PO-1485 Radiotherapy for Ledderhose disease: long-term efficacy, side effects and patient-rated outcome

2021 ◽  
Vol 161 ◽  
pp. S1216
Author(s):  
A. de Haan ◽  
J. van Nes ◽  
P. Werker ◽  
J. Langendijk ◽  
R. Steenbakkers
Lung ◽  
2014 ◽  
Vol 193 (1) ◽  
pp. 105-112 ◽  
Author(s):  
Mona Lichtblau ◽  
Dominik Harzheim ◽  
Nicola Ehlken ◽  
Alberto Marra ◽  
Fabiola Pena Pinado ◽  
...  

Author(s):  
Valeria B. Campos ◽  
Christine C. Dierickx ◽  
William A. Farinelli ◽  
Tai-Yuan D. Lin ◽  
Woraphong Manuskiatti ◽  
...  

2016 ◽  
Vol 38 (2) ◽  
pp. 325-330 ◽  
Author(s):  
Xiaoyong Tao ◽  
Wei Wang ◽  
Feng Jing ◽  
Zhongkui Wang ◽  
Yuping Chen ◽  
...  

Author(s):  
Alfonso Luca Pendolino ◽  
Glenis K. Scadding ◽  
Bruno Scarpa ◽  
Peter J. Andrews

Abstract Purpose Aspirin treatment after desensitization (ATAD) represents an effective therapeutic option suitable for NSAID-exacerbated respiratory disease (N-ERD) patients with recalcitrant disease. Intranasal administration of lysine-aspirin (LAS) has been suggested as a safer and faster route than oral ATAD but evidence for its use is less strong. We investigated nasal LAS therapy long-term efficacy based on objective outcomes, smell function, polyp recurrence and need for surgery or rescue therapy. Clinical biomarkers predicting response to intranasal LAS, long-term side effects and consequences of discontinuing treatment have been evaluated. Methods A retrospective analysis of a database of 60 N-ERD patients seen between 2012 and 2020 was performed in March 2021. They were followed up at 3-months, 1-, 2- and 3-years with upper and lower airway functions assessed at each follow-up. Results Higher nasal airflow and smell scores were found at each follow-up in patients taking LAS (p < 0.001 and p = 0.048 respectively). No influence of LAS on pulmonary function measurements was observed. Patient on intranasal LAS showed a lower rate of revision sinus surgery when compared to those who discontinued the treatment (p < 0.001). None of the variables studied was found to influence LAS treatment response. Conclusion Our study demonstrates the clinical effectiveness of long-term intranasal LAS in the management of N-ERD in terms of improved nasal airflow and olfaction and a reduced need for revision sinus surgery. Intranasal LAS is safe, being associated with a lower rate of side effects when compared to oral ATAD. However, discontinuation of the treatment at any stage is associated with a loss of clinical benefit.


2016 ◽  
Vol 23 (2) ◽  
pp. R131-R142 ◽  
Author(s):  
Carole Guerin ◽  
David Taieb ◽  
Giorgio Treglia ◽  
Thierry Brue ◽  
André Lacroix ◽  
...  

Therapeutic options available for the treatment of Cushing's syndrome (CS) have expanded over the last 5 years. For instance, the efficient management of severe hypercortisolism using a combination of fast-acting steroidogenesis inhibitors has been reported. Recent publications on the long-term efficacy of drugs or radiation techniques have also demonstrated low toxicity. These data should encourage endocrinologists to reconsider the place of bilateral adrenalectomy in patients with ACTH-dependent aetiologies of CS; similarly, the indication of bilateral adrenalectomy is reassessed in primary bilateral macronodular adrenal hyperplasia. The objective of this review is to compare the efficacy and side effects of the various therapeutic options of hypercortisolism with those of bilateral adrenalectomy, in order to better define its indications in the 21st century.


2020 ◽  
Author(s):  
Hyun-Tae Shin ◽  
Si Hyub Lee ◽  
Hee Seong Yoon ◽  
Ji Hye Heo ◽  
Seon Bok Lee ◽  
...  

Abstract Atopic dermatitis is a chronic and relapsing inflammatory skin disease that is treated with immunosuppressants. However, long-term use of immunosuppressants may cause toxicity and severe side effects. To confirm the long-term efficacy and safety of clonal mesenchymal stem cell therapy, we performed investigator-initiated clinical trials and long-term observation in five adult patients with moderate to severe atopic dermatitis that was refractory to conventional treatments. The clinical response assessment values such as eczema area and severity index (EASI) improved significantly at 16 weeks, and 80% (4/5) of the patients achieved EASI-50 after one or two treatment cycles. Patients were observed for long-term efficacy and safety for an average of 38 weeks (range: 16–86 weeks) and showed no serious side effects. Among the cytokines tested, CCL-17, IL-13 and IL-22 significantly decreased at the endpoint of the five participants, two patients who maintained good clinical response over 84 weeks showed increased IL-17 cytokine levels in the blood.


PEDIATRICS ◽  
1993 ◽  
Vol 92 (3) ◽  
pp. 420-425
Author(s):  
M. E.K. Moffatt ◽  
S. Harlos ◽  
A. J. Kirshen ◽  
L. Burd

Objectives. Desmopress in acetate (DDAVP) is promoted to treat nocturnal enuresis but indications for its use are unclear. We reviewed all randomized controlled trials to determine (1) short- and long-term efficacy, (2) responders, (3) dose-response curve, (4) side effects, and (5) comparative efficacy with other treatments. Methods. A Medline search of the English language literature from January 1966 to August 1992, supplemented by contact with the drug companies, yielded 18 articles which were true randomized controlled trials (11 cross-over and 7 parallel studies). Results. The 18 randomized controlled trials included 689 subjects for most of whom some other type of treatment had failed. All studies found decreased mean frequency of wetting ranging from 10% to 91%, but only 24.5% of subjects achieved short-term dryness. One study of DDAVP responders directly tested long-term dryness and 21% stayed dry. In three studies that incidentally reported on long-term effects 5.7% stayed dry after stopping DDAVP. There was wide variation in the type of patient included. Seven studies addressed prognostic factors. Children more than 9 years old and with fewer initial wet nights do better. Four studies seem to include almost exclusively monosymptomatic children with nocturnal enuresis (ie, primary nocturnal enuresis, positive family history, and no urinary symptoms). Results were no better than those which included mixed symptoms. Five studies attempted to address the dose-response issue. Despite some methodological issues, there is probably some dose-response effect. Side effects were infrequent in the 589 subjects who received DDAVP as opposed to placebo. No cases of water intoxication and no significant shifts in electrolytes were reported in the four studies which measured them. Nasal stuffiness, headache, epistaxis, and mild abdominal pain seem to be the only side effects noted, and these were uncommon. Only one study compared DDAVP with conditioning alarms. Alarm patients had 10% fewer wet nights and a better long-term result. Conclusions. DDAVP reduces wet nights in children for whom other treatments have failed but it produces complete dryness in a minority, and this is often a temporary effect. The literature focuses on short-term efficacy. The true role of DDAVP will be known when samples are carefully selected, prognostic factors are examined, and more comparisons with other treatments are conducted focusing on long-term outcomes. On the basis of current knowledge, DDAVP is inferior to conditioning alarms as a primary therapy.


2018 ◽  
pp. 1-6
Author(s):  
Nagaendran Kandiah ◽  
Laura Tan ◽  
Chathuri J Yatawara ◽  
Debby Ng ◽  
Nagaendran Kandiah

Background: Donepezil is a routinely prescribed cognitive enhancer for patients with Alzheimer’s disease (AD), however the effectiveness and safety of long-term high doses remains largely unexplored. Objective: We investigated the long-term efficacy and safety of Donepezil dose escalation in reducing global cognitive decline for patients with AD in a clinical setting. Method: In a naturalistic, open-label, controlled study design, 71 mild to moderate AD patients from a tertiary clinic were prescribed Donepezil 5mg/day for 12 months (phase 1), while 9 AD patients received no treatment. Patients who showed limited benefits (N=30) with Donepezil 5mg/day were titrated up to 10mg/day for a subsequent 12 months (phase 2) and the remaining (N=41) patients continued on 5mg/day. The primary outcome was global cognition, indexed using the Mini-Mental State Examination (MMSE). Results: Phase 1 trends confirmed Donepezil 5mg/day was better than no treatment at reducing cognitive decline (p = .09, f=.18). Phase 2 trends indicated that for patients who showed limited response to Donepezil 5mg/day, Donepezil 10mg/day was more effective in reducing slope of cognitive decline (p = 0.13, f= .42). Additionally, the patients that were titrated up to 10mg/day had comparable treatment benefits to those patients that remained on 5mg/day during phase 2 (p = .32, f =.12). Side effects in the 10mg/day group were not significantly different from the side effects in the 5mg group (t (67)=-1.27, p=.21). Conclusion: Donepezil dose escalation in patients with AD is safe and may result in large noticeable effects on cognition, with effects comparable to patients who initially responded well to 5mg/day.


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