plays a role in UVB-mediated induction of apoptosis and is a strong inducer of the c-Jun N-terminal kinase (JNK) pathway, which eventually leads to the loss of dermal collagen and elastin content. Recently chimeric anti-TNF-alpha has been introduced as a therapy for rheumatoid arthritis. The aim of the present study was to investigate the effect of anti-TNF-alpha treatment on UV-induced DNA damage, apoptosis, and induction of matrix metallo proteinases. Twelve patients with rheumatoid arthritis were included and irradiated with 2 MED broadband UVB before and after administration of 0.5 mg/kg anti-TNF-alpha monoclonal antibody. Twenty-four hours after irradiation biopsies were taken. Frozen and paraffin sections were stained for p53, c-Jun, phosphorylated c-Jun, sunburn cells and MMP-1. No significant changes were observed in the expression of p53 and sunburn cells and MMP-1 content after treatment with anti-TNF-alpha, whereas a slight but significant decrease in c-Jun and phosphorylated c-Jun expression was noted (P = 0.0250 and P = 0.0431, respectively). Our results showed no influence of anti-TNF-alpha on UV response at therapeutic doses in patients with rheumatoid arthritis.


Subject(s)
Antibodies, Monoclonal/therapeutic use , Arthritis, Rheumatoid/immunology , Arthritis, Rheumatoid/therapy , Skin/immunology , Skin/radiation effects , Tumor Necrosis Factor-alpha/antagonists & inhibitors , Ultraviolet Rays/adverse effects , Adalimumab , Antibodies, Monoclonal/administration & dosage , Antibodies, Monoclonal, Humanized , Arthritis, Rheumatoid/metabolism , Arthritis, Rheumatoid/pathology , DNA Damage , Humans , JNK Mitogen-Activated Protein Kinases , Matrix Metalloproteinase 1/metabolism , Mitogen-Activated Protein Kinases/metabolism , Skin/pathology , Sunburn/etiology , Sunburn/immunology , Sunburn/pathology , Tumor Suppressor Protein p53/metabolism
7.
Exp Dermatol ; 12(6): 729-33, 2003 Dec.
Article in English | MEDLINE | ID: mdl-14714551

ABSTRACT

Since Fischer reported on the superiority of 313 nm UVB compared with broad band UVB in the treatment of psoriasis, narrow band UVB has become the main phototherapeutical modality in several countries. There is some discussion about the safety and photobiological effects of narrow band UVB. In the present study, narrow and broad band UVB have been compared with respect to parameters for photodamage and inflammation. Fourteen healthy volunteers were randomized in two groups. Both groups were irradiated with three minimal erythema doses (MED) of narrow or broad brand UVB, respectively. Before and 4, 24 and 48 h after irradiation, 6 mm biopsies were taken from immunohistochemical analysis of p53, apoptosis and p16 (photodamage parameters) and T-cells, polymorphonuclear leukocytes (PMN) and Langerhans' cells (inflammatory cells). Mean MED for narrow band UVB was 8.125 times higher than broad band UVB. Significant changes in expression were seen for all parameters except for p16. P53, apoptosis, T-cells and PMN increased, while Langerhans' cell count decreased significantly. No significant differences were seen between the narrow band UVB. In conclusion, following irradiation of three MED narrow band UVB and broad band UVB safety parameters for carcinogenesis and inflammation were induced to the same extent. As narrow band UVB is more effective than broad band UVB, the present study suggests superiority of narrow band UVB as a treatment with a better benefit risk ration.


Subject(s)
Erythema/pathology , Inflammation , Ultraviolet Rays , Antibodies, Monoclonal/metabolism , Apoptosis , Cyclin-Dependent Kinase Inhibitor p16/biosynthesis , Dermatitis/pathology , Humans , Immunohistochemistry , Langerhans Cells/metabolism , Neutrophils/metabolism , Pancreatic Elastase/biosynthesis , T-Lymphocytes/metabolism , Time Factors , Tumor Suppressor Protein p53/metabolism
8.
Acta Derm Venereol ; 82(5): 369-72, 2002.
Article in English | MEDLINE | ID: mdl-12430737

ABSTRACT

Narrow band UVB is succeeding psoralen and UVA irradiation as the main treatment of vitiligo vulgaris in several European countries. Vitamin B12 and folic acid deficiency in some vitiligo patients has prompted researchers to investigate the efficacy of these vitamins in the treatment of vitiligo. In the present controlled study we investigated the value of narrow band UVB phototherapy in the treatment of vitiligo and the possible additive effect of vitamin B12 and folic acid. Twenty-seven patients with long-term stable vitiligo were included and randomized in a "UVB only" (UVB) or "UVB combined with vitamin B12 and folic acid" (UVB+) group. Patients were irradiated thrice weekly for one year, whilst repigmentation was carefully monitored. In 92% (25/27) of the patients up to 100% repigmentation was seen. Repigmentation was notable in lesions on the face, neck and throat, lower arm, chest, back and lower legs, whilst repigmentation on the hands, wrists, feet and ankles proved to be minimal. Maximum repigmentation rates did not differ significantly between the UVB group and the UVB+ group. Our study reconfirms that narrow band UVB phototherapy is an effective treatment for vitiligo and shows that co-treatment with vitamin B12 and folic acid does not improve the outcome of treatment of vitiligo with narrow band UVB phototherapy.


Subject(s)
Folic Acid/therapeutic use , Ultraviolet Therapy/methods , Vitamin B 12/therapeutic use , Vitiligo/drug therapy , Vitiligo/radiotherapy , Analysis of Variance , Chemotherapy, Adjuvant , Combined Modality Therapy , Female , Follow-Up Studies , Humans , Long-Term Care , Male , Radiation Dosage , Reference Values , Sensitivity and Specificity , Severity of Illness Index , Sweden , Treatment Outcome , Vitiligo/diagnosis
9.
Hepatogastroenterology ; 39(5): 429-32, 1992 Oct.
Article in English | MEDLINE | ID: mdl-1459525

ABSTRACT

In order to analyze the results of treatment of patients with locoregional recurrence after intentional curative resection of pancreatic cancer, a retrospective study was performed. During the period 1978-1988, 108 patients underwent an intentional curative resection fo the pancreas. In 34 patients locoregional recurrence occurred, all within a period of three years (cumulative recurrence rate 56%). Sixty-eight percent of the patients presented with upper abdominal pain, and 62% with weight loss. Survival was significantly better (p = 0.02) in the group of 18 patients without distant metastases (1-year survival 22%) than in the 16 patients with distant metastases (1-year survival 0%). Five patients without proven distant metastases were treated by resection or chemotherapy. The mean survival was 33 months (range 6-74) in the treated group, and 4 months (0.4-7 months) in the untreated group, p = 0.002. In this retrospective study the longest survival was seen after radical resection of locoregional tumor recurrence. We therefore recommend that patients with locoregional recurrence without distant metastases after intentional curative resection of pancreatic cancer be treated.


Subject(s)
Neoplasm Recurrence, Local/surgery , Pancreatic Neoplasms/surgery , Adult , Aged , Female , Humans , Incidence , Male , Middle Aged , Neoplasm Metastasis , Neoplasm Recurrence, Local/epidemiology , Neoplasm Recurrence, Local/pathology , Pancreatic Neoplasms/pathology , Retrospective Studies , Survival Rate
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