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Essential Medical Issues Related to HIV in Dentistry


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Essential Medical Issues Related to HIV in Dentistry

Arthur H. Moswin, MD, FACP; Joel B. Epstein, DMD, MSD, FRCD(C), FDS RCSE


Management of HIV infection has progressed dramatically since the disease was first recognized, to the point that HIV infection is now considered a chronic condition. Some of these new approaches in management are related to the strides that have been made in understanding the pathogenesis of this condition. Such changes in medical care may also affect the provision of oral health care. Dental providers must therefore be aware of current management practices. This paper reviews current approaches to managing HIV-related disease.

Dr. Epstein

Email: jepstein@uic.edu

For citation purposes, the electronic version is the definitive version of this article: www.cda-adc.ca/jcda/vol-73/issue-10/945.html


IV infection is now a chronic manage- able illness. Affected patients are living longer and increasingly normal lives, thanks largely to highly active antiretroviral therapy (commonly called HAART). It is esti- mated that a 21-year-old person infected with HIV today will live to 60 years of age.1 Regular dental care is an important aspect of the man- agement of HIV infection. Oral lesions can be among the earliest manifestations of this infection and may develop anytime during the course of the illness. This article summar- izes medical issues related to HIV infection of which the dentist should be aware.

Overview of �ental �are in the

�ontext of HIV-Related �isease

As many as one-quarter of people infected with HIV are unaware of their condition.2 In a survey of patients with HIV/AIDS conducted in 2000, the Rand Corporation found that 58% did not see a dentist regularly (i.e., had not seen a dentist in the past 6 months), and 20% reported having had an unmet need for

dental care in the previous 6 months.3 Not surprisingly, dental programs that were af- filiated with a comprehensive HIV treatment program were most successful, probably be- cause of greater referrals and greater funding available for care in those settings.

There are various reasons for the disparity between need for and availability of dental care, including lack of dental insurance and competing medical and social needs; however, reticence on the part of the dentist should not be a factor. Although universal precautions should be used for all patients, regardless of HIV status, occupational transmission of HIV in the course of providing dental care is ex- tremely unlikely,4 despite the fact that some pa- tients will have HIV infection and despite the frequency of accidental skin punctures from instruments. This is probably because HIV is rarely transmitted through saliva and because of the small quantities of blood involved. In fact, it appears that most percutaneous in- juries associated with dental care occur during extraoral procedures such as laboratory work


or clean-up.5 Any patient in the dental chair could be among those with HIV who do not know they are HIV- positive. Therefore, every office should have a plan in case of needlestick injury or other exposure to blood or body fluids (Fig. 1; see also Appendix 1, Recommendations on managing occupational HIV exposure, at www.cda-adc.

ca/jcda/vol-73/issue-10/945.html). Studies suggest that the risk of contracting HIV from a needlestick injury is 1 in 200 (0.3%) overall.7 Stated another way, 99.7% of exposures through needlestick injuries and cuts do not lead to HIV infection. In contrast, the risk of contracting hepatitis B from a needlestick injury (which has always been a risk in medical and dental care) during care of an infected patient may be as high as 30%.7 The risks of some other modes of HIV transmission are shown in Table 1.

Certain types of needlestick exposure are more risky than others, as outlined in Table 2. Wearing gloves may

reduce the volume of blood transmitted by 50%, even if a puncture through the glove does occur.

Starting antiretroviral therapy within 1–4 hours of an exposure can drastically reduce (by more than 80%) the incidence of HIV transmission.9 A procedure should be in place for testing the source patient, should a sharps injury occur. It is important to determine, in consultation with medical personnel familiar with HIV exposure, the severity of the exposure and, if indicated, to start prophylactic antiretroviral therapy within 1 or 2 hours. HAART should be continued for 4 weeks if the source patient is positive. It may be discontinued if the patient’s status is found to be negative.

Preoperative Management

When undertaking dental care of an HIV- positive patient, communication with the primary treating physician is imperative and should cover more than the usual (though still important) questions about bleeding, allergies, cardiac history and antibiotic prophylaxis. Such communication should also include informa- tion about recent CD4 (T cell) count, HIV viral load, any other medical issues (e.g., hepa- titis, cardiac problems) and the patient’s cur- rent medication list (to allow identification of potential drug–drug interactions). As patients with HIV age, the incidence of renal disease, liver disease (often from concomitant hepatitis), cardiomyopathy and lipid abnormalities such as high cholesterol tends to increase. There may also be a higher incidence of coronary artery disease (although this is controversial because of the conflicting evidence) and a higher inci- dence of osteoporosis, especially among men;

these latter patients may be taking bisphosphon- ates, such as alendronate (Fosamax). In light of recent cases of jaw osteonecrosis in non-HIV patients taking these drugs, vigilance is advised.10 An otherwise fit HIV- positive person with good muscle mass probably has the same risk of wound complications as an HIV-negative person.11

Minor laboratory abnormalities are common in HIV- positive patients, whether or not they are receiving an- tiretroviral therapy. Abnormalities in the complete blood count, such as mild anemia, neutropenia and, less often, thrombocytopenia, are common; unless these problems are severe, they should not delay delivery of care. Usually, no further work-up is required, as long as the primary medical provider is experienced in the care of HIV- infected patients, is aware of the issues and agrees that there is no contraindication to surgery. However, a hemoglobin level less than 0.007 g/dL (0.07 g/L), an

PEP not indicated, no follow-up


Assess risk: Did a percutaneous or mucous membrane exposure occur that carries significant risk of HIV transmission?

PEP probably not useful.

Optimum start time is 1–

4 hours after exposure.

No effect after 36 hours.

Arrange for immediate HIV testing of source, using rapid test if available. Is result of

rapid test negative?

If result of rapid test is positive or rapid test is not available, consult medical or infectious disease resource to determine best regimen.

Start PEP immediately.



No Did the exposure happen

less than 36 hours ago?

Is HIV status of the source patient known?

• Perform confidential baseline HIV testing of the exposed health care worker within 72 hours of initiating HAART.

• Providesource patient with appropriate referral for post-test counselling.-

• Refer health care worker to an HIV specialist within 72 hours of initiating HAART.

If Western blot testing of source patient is negative, with

no evidence of acute seroconversion in source

patient, stop PEP.

If Western blot testing of source patient is positive or indeterminate, continue PEP

for 4 weeks.

No Yes



HIV status known to be positive.

Start PEP immediately, and continue for 4 weeks.

If result of rapid test is negative and there is no evidence of acute seroconversion in source patient, there is no need for PEP.

Figure 1: Management of occupational exposure to HIV. PEP = Postexposure prophylaxis. Adapted from reference 6.


––– HIV: Medical Issues –––

absolute neutrophil count (total leukocytes × % polymorph- onuclear leukocytes + bands) of less than 1.5 × 103/μL (1.5 × 109/L) or a platelet count less than 100 × 103/μL (100 × 109/L) may require special attention by the primary provider before surgical procedures12 but usually not before routine dental care.

Another laboratory abnormality in patients who are receiving HAART is an isolated increase in bilirubin in association with normal levels of aspartate aminotrans- ferase and alanine aminotransferase, a phenomenon that may be seen in patients taking atazanavir (Reyataz); how- ever, this abnormality is of no medical consequence. It (and, though more rarely, frank jaundice) is being seen more frequently as use of HAART increases. Patients with concomitant hepatic or renal dysfunction may be at higher risk of bleeding and other complications, but the usual caveats apply; there is no increase in risk due solely to HIV status.

Another important test for patients with HIV is the purified protein derivative (PPD) test, also known as the Mantoux skin test, for tuberculosis (TB). Patients with HIV are at higher risk for active TB if the PPD test result is positive; therefore, they should undergo PPD testing annually. The patient’s TB status and most recent PPD test result should be ascertained from the primary pro- vider; if the test result is positive, the dental care provider

should confirm that the results of chest radiography are normal (i.e., that the patient does not have active TB) and that prophylaxis with isoniazid has been started before initiating dental care.

Medication-Related Issues

The continued success of a patient’s HIV therapy de- pends on strict adherence to the medication regimen, with no missed doses. Missing 10% of doses (essentially 1 or 2 doses a month) or more can cause selection of resistant virus and lead to regimen failure. Adherence is one of the guiding principles of HIV therapy, and every attempt should be made to minimize missed doses and to encourage patients to take all scheduled medication doses. Patients who are receiving therapy and who must fast in preparation for laboratory testing or who must take nothing by mouth in advance of surgery should be allowed to take their HIV medications with sips of water, if at all possible. In cases where the patient must miss one or more doses, as when the jaw has been wired after fracture, consultation with the treating physician is important. Standard antibiotics and pain medications usually pose no additional concerns for patients with HIV. However, the dental care provider must be aware of the possibility of current or prior drug abuse, which may affect the choice of pain medication. Although the com- bination drug trimethoprim–sulfamethoxazole (Bactrim) is not frequently used by dentists, up to 50% of patients with HIV may be allergic to this drug, a problem that may be discovered by the dentist if he or she unknow- ingly prescribes it for an allergic patient. The allergic reaction usually resolves on its own once the drug is discontinued.

The most important drug with potential for drug–

drug interactions is ritonavir (Norvir), which may be ad- ministered alone or combined with lopinavir in the drug Kaletra. This agent is involved in many known drug–drug interactions and has many contraindications. The full list of potential problems is given in the package insert avail- able online (www.norvir.com) or in various drug refer- ences. Among drugs that may be used in dentistry and that can interact with ritonavir or lopinavir–ritonavir, meperidine (Demerol) should not be used at all, whereas acetaminophen, ibuprofen, tramadol and oxycodone all seem to be minimally affected. Proxyphene levels may be increased by ritonavir or lopinavir–ritonavir, and this drug should therefore be used with caution in patients taking either of these HIV drugs. Antibiotics require no dose adjustments, although levels of clarithromycin (Biaxin) are increased. All ergot derivatives and the sedatives midazolam (Versed) and triazolam (Halcion) are contraindicated for patients taking ritonavir or lopinavir–ritonavir and should be used with extreme caution or avoided altogether.

Table 1 Risk of HIV transmission for various modes of transmissiona

Mode of transmission

Risk per 10,000 exposuresb

Percutaneous (blood) 30

Mucocutaneous (blood) < 1

Receptive anal intercourse 50

Receptive vaginal intercourse 10

Insertive vaginal intercourse 5

aAdapted from reference 8

bAssuming an infected source and, for intercourse-related modes of transmission, no condom use.

Table 2 Risk of HIV transmission after percutaneous (needle- stick) exposurea

Risk factor Odds ratio

Deep injury 16.1

Visible blood on needle 5.2

Device in artery or vein (vs. sub-

cutaneous or intramuscular injection) 5.1 Source patient with high viral load 5.4 Use of zidovudine after exposure 0.2

aAdapted from reference 9



p r a c t i c E The Road ��head

There are many new and promising drugs in the phar- maceutical “pipeline.” These drugs, combined with on- going vaccine research, may further revolutionize the care of patients with HIV and prolong their life expect- ancies. These include entirely new classes of drugs such as fusion inhibitors (e.g., the recently approved enfu- virtide [Fuzeon]), integrase inhibitors (e.g., raltegravir [Isenstress]), HIV receptor antagonists (e.g., maraviroc [Selzentry]) and others13 that are coming to market. As the number of people living with HIV infection and AIDS continues to increase, we must work to reduce their unmet needs for dental care. a


Acknowledgments: The authors wish to thank Norma Rolfsen, FNP, ACRN, for her help in preparing this manuscript.

Dr. Moswin is medical director, HIV Program, Provident Hospital of Cook County, Chicago, Illinois, and medical dir- ector, HIV Care Program, Michael Reese Hospital, Chicago, Illinois.

Dr. Epstein is professor and head, department of oral medi- cine and diagnostic sciences, College of Dentistry, and dir- ector, interdisciplinary program in oral cancer, College of Medicine, Chicago Cancer Center, University of Illinois at Chicago, Chicago, Illinois.

Correspondence to: Dr. Joel Epstein, UIC College of Dentistry, Oral Medicine, MC-838, 801 South Paulina St., Chicago, IL 60091, USA.

The authors have no declared financial interests in any company manufac- turing the types of products mentioned in this article.

This article has been peer reviewed.


1. Lohse N, Hansen AB, Pedersen G, Kronborg G, Gerstoft J, Sorensen HT, and others. Survival of persons with and without HIV infection in Denmark, 1995–2005. Ann Intern Med 2007; 146(2):87–95.

2. Department of Human Health and Services. Centers for Disease Control and Prevention. HIV/AIDS prevention at CDC. 2007. Available: www.cdc.

gov/hiv/aboutDHAP.htm (accessed 2007 Oct 30).

3. Rand Corporation. Do people with HIV get the dental care they need?

Results of the HCSUS study. 2005. Available: www.rand.org/pubs/research_

briefs/RB9067/index1.html (accessed 2007 Oct 30).

4. Cleveland JL, Barker L, Gooch BF, Beltrami EM, Cardo D; National Surveillance System for Health Care Workers Group of the Centers for Disease Control and Prevention. Use of HIV postexposure prophylaxis by dental health care personnel: an overview and updated recommendations.

J Am Dent Assoc 2002; 133(12):1619–26.

5. McCarthy GM, Ssali CS, Bednarsh H, Jorge J, Wangrang Simakulk K, Page-Shafer K. Transmission of HIV in the dental clinic and elsewhere. Oral Dis 2002; 8 Suppl 2:126–35.

6. HIV Clinical Resource. Office of the Medical Director, New York State Department of Health AIDS Institute in collaboration with the Johns Hopkins University Division of Infectious Diseases. HIV prophylaxis following occupa- tional exposure. December 2005. Available: www.hivguidelines.org.

7. U.S. Public Health Service. Updated U.S. Public Health Service guidelines for the management of occupational exposures to HBV, HCV, and HIV and recommendations for postexposure prophylaxis. MMWR Recomm Rep 2001;


8. Antiretroviral postexposure prophylaxis after sexual, injection-drug use, or other nonoccupational exposure to HIV in the United States: recommen- dations from the U.S. Department of Health and Human Services. MMWR Recomm Rep 2005; 54(RR-2):1–20.

9. Centres for Disease Control and Prevention (CDC). Case-control study of HIV seroconversion in health-care workers after percutaneous exposures to HIV-infected blood — France, United Kingdom, and United States, January 1988–August 1994. MMWR Morb Mortal Wkly Rep 1995; 44(50):929–33.

10. Ruggiero SL, Mehrotra B, Rosenberg TJ, Engroff SL. Osteonecrosis of the jaws associated with the use of bisphosphonates: a review of 63 cases. J Oral Maxillofac Surg 2004; 62(5):527–34.

11. Schecter WP, Stock P. Surgery in patients with HIV. HIV InSite Knowledge Base Chapter. February 2003. Available: http://hivinsite.ucsf.

edu/InSite?page=kb-03-03-02 (accessed 2007 Oct 30).

12. Practice Guidelines for blood component therapy. A report by the American Society of Anesthesiologists Task Force on Blood Component Therapy. Anesthesiology 1996; 84(3):732–47.

13. Treatment Action Group. The 2007 Pipeline Report. Experimental treat- ments and preventive therapies for HIV, hepatitis C, and tuberculosis. New York, NY. Available: www.aidsinfonyc.org/tag/tx/pipeline2007b.pdf.


––– HIV: Medical Issues –––

��ppendix 1 Recommendations on managing occupational HIV exposure


ound and skin sites should be cleansed with soap and water immediately. Exposed mucous mem- branes should be flushed with water.

Postexposure prophylaxis (PEP) is recommended if there has been exposure to blood, visibly bloody fluid or other potentially infectious material (e.g., semen, vaginal secretions, or cerebrospinal, synovial, pleural, peritoneal, pericardial or amniotic fluid) associated with potential HIV transmission and in any of the following exposure situations:

• break in the skin caused by a sharp object (including both hollow-bore and cutting needles or broken glass- ware) that is contaminated with blood, visibly bloody fluid or other potentially infectious material or that has been in the source patient’s blood vessel

• bite from an HIV-infected patient with visible bleeding in the mouth that causes bleeding in the health care worker

• splash of blood, visibly bloody fluid or other pot- entially infectious material onto a mucosal surface (mouth, nose or eyes)

• exposure to blood, visibly bloody fluid or other poten- tially infectious material through nonintact skin (e.g., dermatitis, chapped skin, abrasion or open wound) If the HIV serostatus of the source is unknown, HIV testing of the source should be sought. If the rapid HIV test is available on site (or at another site nearby), it should be used to determine the HIV status of the source patient. Results are usually available within 30 minutes of testing. If the result of a rapid HIV test is negative, and there is no evidence of acute symptoms of seroconver- sion, PEP is not necessary.

If the preliminary rapid test result is positive, the health care worker should start PEP immediately. Post- test counselling should be given to the source patient.

To establish a diagnosis of HIV infection, the test must be confirmed by a Western blot assay, which should be performed as soon as possible. PEP should be continued for 4 weeks.

If the result from testing the source patient is not im- mediately available and PEP is indicated on the basis of an initial assessment, PEP should not be delayed pending receipt of the test result.

If the source patient’s HIV test result is negative and the source patient was infected recently, the health care worker should be informed of the small chance that it is a false-negative result. PEP should be recommended in situations when an exposure with significant risk has oc- curred and the clinician suspects a strong likelihood that the source patient acquired the HIV infection recently.

The critical decision point should be based on whether the health care worker has had a percutaneous,

mucocutaneous or nonintact skin exposure to potentially HIV-infected blood, visibly bloody fluid or other poten- tially infectious material. For these exposures, prompt initiation of PEP, followed by telephone or in-person consultation with a clinician experienced in HIV PEP, is recommended.

Implementing PEP

PEP should be initiated as soon as possible, ideally within 2 hours and no later than 36 hours after exposure, after which there is little efficacy. The prescribing pro- vider should ensure that the patient has access to the full course of antiretroviral medications.

PEP medications should be readily available to health care workers who sustain a known or highly suspect oc- cupational exposure to HIV. In establishing plans for pro- viding PEP, employers should determine the following:

• how PEP will be made available within 1 to 2 hours of an exposure

• how a 24- to 48-hour supply of PEP will be made available for urgent use

• how the health care worker will obtain PEP drugs to complete the 4-week regimen (given that some individuals may be reluctant to go to their local pharmacy)

Confidential baseline HIV antibody testing of the health care worker should be obtained at the time the occupational exposure is reported or within 72 hours of initiating PEP.

If a recommendation to begin PEP is declined, this decision should be documented in the health care work- er’s medical record.

All patients who start receiving PEP should be re- evaluated within 72 hours of their exposure. This allows further clarification of the nature of the exposure, review of available serologic test results from the source patient and evaluation of adherence to and toxicities associated with the PEP regimen.

If a health care worker presents for evaluation of a high-risk exposure more than 36 hours after the incident, close monitoring for signs and symptoms of acute HIV infection is recommended, with subsequent introduction of highly active antiretroviral therapy (HAART) if acute seroconversion occurs. a

Adapted from: HIV Clinical Resource. Office of the Medical Director, New York State Department of Health AIDS Institute in collaboration with the Johns Hopkins University Division of Infectious Diseases. HIV prophylaxis following occupational exposure. December 2005. Available: www.hivguidelines.org.



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