Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 20 de 21
Filter
1.
Expert Opin Biol Ther ; 23(12): 1307-1315, 2023.
Article in English | MEDLINE | ID: mdl-38108300

ABSTRACT

BACKGROUND: Tralokinumab is a human monoclonal antibody targeting interleukin-13 that is approved for the treatment of moderate-severe atopic dermatitis. Studies analyzing the efficacy and safety of tralokinumab in a real-world setting are scarce. RESEARCH DESIGN AND METHODS: A European, multicentric, real-world, retrospective cohort study was defined to assess the effectiveness and safeness profile of tralokinumab, investigating the achievement of pre-specified treatment goals; and to detect potential differences in terms of effectiveness and safeness across some selected patient subcohorts. RESULTS: A total of 194 adult patients were included in this study. A significant improvement in physician-assessed disease severity was detected at each follow-up visit as compared with baseline and similar trend was observed for patient-reported outcomes and quality of life. No meaningful difference in effectiveness was found when considering patient age (<65 versus ≥65 years), neither dissecting patient cohort in dupilumab-naive vs dupilumab-treated subjects. Among tralokinumab-treated patients, 88% achieved at least one currently identified real-world therapeutic goal at week 16. CONCLUSIONS: This retrospective multicenter study confirmed the effectiveness and safeness of tralokinumab throughout 32 weeks of observation, showing the achievement of therapeutic goals identified in both trial and real-world settings in a large proportion of tralokinumab-treated patients.


Subject(s)
Dermatitis, Atopic , Adult , Humans , Aged , Dermatitis, Atopic/diagnosis , Dermatitis, Atopic/drug therapy , Retrospective Studies , Goals , Cohort Studies , Quality of Life , Treatment Outcome , Antibodies, Monoclonal/adverse effects , Severity of Illness Index , Double-Blind Method
9.
J Eur Acad Dermatol Venereol ; 34(1): 188-191, 2020 Jan.
Article in English | MEDLINE | ID: mdl-31494978

ABSTRACT

BACKGROUND: 'Braun' is an illegal injectable dihydrocodeinone-enriched drug mixture of semi-synthetic opioids. It is prepared by palladium-catalysed hydrogenation from codeine-containing tablets. OBJECTIVE: We aimed to characterize the dermatologic consequences of long-term abuse of 'Braun'. METHODS: Skin biopsies of two long-term 'Braun' abusers were evaluated histopathologically, immunohistochemically and ultrastructurally. Palladium skin content was assessed by X-ray fluorescence (XRF) spectrometry. RESULTS: Both patients showed generalized diffuse dark blue-grey hyperpigmentation of the skin. In both, an abnormal population of cells containing intracytoplasmic brownish granular material was identified in the papillary dermis by light microscopy. Electron microscopy revealed a dense and minimally structured material that predominantly accumulated in macrophages, fibroblasts and vascular endothelial cells. XRF analysis confirmed elevated levels of palladium in the patient's skin in comparison to healthy controls. CONCLUSION: Long-term abuse of palladium-contaminated dihydrocodeinone ('Braun') results in excessive accumulation of granular material in various dermal cell types and causes generalized diffuse skin hyperpigmentation.


Subject(s)
Hydrocodone/adverse effects , Hyperpigmentation/chemically induced , Illicit Drugs/adverse effects , Narcotics/adverse effects , Palladium/adverse effects , Synthetic Drugs/adverse effects , Female , Humans , Hyperpigmentation/metabolism , Hyperpigmentation/pathology , Male , Middle Aged , Narcotic-Related Disorders/complications , Palladium/metabolism , Spectrometry, Fluorescence
SELECTION OF CITATIONS
SEARCH DETAIL