European Journal of Medical Research - Deutsche AIDS ...
European Journal of Medical Research - Deutsche AIDS ...
European Journal of Medical Research - Deutsche AIDS ...
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66 EUROPEAN JOURNAL OF MEDICAL RESEARCH<br />
June 27, 2007<br />
tained and min 3 NRTI were chosen for next treatment cycle<br />
according to the results. We compared CD4+ T-cell count and<br />
VL developing in each cycle with BL values.<br />
Results: We included 30 pt (1/30 female; 29/30 male). 12/30<br />
were excluded for various reasons: new treatment options,<br />
protocol violation etc.. 17 patients completed week 48 and<br />
were analyzed. Mean CD4-T-cellcount was 160/l (R: 10-<br />
580/l), mean VL was 4,99 log (R: 2,4 – 5,88 log) at BL. The<br />
time-on-NRTI/PI-cycle- ratio was 1,84. Due to permissive VL<br />
elevation we could see a mean VL reduction in each cycle:<br />
C1: -0,64 log (R: + 1,71 to – 4,18log), C2: -0,51log (R: +0,74<br />
to – 1,72log), C3:-0,64log (R:+0,67 to -1,69log), C4: -0,78log<br />
(R:+ 0,42 to -2,67log), C5: -0,82log (R: +0,01 to -3.04log)<br />
compared to the VL at the end <strong>of</strong> the prior cycle.<br />
Conclusion: We could see a significant decline within each cycle<br />
attributed to a rest activity <strong>of</strong> the drug combinations. In<br />
8/17 patients we could see a mild to moderate increase <strong>of</strong> CD4<br />
T-cell within the cycles. Therefore we consider this strategy as<br />
a further option in the mosaic <strong>of</strong> deep salvage therapy.<br />
B.35 (Poster)<br />
Frequency and reasons for ARV switch in heavily<br />
pretreated patients in a 24 months observation<br />
period. Results <strong>of</strong> the Radata-cohort<br />
Lorenzen T. 1 , Staszewski S. 2 , Faetkenheuer G. 3 ,<br />
Bogner J.R. 4 , van Lunzen J. 5 , Mutz A. 6 , Gute P. 7 ,<br />
Arbter P. 8 , Bähr D. 1 , Stoehr A. 1 , H<strong>of</strong>fmann C. 1 ,<br />
Plettenberg A. 1 , for the Radata-studygroup<br />
1 ifi-Institut für interdisziplinäre Medizin, Hamburg, Germany,<br />
2 Universität Frankfurt, HIV-Center, Frankfurt, Germany,<br />
3 Klinikum der Universität zu Köln, Klinik I für Innere<br />
Medizin, Köln, Germany, 4 Medizinische Poliklinik, Klinikum<br />
der Universität München Innenstadt, Infektionsambulanz,<br />
München, Germany, 5 Universitätsklinikum Hamburg-<br />
Eppendorf, Ambulanzzentrum Infektiologie, Hamburg,<br />
Germany, 6 Klinikum Osnabrück, Infektionsambulanz,<br />
Osnabrück, Germany, 7HIV-Schwerpunktpraxis, Frankfurt,<br />
Germany, 8 Praxis für Allgemeinmedizin, Krefeld, Germany<br />
Objective: Radata is an internet-based system which provides<br />
planning <strong>of</strong> antiretroviral therapy (ART), according to resistance<br />
analysis, adherence questionnaire, therapeutic drug<br />
monitoring and external expert advice.<br />
Methods: Of 637 patients included in the radata database,<br />
224 patients with a follow up <strong>of</strong> at least 24 months were selected<br />
and were analysed according to frequency and reasons<br />
for switches <strong>of</strong> ART. All patients were put on a new ART at<br />
the time <strong>of</strong> enrolment.<br />
Results: Within the 24 months period <strong>of</strong> follow-up, 317 ART<br />
switches in 146/224 patients (1.4 switches per patient, range<br />
0-7) were observed. The main reason for switch was therapeutical<br />
failure (n = 180, 50.4 %). Within this subgroup, elevated<br />
viral load was the main reason in 117, CD4-T-cell decline in<br />
17 and clinical progression in 7 cases. For 39 cases, the detailed<br />
reason for switch due to therapeutical failure was not<br />
stated by treating physician. Besides therapeutical failure,<br />
switches due to drug related side effects were noted in 75 cases<br />
(21.0 %). In 27 cases (7.6 %) simplification <strong>of</strong> regimen was<br />
the primary reason for therapeutic change, 25 cases (7.0 %)<br />
were switched due to inadequate adherence <strong>of</strong> patients and for<br />
13 cases (3.6 %) study related conditions (protocol requirement)<br />
were responsible. In 12 cases (3.4 %), comorbidities<br />
such as acute illnesses or newly diagnosed gravidity led to the<br />
switch. In 6 cases (1.7 %) physicians assumed unfavourable<br />
drug interactions. In 19 cases (5.3 %) physicians did not state<br />
a specific reason for change <strong>of</strong> therapy.<br />
Conclusions: Despite intensive pre-treatment <strong>of</strong> the patients,<br />
only half <strong>of</strong> the therapy switches over a period <strong>of</strong> 24 months<br />
in this cohort were due to therapeutic failure. Other predominant<br />
reasons were side effects, treatment simplification and<br />
inadequate patient adherence.<br />
B.36 (Vortrag)<br />
Sexually transmitted infections in men having sex<br />
with men with primary HIV infection<br />
Lenz J.C.C. 1 , Jessen H. 1 , Jessen A.B. 1<br />
1 Praxis Jessen/Jessen/Stein, Berlin, Germany<br />
Objective: In the very early stage <strong>of</strong> HIV infection high levels<br />
<strong>of</strong> HI virus are measured. Also at this stage individuals<br />
with HIV are <strong>of</strong>ten not aware <strong>of</strong> their infection. Both may<br />
contribute to the high proportions <strong>of</strong> HIV transmission in this<br />
phase. Sexually transmitted infections (STI) are known to increase<br />
both the risk to acquire HIV as well as to transmit HIV<br />
to sex partners. Co-infections <strong>of</strong> HIV and STI in patients with<br />
primary HIV infection (PHI) may represent an individual risk<br />
factor that facilitated acquiring the new HIV infection as well<br />
as a risk factor to transmit HIV to other sex partners. In this<br />
study we want identify the rate <strong>of</strong> STI in patients with primary<br />
HIV infection.<br />
Methods: We performed a retrospective analysis <strong>of</strong> all men<br />
having sex with men (MSM) with PHI in the years 2005 and<br />
2006 in the database <strong>of</strong> a single center (Praxis Jessen, Berlin)<br />
an HIV and STI practice. PHI was defined as presence <strong>of</strong> HIV<br />
(measured by PCR) and three or less HIV specific bands in the<br />
western blot. For these patients the charts were reviewed for<br />
clinical signs and laboratory test (Syphilis, Gonorrhea, Chlamydia,<br />
Hepatitis B and C) results indicative <strong>of</strong> symptomatic STI.<br />
Results: We identified 22 individuals with PHI. In 4 (18%)<br />
active infection with syphilis, chlamydia or gonorrhea was<br />
found. In two other possibly sexually transmitted diseases<br />
were present (campylobacter, unspecific urethritis). Over all<br />
1/3 <strong>of</strong> the patients with PHI had infections that are possibly<br />
sexually transmitted.<br />
Conclusions: The presence <strong>of</strong> STI in about 1/3 <strong>of</strong> patients<br />
with PHI in this center may represent an individual risk that<br />
led to the HIV infection. It may also indicate that HIV and<br />
STI have been acquired at the same time. This finding leads<br />
us to conclude that screening for STI should be performed in<br />
PHI. The identification and subsequent treatment <strong>of</strong> STI will<br />
not only prevent negative consequences <strong>of</strong> STI, but also may<br />
help to reduce the additional risk for onward transmission <strong>of</strong><br />
HIV caused by an active STI.<br />
B.37 (Poster)<br />
Antiretroviral (AR) treatment (ART) in the<br />
German ClinSurv multicenter cohort -<br />
An overview <strong>of</strong> HAART in Germany over the last<br />
ten years<br />
Kollan C. 1 , Kühne A. 1 , Hamouda O. 1 , for the ClinSurv<br />
Study Group<br />
1 Robert Koch Institut, Infektionsepidemiologie, Berlin,<br />
Germany<br />
Objective: With the available number <strong>of</strong> different AR-substances<br />
(S) the number <strong>of</strong> drugs (ARV) and AR-regimen (R)