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1.
Photodermatol Photoimmunol Photomed ; 36(1): 14-20, 2020 Jan.
Article in English | MEDLINE | ID: mdl-31206787

ABSTRACT

PURPOSE: To compare the efficacy and safety of narrowband ultraviolet B (NB-UVB) phototherapy in home vs in hospital for the management of limited new-onset vitiligo. METHODS: Patients with new-onset vitiligo (<3 months) with <5% body surface area involvement were recruited and randomly assigned to either a home-based or a hospital-based treatment group. Both groups were administered NB-UVB phototherapy thrice a week. The body surface area (BSA) involved with vitiligo, Vitiligo Area Scoring Index (VASI), the effectiveness of repigmentation, Vitiligo Quality of Life index (VitiQoL), and the cost of treatment were examined. RESULTS: A total of 100 patients completed the study. Patients in both groups exhibited improvements demonstrated by BSA and VSAI decrease. No significant differences were found between the two groups in terms of skin repigmentation (P > 0.05). Improvements in the VitiQoL scores were reduced to the greatest degree at week 8 for all patients in both groups. Adverse events, such as painful erythema, burning, blistering, and excessive hyperpigmentation, were more frequently observed in the home-based treatment group than in the hospital-based treatment group. The cost of phototherapy in hospital exceeded the cost of home phototherapy after 7 weeks of treatment. CONCLUSIONS: Home NB-UVB phototherapy treatment was as effective as treatment in hospital, but exhibited cost-effective and a better compliance. However, the education of the patients should be strengthened to avoid excessive UVB exposure and related adverse events.


Subject(s)
Quality of Life , Ultraviolet Therapy/economics , Vitiligo , Adolescent , Adult , Child , Child, Preschool , Female , Humans , Hyperpigmentation/economics , Hyperpigmentation/therapy , Male , Middle Aged , Pilot Projects , Vitiligo/economics , Vitiligo/radiotherapy
2.
J Eur Acad Dermatol Venereol ; 33(1): 191-197, 2019 Jan.
Article in English | MEDLINE | ID: mdl-30242917

ABSTRACT

BACKGROUND: Vitiligo has a complex bidirectional relationship with mental health (MH) disturbances. However, little is known about the relationship between vitiligo and MH emergencies. OBJECTIVE: To examine the associations of vitiligo and MH hospitalizations in the United States. METHODS: Data from the 2002 to 2012 National Inpatient Sample were analysed, including a ~20% sample of all US hospitalizations (n = 87 053 155 children and adults). Prevalence of hospitalization for MH disorders, their length of stay (LOS) and cost of care were determined for those with vitiligo compared to those without vitiligo. RESULTS: Hospitalization for MH disorders occurred more commonly in those with vitiligo compared to those without vitiligo (4.17% vs. 2.18%). In multivariable logistic regression models, vitiligo was associated with higher odds of admission for any MH disorder [adjusted odds ratio (95% confidence interval): 1.69 (1.61-1.78)], including 14 of 15 MH disorders examined. Associated MH disorders included anxiety, schizophrenia, depression, suicidal risk, personality disorder, ADD/ADHD and conduct disorder, substance use disorder, childhood and adolescent psychiatric illnesses, alcohol-related disorders, adjustment disorders, developmental disorders, impulse control disorders, history of mental health disorders and miscellaneous mental health disorders. Vitiligo patients hospitalized with any MH disorder had higher geometric-mean (95% confidence interval) cost of inpatient care [$10 992 ($10 477-$11 507) vs. $10 082 ($9728-$10 435)] and LOS [5.6 (5.3-5.8) vs. 4.8 (4.6-4.9); P < 0.0001] compared to those without vitiligo, with $10.5 million excess annual costs from hospitalization with MH disorders in persons with vitiligo. CONCLUSIONS: Persons with vitiligo had increased hospitalization for multiple MH disorders, which were associated with a considerable cost burden.


Subject(s)
Hospitalization/economics , Hospitalization/statistics & numerical data , Mental Disorders/economics , Mental Disorders/epidemiology , Vitiligo/economics , Vitiligo/epidemiology , Adult , Aged , Comorbidity , Female , Hospital Costs/statistics & numerical data , Humans , Length of Stay/statistics & numerical data , Male , Middle Aged , United States/epidemiology
3.
Dermatol Ther ; 31(5): e12620, 2018 09.
Article in English | MEDLINE | ID: mdl-30253018

ABSTRACT

Vitiligo is a non-lethal, non-communicable, immune-mediated, and generally progressive skin disease, with poorly understood etiopathogenesis and weak evidence base. The aim of the study is to contribute to the scant research on the patient-reported outcomes in vitiligo, and to examine the presence of associations between various inputs for possible use in clinical practice. The study was designed as a web-based questionnaire with 40 inputs across seven dimensions. The questions include demographics, skin type, eye and natural hair color, age of respondent and age of onset, possible triggers, disease extent, localization, progression and activity, the efficacy of most common treatment modalities, medication side-effects, heredity and diseases among parents, and out-of-pocket expenses for treatments to date. The analysis presented with this work contributes to the discussion about the relation between therapies, socio-economic factors, and treatment outcomes in vitiligo. All physicians should adequately manage patient expectations in terms of overall treatment duration and expected out-of-pocket expenses, and actively evaluate patients at shorter intervals. A more aggressive therapeutic approach using telehealth devices should be considered to supplement therapy, monitor treatment progress, and protocol compliance.


Subject(s)
Patient Reported Outcome Measures , Vitiligo/therapy , Adolescent , Adult , Age of Onset , Aged , Aged, 80 and over , Child , Female , Health Services Needs and Demand , Humans , Internet , Male , Middle Aged , Patient Acceptance of Health Care/statistics & numerical data , Severity of Illness Index , Skin Pigmentation , Treatment Outcome , Vitiligo/economics , Vitiligo/genetics , Young Adult
4.
Dermatol Ther ; 29(6): 413-418, 2016 Nov.
Article in English | MEDLINE | ID: mdl-27594551

ABSTRACT

Vitiligo is a chronic disorder of depigmentation that has different treatment modalities, but patients' nonadherence is common. This study aimed to assess the influence of patients' medication beliefs on patients' adherence to topical, oral medications, and phototherapy in vitiligo. Between September 2015 and February 2016, 260 patients with vitiligo were asked to fill in the Beliefs about Medicines Questionnaire (BMQ) to assess their beliefs about therapy for vitiligo. Their adherence to the therapy was examined using the 8-item Morisky Medication Adherence Scale (MMAS-8). RESULTS: The MMAS-8 scale and BMQ had good internal consistency (Cronbach's α = 0.78 and 0.66, respectively). Using Morisky's recommended cutoff point, 71% of patients were categorized as low or nonadherent to the scheduled therapy. Patients who perceived specific necessity of dermatological medicines significantly adhered to their therapy (OR 1.23; 95% CI 1.09, 1.38; p = 0.001) whereas patients who had specific concerns about the adverse effects exhibited significant low adherence (OR 0.65; 95% CI 0.56, 0.76; p < 0.001). CONCLUSION: Positive beliefs about the necessity of medications in vitiligo do not necessarily reflect high adherence. Patients' adherence behavior is a multidimensional and dynamic process. The prolonged course of treatment, its cost, and unsatisfactory outcomes influenced the patients' adherence.


Subject(s)
Dermatologic Agents/therapeutic use , Health Knowledge, Attitudes, Practice , Medication Adherence , Perception , Vitiligo/drug therapy , Adolescent , Adult , Aged , Chi-Square Distribution , Cross-Sectional Studies , Dermatologic Agents/adverse effects , Dermatologic Agents/economics , Drug Costs , Egypt , Female , Humans , Logistic Models , Male , Middle Aged , Multivariate Analysis , Odds Ratio , Risk Assessment , Risk Factors , Surveys and Questionnaires , Time Factors , Treatment Outcome , Vitiligo/diagnosis , Vitiligo/economics , Vitiligo/psychology , Young Adult
5.
Br J Dermatol ; 170(3): 581-5, 2014 Mar.
Article in English | MEDLINE | ID: mdl-24641482

ABSTRACT

BACKGROUND: Despite continued progress towards an elucidation of pathogenetic pathways in vitiligo, a definitive cure remains elusive. Noncultured epidermal cell suspension (NCECS) is emerging as the treatment of choice for surgical management of both stable and segmental vitiligo. NCECS is very effective in repigmenting stable vitiligo, but the technique requires an expert and the support of a laboratory facility. OBJECTIVES: To investigate a simplified and more cost-effective method for NCECS. METHODS: We simplified the conventional NCECS method and made it more cost-effective and simple enough to be performed in the clinic without laboratory equipment. We named this the four compartment (FC) method. Six patients with vitiligo were treated with this FC method. RESULTS: The FC method for NCECS is highly cost-effective and simple. Six patients with vitiligo were treated and the results showed marked to complete repigmentation in four patients and > 50% repigmentation in two patients in 3 months. CONCLUSIONS: The FC method is a cost-effective and simple procedure to prepare epidermal cell suspensions. In this modified method we showed that there is no need for pipette, tips, centrifuge tube and most importantly a centrifuge machine or any other expensive laboratory equipment.


Subject(s)
Cell Transplantation/methods , Epithelial Cells/transplantation , Vitiligo/therapy , Adult , Cell Transplantation/economics , Cost-Benefit Analysis , Female , Follow-Up Studies , Humans , Male , Skin Transplantation/economics , Skin Transplantation/methods , Tissue and Organ Harvesting/economics , Tissue and Organ Harvesting/methods , Transplantation, Autologous , Vitiligo/economics
7.
Dermatol Ther ; 25 Suppl 1: S1-9, 2012.
Article in English | MEDLINE | ID: mdl-23237032

ABSTRACT

A global interest in therapies for neglected diseases is rising, but traditional biopharma research and development (R&D) process is prohibitively expensive to justify cost of their development. Vitiligo is a multifactorial orphan disease that affects at minimum 35 million people worldwide, yet no therapeutic solutions exist. The present authors describe a budget-minded pursuit of the new therapy development for vitiligo, which includes a multidiscipline collaboration and effective bridging between academic research, biobanking, and bioinformatics. The present authors anticipate that the present authors' "theoretically induced and empirically guided" discovery process will enable development of more leads, with a much greater probability of success and under tighter budgets compared with those of the biopharma company. Ultimately, the multidisciplinary approach described below facilitates the collaborative development of personalized treatments for different patient subpopulations in vitiligo and other neglected diseases.


Subject(s)
Biomedical Research/economics , Drug Design , Orphan Drug Production/economics , Vitiligo/therapy , Biomedical Research/methods , Biopharmaceutics/economics , Biopharmaceutics/methods , Computational Biology/economics , Computational Biology/methods , Humans , Medical Informatics/economics , Medical Informatics/methods , Neglected Diseases/economics , Neglected Diseases/physiopathology , Neglected Diseases/therapy , Orphan Drug Production/methods , Rare Diseases/economics , Rare Diseases/physiopathology , Rare Diseases/therapy , Vitiligo/economics , Vitiligo/physiopathology
9.
Br J Dermatol ; 161(1): 134-9, 2009 Jul.
Article in English | MEDLINE | ID: mdl-19298268

ABSTRACT

BACKGROUND: Vitiligo is a chronic pigmentary disorder of the skin, affecting 1-2% of the general population. Although not life threatening, vitiligo may considerably influence patients' health-related quality of life (QoL) and psychological well-being. Willingness-to-pay (WTP) is a construct reflecting disease burden and QoL reduction which has not yet been used in vitiligo. OBJECTIVES: To assess the WTP and the QoL of patients with vitiligo. METHODS: Patients with vitiligo were included in a nationwide German postal survey. WTP was assessed by two standardized items, and QoL was evaluated using the Dermatology Life Quality Index (DLQI) and the EuroQol (EQ-5D) questionnaire. QoL data were compared with n = 1,511 patients from a national survey on psoriasis. RESULTS: The questionnaire was completed by 1,023 patients (71.5% women, mean age 44.4 years, mean disease duration 20.3 years) with vitiligo. The mean DLQI was 7.0 (7.5 in women, 5.5 in men) compared with 8.6 in psoriasis. Of the patients with vitiligo, 24.6% had a DLQI > 10 which indicates severe QoL reductions, compared with 34.1% in patients with psoriasis. The highest mean DLQI value was observed in the patient group aged 20-29 years. EQ-5D mean score was 83.6 compared with 75.3 in psoriasis. Of the patients with vitiligo, 32.9% would pay more than 5,000 Euro in order to achieve complete disease remission. WTP was highest among middle-aged patients (30-60 years). There was a significant correlation between DLQI scores and WTP (chi(2) = 65.43, P < 0.001). Moreover, WTP significantly correlated with duration of disease, and with body surface area affected (P < 0.001). CONCLUSIONS: Vitiligo causes substantial disease burden as reflected by QoL impairment and high WTP, especially in women. These results should draw the attention of physicians to this disease, as appropriate education and treatment are likely to improve the QoL of patients with vitiligo and may support patients' compliance and empowerment.


Subject(s)
Fees and Charges , Quality of Life , Vitiligo/psychology , Adolescent , Adult , Aged , Aged, 80 and over , Child , Female , Germany , Humans , Male , Middle Aged , Psoriasis/economics , Psoriasis/psychology , Severity of Illness Index , Surveys and Questionnaires , Vitiligo/economics , Vitiligo/therapy , Young Adult
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