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    المصدر: Meyer, S I R, Jørgensen, C S, Kamperis, K, Andersen, R F, Pedersen, M J, Faerch, M & Rittig, S 2021, ' Efficacy and safety of multimodal treatment in nocturnal enuresis-A retrospective cohort study ', Journal of Pediatric Urology, vol. 17, no. 4, pp. 447.e1-447.e7 . https://doi.org/10.1016/j.jpurol.2021.03.005Test

    الوصف: Summary Introduction and aim of the study Most treatments of nocturnal enuresis (NE) are targeting the main pathophysiological mechanisms, i.e., excess nocturnal urine production, bladder reservoir dysfunction and inability to awaken to a full bladder. Although many children can be effectively treated with only one treatment modality, there is a significant number of treatment-refractory cases. We experience an increasing tendency to combine treatment modalities in those children. However, there is limited evidence regarding the efficacy and safety of such strategies. Materials and methods We reviewed files from all NE children seen in our outpatient incontinence clinic between January 1st and December 31st 2017 and identified children refractory to first line treatment receiving a combination of at least two treatment modalities concurrently. Age, gender, wet nights per week before treatment, follow-up time, previous treatment with desmopressin or alarm, phenotype of NE, number of simultaneous treatments tried and response as well as registered side effects during treatment was noted. We registered the outcomes and safety of the treatment modalities and evaluated prognostic factors. Results We identified 59 children (13 girls) aged 6–15 yrs (mean 9.6 yrs) of whom 30 were monosymptomatic NE (MNE) and 29 were non-monosymptomatic NE (NMNE) patients. They all suffered at least three wet nights per week before treatment. In total, 38 children (61%) became dry on multimodal therapy. Eighteen children (30%) became dry on a combination of two treatment modalities, 16 (27%) on three modalities, and two (3%) on four modalities. Nine children (15%) achieved partial response whereas three (5%) showed no response despite multiple tries with combination therapies. A total of 18 children (30%) reported side effects to one or more of the modalities tried. Side effects that led to discontinuation of the treatment were uncommon (three patients). Conclusions Treatment refractory NE represents a challenge for the clinician. Although it seems possible to adequately treat refractory NE patients with multimodal treatment one should be aware of side effects as well as inform the families of the challenges in the treatment of refractory enuresis patients. Future RCT's should focus on providing further evidence for the role of multimodal therapy in NE treatment. Download : Download high-res image (119KB) Download : Download full-size image Summary Figure 1 . EN treatment modalities and their target.

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    المصدر: Meyer, S I R, Fuglsang, K & Blaakær, J 2014, ' Cell-mediated immune response: a clinical review of the therapeutic potential of human papillomavirus vaccination ', Acta Obstetricia et Gynecologica Scandinavica (AOGS), pp. 1209-1218 . https://doi.org/10.1111/aogs.12480Test
    Meyer, S I, Fuglsang, K & Blaakaer, J 2014, ' Cell-mediated immune response : a clinical review of the therapeutic potential of human papillomavirus vaccination ', Acta Obstetricia et Gynecologica Scandinavica, vol. 93, no. 12, 93, pp. 1209-1218 . https://doi.org/10.1111/aogs.12480Test

    الوصف: Objective This clinical review aims to assess the efficacy of human papillomavirus 16/18 (HPV16/18) vaccination on the cell-mediated immune response in women with existing cervical intraepithelial neoplasia or cervical cancer induced by HPV16 or HPV18. Data sources and study selection A focused and thorough literature search conducted in five different databases found 996 publications. Six relevant articles were chosen for further review. In total, 154 patients (>18 years of age) were enrolled in prospective study trials with 3–15 months of follow up. The vaccine applications were administered two to four times. The vaccines contained different combinations of HPV16 and HPV18 and early proteins, E6 and E7. The primary outcome was the cell-mediated immune response. Correlation to clinical outcome (histopathology) and human leukocyte antigen genes were secondary endpoints. Results All vaccines triggered a detectable cell-mediated immune response, some of which were statistically significant. Correlations between immunological response and clinical outcome (histopathology) were not significant, so neoplasms may not be susceptible to vaccine-generated cytotoxic T cells (CD8+). Conclusions Prophylactic HPV vaccines have been introduced to reduce the incidence of cervical cancer in young women. Women already infected with HPV could benefit from a therapeutic HPV vaccination. Hence, it is important to continue the development of therapeutic HPV vaccines to lower the rate of HPV-associated malignancies and crucial to evaluate vaccine efficacy clinically. This clinical review represents an attempt to elucidate the theories supporting the development of an HPV vaccine with a therapeutic effect on human papillomavirus-induced malignancies of the cervix.

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    المؤلفون: Sonja Izquierdo Riis Meyer

    المصدر: Aarhus University
    Meyer, S I R 2018, ' Efficacy and safety of multimodal treatment in nocturnal enuresis-A retrospective cohort study ', International Children Continence Society Conference, Rome, Italien, 26/09/2018-29/09/2018 s. 447.e1-447.e7 . < http://i-c-c-s.org/events-archiveTest/ >