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European Journal of Medical Research - Deutsche AIDS ...

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June 27, 2007 EUROPEAN JOURNAL OF MEDICAL RESEARCH<br />

83<br />

D.11 (Poster)<br />

Virological medical quality management -<br />

7 year follow-up <strong>of</strong> HIV treatment<br />

Knechten H. 1 , Höhn C. 1 , Ehret R. 1 , Wiesmann F. 1 ,<br />

Braun P. 1<br />

1 PZB Aachen, Aachen, Germany<br />

Purpose: The HIV treatment guidelines have been modified recently<br />

and recommend that a viral load 1 diarrhea per day prior to switching vs. 32.8 % <strong>of</strong> pts after<br />

switching. 40.3 % <strong>of</strong> pts used antidiarrheal medication before<br />

switching vs. 30.3 % <strong>of</strong> those afterwards.<br />

Overall Quality <strong>of</strong> Life improved in 27 % and deteriorated<br />

in 10 % <strong>of</strong> pts. 29 % <strong>of</strong> pts experienced fewer loose stools and<br />

11 % reported more. 29 % <strong>of</strong> pts reported less diarrhea and 6<br />

% reported more. In 20 % <strong>of</strong> pts use <strong>of</strong> antidiarrheal medication<br />

was reduced vs. 2 % <strong>of</strong> pts in which the use increased.<br />

75.4 % <strong>of</strong> pts preferred LPV/r TAB therapy, 2.7 % preferred<br />

therapy with LPV/r SGC and 20.3 % judged both therapies<br />

equal (1.5 % n. a.).<br />

Conclusion: In this unselected group <strong>of</strong> patients a trend to<br />

improved Quality <strong>of</strong> Life and reduced GI side effects is observed<br />

after switch from LPV/r SGC to LPV/r TAB.<br />

D.13 (Vortrag)<br />

Long-term efficacy <strong>of</strong> Enfurvitide – final results <strong>of</strong><br />

the RADATA-Fuzeon cohort<br />

H<strong>of</strong>fmann C. 1 , Lorenzen T. 1 , Bogner J.R. 2 , van Lunzen J. 3 ,<br />

Staszewski S. 4 , Arbter P. 5 , Faetkenheuer G. 6 , Gute P. 7 ,<br />

Stoll M. 8 , Hintsche B. 9 , Walther I. 1 , Waesle B. 10 ,<br />

Stoehr A. 1 , Plettenberg A. 1<br />

1 ifi-Institut für interdisziplinäre Medizin, Hamburg, Germany,<br />

2 Medizinische Poliklinik, Klinikum der Universität München<br />

Innenstadt, Infektionsambulanz, München, Germany,<br />

3 Universitätsklinikum Hamburg-Eppendorf,<br />

Ambulanzzentrum Infektiologie, Hamburg, Germany,<br />

4 Universität Frankfurt, HIV-Center, Frankfurt, Germany,<br />

5 Praxis für Allgemeinmedizin, Krefeld, Germany, 6 Klinikum<br />

der Universität zu Köln, Klinik I für Innere Medizin, Köln,<br />

Germany, 7 HIV-Schwerpunktpraxis, Frankfurt, Germany,<br />

8 Medizinische Hochschule Hannover, Abteilung Klinische<br />

Immunologie, Hannover, Germany, 9 Praxis für Innere<br />

Medizin, Berlin, Germany, 10 Roche-Pharma AG, Grenzach-<br />

Wyhlen, Germany<br />

Background: Data on long-term efficacy <strong>of</strong> enfuvirtide outside<br />

clinical trials is limited. In the Radata-Fuzeon cohort,<br />

data <strong>of</strong> HIV-1-infected patients (pts) treated with enfuvirtide<br />

in clinical practice were collected from 32 German centers.<br />

The setting <strong>of</strong>fered planning <strong>of</strong> background therapy according<br />

to resistance analysis, adherence questionnaire, therapeutic<br />

drug monitoring and external expert advice.<br />

Methods: All pts in whom a switch to a new enfuvirtidebased<br />

antiretroviral therapy (ART) was intended were included<br />

in this prospective cohort study. Clinical, immunological<br />

and virological outcomes were measured every three months.<br />

Results: Of 233 pts included, 173 received enfuvirtide and<br />

were eligible for analysis. Pts were heavily pretreated at baseline<br />

(median time on ART: 80 months, number <strong>of</strong> prior regimens:<br />

10), showing a median <strong>of</strong> 7 (range, 1-18) and 2 (range,<br />

1-4) resistance mutations in the reverse transcriptase and in<br />

the protease gene locus, respectively. Pts had a median viral

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