Abstracts Vol. 1 [International Conference on AIDS (11th: 1996: Vancouver, Canada)]

Mo.B.1367 - Mo.B.1372 Monday, July 8, 1996 Five patients have been treated with coprofloxacin/ofloxacin plus clarithromycin (+ amikacin), 4 are still alive by Dec. 1995. Conclusion: Our experience should alert the physicians in developing countries that MAC is also common in HIV patients, at least in South East Asia region. Cases emnerge when we look harder for them and perhaps our AIDS patients survive longer B Sathapatayavongs, Rama VI Rd, Bangkok, 10400 Thailand Tel: 66-2-201-I 58 I; Fax: 66-2-201 1715 Mo.B. 1367 BONE MARROW SAMPLING AS A DIAGNOSTIC TOOL IN HIV-POSITIVE PATIENTS WITH PYREXIA OF UNKNOWN ORIGIN (PUO) Brook, M Gary*, Ayles H**, Harrison C***, Rowntree C***, Miller RF*/**. * Mortimer Market Centre; * Middlesex Hospital, ** University College Hospital, London Objectives: To assess the effectiveness of bone marrow sampling in the diagnosis of the causes of PUO in HIV positive patients. Methods: Patients who had undergone bone marrow sampling as one of the investigations for PUO between 1987 and 1995 were identified. From patient records and computer data the value of the marrow samples in achieving a diagnosis of the cause of the PUO was assessed. Results: I 17 patients had 121 imarrow aspiration and 1 13 marrow trephine samples. Microscopic examination of the marrow revealed the cause of the pyrexia in 33 (27%) of patients from 30 (27%) trephine and 4 (3%) aspiration samples.The diagnoses made were: mycobacterial infection (25), lymphoma (7) and toxoplasmosis (1). Factors more commonly found in patients with positive marrow samples than those with negative samples were low haemoglobin (mean 8.5 g/dl Vs 9.9 g/dl, p<0.05), low CD4 count (mean 0.06 Vs 0.102 x 10 /I,p<0.05) and recent significant fall in any of the haemoglobin (<8g/dl), white cell (<2xl0 /I1) or platelet count (<80x109/1) (18/33 [55%] Vs 27/88 [31%] of patients with diagnostic and non-diagnostic samples respectively p<0.05).When mycobacterial infection was diagnosed by microscopy of a marrow sample, this was achieved a mean (range) of 25 (8-60) days earlier than the first positive culture. Marrow trephine samples had a sensitivity of 25/39 (64%) for the detection of mycobacterial infection. Conclusion: Marrow sampling, especially marrow trephines, contributed significantly to the early diagnosis of the cause of PUO.This success was due to the detection of mycobacterial infection, lymphoma and disseminated toxoplasmosis Samples were most likely to be positive in patients with anaemia, low CD4 count or recent fall in platelet, red or white blood cell count. M Gary Brook, Mortimer Market Centre, Mortimer Market, Off Capper Street, London WCI E 6AU UK.KTel (0)171 530 5077/5014 Fax (0) 171 530 5044 Mo.B. 1368 EVALUATION OF PPD-BATTEY AS A DIAGNOSTIC TOOL IN PERSONS WITH SMALL INDURATION SIZES TO CONVENTIONAL PPD Gourevitch, Marc N, Steinhart R, Schoenbaum EE, Hartel D, Klein RS. Montefiore Medical Center/Albert Einstein College of Medicine, Bronx, NY, USA Objective: To determine whether small (< 10 mm) reactions to PPD reflect cross reactivity to a common nontuberculous mycobacterial antigen in persons with and without HIV infection. Methods: Persons enrolled in a study of M. tuberculosis infection in drug users were tested at baseline with PPD (5 TU, Mantoux method) and PPD-Battey (PPD-B, manufactured by Connaught Laboratories, Ontario) derived from M. avium intracellulare (0.05 mcg in 0. I ml, Mantoux method) and the MultitestR CMI device (to assess cutaneous anergy). Induration was assessed at 48 72 hours. Pts developing >2 mm induration to PPD or PPD-B were classified as reactors. Reactions to one skin test exceeding the other by >5 mm were classified as dominant. HIV serology was also performed. Results: Complete data were available for 32 1/330 subjects enrolled to date. Of these, 60 had cutaneous aner gy and were excluded from analysis. Of the 270 remaining patients, 93 (34%) reacted to PPD, 1 18 (44%) to PPD--B, and 76 (28%) to both. Only I12 (I 3%) PPD reactors (9 HIV positive and 3 HIV negative) had indurations of 2-9 mm. Among these, only I was dominant to PPD-B, 5 were dominant to PPD, and 3 were non-dominant. Among all 270 reactors, induration sizes to PPD and PPD B were well-correlated [Spearman's r=0.66 (95% CI 0.58 0.72)].This correlation did not differ between HIV positive and HIV-negative patients when examined separately Conclusions: Few reactors have small induration sizes to PPD. Reaction to PPD-Battey is common in this population.These data do not suggest that small PPD reaction sizes reflect infection with M. aviur. Further study is needed to define the significance of PPD- Battey reactions among persons reacting to PPD. MN Gourevitch, Montefiore Med Ctr; Il Fast 210th Street, Bronx, NY, USA 10467. Tele: (718) 920 6481 Fax: (718) 652 1343 email: gourevitarecom.yu.edu Mo.B. 1369 INTERACTIVE EFFECTS OF RIFABUTIN COMBINED WITH OTHER ANTIMICROBIAL AGENTS AGAINST MYCOBACTERIUM AVIUM COMPLEX (MAC) Yajko, David M, Cawthon VL, Madej JJ, Hadley VWK. University of California, San Francisco General H spita, San Francisco, CA USA Objective: It has been recommended that treatment of disseminated MAC infection in patients with AIDS include at least two Cntimicrobial agents.When used in combination, deugs an nterarct is an addive, synergistic, or antagonistic mannerThe interactive effects of drugs rgainst MAC are poorly understood. Rifabutin, clarithromycin (CLA), azithromycin (AZI), ciprofloxarin (CIR), ethambutol (FMB), and clofazimine (CLO) have all beers suiggested for- use ira the treartment of disseminated MAC infectronThe objective of this study was to determine the effect on intracellular MAC survival of the combination of each one of these agents with rfabutinTo accomplish this, we first determined the concentration of each drug which caused a small but measurable decrease in intracellular MAC survival. We then combined the 2 drugs at these concentrations and determined whether the combined effect on MAC survival was greater than (synergistic), equal to (additive), or less than (antagonistic) the effect of each drug used alone. Methods: Three MAC strains with varying levels of drug susceptibility were used to infect cells of the macrophage derived mouse cell line J774. Macrophages were treated with single drugs, and the concentration of each drug that caused a 25% reduction in intracellular MAC survival was determninecl Experiments were then repeated using a mixture of 2 drugs. each drug being used at the, oncentration which caused a 25% reduction in survival. Results: For 2 MAC stras r the interaction of rifabutin + CIP was consistent with the 2 drugs acting inr an addii.e, anner For one MAC strain the combination of rifabutin + EMB was additive. For all other ombinations (and all 3 strains of MAC) the interaction of drugs with rifabutin appeared to be synergistic. Differences among strains in level of susceptibility to rifabutin seemed to have little effect on combination results. Conclusions: This study provides evidence that rifabutin acts synergistically with CLA, AZI, and CLO against MAC in vitro, and may act in an additive manner with CIP and EMB against some strains.There was no evidence of antagonism between rifabutin and any of the drugs tested. DavidYajko, Clin. Labs Rm 2M35 Son Francisco Gen. Hosp. 1001 Potrero Ave. San Francisco, California, USA 94110 Telephone: 4 I 5-476 4604 Fax:415 206-3045 e-mail: [email protected] Mo.B. 1370 PREVALENCE AND RISK FACTORS FOR TUBERCULIN POSITIVITY IN A COHORT OF HIV INFECTED AND UNINFECTED AT-RISK WOMEN. Anastos Kathryn,Telzak E, Chirgwin K, Benson C, Delapenha B, Palacio H. Stonis L, Kalish L. The Women's Interagency HIV Study (WIHS) Objective: To determine the prevalence of and risk factors for tuberculin (PPD) positivi ty among HIV seropositive and seronegative at-risk women enrolled in a prospective cohort study Methods: The WIHS, a multi-site study of HIV infected and uninfected at-risk women, enrolled 1,761 women at six sites in the U.S. from October I, 1994 to May 1, 1995 This analysis reports results for 885 women who received intradermal tuberculin skin tests with 0. I ml 5-tuberculin-unit purified protein derivative (PPD), and delayed type hypersensitivity testing (DTH) by separate intradermal injection of mumps, tetanus, and candida antigens, whose HIV serostatus was confirmed and readings of skin testing at 48 to 72 hours were available. PPD reactivity (PPD+) is defined as induration of >10 mm in HIV- women, and of >5 mm in HIV+ women. DTH negative (DTH-) status is defined as failure to respond to non-PPD antigens. Results: The prevalence of PPD+ was 3% in the 750 HIV+ and 15% in the 135 HIV women. PPD+ was 7% in African American women (N -= 468), 4% in Latinas (N - 22 I) and 1% in white women (N - 173). 42% of HIV+ and 14% of HIV- women were DTH negative. PPD+ in HIV- women was not associated with DTH status (I 6% in DTH+ and 15% in DTH- women), Among HIV+ women, 4.4% of DTH+ and 1.6% of DTH- women were PPD+, p = 0.04. Among HIV+ women, 7 of the 32 (22%) reactive PPD's were in DTH- women. Independent predictors of PPD+ in multivariate logistic regression analyses were: HIV serostatus (p<.00 I); race/ethnicity (p =.006), low CD4 cell count (p-. 001), location (Calif., <1%, vs other sites 4% to 9%, p -.007), and a prior history of tuberculosis (by self-report), 5% vs 16%, p -.03.There was not an observed association of PPD reactivity with foreign birth, history of IDU, use of crack/cocaine, number of sexual partners, exchange of sex for money or drugs, or household history of TB. Conclusion: PPD+ in this cohort of HIV infected and at risk women was associated most strongly with HIV negative serostatus and CD4 cell count > 500/nam as well as geographic site, non-white race, a personal history of TB, and in HIV+ women, DTH+ status. DTH- status may not be an indication to discontinue PPD skin tests in HIV+ women. Kathryn Anastos, MD (718) 920-6062 FAX #(718) 515-7741 3544 Jerome Avenue, Bronx New York 10467 Mo.B.137 I MAIC AND THE EFFECT OF PREDNISONE ON DISEASE PROGRESSION IN AIDS PATIENTS Graves, Marilyn, Salvato, P,Thompson, C. Twelve Oaks Hospital. Houston,Texas, USA. Objective: To assess the effect of steroid therapy in combination with standard MAIC therapy in patients with AIDS. Methods: 52 patients infected with HIV (CD4 8-I21) who received oral prednisone (.5 mg/kg daily) with standard 3-5 drug treatment for MAIC were compared to 4 I patients who received only standard 3-5 drug MAIC treatment. After one (I ) year of treatment medical records were reviewed to evaluate death rate, CD4 count changes, and weight changes. 86% of all patients were on combination antiviral therapy for the I year data collection period. Results: Patients on standard 3-5 drug MAIC therapy without prednisone adjunct therapy experienced a 34% increase in deaths as compared to those patients receiving both stan dard MAIC therapy and adjunctive treatment with prednisone. Increase in mean CD4 counts and weight were greater in the group receiving prednisone. Type Therapy # Patients Prednisone.5mg/kg QD 52 No Prednisone 41 Parameters Measured Deaths CD4 Count A #23 %44 xT 27 #32 %78 x,39 Weight A x 14 Ibs x 31 Ilbs Conclusions: Treating HIV patients with steroids presents considerable challenge to most clinicians.This study demonstrates significant survival advantages in the treatrment of MAIC with the addition of once daily.5 mg/kg prednisone to standard treatment regirsen. In addition, weight gain was significantly improved as were CD4 counts. Steroid treatment in patients with MAIC clearly warrant further study. Marilyn Graves, 4120 Southwest Fwy, Suite 200, Houston,Texas. 77027 Tel: (713) 960 7900, Fax: (713) 960 7910 Mo.B. 1372 COMBINATION CLARITHROMYCIN AND A QUINOLONE IN THE TREATMENT OF DISSEMINATED MYCOBACTERIUM AVIUM-INTRACELLULARE INFECTION Alkhal, AM*, Ross. ack W*, Sherwood, DJ**. *Hartford Hospital, Hartford, CT USA;**University of Connecticut, Farmington, CT USA. Objective: To determine the efficacy of combination therapy of oral clarithromycin and a quinolone in the treatment of disseminated mycobacterium-avium intracellulare complex (MAC) infection in patients with AIDS.

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Abstracts Vol. 1 [International Conference on AIDS (11th: 1996: Vancouver, Canada)]
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International AIDS Society
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1996
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