<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>36(1)</volume><submitter>Ricciardelli G</submitter><pubmed_abstract>&lt;h4>Objectives&lt;/h4>To analyze the effect of the employment of polyvinylpyrrolidone-iodine (PVP-I) 0.6% eye drop on the clinical course of patients affected by Adenoviral Keratoconjunctivitis (AKC).&lt;h4>Methods&lt;/h4>Consecutive patients with clinical signs of AKC and positive results of AdenoPlus test were enrolled from four Italian Centres. Patients were randomized to receive: PVP-I 0.6% eye drops four times/daily for 20 days (Group A) or hyaluronate-based tear substitutes four times/daily for 20 days (Group B). Best-corrected visual acuity (BCVA), optical coherence tomography (OCT) Optovue iVue pachymetry map; corneal haze; conjunctival injection and chemosis; subepithelial corneal infiltrates (SEIs); corneal and conjunctival staining and corneal densitometry were recorded at diagnosis and </pubmed_abstract><journal>Eye (London, England)</journal><pagination>160-166</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8727611</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Efficacy and tolerability of polyvinylpyrrolidone-iodine 0.6% treatment in adenoviral keratoconjunctivitis: a Prospective Randomized Controlled Study.</pubmed_title><pmcid>PMC8727611</pmcid><pubmed_authors>Ricciardelli G</pubmed_authors><pubmed_authors>Giannaccare G</pubmed_authors><pubmed_authors>Allegrini D</pubmed_authors><pubmed_authors>Cennamo M</pubmed_authors><pubmed_authors>Antonini M</pubmed_authors><pubmed_authors>Bernabei F</pubmed_authors><pubmed_authors>Morelli A</pubmed_authors><pubmed_authors>Scorcia V</pubmed_authors><pubmed_authors>Mencucci R</pubmed_authors><pubmed_authors>Coassin M</pubmed_authors><pubmed_authors>Di Zazzo A</pubmed_authors><pubmed_authors>Romano MR</pubmed_authors></additional><is_claimable>false</is_claimable><name>Efficacy and tolerability of polyvinylpyrrolidone-iodine 0.6% treatment in adenoviral keratoconjunctivitis: a Prospective Randomized Controlled Study.</name><description>&lt;h4>Objectives&lt;/h4>To analyze the effect of the employment of polyvinylpyrrolidone-iodine (PVP-I) 0.6% eye drop on the clinical course of patients affected by Adenoviral Keratoconjunctivitis (AKC).&lt;h4>Methods&lt;/h4>Consecutive patients with clinical signs of AKC and positive results of AdenoPlus test were enrolled from four Italian Centres. Patients were randomized to receive: PVP-I 0.6% eye drops four times/daily for 20 days (Group A) or hyaluronate-based tear substitutes four times/daily for 20 days (Group B). Best-corrected visual acuity (BCVA), optical coherence tomography (OCT) Optovue iVue pachymetry map; corneal haze; conjunctival injection and chemosis; subepithelial corneal infiltrates (SEIs); corneal and conjunctival staining and corneal densitometry were recorded at diagnosis and </description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Jan</publication><modification>2025-04-22T10:08:48.318Z</modification><creation>2025-04-05T23:29:35.693Z</creation></dates><accession>S-EPMC8727611</accession><cross_references><pubmed>33654316</pubmed><doi>10.1038/s41433-020-01344-6</doi></cross_references></HashMap>