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Clinical Manual for Management of the HIV-Infected ... - myCME.com

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CMV retinitis<br />

Treatment consists <strong>of</strong> 2 phases: initial <strong>the</strong>rapy and<br />

chronic maintenance <strong>the</strong>rapy.<br />

Initial <strong>the</strong>rapy<br />

Be<strong>for</strong>e <strong>the</strong> advent <strong>of</strong> valganciclovir, <strong>the</strong> preferred<br />

strategy <strong>for</strong> treating CMV retinitis involved ganciclovir<br />

intraocular implants and systemic <strong>the</strong>rapy. Because<br />

implants deliver a higher dose <strong>of</strong> drug to <strong>the</strong> retina<br />

than any o<strong>the</strong>r modality (1.4 mcg/hour <strong>for</strong> up to 8<br />

months), many experts still prefer <strong>the</strong>m <strong>for</strong> patients<br />

with sight-threatening (zone 1) disease. About half<br />

<strong>of</strong> patients treated with implants develop disease in<br />

<strong>the</strong> contralateral eye, and a third experience systemic<br />

disease, within 3 months <strong>of</strong> implantation. There<strong>for</strong>e,<br />

patients with implants should be treated systemically<br />

with valganciclovir (900 mg once daily; some experts<br />

increase this to 900 mg twice daily <strong>for</strong> patients with<br />

vision-threatening disease).<br />

For patients with peripheral retinitis (beyond zone 1),<br />

oral valganciclovir (see below) is <strong>the</strong> preferred treatment<br />

because it is easy to administer and is not associated<br />

with <strong>the</strong> surgery- or ca<strong>the</strong>ter-related <strong>com</strong>plications seen<br />

with intraocular treatments and intravenous <strong>the</strong>rapies.<br />

This <strong>for</strong>mulation quickly converts to ganciclovir in <strong>the</strong><br />

body and has good bioavailability. Valganciclovir should<br />

be used only if <strong>the</strong> patient is thought to be capable <strong>of</strong><br />

strict adherence. O<strong>the</strong>r possible intravenous treatments<br />

include ganciclovir, ganciclovir followed by oral<br />

valganciclovir, foscarnet, and cid<strong>of</strong>ovir. See below <strong>for</strong><br />

dosing re<strong>com</strong>mendations.<br />

For sight-threatening disease, treat with ganciclovir<br />

intraocular implants plus valganciclovir 900 mg orally<br />

once daily or twice daily.<br />

For peripheral disease, treat with valganciclovir 900 mg<br />

orally twice daily <strong>for</strong> 14-21 days.<br />

Alternatives <strong>for</strong> initial <strong>the</strong>rapy<br />

♦<br />

♦<br />

♦<br />

Intravenous ganciclovir 5 mg/kg every 12 hours <strong>for</strong><br />

14-21 days<br />

Intravenous foscarnet 60 mg/kg every 8 hours or 90<br />

mg/kg every 12 hours <strong>for</strong> 14-21 days<br />

Intravenous cid<strong>of</strong>ovir 5 mg/kg weekly <strong>for</strong> 2<br />

weeks, <strong>the</strong>n every o<strong>the</strong>r week (must be given with<br />

probenecid [2 g orally 3 hours be<strong>for</strong>e, 1 g orally 2<br />

hours after, and 1 g orally 8 hours after <strong>the</strong> cid<strong>of</strong>ovir<br />

infusion] and intravenous saline to decrease <strong>the</strong> risk<br />

<strong>of</strong> renal toxicity)<br />

Section 6—Disease-Specific Treatment | 6–27<br />

Note: Valganciclovir, ganciclovir, and foscarnet require<br />

dosage adjustment in patients with renal insufficiency.<br />

Cid<strong>of</strong>ovir is contraindicated in patients with renal<br />

insufficiency or proteinuria.<br />

Monitor patients closely to gauge <strong>the</strong> response to<br />

<strong>the</strong>rapy. Repeat <strong>the</strong> dilated retinal examination after<br />

<strong>the</strong> <strong>com</strong>pletion <strong>of</strong> induction <strong>the</strong>rapy, 1 month after<br />

initiation <strong>of</strong> <strong>the</strong>rapy, and monthly during anti-CMV<br />

<strong>the</strong>rapy. Consult with a specialist if <strong>the</strong> response to<br />

<strong>the</strong>rapy is suboptimal.<br />

Note: Retinal detachment may occur in up to 50-60% <strong>of</strong><br />

patients in <strong>the</strong> first year after diagnosis. Regular followup<br />

with an ophthalmologist is required <strong>for</strong> all patients.<br />

Patients should report any vision loss immediately.<br />

Chronic maintenance <strong>the</strong>rapy<br />

After initial CMV treatment, lifelong maintenance<br />

<strong>the</strong>rapy with valganciclovir or intravenous foscarnet<br />

should be given to prevent recurrence, and <strong>the</strong> patient<br />

needs regular reevaluation by an ophthalmologist.<br />

Re<strong>com</strong>mended dosages <strong>for</strong> maintenance <strong>the</strong>rapy are as<br />

follows:<br />

♦<br />

♦<br />

Valganciclovir 900 mg orally once daily<br />

Intravenous foscarnet 90-120 mg/kg once daily<br />

Discontinuation <strong>of</strong> maintenance <strong>the</strong>rapy can be<br />

considered <strong>for</strong> patients with inactive CMV and<br />

sustained immune reconstitution during ART (CD4<br />

count <strong>of</strong> >100-150 cells/µL <strong>for</strong> at least 6 months).<br />

However, <strong>the</strong> decision should be guided by factors such<br />

as <strong>the</strong> extent and location <strong>of</strong> <strong>the</strong> CMV lesions and<br />

<strong>the</strong> status <strong>of</strong> <strong>the</strong> patient’s vision. An ophthalmologist<br />

who is experienced in caring <strong>for</strong> <strong>HIV</strong>-infected<br />

patients should be involved in making any decision to<br />

discontinue <strong>the</strong>rapy, and patients should receive regular<br />

ophthalmologic follow-up. Maintenance <strong>the</strong>rapy should<br />

be resumed if <strong>the</strong> CD4 count drops below 100-150<br />

cells/µL or <strong>the</strong> patient develops o<strong>the</strong>r signs <strong>of</strong> <strong>HIV</strong><br />

progression.<br />

Gastrointestinal and pulmonary CMV disease<br />

These infections are usually treated with intravenous<br />

ganciclovir or foscarnet <strong>for</strong> 21-28 days unless <strong>the</strong><br />

patient is able to absorb oral medications, in which<br />

case oral valganciclovir is an option (refer to <strong>the</strong> dosing<br />

suggestions above). Some specialists re<strong>com</strong>mend a<br />

follow-up endoscopy to verify regression <strong>of</strong> lesions<br />

be<strong>for</strong>e discontinuing <strong>the</strong>rapy. Many experts do not<br />

re<strong>com</strong>mend maintenance <strong>the</strong>rapy <strong>for</strong> gastrointestinal<br />

CMV infections unless <strong>the</strong> disease recurs.

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