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1.
Lasers Surg Med ; 53(10): 1356-1363, 2021 12.
Artículo en Inglés | MEDLINE | ID: mdl-34082477

RESUMEN

BACKGROUND AND OBJECTIVES: To evaluate the efficacy and safety of fractional 1064 nm Nd:YAG picosecond laser combined with intense pulsed light (IPL) in the treatment of atrophic acne scar with post-inflammatory erythema (PIE). © 2021 Wiley Periodicals LLC. STUDY DESIGN/MATERIALS AND METHODS: Seventeen patients received five sessions of treatment at weeks 0, 4, 8, 12, 16 and were followed up at week 28. One half of the face was randomly treated by fractional 1064 nm Nd:YAG picosecond laser combined with IPL (FxPico + IPL), and the other by IPL alone as a control. RESULTS: For the 15 patients who completed the study, the FxPico + IPL side demonstrated significant median Échelle D'évaluation clinique des cicatrices D'acné (ECCA) score improvement (P < 0.01), while IPL alone side did not (P = 0.1250). The pore counts for both sides decreased but more pore count reduction was seen on the FxPico + IPL side (P < 0.05). Better scar improvement was observed on the FxPico + IPL-treated side (P < 0.05) while no difference in erythema improvement was seen between the two sides. There was no difference between the two treatments in terms of overall satisfaction. Pain, erythema, edema, petechiae, crusting, reactive acneiform eruptions, and pruritus were common adverse effects and were mild to moderate. CONCLUSION: FxPico + IPL is an effective, efficient, and safe treatment regimen for atrophic acne scars complicated by PIE.


Asunto(s)
Acné Vulgar , Láseres de Estado Sólido , Terapia por Luz de Baja Intensidad , Acné Vulgar/complicaciones , Cicatriz/etiología , Cicatriz/patología , Cicatriz/terapia , Humanos , Láseres de Estado Sólido/uso terapéutico , Resultado del Tratamiento
2.
Eur J Dermatol ; 30(1): 24-31, 2020 Feb 01.
Artículo en Inglés | MEDLINE | ID: mdl-32031529

RESUMEN

BACKGROUND: Cutaneous adverse drug reactions (CADRs) are drug-induced skin reactions with or without systemic involvement, ranging from mild maculopapular exanthema (MPE) to life-threatening severe CADRs (S-CADRs). Due to their unpredictability and severity, early recognition of suspected causative drugs is highly recommended. However, the profile of CADRs remains unknown in China. OBJECTIVES: To assess the clinical profile, predominant causative drugs, and cost associated with CADRs in Shanghai, China. MATERIALS AND METHODS: Clinical records of inpatients admitted with a diagnosis of CADRs to the dermatology ward of Huashan Hospital from January 2007 to December 2016 were retrospectively studied. RESULTS: A total of 1,883 patients (1,231 female and 652 male), admitted with a diagnosis of CADR, were investigated. S-CADRs made up 21.99% of all cases (n=414), and urticaria (27.19%) was the most frequent reaction. Of the patients, 53.43% suffered from multiple drug-induced drug eruptions and the rest (45.83%) from single drug-induced drug eruptions. Overall, antimicrobials (28.85%) was the main drug group involved, and for S-CADRs, this was antiepileptic drugs (36.15%). The total cost for CADRs was RMB23,718,788.83 ($3,588,319.04). Both age and sex were related to admission cost (p=0.005 and p=7.84E-8, respectively). Antimicrobials were the most common treatment causing CADRs. CONCLUSION: The management of CADRs requires considerable medical cost. CADRs are not only a health problem but also a significant financial burden for affected individuals.


Asunto(s)
Antibacterianos/efectos adversos , Anticonvulsivantes/efectos adversos , Erupciones por Medicamentos/economía , Erupciones por Medicamentos/etiología , Adolescente , Adulto , Factores de Edad , Anciano , Anciano de 80 o más Años , Alopurinol/efectos adversos , Analgésicos/efectos adversos , Antipiréticos/efectos adversos , Niño , China , Medicamentos Herbarios Chinos/efectos adversos , Femenino , Supresores de la Gota/efectos adversos , Costos de la Atención en Salud , Hospitalización , Humanos , Masculino , Persona de Mediana Edad , Pronóstico , Estudios Retrospectivos , Factores Sexuales , Urticaria/inducido químicamente , Adulto Joven
4.
Pharmacogenomics J ; 19(3): 277-285, 2019 06.
Artículo en Inglés | MEDLINE | ID: mdl-30237582

RESUMEN

Xuesaitong (XST) is mainly used to treat cardiovascular and cerebrovascular diseases, sometimes causing cutaneous adverse drug reactions (cADRs) with unknown mechanisms of pathogenicity or risk factors. We aimed to verify whether human leukocyte antigen (HLA) alleles are associated with XST-related cADRs in Han Chinese population. We carried out an association study including 12 subjects with XST-induced cADRs, 283 controls, and 28 XST-tolerant subjects. Five out of 12 patients with XST-induced cADRs carried HLA-C*12:02, and all of them received XST via intravenous drip. The carrier frequency of HLA-C*12:02 was significantly high compare to that of the control population (Pc = 4.4 × 10-4, odds ratio (OR) = 21.75, 95% CI = 5.78-81.88). Compared with that of the XST-tolerant group, the patients who received XST through intravenous drip presented a higher OR of cADRs (Pc = 0.011, OR = 27.00, 95% CI = 2.58-282.98). The results suggest that HLA-C*12:02 is a potentially predictive marker of XST-induced cADRs in Han Chinese, especially when XST is administered via intravenous drip.


Asunto(s)
Erupciones por Medicamentos/genética , Efectos Colaterales y Reacciones Adversas Relacionados con Medicamentos/genética , Medicamentos Herbarios Chinos/efectos adversos , Predisposición Genética a la Enfermedad/genética , Antígenos HLA-C/genética , Saponinas/efectos adversos , Adulto , Anciano , Anciano de 80 o más Años , Alelos , Pueblo Asiatico/genética , Femenino , Frecuencia de los Genes/genética , Genotipo , Humanos , Masculino , Persona de Mediana Edad , Adulto Joven
5.
Dermatol Ther ; 30(6)2017 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-29047198

RESUMEN

Few studies have been conducted in chronic actinic dermatitis (CAD) treated with narrowband ultraviolet B (NB UVB) phototherapy, especially in Asian patients. We aim to evaluate the efficacy and safety of NB UVB phototherapy in Chinese patients with CAD. 19 CAD patients of Fitzpatrick skin phototype IV received NB UVB phototherapy in spring and treatments were given 3 times weekly with incremental dose and maintenance therapy was given twice weekly for 3-4 weeks. The mean initial, endpoint, and cumulative dose of NB UVB was 0.08, 0.33, and 6.0 J/cm2 , respectively. Patients totally received 27 times of treatments in average. 87.5% of previously ultraviolet B(UVB) sensitive patients and 75% of previously ultraviolet A(UVA) sensitive patients had normal or improved MED after phototherapy. The percentage of patients returned to normal UVB phototesting was higher than that of patients returned to normal UVA phototesting (68.8% vs. 37.5%). The mean 1-week DLQI and the need for using immunosuppressive agents and antihistamines were significantly reduced after treatment (p < .01 or p < .05). In conclusion, prophylactic NB UVB phototherapy is effective and safe in treatment of CAD in Chinese patients with Fitzpatrick skin phototype IV.


Asunto(s)
Trastornos por Fotosensibilidad/radioterapia , Terapia Ultravioleta/métodos , Anciano , China , Femenino , Antagonistas de los Receptores Histamínicos/uso terapéutico , Humanos , Inmunosupresores/uso terapéutico , Masculino , Persona de Mediana Edad , Trastornos por Fotosensibilidad/diagnóstico , Inducción de Remisión , Factores de Tiempo , Resultado del Tratamiento , Terapia Ultravioleta/efectos adversos
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