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European Journal of Medical Research - Deutsche AIDS ...

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

101<br />

sons. For on <strong>of</strong> the three patients still on TPV/r and without<br />

showing any other obvious conditions or comedication, aggregation<br />

<strong>of</strong> platelets showed a decrease in ADP and collagen<br />

induced aggregation.<br />

In contrast to our laboratory findings, clinically only mild<br />

episodes <strong>of</strong> epistaxis and menorrhagia were observed in only<br />

one patient respectively. Nevertheless the effect <strong>of</strong> ART on<br />

coagulation parameters needs to be taken into account and<br />

further studies are needed to evaluate and understand this interaction.<br />

D.55 (Poster)<br />

Determination <strong>of</strong> HLA-B*5701 status prior to<br />

Abacavir exposure results in higher prescription<br />

frequencies and lower rates early therapy<br />

terminations<br />

Kohrgruber N. 1 , Fischer G. 2 , Rieger A. 1<br />

1 Univ. Klinik für Dermatologie, Medizinische Universität<br />

Wien, Abteilung für Allergologie, Immunologie und infektiöse<br />

Hauterkrankungen, Wien, Austria, 2 Univ. Klinik für<br />

Blutgruppenserologie und Transfusionsmedizin, Medizinische<br />

Universität Wien, Wien, Austria<br />

Background: Treatment with Abacavir (ABC) results in a<br />

hypersensitivity reaction (HSR) in about 8% <strong>of</strong> patients. The<br />

risk <strong>of</strong> HSR may limit ABC prescription or may result in premature<br />

treatment cessation, both due to precaution <strong>of</strong> physicians<br />

and patients. Pretesting for HLA-B*5701 prior to ABC<br />

initiation results in significant reduction <strong>of</strong> HSR incidence<br />

and thus may lead to a change <strong>of</strong> prescription frequencies and<br />

a more sustained adherence to ABC.<br />

Methods: In this single centre study, we prospectively collected<br />

data about ABC prescription frequencies and early<br />

therapy cessations after a pre-test for HLA-B*5701 was introduced<br />

in August 2005. Those data were compared to retrospectively<br />

evaluated data about the period before HLA-<br />

B*5701 testing was performed. All patients with > 60 days <strong>of</strong><br />

follow-up were included.<br />

Results: After HLA-B*5701 testing was introduced, 141<br />

ABC naïve patients started ABC therapy between August 05<br />

and November 06. 5 (3.5%) patients discontinued ABC in <<br />

42 days based on patients (n=3) or physicians decisions<br />

(n=2). Reasons for patients driven terminations were anticipation<br />

<strong>of</strong> HSR (n=1) or misinterpretation <strong>of</strong> unrelated symptoms<br />

(n=2), physicians withdrew ABC because <strong>of</strong> symptoms<br />

highly presumptive HSR (n=1) or secondary syphilis misdiagnosed<br />

as HSR (n=1). In comparison, 157 patients initiated<br />

ABC without HLA-B*5701 prescreening between 1997 and<br />

2005 at a mean per year prescription rate <strong>of</strong> 19.9 (± 12.3; 1-<br />

38). A mean <strong>of</strong> 15.7 % (± 7.9; 6-30) stopped ABC thereafter<br />

during the first 42 treatment days because <strong>of</strong> HSR related<br />

reasons. Retrospectively, 5 ABC treated patients <strong>of</strong> initially<br />

undetermined HLA status were tested B*5701 positive.<br />

Three <strong>of</strong> those 5 subjects stopped ABC during the initial 42<br />

days, 2/5 HLA-B*5701+ patients tolerated ABC for 3 and 4<br />

years, respectively.<br />

Conclusion: HLA-B*5701 predetermination results in more<br />

confident and thus more frequent ABC prescriptions and decreased<br />

rates <strong>of</strong> ABC terminations unrelated and related to<br />

HSR.<br />

D.56 (Poster)<br />

Gastrointestinal bleeding due to livercirrosis<br />

under HAART- a case report<br />

Degen O. 1 , Hertling S. 1 , Kreuzberg C. 1 , Zoufaly A. 1 ,<br />

van Lunzen J. 1<br />

1 University medical center Hamburg-Eppendorf, Hamburg,<br />

Germany<br />

Objective: Liver-relate death in HIV positive patients was the<br />

most frequent cause <strong>of</strong> non-<strong>AIDS</strong>-related death in the D:A:D<br />

Study. Most <strong>of</strong> the patients in this trial were HBV or HCV<br />

coinfected. However in clinical practice there are increasing<br />

numbers <strong>of</strong> patients with steatosis or fibrosis <strong>of</strong> the liver without<br />

comorbidity as viral hepatitis or alcohol abuse. We report<br />

a patient with development <strong>of</strong> esophageal bleeding due to cirrhosis<br />

<strong>of</strong> the liver under long term HAART.<br />

Case report: Case report <strong>of</strong> a 76 year old Caucasian patient<br />

HIV positive since 1987. Risk <strong>of</strong> infection was MSM. He is<br />

after esophageal candidiasis in stage CDC C3. In 1987 a<br />

healed hepatitis B was found. ART was started in 1996 and he<br />

was treated with more than 18 drugs from all available classes.<br />

Until today the liver function was normal without elevation<br />

<strong>of</strong> liver enzymes and normal blood coagulation and other<br />

synthesis factors. The patient is rare drinking alcohol. 1999 a<br />

abdominal ultrasound was performed with signs <strong>of</strong> liver<br />

steatosis, a gastroscopy in 2002 was without pathological<br />

findings. In 2004 the ART was switched to AZT, 3TC, TFV<br />

and Tipranavir. In Mai 2006 we found anemia with Hb <strong>of</strong><br />

10.8 g/dl, the haemocult-test was positive.<br />

The ultrasound showed advanced damage <strong>of</strong> the liverparenchym<br />

without singes <strong>of</strong> decompensation. No thrombosis<br />

<strong>of</strong> the V. portae in the Duplex. The hepatitis serology was<br />

negative for B and A, as 1987 with a healed hepatitis B. No<br />

autoimmunhepatits or lack <strong>of</strong> alpha-1 antitrypsin. In liverbiopsie<br />

the parenchyma was fine dropted fatty degenerated.<br />

The gastroscopy showed hypertensive gastropathie and III°<br />

esophageal varicosis with red spots. A ligation therapy <strong>of</strong> the<br />

varicosis was done and a beta blocker was added to therapy.<br />

The PI in the ART was switched from Tipranavir to<br />

Darunavir.<br />

Discussion: In this case we report a HIV positive patient with<br />

gastrointestinal bleeding due to hypertensive gastropathie and<br />

esophageal varicosis by liver cirrosis. The only known risk<br />

factor is HAART over 10 years. Physicians should be aware<br />

<strong>of</strong> liver damage in patient under HAART also when the routinely<br />

performed liver function test and enzymes were normal.<br />

D.57 (Poster)<br />

Attenuation kognitiver Funktionen unter HAART<br />

mit ddI, ddC und d4T im Vergleich zu HAART<br />

ohne ddI, ddC und d4T<br />

Hudelmaier B. 1 , Reichelt D. 2 , Oelker-Güneberg U. 3 ,<br />

Klönne K. 4 , Gregor N. 1 , Summ O. 1 , Biehl K. 1 , Evers S. 1 ,<br />

Husstedt I.W. 1<br />

1 UKM Münster, Neurologie, Münster, Germany, 2 UKM<br />

Münster, Innere Medizin D, Münster, Germany, 3 UKM<br />

Münster, Medizin D, Münster, Germany, 4 UKM Münster,<br />

Medizin B, Münster, Germany<br />

Seit der Einführung von HAART hat sich die Überlebenszeit<br />

nach Feststellung der Diagnose HIV-assoziierte Enzephalopathie<br />

(HIVE) von ca. 12 Monaten auf ca. 43 Monate erhöht.

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