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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)

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