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