The Journal of the American Dental Association
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


J Am Dent Assoc, Vol 138, No 11, 1468-1475.
© 2007 American Dental Association

This Article
Right arrow Abstract Freely available
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Magalhães, M. G.
Right arrow Articles by Glick, M.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Magalhães, M. G.
Right arrow Articles by Glick, M.
Related Collections
Right arrow Periodontics

RESEARCH

JADA Continuing Education

Comorbidities in older patients with HIV

A retrospective study



Marina Gallottini Magalhães, DMD, Barbara Greenberg, MSc, PhD, Heidi Hansen, Cand Odont and Michael Glick, DMD


   ABSTRACT
 TOP
 ABSTRACT
 SUBJECTS AND METHODS
 RESULTS
 DISCUSSION
 CONCLUSIONS
 REFERENCES
 
Background. The number of older adults with HIV is increasing. The authors conducted a retrospective study to determine the prevalence of selected comorbidities that may affect the delivery of oral health care to this population.

Methods. The authors reviewed the charts of 162 patients with HIV who were 50 years or older who had sought dental treatment from 2000 through 2006. The authors abstracted patients’ self-reported clinical comorbidities and laboratory-verified HIV-related and hematologic values.

Results. A total of 88.8 percent of the study subjects had at least one comorbidity. Comorbidity prevalence was 44.4 percent for hepatitis C virus, 41.4 percent for hypertension, 16.7 percent for psychiatric disorders, 16.1 percent for chronic obstructive pulmonary disease, 15.4 percent for anemia and 14.8 percent for heart disease. Significantly more subjects with a CD4+ cell count of less than 200 per cubic millimeter were anemic compared with subjects with counts of 200/mm3 or more.

Conclusions. HIV-positive patients 50 years or older have a broad range of comorbidities that may affect the provision of oral health care.

Clinical Implications. Whether these patients have clinically severe or less well-controlled comorbidities that may require modification of oral health care treatment remains to be determined.

Key Words: HIV infection; aging; cardiovascular diseases; hypertension; hepatitis virus; anemia

Abbreviations: ALT: Alanine aminotransferase • ANC: Absolute neutrophil count • AST: Aspartate aminotransferase • COPD: Chronic obstructive pulmonary disease • HAART: Highly active antiretroviral therapy • HCV: Hepatitis C virus • Hgb: Hemoglobin • IDU: Injecting drug users • MSM: Men who have sex with men • VL: Viral load • WBC: White blood cell count

The HIV/AIDS epidemic in the United States has changed dramatically over the last decade. Significant improvements in the clinical management of HIV and advances in pharmacotherapy have changed the course of HIV, transforming it from a highly fatal disease to a chronic condition that can be managed over time. At the threshold of the HIV/AIDS epidemic’s fourth decade, the number of people who receive diagnoses of HIV/AIDS and the number of deaths continues to decline in the United States, while the number of older adults living with HIV/AIDS continues to grow. The Centers for Disease Control and Prevention has indicated that the cumulative number of AIDS cases among American adults older than 50 years of age quintupled over the last decade.1 More recently, the estimated number of AIDS cases by year of diagnosis increased 3.8 percent from 2000 to 2004 in the 20- to 49-year-old age group and 29 percent from 2000 to 2004 in the 50-year-old or older group. Approximately one in five people with HIV in the United States is 50 years or older.13

Concomitant with the changes in the course of HIV/AIDS are changes in the types and presentations of comorbidities seen in these patients. People with HIV may have comorbidities owing to the presence of underlying conditions that were present before they developed HIV, coinfection with other infectious diseases such as hepatitis B virus and hepatitis C virus (HCV), HIV-related medical consequences and central nervous system complications, or the adverse effects of certain medical treatments. As a result of the widespread use of new pharmacotherapies and the aging of the infected population, new comorbidities such as cardiovascular disease and diabetes have emerged.46

Given the interrelationships between oral health and general health that involve most organ systems, many diseases can affect oral health care delivery. HIV provides a dramatic example of this medical-dental interaction. The consideration of comorbidities is particularly important in the delivery of oral health care to older patients with HIV, as they may have a greater array of and more complex medical conditions associated with their HIV infection or the aging process. To date, no studies have assessed the presence of comorbidities that are important in oral health care delivery to older patients with HIV post–highly active antiretroviral therapy (HAART) era.

At a time when the prevalence of comorbidities in people with HIV is changing, dental professionals should assess the prevalence and presentation of comorbidities to determine the need for dental treatment modifications.7,8 We conducted a retrospective study to determine the prevalence of selected clinical and hematologic comorbidities that may affect the delivery of oral health care to older patients with HIV.


   SUBJECTS AND METHODS
 TOP
 ABSTRACT
 SUBJECTS AND METHODS
 RESULTS
 DISCUSSION
 CONCLUSIONS
 REFERENCES
 
We conducted a retrospective review of the dental charts of 162 patients 50 years or older who sought treatment at the Oral Medicine Clinic of the New Jersey Dental School, University of Medicine and Dentistry of New Jersey, Newark, from 2000 through 2006. The institutional review board of the University of Medicine and Dentistry of New Jersey, Newark, approved our study.

A trained oral health care professional (M.G.M.) abstracted data from medical history forms, laboratory reports and notes from the dental chart. Specifically, she abstracted demographic information (age, sex, race/ethnicity), clinical data (self-reported primary route of HIV transmission, alcohol and tobacco use, illicit drug use, self-reported comorbidities, antiviral medication use), laboratory-verified HIV-related data (CD4+ cell counts, HIV viral load [VL] levels) and other laboratory information (total white blood cell count [WBC]), hemoglobin level [Hgb], absolute neutrophil count [ANC], alanine aminotransferase level [ALT], aspartate aminotransferase level [AST] and platelet count) from the initial visit. She abstracted laboratory values within one month of the initial visit.

The comorbidities that had the potential to warrant dental modifications9 included viral hepatitis, hypertension, psychiatric disorders, chronic obstructive pulmonary disease (COPD), anemia, heart disease (coronary artery disease, including myocardial infarction, cardiomyopathy, heart murmur), stroke, diabetes mellitus, kidney disease, neurological disorders, orthopedic disease, bleeding disorders, cancer and tuberculosis. We determined the prevalence of each comorbidity among people 50 years or older who had HIV, as well as their immune, anemia (Hgb < 13 grams per deciliter for men and < 12 g/dL for women), leukopenia (WBC < 4.0 x 109/liter), neutropenia (ANC < 1,000 microliters) and thrombocytopenia (platelet count < 50 x 109/L) statuses. We also determined the incidence of critically low levels of Hgb that are considered important in the delivery of oral health care (< 9.0 g/dL).10

We used {chi}2 or Fisher exact tests, as appropriate, to test the association among the sex distributions for the clinical comorbidities, hematologic comorbidities and HIV-related laboratory data (CD4+ cell count, VL). We also used {chi}2 or Fisher exact tests to assess the relationship between CD4+ cell counts and VL with select hematologic variables (ANC, Hgb level and platelet count); we separated the CD4+ cell counts into three categories (< 200 per cubic millimeter, 200–499/mm3 and ≥ 500/mm3), and we separated VL into three categories (undetectable, < 10,000 copies per milliliter and ≥ 10,000 copies/mL). We set a significance level of P < .05 for all statistical tests. We performed all statistical analyses by using a software package (SAS, Version 9.1, SAS Institute, Cary, N.C.).


   RESULTS
 TOP
 ABSTRACT
 SUBJECTS AND METHODS
 RESULTS
 DISCUSSION
 CONCLUSIONS
 REFERENCES
 
Among 162 subjects 50 years or older, 119 (73.5 percent) were men and 43 (26.5 percent) were women (Table 1Go). The racial/ethnic distribution was 130 (80.3 percent) African-American, 14 (8.6 percent) white, 16 (9.9 percent) Hispanic and 2 (1.2 percent) unknown. The subjects’ ages ranged from 51 to 84 years, with a mean of 57 years. The primary HIV transmission categories were injecting drug users (IDU) (n = 50, 30.9 percent) and heterosexual behavior (n = 48, 29.6 percent). They were followed by men who have sex with men (MSM) (n = 8, 4.9 percent) and blood transfusion recipients (n = 3, 1.9 percent). Twelve (7.4 percent) subjects reported having multiple risk factors, and 41 (25.3 percent) reported having an unknown risk or had no information. Of the 160 subjects who reported tobacco use, 80 (50 percent) were current smokers. Of the total study sample of 162 subjects, 74 (45.7 percent) reported past injected drug use, nine (5.6 percent) reported current use, and 79 (48.8 percent) reported that they had never used any injected drugs. Among the 162 subjects, 117 (72.2 percent) were receiving HAART therapy.


View this table:
[in this window]
[in a new window]

 
TABLE 1 Demographic data and type of therapy.

 
Table 2Go shows the prevalence of comorbidities reported for all study subjects and the distribution by sex. A total of 144 of the 162 study subjects (88.8 percent) reported having at least one comorbidity. Among those who reported having a comorbidity, 26 (18.0 percent) reported having one, 40 (27.8 percent) reported having two, and 78 (54.2 percent) reported having three or more. Among all study subjects, 72 (44.4 percent) reported having HCV, 67 (41.4 percent) reported having hypertension, 27 (16.7 percent) reported having psychiatric disorders, 26 (16.1 percent) reported having COPD, 25 (15.4 percent) reported having anemia, and 24 (14.8 percent) reported having heart disease. The rate of HCV ranged from 37.5 percent among MSM to 66.7 percent among blood transfusion recipients.


View this table:
[in this window]
[in a new window]

 
TABLE 2 Self-reported comorbidity prevalence for total study population.

 
Men reported having HCV more frequently than did women (49.6 percent versus 30.2 percent, respectively; P = .03), while women reported having hypertension more frequently than did men (55.8 percent versus 36.1 percent, respectively; P = .02). We did not find sex differences for the remaining comorbidities.

The CD4+ cell count, HIV VL and hematologic profile of subjects with available data are shown in Table 3Go (page 1472). Among the 124 subjects with available data on CD4+ cell counts, 91 (73.0 percent) had cell counts of less than 500/mm3, and 37 (29.8 percent) had cell counts of less than 200/mm3. Sixty-three (52.1 percent) of the 121 study subjects with available data on VL counts had undetectable VL, and 11 (9.1 percent) had a VL count of 10,000 copies/mL or greater. Among the 137 subjects with available data on Hgb levels, 53 (38.7 percent) had abnormal levels, and four (2.9 percent) had critically low levels. Among the 118 subjects with available on AST data, 74 (62.7 percent) had abnormal values. Among the 117 subjects with available ALT data, 60 (51.3 percent) had abnormal values. Among the 140 subjects with available WBC data, 42 (30 percent) had low levels of WBC (< 4,000/mL). Among the 118 subjects with available ANC data, 13 (11 percent) had critically low levels (< 1,000 µL). Among the 132 subjects with available platelet count data, 1 (0.8 percent) had critically low platelet counts (< 50,000). We found no sex differences for any variable.


View this table:
[in this window]
[in a new window]

 
TABLE 3 Laboratory-verified data, by sex.

 
When we analyzed CD4+ cell count distribution with each clinical comorbidity listed in Table 2Go, we found no association (data not shown). Table 4Go (page 1473) shows the results of our analysis of CD4+ cell count and HIV VL with ANC, platelet count, abnormal Hgb level (anemic) and critically low Hgb level. We found that 60.0 percent of subjects with a CD4+ cell count of less than 200/mm3 were anemic compared with 23.5 percent of subjects with a CD4+ cell count of 200/mm3 or greater (P < .001). In an analysis of the three categories of CD4+ cell count categories, we found that 60 percent of subjects in the lowest CD4+ cell count category (< 200/mm3) had anemia compared with 7 percent of subjects in the highest CD4+ cell count category (≥ 500/mm3) (data not shown). We found no associations between CD4+ cell count and ANC or platelet count. We used logistic regression to assess the relationship of CD4+ cell count and abnormal Hgb levels, adjusting for VL. Subjects with a CD4+ cell count of less than 200/mm3 had five times greater odds of having abnormal Hgb levels compared with subjects with a CD4+ cell count of 200/mm3 or greater (odds ratio = 5.20; 95 percent confidence interval = 1.94 to 13.96). We detected no significant associations between the CD4+ cell count and ANC. We found no significant association of VL with ANC, Hgb levels or platelet counts.


View this table:
[in this window]
[in a new window]

 
TABLE 4 Distribution of absolute neutrophil count, hemoglobin and platelet count, by CD4+ cell count and HIV viral load.

 

   DISCUSSION
 TOP
 ABSTRACT
 SUBJECTS AND METHODS
 RESULTS
 DISCUSSION
 CONCLUSIONS
 REFERENCES
 
We conducted our study to document the prevalence of select comorbidities in adults 50 years or older who had HIV and sought treatment at an urban dental school clinic. In this population, the most commonly reported comorbidities were HCV (44.4 percent), hypertension (41.4 percent), psychiatric disorders (16.7 percent), COPD (16.1 percent), anemia (15.4 percent) and heart disease (14.8 percent). The potential concerns from the perspective of oral health care delivery depend on the severity of these conditions and how well they are controlled.

Viral hepatitis. Authors from France who produced a mortality report of all hospital wards known to treat patients with HIV identified cancer, viral hepatitis and cardiovascular disease as the top three non–AIDS-defining causes of death in the era of HAART.11 Authors of a recent study of 23,441 patients with HIV who were followed prospectively found that liver-related deaths were the most common cause of death after AIDS.12

Since HCV and HIV have common transmission risk factors, HCV is a common comorbidity among patients with HIV. Among IDUs and patients with hemophilia, rates of coinfection may be as high as 70 to 95 percent, as compared with 1 to 12 percent among MSM.13 In the population of urban older people with HIV who we studied, the rate of HCV ranged from 37.5 percent among MSM to 66.7 percent among those who had received blood transfusions, while the HCV rate ranged from 46 percent for IDUs and 50 percent for heterosexual patients (data not shown). As subjects self-reported their primary route of HIV transmission, we do not know if this is a true reflection of the prevalence among particular risk groups. The reported prevalence rate among the general population in the United States, however, is markedly lower (approximately 2.5 percent).14 Although our study population had a higher prevalence of HCV infection than did the general population, it was lower than that reported for patients coinfected with HIV. It is possible that our older study population includes those who have survived longer, owing to less severe HCV-induced liver disease. Our study population’s relatively low liver transaminase levels may support such a conclusion.

While modifications to dental treatment are not necessary for patients with asymptomatic viral hepatitis,15 dental professionals should request a medical consultation with the patient’s physician to determine the severity of any associated liver disease before providing dental care. Patients with HCV may have chronic active hepatitis, which can lead to compromised liver function and may interfere with hemostasis and altered drug metabolism.

Hypertension. The prevalence of hypertension, a primary risk factor for cardiovascular disease and stroke, is likely to increase as the population with HIV ages. The prevalence of hypertension in patients with HIV also has increased as a result of the more widespread use of HAART, particularly with certain classes of drugs. The 41.4 percent prevalence of hypertension among our study population is higher than that reported for adults older than 20 years with HIV (33 percent),16 but lower than that reported among the general older adult population in the United States (men aged 55–64 years, 45.8 percent; aged 65–74 years, 58.5 percent; 75 years and older, 68.8 percent; and women aged 55–64 years, 54.6 percent; aged 65–74 years, 74.3 percent; 75 years and older, 81.7 percent).16 It is not clear why there is such a discrepancy between our study population and other people of the same age groups. This, however, may be an indication of patients with HIV seeing a physician more often and addressing early signs of high blood pressure.

Important considerations for assessing the delivery of oral health care in older patients with HIV and hypertension include the patient’s clinical disease status (for example, controlled or uncontrolled, presence of signs or symptoms), the length of time that the patient has been hypertensive, and the presence or history of target organ disease. For patients with controlled hypertension, modifications to dental treatment are not necessary. However, depending on the patient’s history of target organ damage and the presence of signs and symptoms of hypertension, clinicians should assess patients individually, as modifications to dental treatment—including avoiding elective dental care—may be warranted.17

Psychiatric disorders. Psychiatric disorders in populations of people with HIV exceed general-population estimates significantly in the United States. Rates of depression range from 20 to 37 percent in people with HIV.18 Cognitive impairment increases as the immune system worsens and HIV progresses.19 Although the use of HAART has been associated with improvements in cognitive performance, data suggest there is no change in the frequency of cognitive abnormalities after widespread use of HAART.20 Furthermore, the prevalence of minor HIV-associated cognitive impairment is rising among patients on HAART as a result of the increased survival time.21

The reported prevalence of psychiatric disorders in our study population was 16.7 percent, which is slightly lower than the 20 to 37 percent in a previous report.18 Dental treatment modifications may be necessary in patients with psychiatric disorders owing to interactions between different analgesic agents and the antidepressant/antipsychotic class of drugs.17 Therefore, clinicians should take a thorough history of medication use when caring for patients with HIV and psychiatric disorders.

COPD. COPD includes chronic bronchitis, emphysema and asthma, which are characterized by chronic obstruction of the flow of air through the airways and out of the lungs. COPD affects more than 5 percent of the general adult population and occurs mainly in elderly people in whom it causes significant morbidity and mortality.22 The authors of a recent study of U.S. veterans found a 10 percent prevalence rate of COPD in people with HIV compared with a 9 percent prevalence rate in people who did not have HIV.23 After adjusting for potential effect modifiers, subjects with HIV had 1.47 greater odds of having COPD compared with subjects who did not have HIV, suggesting that HIV is an independent risk factor.

Current smoking was associated with increased mortality and decreased quality of life, as well as increased respiratory symptoms, COPD and bacterial pneumonia.24 These findings suggest that smoking cessation should be emphasized for patients with HIV.

A total of 16.1 percent of our study population reported having COPD, suggesting that COPD may be more common in older patients with HIV than in patients who did not have HIV or in the general U.S. adult population. When determining oral health care delivery strategies in these patients, clinicians should establish whether the disease is stable or unstable. Patients with unstable COPD (for example, those having a shortness of breath, a productive cough or an oxygen saturation level less than 91 percent) should avoid elective dental treatment. When treating patients with COPD, clinicians should monitor oxygen saturation levels, have an extra oxygen tank available and give careful consideration to the patient’s use of additional medications.17

Anemia. The prevalence of anemia among people with HIV varies widely by sex and race/ethnicity, with rates ranging from 12 to 95 percent, depending on the study setting.25 In general, reported rates are higher among blacks and among women. Data from a large cohort of women with HIV indicated a 71 percent greater prevalence of anemia among women compared with men. Although the use of HAART has been associated with a reduction in the prevalence of anemia in women with HIV, anemia remains an important comorbidity.

Our data suggest that anemia, as determined by abnormal Hgb levels, is common (38.7 percent) among adults 50 years or older who have HIV. We found critically low levels (< 9 g/dL), which are important when determining dental treatment, in only 2.9 percent of the subjects.

Although there is little risk of exacerbating anemia with routine dental procedures, depending on the severity and underlying cause of the anemia, dental treatment modifications that minimize blood loss may be warranted. The underlying cause of the anemia, specifically whether bone marrow suppression is involved, and the severity of the condition are important factors for clinicians to consider when planning treatment for these patients. The potential impact of people with HIV’s having anemia is highlighted in longitudinal studies of women with HIV in which anemia (< 12 g/dL) was associated independently with decreased survival or increased mortality.26,27

Neutropenia. The prevalence of neutropenia varies widely in patients with HIV; reported prevalence ranges from 10 to 50 percent.28,29 The authors of a recent longitudinal study of women with HIV suggests that the progression of HIV, as measured by deceasing CD4+ cell counts and increasing HIV RNA levels, is associated significantly with developing neutropenia, while HAART was associated with resolving neutropenia.30 ANCs less than 1,500/µL are associated with patients’ increased susceptibility to bacterial and fungal infections, and lower neutrophil counts are associated with increased risks.31 Eleven percent of our study subjects had an ANC of less than 1,000/µL, which was slightly higher than the 7 percent rate reported in the longitudinal study of women with HIV.30 While older patients with HIV may not have a greater rate of neutropenia than do younger patients with HIV, given the increased susceptibility to infection patients with neutropenia have, clinicians should recognize this condition and consider administering antibiotic prophylaxis to patients when warranted.17

Cytopenia. The incidence and severity of cytopenia generally are correlated to the stage of the HIV infection.31 Our results confirmed that among older patients with HIV, those with CD4+ cell counts of less than 200/mm3 were the most likely to have anemia, suggesting that a Hgb level assessment is warranted among older patients with HIV who have low CD4+ cell counts (less than 200/mm3).


   CONCLUSIONS
 TOP
 ABSTRACT
 SUBJECTS AND METHODS
 RESULTS
 DISCUSSION
 CONCLUSIONS
 REFERENCES
 
HIV-positive patients 50 years or older may have a broad range of comorbidities that can affect the provision of oral health care. In our study, we found that 88.8 percent of patients 50 years or older who had HIV had at least one clinical comorbidity, and 59.0 percent had multiple comorbidities. The reported prevalence of selected comorbidities in our study population was different, and in many instances higher, than those in reports for the overall population with HIV or the general U.S. population. Whether older people with HIV have clinically severe or less well-controlled comorbidities that may require modification of oral health care treatment remains to be determined through a systematic prospective study.


   FOOTNOTES
 

Dr. Magalhães is a professor, Oral Pathology, School of Dentistry, University of São Paulo, Av Professor Lineu Prestes, 2227, São Paulo, SP, 055800-900, Brazil, e-mail "mhcgmaga{at}usp.br". Address reprint requests to Dr. Magalhães.


Dr. Greenberg is an associate professor, University of Medicine and Dentistry of New Jersey, New Jersey Dental School, Newark.


Dr. Hansen is a postgraduate student, Department of Diagnostic Sciences, Division of Oral Medicine, University of Medicine and Dentistry, New Jersey Dental School, Newark.


Dr. Glick is a professor of oral medicine, Arizona School of Dentistry and Oral Health, and associate dean for Oral-Medical Sciences, School of Osteopathic Medicine—Arizona, A.T. Still University, Mesa, Ariz. He also is editor of The Journal of the American Medical Association.


Dr. Magalhães received a CAPES (Coordenação de Aperfeiçoamento de Pessoal de Nível Superior) fellowship for a three-month postdoctoral developmental research project at University of Medicine and Dentistry of New Jersey, New Jersey Dental School, Newark.


   REFERENCES
 TOP
 ABSTRACT
 SUBJECTS AND METHODS
 RESULTS
 DISCUSSION
 CONCLUSIONS
 REFERENCES
 

  1. Centers for Disease Control and Prevention. National Prevention Information Network. Communities at risk: The elderly. Available at: "www.cdcnpin.org/scripts/population/elderly.asp". Accessed Feb. 28, 2007.

  2. Shah S, Mildvan D. HIV and aging. Curr Infect Dis Rep 2006;8(3): 241–7.[Medline]

  3. Manfredi R. HIV infection and advanced age emerging epidemiological, clinical, and management issues. Ageing Res Rev 2004;3(1): 31–54.[Medline]

  4. Palácios R, Santos J, García A, et al. Impact of highly active anti-retroviral therapy on blood pressure in HIV-infected patients: a prospective study in a cohort of naive patients. HIV Medicine 2006; 7(1):10–5.[Medline]

  5. Goodroad BK. HIV and AIDS in people older than 50: a continuing concern. J Gerontol Nurs 2003;29(4):18–24.[Medline]

  6. Grabar S, Kousignian I, Sobel A, et al. Immunologic and clinical responses to highly active antiretroviral therapy over 50 years of age: results from the French Hospital Database on HIV. AIDS 2004;18 (15):2029–38.[Medline]

  7. Armstrong GL, Wasley A, Simard EP, McQuillan GM, Kuhnert WL, Alter MJ. The prevalence of hepatitis C virus infection in the United States, 1999 through 2002. Ann Intern Med 2006;144 (10):705–14.[Abstract/Free Full Text]

  8. Lacombe K, Pacanowski J. HIV infection and comorbidities (in French). Rev Prat 2006;56(9):995–1004.[Medline]

  9. Greenberg MS, Glick M, eds. Burket’s oral medicine: Diagnosis and treatment. Hamilton, Ontario, Canada: Decker; 2003.

  10. Dighe AS, Rao A, Coakley AB, Lewandrowski KB. Analysis of laboratory critical value reporting at a large academic medical center. Am J Clin Pathol 2006;125(5):758–64.[Medline]

  11. Lewden C, Salmon D, Morlat P, et al. Causes of death among human immunodeficiency virus (HIV)-infected adults in the era of potent antiretroviral therapy: emerging role of hepatitis and cancers, persistent role of AIDS. Int J Epidemiol 2005;34(1):121–30.[Abstract/Free Full Text]

  12. Weber R, Sabin CA, Friis-Moller N, et al. Liver-related deaths in persons infected with the human immunodeficiency virus: the D:A:D study. Arch Intern Med 2006;166(15):1632–41.[Abstract/Free Full Text]

  13. Alter MJ. Epidemiology of viral hepatitis and HIV co-infection. J Hepatol 2006;44(1 supplement):S6–S9.[Medline]

  14. Hagan H, Campbell J, Thiede H, et al. Self-reported hepatitis C virus antibody status and risk behavior in young injectors. Public Health Rep 2006;121(6):710–9.[Medline]

  15. Demas P, McClain JR. Hepatitis: implications for dental care. Oral Surg Oral Med Oral Pathol Oral Radiol Endod 1999;88(1):2–4.[Medline]

  16. National Center for Health Statistics, National Center for Health Services Research. Health, United States, 2006: With chartbook on trends in the health of Americans. Rockville, Md.: U.S. Department of Health, Education, and Welfare, Public Health Service, Health Resources Administration, National Center for Health Statistics; 2006:279.

  17. Glick M. Medical considerations for dental practice. Chicago: Quintessence; 2005.

  18. Olatunji BO, Mimiaga MJ, O’Cleirigh C, Safren SA. Review of treatment studies of depression in HIV. Top HIV Med 2006;14(3): 112–24.[Medline]

  19. Odiase F, Ogunrin O, Ogunniyi A. Effect of progression of disease on cognitive performance in HIV/AIDS. J Natl Med Assoc 2006;98(8): 1260–2.[Medline]

  20. Sacktor N, McDermott MP, Marder K, et al. HIV-associated cognitive impairment before and after the advent of combination therapy. J Neurovirol 2002;8(2):136–42.[Medline]

  21. Bell JE. An update on the neuropathology of HIV in the HAART era. Histopathology 2004;45(6):549–59.[Medline]

  22. Sin DD, McAlister FA, Man SF, Anthonisen NR. Contemporary management of chronic obstructive pulmonary disease: scientific review. JAMA 2003;290(17):2301–12.[Abstract/Free Full Text]

  23. Crothers K, Butt AA, Gibert CL, Rodriquez-Barradas MC, Crystal S, Justice AC; Veterans Aging Cohort 5 Project Team. Increased COPD among HIV-positive compared to HIV-negative veterans. Chest 2006; 130(5)1326–33.[Medline]

  24. Crothers K, Griffith TA, McGinnis KA, et al. The impact of cigarette smoking on mortality, quality of life, and comorbid illness among HIV-positive veterans. J Gen Intern Med 2005;20(12):1142–5.[Medline]

  25. Sullivan PS, Hanson DL, Chu SY, Jones JL, Ward JW. Epidemiology of anemia in human immmunodeficiency virus (HIV)-infected persons: results from the multistate adult and adolescent spectrum of HIV disease surveillance project. Blood 1998;91(1):301–8.[Abstract/Free Full Text]

  26. Berhane K, Karim R, Cohen MH, et al. Impact of highly active antiretroviral therapy on anemia and relationship between anemia and survival in a large cohort of HIV-infected women. J Acquir Immune Defic Syndr 2004;37(2):1245–52.[Medline]

  27. Semba RD, Shah N, Klein RS, Mayer KH, Schuman P, Vlahov D; Human Immunodeficiency Virus Epidemiology Research Study Group. Prevalence and cumulative incidence of and risk factors for anemia in a multicenter cohort study of human immunodeficiency virus-infected and-uninfected women. Clin Infect Dis 2002;34(2):260–6.[Medline]

  28. Zon LI Groopman JE. Hematologic manifestations of the human immune deficiency virus (HIV). Semin Hematol 1988;25(3):208–18.[Medline]

  29. Moses A, Nelson J, Bagby GC Jr. The influence of human immunodeficiency virus-1 on hematopoieses. Blood 1998;91(5):1479–85.[Free Full Text]

  30. Levine AM, Karim R, Mack W, et al. Neutropenia in human immunodeficiency virus infection: data from the women’s interagency HIV study. Arch Intern Med 2006;166(4):405–10.[Abstract/Free Full Text]

  31. Patton LL. Hematological abnormalities among HIV-infected patients: associations of significance for dentistry. Oral Surg Oral Med Oral Pathol Oral Radiol Endod 1999;88(5):561–7.[Medline]





This Article
Right arrow Abstract Freely available
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Magalhães, M. G.
Right arrow Articles by Glick, M.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Magalhães, M. G.
Right arrow Articles by Glick, M.
Related Collections
Right arrow Periodontics


HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS