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New Canadian guideline provides evidence-based approach to non-occupational HIV prophylaxis

Published online by Cambridge University Press:  20 November 2018

Shannon O’Donnell*
Affiliation:
Department of Emergency Medicine, St. Paul’s Hospital, Vancouver, BC
Darrell H. S. Tan
Affiliation:
Division of Infectious Diseases, St. Michael’s Hospital, Toronto, ON
Mark W. Hull
Affiliation:
BC Centre for Excellence in HIV/AIDS, Vancouver, BC.
*
Correspondence to: Dr. Shannon O’Donnell, Providence Health Care – St. Paul’s Hospital Site, 1081 Burrard Street, Vancouver, BC V6Z1Y6; Email: odonnell.shannon1@gmail.com

Abstract

The incidence of HIV infections in Canada has increased yearly since 2014. New cases of HIV have resulted almost exclusively from non-occupational exposures, including sexual contact and needle sharing. Appropriate HIV post-exposure prophylaxis is under-prescribed to patients who present to the emergency department after a high-risk exposure. In November of 2017, a Canadian guideline on HIV pre-exposure prophylaxis (PrEP) and non-occupational post-exposure prophylaxis (nPEP) was published. The guideline presents a standardized, evidence-based approach to assessing risk for HIV transmission and prescribing HIV prophylaxis. This summary highlights the key points from the guideline that are relevant to the practice of emergency medicine in Canada.

Résumé

L’incidence des infections à VIH au Canada croît sans cesse chaque année depuis 2014. La hausse du nombre de nouveaux cas d’infection s’explique presque exclusivement par des expositions non professionnelles au virus, attribuables par exemple à des contacts sexuels ou au partage de seringues. Toutefois, les médecins ne prescrivent pas suffisamment de mesures prophylactiques appropriées de postexposition aux patients qui consultent au service des urgences après une exposition à haut risque au VIH. Une nouvelle ligne directrice canadienne sur la prophylaxie préexposition au VIH et sur la prophylaxie postexposition non professionnelle a été publiée en novembre 2017. Elle porte sur une démarche uniforme et fondée sur des données probantes pour évaluer le risque de transmission du VIH et pour prescrire des mesures prophylactiques anti-VIH. Sera présenté dans l’article un résumé des principaux éléments de la ligne directrice, qui trouvent application dans la pratique de la médecine d’urgence au Canada.

Type
Commentary
Copyright
Copyright © Canadian Association of Emergency Physicians 2018 

BACKGROUND

In the last decade, the number of new human immunodeficiency virus (HIV) infections in Canada decreased yearly from 2,599 in 2008 to 2,053 in 2014. Since 2014, however, there has been an uptick in the annual incidence, and in 2016, there were 2,344 new cases of HIV reported in Canada.Reference Bourgeois, Edmunds and Awan1 While it is theoretically possible to acquire HIV after occupational exposure (e.g., a needlestick injury in a health care setting), new HIV infections occur almost exclusively as a result of non-occupational exposures (e.g., sexual contact or needle sharing). Only one case of HIV transmission from an occupational exposure has been confirmed in the United States since 1999.Reference Joyce, Kuhar and Brooks2

New HIV infections are disproportionately concentrated among certain populations. Recent Canadian data revealed that nearly one-half of all new infections (44.1%) occur among men who have sex with men (MSM). Heterosexual contact represents the next most common route of transmission (32.3%), with one-third of these cases (10.5%) occurring in people from HIV-endemic countries. Finally, 15.1% of new HIV infections are identified in people who inject drugs (PWID), more than one-half of whom are indigenous. The remaining new infections result from a combination of injection drug use and sexual contact between MSM and from unspecified exposure routes.Reference Bourgeois, Edmunds and Awan1

While emergency departments (ED) serve as an important resource for timely access to HIV post-exposure prophylaxis (PEP), the literature suggests that emergency physicians have not felt confident determining the need for PEP when patients present after sexual contact or the use of injection drugs.Reference McCausland, Linden and Degutis3 Consistent with this finding, recent data show that emergency physicians under prescribe HIV PEP when indicated: in a review of patients presenting to a Vancouver ED, more than one-quarter of those who should have received HIV PEP after a high-risk non-occupational exposure (based on 2005 Centers for Disease Control and Prevention recommendationsReference Smith, Grohskopf and Black4) did not.Reference O’Donnell, Bhate and Grafstein5

In 2017, a Canadian guideline on HIV pre-exposure prophylaxis (PrEP) and non-occupational post-exposure prophylaxis (nPEP)Reference Tan, Hull and Yoong6 was published to provide clinicians with an evidence-based approach for assessing the risk for HIV, providing antiretroviral medications as a preventative measure, conducting baseline and follow-up testing, and monitoring medication safety. The guidelineReference Tan, Hull and Yoong6 is the first of its kind in Canada and is broadly consistent with guidelines from Europe, the United Kingdom, the United States, and Australia.Reference Brady, Rodger and Asboe710 In this article, we outline the key points that are relevant to the practice of emergency medicine in Canada, with a focus on determining which patients should be treated with nPEP.

DESCRIPTION

The guideline was developed by a panel of 25 experts from across Canada, with representatives from infectious diseases, primary care, emergency medicine, public health, pharmacy, nursing, and the community. Funding for the work was provided by the Canadian Institutes of Health Research (CIHR; grant number PCS 142089), with in-kind support from the CIHR Canadian HIV Trials Network and a New Investigator Award from the CIHR/Ontario HIV Treatment Network (D.H.S.T.).

Methods for development of the guideline are described in detail.Reference Tan, Hull and Yoong6 The Grading of Recommendation, Assessment, Development and Evaluation (GRADE) systemReference Atkins, Best and Briss11 was used to specify two categories of strength of recommendation and four categories of quality of evidence for each of the recommendations (Appendix 1).

Non-occupational post-exposure prophylaxis

The guideline recommends that nPEP be started in patients who are HIV negative and present within 72 hours of an exposure that is of a moderate or high risk and involves a source person who is HIV positive or at risk for having transmissible HIV (see Table 1). HIV nPEP is not recommended in any other scenarios nor is it recommended beyond 72 hours from the exposure.Reference Tan, Hull and Yoong6

Table 1 Risk that a person has transmissible HIV infectionReference Gray, Wawer and Brookmeyer15Reference Cohen, Chen and McCauley17

HIV=human immunodeficiency virus; STI=sexually transmitted infection; VL=viral load, copies/mL.

The risk for a given exposure type is based on estimates of per-act HIV transmission risk from a known HIV positive source. Receptive anal sex carries the highest risk for transmission, followed (in decreasing order of risk) by needle sharing, insertive anal sex, receptive vaginal sex, and insertive vaginal sex. nPEP is not indicated after oral sex. (See Table 2).

Table 2 Risk of HIV transmission per act by exposure type from an HIV-positive sourceReference Patel, Borkowf and Brooks14

Determining the involved source person’s risk for having transmissible HIV in the ED is often difficult. Very rarely is the source person available for interviewing or HIV testing, and, often, the source is not known to the patient. In these cases, a determination of whether the source is at high epidemiologic risk for HIV must be made. In Canada, HIV prevalence is elevated among MSM, PWID, individuals from HIV-endemic countries, and certain indigenous populations.Reference Bourgeois, Edmunds and Awan1 The HIV epidemic varies geographically across Canada, however, and clinicians should be aware of local epidemiology. In addition, caution is advised when applying epidemiologic constructs to individuals, as this may contribute to stigma and discrimination and may not apply to the source person in question.

The guidelineReference Tan, Hull and Yoong6 provides recommendations for nPEP after consensual exposures only and does not include specific directives for treating patients after a sexual assault. In centres where sexual assault services are available, patients should be referred accordingly.Reference Tan, Hull and Yoong6 If these services are not available, the ED physician should consider that circumstances often associated with assault (trauma or bleeding, multiple assailants, or possible presence of a sexually transmitted infection [STI] in the assailant) increase the risk for HIV transmission.

Another scenario not addressed in the guidelineReference Tan, Hull and Yoong6 is the patient who presents after a needlestick injury from a discarded or abandoned needle (found in a park or garbage). There have not been any documented cases of HIV infection from such injuriesReference Dominguez, Smith and Vasavi12 and, in general, they are a very low risk for transmission of HIV because the needles in question are often small-bore needles, there is usually minimal blood in the syringe, and HIV does not survive outside the body for prolonged periods.

Certainly not all patient presentations fit neatly into the scenarios defined by the guideline,Reference Tan, Hull and Yoong6 and nPEP should involve shared decision making with the patient. Each case should be considered on an individualized basis, and if there is uncertainty about whether nPEP is indicated, the emergency physician should obtain subspecialty support.

In addition to HIV serology, baseline laboratory investigations in the ED should include thorough STI testing (urine and mucosal swabs for gonorrhea and chlamydia; serology for syphilis and hepatitis A, B, and C), complete blood count, creatinine, alanine aminotransferase, and pregnancy testing as applicable. Emergency physicians should make onward referrals to other providers who can conduct follow-up testing 12 weeks after the exposure and manage other considerations regarding special populations, ongoing monitoring while on nPEP, and indications for stopping nPEP.Reference Tan, Hull and Yoong6

When indicated, medications should be started as soon as possible. When patients are dispensed the full 28-day course of nPEP rather than a starter pack of medications, PEP completion rates are better and there are fewer PEP refusals.Reference Ford, Venter, Irvine, Beanland and Shubber13 However, if the need for continued prophylaxis will be reassessed pending source testing, if there is a concern for drug resistance, or if drug coverage does not include nPEP, starter packs dispensed in the ED are recommended.Reference Tan, Hull and Yoong6

Twenty-eight-day nPEP regimens include two nucleoside reverse transcriptase inhibitors (tenofovir disoproxil fumarate [TDF]/emtricitabine [FTC] 300/200 mg orally once daily), plus a third drug (darunavir 800 mg orally once daily plus ritonavir 100 mg orally once daily, Grade 1A) dolutegravir 50 mg orally once daily, Grade 1C; or raltegravir 400 mg orally twice daily, Grade 1A).Reference Tan, Hull and Yoong6 See Table 3.

Table 3 Preferred nPEP drug regimens*

CK=creatine kinase; NRTI=nucleoside reverse transcriptase inhibitors; nPEP=non-occupational post-exposure prophylaxis.

* A thorough medication history (including prescription drugs, supplements, and herbal preparations) should be taken prior to selecting an nPEP regimen because of the potential for drug-drug interactions.

Pre-exposure prophylaxis

PrEP is the use of TDF/FTC 300/200 mg orally either once daily or “on demand” on the days surrounding sexual encounters to prevent transmission of HIV. The guidelineReference Tan, Hull and Yoong6 lists indications for the use of PrEP by MSM and transgender women at high risk for infection, as well as at-risk HIV-negative partners in heterosexual serodiscordant relationships, and certain PWID.

Because individuals taking PrEP should be assessed clinically at regular intervals, the ED is not the appropriate setting for initiation of PrEP. It is important, however, that emergency physicians be able to recognize patients who may be candidates for PrEP (for instance, gay, bisexual, or other MSM with recurrent use of nPEP, rectal bacterial STIs, or early syphilis) and refer these patients to their primary care physician or another suitably trained provider for consideration of PrEP initiation.

SUMMARY

Patients with non-occupational exposures to HIV often present to the ED and are cared for by emergency physicians. Preventing the transmission of HIV is of social and economic importance, given the high cost of treating HIV and the young age at which most infections occur (age 30–39 yearsReference Bourgeois, Edmunds and Awan1). Canadian research has shown that there are patients who have had high-risk exposures and were discharged without appropriate treatment.Reference O’Donnell, Bhate and Grafstein5 The goal of this article was to update emergency physicians on the new Canadian guideline for nPEP and PrEP to enable the highest standard of care possible. (Figure 1)

Figure 1. Algorithm for HIV nPEP assessment

Competing interests

None declared.

SUPPLEMENTARY MATERIALS

To view supplementary material for this article, please visit https://doi.org/10.1017/cem.2018.462

References

REFERENCES

1.Bourgeois, AC, Edmunds, M, Awan, A, et al. HIV in Canada – surveillance report, 2016. Can Commun Dis Rep 2017;43(12):248-256.10.14745/ccdr.v43i12a01Google Scholar
2.Joyce, MP, Kuhar, D, Brooks, JT. Notes from the field: occupationally acquired HIV infection among health care workers – United States, 1985–2013. MMWR Mort Wkly Rep 2015;63(53):1245-1246.Google Scholar
3.McCausland, JB, Linden, JA, Degutis, LC, et al. Nonoccupational postexposure HIV prevention: emergency physicians’ current practices, attitudes, and beliefs. Ann Emerg Med 2003;42(5): 651-666.10.1016/S0196-0644(03)00338-XGoogle Scholar
4.Smith, DK, Grohskopf, LA, Black, RJ, et al. Antiretroviral postexposure prophylaxis after sexual, injection-drug use, or other nonoccupational exposure to HIV in the United States: recommendations from the U.S. Department of Health and Human Services. MMWR Recomm Rep 2005;54(RR-2 No. RR-2):1-20.Google Scholar
5.O’Donnell, S, Bhate, TD, Grafstein, E, et al. Missed opportunities for HIV prophylaxis among emergency department patients with occupational and nonoccupational body fluid exposures. Ann Emerg Med 2016;68(3):315-323.10.1016/j.annemergmed.2016.03.027Google Scholar
6.Tan, DH, Hull, MW, Yoong, D, et al. Canadian guideline on HIV pre-exposure prophylaxis and nonoccupational postexposure prophylaxis. CMAJ. 2017;189(47):E1448-E1458.10.1503/cmaj.170494Google Scholar
7.Brady, M, Rodger, A, Asboe, D, et al. Consultation version of the BHIVA/BASHH guidelines on the use of HIV pre-exposure prophylaxis (PrEP). London, UK: British HIV Association; 2017.Google Scholar
8.Wright, E, Grulich, A, Roy, K, et al. Australasian Society for HIV, Viral Hepatitis and Sexual Health Medicine HIV pre-exposure prophylaxis: clinical guidelines. J Virus Erad 2017;3(3):168-184.Google Scholar
9.Gunthard, HF, Saag, MS, Benson, CA, et al. Antiretroviral drugs for treatment and prevention of HIV infection in adults: 2016 recommendations of the International Antiviral Society-USA Panel. JAMA 2016;316(2):191-210.10.1001/jama.2016.8900Google Scholar
10.Guidelines version 8.2 January 2017. London, UK: European AIDS Clinical Society; 2017.Google Scholar
11.Atkins, D, Best, D, Briss, PA, et al. Grading quality of evidence and strength of recommendations. BMJ 2004;328(7454):1490.Google Scholar
12.Dominguez, KL, Smith, DK, Vasavi, T, et al. Updated guidelines for antiretroviral postexposure prophylaxis after sexual, injection drug use, or other nonoccupational exposure to HIV–United States, 2016. CDC, April 2016.Google Scholar
13.Ford, N, Venter, F, Irvine, C, Beanland, RL, Shubber, Z. Starter packs versus full prescription of antiretroviral drugs for postexposure prophylaxis: a systematic review. Clin Infect Dis 2015;60 Suppl 3:S182-S186.10.1093/cid/civ093Google Scholar
14.Patel, P, Borkowf, CB, Brooks, JT, et al. Estimating per-act HIV transmission risk: a systematic review. AIDS 2014;28(10):1509-1519.10.1097/QAD.0000000000000298Google Scholar
15.Gray, RH, Wawer, MJ, Brookmeyer, R, et al. Probability of HIV-1 transmission per coital act in monogamous, heterosexual, HIV-1-discordant couples in Rakai, Uganda. Lancet 2001;357(9262):1149-1153.10.1016/S0140-6736(00)04331-2Google Scholar
16.Rodger, AJ, Cambiano, V, Bruun, T, et al. Sexual activity without condoms and risk of HIV transmission in serodifferent couples when the HIV-positive partner is using suppressive antiretroviral therapy. JAMA 2016;316(2):171-181.10.1001/jama.2016.5148Google Scholar
17.Cohen, MS, Chen, YQ, McCauley, M, et al. Prevention of HIV-1 infection with early antiretroviral therapy. N Engl J Med 2011;365(6):493-505.10.1056/NEJMoa1105243Google Scholar
Figure 0

Table 1 Risk that a person has transmissible HIV infection1517

Figure 1

Table 2 Risk of HIV transmission per act by exposure type from an HIV-positive source14

Figure 2

Table 3 Preferred nPEP drug regimens*

Figure 3

Figure 1. Algorithm for HIV nPEP assessment

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