Background Guidelines for drug therapy in human immunodeficiencyvirus (HIV) disease are based primarily on the stage of thedisease. To determine whether sociodemographic characteristicsof patients influence drug therapy in practice, we analyzedthe use of antiretroviral therapy and prophylactic therapy forPneumocystis carinii pneumonia (PCP) in an urban populationinfected with HIV.
Methods All patients presenting for the first time to our HIVclinic from March 1990 through December 1992 were enrolled.Data on sociodemographic and clinical variables and on druguse were collected at the time of presentation and after sixmonths. We asked whether patients with CD4+ cell counts of 500or less per cubic millimeter were receiving antiretroviral therapyat the time of presentation, and whether patients with CD4+cell counts of 200 or less per cubic millimeter were receivingPCP prophylaxis.
Results Among the 838 patients enrolled, 656 (79 percent) wereblacks, 167 (20 percent) were non-Hispanic whites, and 15 (2percent) were Asian or Hispanic or were not racially classified.There were no racial differences in the stage of HIV diseaseat the time of presentation. However, there were racial disparitiesin the receipt of antiretroviral therapy: 63 percent of eligiblewhites but only 48 percent of eligible blacks received suchtherapy (P = 0.003). PCP prophylaxis was received by 82 percentof eligible whites but only 58 percent of eligible blacks (P<0.001).There were no significant differences in the receipt of drugtherapy with respect to age, sex, mode of HIV transmission,type of insurance, income, education, or place of residence.In a logistic-regression analysis, race was the feature moststrongly associated with the receipt of drug therapy. When blackswere compared with whites, the adjusted relative odds were 0.59(95 percent confidence interval, 0.38 to 0.93) for the receiptof an antiretroviral agent and 0.27 (95 percent confidence interval,0.13 to 0.56) for the receipt of PCP prophylaxis.
Conclusions Among patients infected with HIV, blacks were significantlyless likely than whites to have received antiretroviral therapyor PCP prophylaxis when they were first referred to an HIV clinic.This disparity suggests a need for culturally specific interventionsto ensure uniform access to care, including drug therapy, anduniform standards of care.
Since the approval in 1987 of zidovudine, the first clinicallyeffective form of antiretroviral therapy,1 a number of prophylacticand therapeutic drugs have been introduced for the treatmentof patients with human immunodeficiency virus (HIV) disease2,3,4,5,6,7,8,9,10,11,12.In addition, over the past few years the most effective drugregimens and dosing schedules have been defined, as well asthe stages of disease at which several of these drugs are mosteffectively used. The guidelines of the National Institute ofAllergy and Infectious Diseases for the treatment of HIV-infectedpersons specify that antiretroviral therapy with zidovudineshould begin when the CD4+ lymphocyte count falls to 500 cellsper cubic millimeter or less13. This recommendation is basedon the results of two clinical trials demonstrating the efficacyof zidovudine therapy for early treatment14,15. One of the mostcommon opportunistic infections associated with advanced HIVinfection is Pneumocystis carinii pneumonia (PCP)16. The guidelinesof the Public Health Service specify that prophylactic treatmentfor PCP should begin when the CD4+ lymphocyte count reaches200 cells per cubic millimeter or less17.
HIV infection has disproportionately affected racial and ethnicminorities in the United States18. Despite clinical recommendationsthat uniform standards of prescription-drug therapy be followedregardless of sociodemographic factors (such as sex, race, andage) or behavioral factors, such as the mode of HIV transmission(e.g., injection-drug use or homosexual contact), there is evidenceto suggest dissimilar demographic patterns of prescription-druguse19,20,21. The reasons for the differences in the use of drugtherapy are unknown. Physicians' prescribing practices may varyinappropriately according to the patient's sociodemographiccharacteristics. The patient's ability to pay, the presenceof certain types of behavior, such as injection-drug use, andother social barriers may also affect access to, and receiptof, appropriate therapy.
To quantify sociodemographic differences in prescription-druguse in patients with HIV infection and to delineate the associatedfactors, we analyzed drug use in a heterogeneous urban cohortof HIV-infected patients presenting for comprehensive HIV care.
Methods
The Johns Hopkins Hospital AIDS Service provides long-term primaryand subspecialty care for the majority of HIV-infected patientsin the Baltimore metropolitan area. To be registered in theclinic, patients must have had HIV infection diagnosed by aMaryland physician. In our patients, the mean interval betweensuch a diagnosis and entry into the clinic was 19 months. SinceDecember 1988, every new patient has undergone a comprehensivemedical and psychosocial evaluation by either a physician ora physician's assistant, along with a nurse and a social worker,using standardized instruments to collect extensive data ondemographic, clinical, laboratory, pharmaceutical, and psychosocialcharacteristics22.
In this study, we assessed data collected at enrollment andalso at follow-up six months later. Data on the use of drugtherapy were obtained for all three antiretroviral drugs licensedat the time of the study: zidovudine, didanosine, and zalcitabine.Data were also collected on the drugs used for PCP prophylaxis:trimethoprim-sulfamethoxazole, aerosolized pentamidine, anddapsone. Information about drug use was obtained from the patients'reports and from accompanying medical records when available.
To determine whether there were demographic differences in thestage of HIV disease at presentation, we divided the patientsinto three groups according to CD4+ lymphocyte count ( 200,201 to 500, and >500 cells per cubic millimeter) and assessedeach group with respect to age, sex, race, mode of HIV transmission,insurance coverage, place of residence, income, and level ofeducation. These variables were categorized as follows: age,as 30 years or less, 31 to 44 years, and 45 or more years; racewas defined as black, white, or other (all the patients in thiscategory were Asian or Hispanic or could not be classified).The mode of HIV transmission was defined as homosexual contact,injection-drug use, homosexual contact combined with injection-druguse, heterosexual contact, or other. Insurance coverage wasdefined as Medicaid coverage, commercial insurance (includingBlue Cross-Blue Shield and private insurance), no insurance,or other (including Medicare and membership in a health maintenanceorganization [HMO]). Level of education was defined as not includinga high-school degree, including a high-school degree, or includingeducation beyond the high-school level. Place of residence wasdefined as East Baltimore (the clinic catchment area), all otherparts of Baltimore, and areas outside Baltimore. Data on incomeincluded legal income only. Some data were missing for race,insurance coverage, education, income, and place of residence.
From interviews with each patient and the medical record, wedetermined whether the patient could identify and name a sourcefrom which he or she had obtained medical care before visitingour clinic for the first time. A usual source of care was definedas a personal physician, physician's assistant, or nurse practitioneror a clinic, HMO, or other practice entity known to providecomprehensive care. However, we did not have information onthe extent or regularity of the care provided by these sources.Determinations of a usual source of care were made only forpatients with base-line CD4+ lymphocyte counts of 500 cellsper cubic millimeter or less.
Since antiretroviral therapy is indicated only for patientswith CD4+ lymphocyte counts of 500 cells per cubic millimeteror less, we restricted our analysis of the use of these drugsto those patients. Since PCP prophylaxis is indicated only forpatients with CD4+ lymphocyte counts of 200 cells per cubicmillimeter or less, we restricted our analysis of the use ofthis prophylaxis to those patients. This was consistent withour subsequent findings, since only 8 percent of patients withCD4+ lymphocyte counts greater than 500 cells per cubic millimeterhad received antiretroviral therapy and only 9 percent of patientswith CD4+ counts greater than 200 cells per cubic millimeterhad received PCP prophylaxis. In our cohort, the most commonlyused antiretroviral drug was zidovudine (92 percent); only asmall number of patients used didanosine (5 percent) or zalcitabine(3 percent). The drugs used for PCP prophylaxis included trimethoprim-sulfamethoxazole(59 percent), aerosolized pentamidine (27 percent), and dapsone(13 percent).
We attempted to determine whether the patients' use of antiretroviraltherapy or PCP prophylaxis at the time of enrollment differedaccording to demographic characteristics. We compared drug usebetween demographic strata by the chi-square test23 and soughtto determine whether differences in other base-line variablescould explain demographic differences in use. The comparisonswere performed again by the chi-square test after the demographicgroups were stratified according to CD4+ lymphocyte counts atenrollment. We performed a multivariate analysis using logisticregression to assess the associations between multiple variablesand drug use23. One of the laboratory values obtained was themean corpuscular volume. This value is elevated in most patientswho take zidovudine and was used as a marker of compliance withzidovudine therapy24. The t-test was used to compare the averagemean corpuscular volume between groups23. Two-tailed P valuesare presented for all statistical analyses.
The research protocol was approved by the Johns Hopkins JointCommittee on Clinical Investigation. Informed consent was notrequired for this observational study.
Results
The demographic characteristics of the HIV-infected patientspresenting to the clinic from March 1990 through December 1992are shown in Table 1. The cohort was predominantly male (69percent) and black (79 percent), with injection-drug use asthe primary mode of HIV transmission (47 percent). The majorityof patients (56 percent) were 31 to 44 years of age. At presentation,the patients were evenly divided into three groups with regardto CD4+ lymphocyte counts: those with 200 cells per cubic millimeteror less (34 percent), those with 201 to 500 cells per cubicmillimeter (36 percent), and those with more than 500 cellsper cubic millimeter (30 percent). We further analyzed the demographiccharacteristics according to the CD4+ lymphocyte count at presentation.Men were more likely than women to present first to the clinicafter the CD4+ lymphocyte count had declined to 500 cells percubic millimeter or less; similarly, persons 31 years old orolder were more likely than younger persons to present aftersuch a decline in the CD4+ count. There were no differencesamong patients according to CD4+ lymphocyte count at presentationwith respect to race or other characteristics, including insurancecoverage, place of residence, annual income, and level of education.
Table 1. Base-Line Characteristics of the 838 HIV-Infected Patients in the Study Cohort.
We examined the frequency of prescription-drug use at presentationaccording to these demographic categories (Table 2). Blackswere less likely than whites (48 vs. 63 percent) to have receivedany of the antiretroviral drugs (P = 0.003). Patients less than30 years old, those without insurance, and those from East Baltimorewere less likely than the other patients to be receiving antiretroviraldrugs at entry, although these differences were not statisticallysignificant. Similarly, blacks were significantly less likelythan whites (58 vs. 82 percent) to have received prophylaxisfor PCP at presentation (P<0.001) (Table 3). No other significantdifferences were found.
Table 3. PCP Prophylaxis at Presentation in Patients with CD4+ Lymphocyte Counts of 200 Cells per Cubic Millimeter or Less.
To determine whether the differences between racial groups inthe use of antiretroviral drugs and PCP prophylaxis were associatedwith other cofactors, we analyzed the use of these therapiesaccording to race and other demographic characteristics. Table 4shows that there was less frequent use of antiretroviral therapyand PCP prophylaxis at the time of first presentation by blacksthan by whites according to most other demographic variables.This suggests that racial differences in drug therapy occurregardless of the patient's other characteristics, includingincome, insurance status, mode of HIV transmission, and placeof residence. We also examined the time from the diagnosis ofHIV infection to entry into the clinic for patients with CD4+lymphocyte counts of 500 cells per cubic millimeter or lessand found that this interval was somewhat shorter for blacks(mean, 20 months; 95 percent confidence interval, 18 to 22)than for whites (mean, 25 months; 95 percent confidence interval,20 to 30).
Table 4. Percentages of Blacks and Whites Receiving Antiretroviral Therapy or PCP Prophylaxis at Presentation.
In a logistic-regression analysis, we examined whether racialdifferences in drug use could be explained by differences inother demographic factors at presentation (Table 5). Racialdifferences continued to be present after adjustment for allthe other factors. The relative odds for the receipt of antiretroviraltherapy by blacks was 0.59 (95 percent confidence interval,0.38 to 0.93), and the relative odds for the receipt of PCPprophylaxis was 0.27 (95 percent confidence interval, 0.13 to0.56) (P = 0.02 and P<0.001, respectively). Significant differenceswere also found for age less than 31 years (relative odds, 0.63;95 percent confidence interval, 0.43 to 0.94) and lack of insurance(relative odds, 0.60; 95 percent confidence interval, 0.39 to0.93) for the receipt of antiretroviral therapy, and residencein East Baltimore (relative odds, 0.55; 95 percent confidenceinterval, 0.32 to 0.94) for PCP prophylaxis.
Table 5. Multivariate Logistic-Regression Analysis of Demographic Characteristics Associated with Drug Use.
To assess whether patients for whom zidovudine had been prescribedwere taking the drug at entry, we compared the mean corpuscularvolume in patients who reported zidovudine use with that inpatients not reporting such use and found means of 95 fl (95percent confidence interval, 94 to 96) and 88 fl (95 percentconfidence interval, 87 to 89), respectively (P<0.001). Notably,among blacks the average mean corpuscular volume in patientsreceiving zidovudine was 93 fl (95 percent confidence interval,91 to 95), as compared with 88 fl (95 percent confidence interval,87 to 89) in patients not receiving zidovudine. Among whites,the average mean corpuscular volume in patients receiving zidovudinewas 101 (95 percent confidence interval, 98 to 104), as comparedwith 89 (95 percent confidence interval, 87 to 91) in patientsnot receiving the drug. The mean difference of 8 fl betweenblacks and whites was significant (P<0.001).
A usual source of care was identified by 67 of 113 whites (59percent) and 150 of 437 blacks (34 percent) (P<0.001). Forty-nineof 67 whites (73 percent) and 92 of 150 blacks (61 percent)who identified a usual source of care had received an antiretroviraldrug (P = 0.092). In the subgroup of patients with CD4+ lymphocytecounts of 200 cells per cubic millimeter or less, 32 of 39 whites(82 percent) and 46 of 78 blacks (59 percent) who identifieda usual source of care had received PCP prophylaxis (P = 0.013).
Finally, the results of the six-month interim follow-up weresimilar among blacks and whites and represented 96 percent and94 percent, respectively, of patients eligible for follow-up.No racial differences in the use of either antiretroviral therapyor PCP prophylaxis were found after six months. Antiretroviraltherapy had been received by 81 percent of the blacks and 84percent of the whites. PCP prophylaxis had been received by92 percent of the blacks and 98 percent of the whites.
Discussion
Our analysis of an HIV-infected urban cohort showed that blackswere less likely than whites to have had either antiretroviraltherapy or PCP prophylaxis prescribed before they came to ourclinic for care. Because a provider may have prescribed a treatmentfor which the patient could not pay, it is notable that thedata on insurance coverage and income did not explain this racialdisparity. Nor did behavior such as injection-drug use, demographiccharacteristics such as sex and age, or socioeconomic factorssuch as the patient's level of education and place of residenceappear to explain the racial difference.
Our HIV service is the principal referral site in Maryland forpatients with HIV infection diagnosed elsewhere. As our analysisof patients' demographic characteristics at presentation shows,both black and white patients are referred to the clinic moreoften in later than in earlier stages of the disease, as demonstratedby the fact that 70 percent of patients had CD4+ lymphocytecounts of 500 cells per cubic millimeter or less. The slightlyshorter interval between the diagnosis of HIV infection andpresentation among blacks than among whites did not explainthe differences in treatment. We learned whether the patientcould identify a physician or comprehensive health care facilityas a usual source of care, but we did not have detailed informationabout the extent to which these patients had used such resourcesbefore their first visit to us. With this qualification, ouranalysis suggested that blacks were less likely than whitesto have a usual source of care through which they could receiveappropriate HIV prophylactic-drug therapy before their referralto our clinic. Recent data indicate that HIV infection increasinglyaffects lower-income residents of inner cities, who are predominantlyyoung and black25. This appears also to describe a group ofpeople who have historically neither sought nor had access tomedical care, particularly preventive medical care26. Blacks,especially younger men, are the group least likely to have aregular primary care physician27. A recent study showed thatHIV-infected non-whites are more likely than whites with comparableCD4+ counts to be admitted to a hospital and less likely touse outpatient care28.
Barriers to the spread of information may also affect blacksmore than whites. Beliefs about the benefits and risks of treatinghypertension relate to differences between blacks and whitesin the use of medical care29. Blacks appear to have less knowledgeof heart-attack symptoms30 and the detection and treatment ofcancer31. Misconceptions about HIV disease and the acquiredimmunodeficiency syndrome (AIDS) have been shown to be morecommon among blacks than whites,32 and distrust of health authoritiesmay also be a barrier33. If we assume that the response of themean corpuscular volume to zidovudine in blacks is similar tothat in whites,24 our finding of a lower average mean corpuscularvolume in blacks suggests that blacks may have lower compliancewith zidovudine therapy than whites.
Still another potential barrier to care for blacks relates tothe prescribing habits of care providers. There is evidenceto suggest that the likelihood of a physician's recommendinga therapeutic regimen may be influenced by the patient's race.Members of minority groups are less likely than non-Hispanicwhites to be offered treatment (surgical or other) for coronaryartery disease,34,35 analgesia for long-bone fractures,36 treatmentof alcoholism,37 erythropoietin for end-stage renal disease,38and rehabilitation after a mastectomy39. Our data indicate thatamong patients who identified a usual source of care, fewerblacks than whites received therapy. This is the case despiteevidence indicating that there are probably no valid reasonsfor racial disparities in drug prescribing for HIV disease40,41,42.
Such barriers to care for young blacks contrast with the carereceived by the predominantly white, middle-class gay community,which has organized support systems through which medical careis actively sought, particularly in the early stages of thedisease. The efforts of the gay community with regard to deliveryof care and research in HIV disease represent a model of involvementby patients in medical care43. Our results suggest that theremay be a need for culturally appropriate efforts to promoteearly preventive care in urban black populations. This needwas emphasized in a recent review of barriers to the treatmentof AIDS in intravenous drug users belonging to ethnic minorities44.One model for such an effort is a community-based partnershipbetween an academic medical center and a high-risk urban blackpopulation, coordinated through churches45. Our six-month follow-updata suggest that without a referral center dedicated to thecomprehensive treatment of HIV disease, inequalities in caremay persist.
Although our results indicate that blacks may not have the sameaccess as whites to recommended therapeutic care, we do notknow whether these differences in access result in differentoutcomes. Our cohort does not have sufficient follow-up to permitus to determine whether rates of survival, progression to AIDS,or the development of PCP and other opportunistic conditionsdiffer over time between blacks and whites. Two previous studiesin urban communities found no racial differences in survivalafter a diagnosis of AIDS, although for the most part thesestudies predated contemporary antiretroviral and other therapy46,47.There are nearly 60,000 excess deaths per year among blacksas compared with whites48. Stroke, diabetes, severe hypertension,and renal failure are all more common in blacks than in whites26.The increasing shift of HIV disease to poor urban communitiesin which the lack of preventive care has resulted in increasedmorbidity and mortality from other diseases underscores theneed for effective intervention to improve access to care.
Supported by a grant (R01-HS07809-01) from the Agency for HealthCare Policy and Research and by a contract from the MarylandDepartment of Health and Mental Hygiene.
We are indebted to Darrell Forney, Sharon McAvinue, and LindaLocklear for their contributions to the creation and analysisof these data.
Source Information
From the Johns Hopkins University School of Medicine, 1830 E. Monument St., Rm. 8059, Baltimore, MD 21205, where reprint requests should be addressed to Dr. Moore.
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