Biological treatments for paediatric psoriasis : a retrospective observational study on biological drug survival in daily practice in childhood psoriasis

2019 ◽  
Vol 33 (10) ◽  
pp. 1984-1992 ◽  
Author(s):  
C. Phan ◽  
A. Beauchet ◽  
A.‐C. Burztejn ◽  
M. Severino‐Freire ◽  
S. Barbarot ◽  
...  
Keyword(s):  
Observational Study ◽  
Daily Practice ◽  
Retrospective Observational Study ◽  
Biological Drug ◽  
Drug Survival ◽  
Biological Treatments

Long‐term safety and drug survival of acitretin in psoriasis: a retrospective observational study

2018 ◽  
Vol 58 (5) ◽  
pp. 593-599 ◽  
Author(s):  
Leena Chularojanamontri ◽  
Narumol Silpa‐archa ◽  
Chanisada Wongpraparut ◽  
Pichaya Limphoka
Keyword(s):  
Observational Study ◽  
Retrospective Observational Study ◽  
Drug Survival

Benefit of statins in daily practice? A six-year retrospective observational study

2009 ◽  
Vol 60 (5) ◽  
pp. 397-401 ◽  
Author(s):  
P. Deambrosis ◽  
G. Terrazzani ◽  
T. Walley ◽  
G. Bader ◽  
P. Giusti ◽  
...  
Keyword(s):  
Observational Study ◽  
Daily Practice ◽  
Retrospective Observational Study

Hemmkörperentwicklung bei Hämophilie-Patienten nach Präparate wechsel

2012 ◽  
Vol 32 (S 01) ◽  
pp. S39-S42 ◽  
Author(s):  
S. Kocher ◽  
G. Asmelash ◽  
V. Makki ◽  
S. Müller ◽  
S. Krekeler ◽  
...  
Keyword(s):  
Risk Factors ◽  
Risk Factor ◽  
Observational Study ◽  
Retrospective Observational Study ◽  
Frequent Change ◽  
Patient Age ◽  
Treatment Regimens ◽  
Patient Âgé ◽  
The Relationship ◽  
Observation Period

SummaryThe retrospective observational study surveys the relationship between development of inhibitors in the treatment of haemophilia patients and risk factors such as changing FVIII products. A total of 119 patients were included in this study, 198 changes of FVIII products were evaluated. Results: During the observation period of 12 months none of the patients developed an inhibitor, which was temporally associated with a change of FVIII products. A frequent change of FVIII products didn’t lead to an increase in inhibitor risk. The change between plasmatic and recombinant preparations could not be confirmed as a risk factor. Furthermore, no correlation between treatment regimens, severity, patient age and comorbidities of the patients could be found.

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