<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>217(10)</volume><submitter>Lynch KD</submitter><pubmed_abstract>&lt;h4>Objectives&lt;/h4>To compare the findings of standard clinical assessments and of complementary clinical and laboratory methods for determining whether community-wide treatment for trachoma is warranted in a remote Queensland community.&lt;h4>Design&lt;/h4>Three cross-sectional screening surveys, 2019-2021, complemented by laboratory pathology testing.&lt;h4>Setting&lt;/h4>Small community in northwest Queensland with geographic and cultural ties to Northern Territory communities where trachoma persists.&lt;h4>Participants&lt;/h4>Children aged 1-14 years; opportunistic screening of people aged 15 years or more.&lt;h4>Main outcome measures&lt;/h4>Prevalence of clinical signs of trachoma, Chlamydia trachomatis infection, ocular non-chlamydial infections, and seropositivity for antibodies to the C. trachomatis Pgp3 protein.&lt;h4>Results&lt;/h4>During the three surveys, 73 examinations of 58 children aged 1-4 years, 309 of 171 aged 5-9 years, and 142 of 105 aged 10-14 years for trachoma were undertaken, as were 171 examinations of 164 people aged 15 years or more; 691 of 695 examinations were of Aboriginal or Torres Strait Islander people (99%), 337 were of girls or young women (48%). Clinical signs consistent with trachomatous inflammation-follicular were identified in 5-9-year-old children 23 times (7%), including in eleven with non-chlamydial infections and one with a C. trachomatis infection. One child (10-14 years) met the criteria for trachomatous scarring. Two of 272 conjunctival swab samples (all ages) were polymerase chain reaction-positive for C. trachomatis (0.7%). Two of 147 people aged 15 years or more examined in 2019 had trichiasis, both aged 40 years or more. Seven of 53 children aged 1-9 years in 2019 and seven of 103 in 2021 were seropositive for anti-Pgp3 antibodies.&lt;h4>Conclusions&lt;/h4>Despite the prevalence of clinical signs consistent with trachomatous inflammation-follicular among 5-9-year-old children exceeding the 5% threshold for community-wide treatment, laboratory testing indicated that childhood exposure to ocular C. trachomatis is rare in this community. Laboratory testing should be integrated into Australian trachoma guidelines.</pubmed_abstract><journal>The Medical journal of Australia</journal><pagination>538-543</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9827872</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Clinical signs of trachoma and laboratory evidence of ocular Chlamydia trachomatis infection in a remote Queensland community: a serial cross-sectional study.</pubmed_title><pmcid>PMC9827872</pmcid><pubmed_authors>Morotti W</pubmed_authors><pubmed_authors>Lambert SB</pubmed_authors><pubmed_authors>Kaldor JM</pubmed_authors><pubmed_authors>Whop LJ</pubmed_authors><pubmed_authors>O'Keefe A</pubmed_authors><pubmed_authors>Kingston K</pubmed_authors><pubmed_authors>Starr M</pubmed_authors><pubmed_authors>Lynch KD</pubmed_authors><pubmed_authors>Ketchup L</pubmed_authors><pubmed_authors>Brian G</pubmed_authors><pubmed_authors>Everill B</pubmed_authors><pubmed_authors>Ware RS</pubmed_authors><pubmed_authors>Asgar N</pubmed_authors></additional><is_claimable>false</is_claimable><name>Clinical signs of trachoma and laboratory evidence of ocular Chlamydia trachomatis infection in a remote Queensland community: a serial cross-sectional study.</name><description>&lt;h4>Objectives&lt;/h4>To compare the findings of standard clinical assessments and of complementary clinical and laboratory methods for determining whether community-wide treatment for trachoma is warranted in a remote Queensland community.&lt;h4>Design&lt;/h4>Three cross-sectional screening surveys, 2019-2021, complemented by laboratory pathology testing.&lt;h4>Setting&lt;/h4>Small community in northwest Queensland with geographic and cultural ties to Northern Territory communities where trachoma persists.&lt;h4>Participants&lt;/h4>Children aged 1-14 years; opportunistic screening of people aged 15 years or more.&lt;h4>Main outcome measures&lt;/h4>Prevalence of clinical signs of trachoma, Chlamydia trachomatis infection, ocular non-chlamydial infections, and seropositivity for antibodies to the C. trachomatis Pgp3 protein.&lt;h4>Results&lt;/h4>During the three surveys, 73 examinations of 58 children aged 1-4 years, 309 of 171 aged 5-9 years, and 142 of 105 aged 10-14 years for trachoma were undertaken, as were 171 examinations of 164 people aged 15 years or more; 691 of 695 examinations were of Aboriginal or Torres Strait Islander people (99%), 337 were of girls or young women (48%). Clinical signs consistent with trachomatous inflammation-follicular were identified in 5-9-year-old children 23 times (7%), including in eleven with non-chlamydial infections and one with a C. trachomatis infection. One child (10-14 years) met the criteria for trachomatous scarring. Two of 272 conjunctival swab samples (all ages) were polymerase chain reaction-positive for C. trachomatis (0.7%). Two of 147 people aged 15 years or more examined in 2019 had trichiasis, both aged 40 years or more. Seven of 53 children aged 1-9 years in 2019 and seven of 103 in 2021 were seropositive for anti-Pgp3 antibodies.&lt;h4>Conclusions&lt;/h4>Despite the prevalence of clinical signs consistent with trachomatous inflammation-follicular among 5-9-year-old children exceeding the 5% threshold for community-wide treatment, laboratory testing indicated that childhood exposure to ocular C. trachomatis is rare in this community. Laboratory testing should be integrated into Australian trachoma guidelines.</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Nov</publication><modification>2025-04-21T17:54:42.422Z</modification><creation>2025-04-05T17:03:28.963Z</creation></dates><accession>S-EPMC9827872</accession><cross_references><pubmed>36180097</pubmed><doi>10.5694/mja2.51735</doi></cross_references></HashMap>