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Helicobacter pylori - Portal Neonatal

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32<br />

Infectious esophagitis<br />

Non-invasive methods to diagnose esophageal<br />

infections without endoscopy are cytology brush<br />

and balloon devices. The latter consists of a tube<br />

with a ridged cytology balloon on the distal end:<br />

when inflated, it can be withdrawn from the<br />

esophagus and the brushings removed and submitted<br />

for cytological evaluation as well as viral<br />

culture. Whereas these methods are useful to identify<br />

Candida, they are less sensitive for viral<br />

disease and have no real advantage over empirical<br />

antifungal therapy. 13<br />

Endoscopy with biopsy is the gold standard for<br />

diagnosing esophageal candidiasis because<br />

mucosal biopsies can be performed. Despite the<br />

fact that gross endoscopic features can suggest a<br />

diagnosis of esophageal candidiasis, this is<br />

confirmed by the presence of hyphae in biopsies.<br />

Cytological specimens, which can be obtained at<br />

the time of endoscopy, are also a sensitive tool for<br />

the diagnosis, especially when organisms are<br />

washed off the tissue surface in mild superficial<br />

candidiasis after processing of bioptic specimens.<br />

When endoscopy is performed in patients with<br />

esophageal candidiasis, removal of plaque material<br />

by scraping with the endoscope is important to<br />

evaluate the underlying mucosa for ulcers. 6 In<br />

general, Candida should not be considered a cause<br />

of esophageal ulcers in HIV-infected patients.<br />

Both oral and intravenous drugs are available for<br />

treating esophageal candidiasis. Oral medications<br />

are generally administered first, whereas intravenous<br />

therapy is reserved for refractory cases or<br />

when oral administration is contraindicated. Nonsystemic<br />

locally acting agents such as nystatin or<br />

clotrimazole are not very effective and must be<br />

reserved for the treatment of oropharyngeal<br />

disease. In patients with mild disease, with<br />

minimal or reversible immunodeficiency, a short<br />

course of therapy with a systemically absorbed<br />

agent can be given, whereas in patients with HIV<br />

infection or with transplantation immunodeficiency,<br />

longer courses of azoles are best given.<br />

Patients with granulocytopenia, at risk for<br />

systemic Candida infection, require the use of<br />

systemically acting intravenous agents such as<br />

azoles or amphotericin B. All available oral agents<br />

(ketoconazole, fluconazole and itraconazole) are<br />

efficacious for the treatment of esophageal<br />

candidiasis (Table 3.3). Ketoconazole and itraconazole<br />

should be avoided in patients requiring anti-<br />

acid therapy, as an alkaline pH limits their<br />

bioavailability. Fluconazole appears to be more<br />

efficacious than itraconazole; a poor response to<br />

fluconazole suggests non-compliance, drug resistance<br />

or other causes for esophageal symptoms. 14<br />

Randomized trials suggest that fluconazole is<br />

significantly more effective for the treatment of<br />

esophageal candidiasis in HIV-infected patients<br />

than ketoconazole and itraconazole. 14 Fluconazole<br />

is available in oral and intravenous preparations,<br />

is minimally metabolized, is highly water soluble<br />

and is slightly protein bound. The new oral<br />

suspension formulations of fluconazole and itraconazole<br />

may have superior efficacy over pills due<br />

to an additional local antifungal effect and<br />

improved absorption. 15 The adverse effects of ketoconazole,<br />

fluconazole and itraconazole are dose<br />

dependent and include nausea, hepatotoxicity,<br />

inhibition of steroid production and cyclosporin<br />

metabolism. 16 The latter effect is more pronounced<br />

with ketoconazole. 17 Minor increases in aminotransferases<br />

are commonly found in patients<br />

treated with oral azoles and do not require drug<br />

discontinuation.<br />

Amphotericin B represents the other family of<br />

antifungal agents (polyene antibiotics), which bind<br />

irreversibly to sterol in fungal cell membranes,<br />

causing cell death. This drug has a limited use for<br />

the treatment of esophageal candidiasis, owing to<br />

its severe side-effects (nephro- and hepatotoxicity).<br />

This drug is now available in an oral<br />

formulation. Patients with esophageal candidiasis<br />

that is resistant to treatment with fluconazole or<br />

other azoles can be treated effectively with lower<br />

doses of intravenous amphotericin B.<br />

The prophylaxis of esophageal candidiasis in<br />

malignancy and transplant patients has yielded<br />

controversial results. 18<br />

Viral infections<br />

HSV and CMV are the most common viral agents<br />

involved in infectious esophagitis, although some<br />

cases have been ascribed to HIV infection of the<br />

esophagus. HSV (HSV I or, rarely, HSV II)<br />

esophagitis causes a self-limited disease in normal<br />

subjects, but it can be severe and prolonged in the<br />

compromised patients.

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