<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>46</volume><submitter>da Silva-Filho LVRF</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>Meconium ileus (MI) is one of the earliest manifestations of cystic fibrosis (CF), affecting 15-20% of individuals. The impact of MI on health outcomes has yet to be elucidated and may vary based on the amount of health care resources. The aim of this study was to investigate the clinical impact of MI on outcomes among Brazilian CF individuals using data from the Brazilian Cystic Fibrosis Patient Registry.&lt;h4>Methods&lt;/h4>This retrospective cohort study included data from individuals with CF from 53 reference centres in Brazil. Data from individuals with a history of MI during the neonatal period were compared to those of the non-MI individuals. Demographic data, genotype, lung function, nutritional data, microbiological data and survival data were compared between groups. The impact of MI on lung function and anthropometric outcomes was evaluated using mixed effects models after adjusting for age. Individual survival data were analyzed by Kaplan-Meier curves, log-rank tests and Cox proportional hazards models.&lt;h4>Findings&lt;/h4>Among the 5128 individuals included in the registry, 369 (7·2%) were diagnosed with MI at birth. The occurrence of MI was associated with an earlier diagnosis of CF but a lower mean Z score for weight (-0·32, 95% CI -0·46 to -0·18, p &lt; 0·0001) and height (-0·28 95% CI -0·40 to -0·15, p &lt; 0·0001). Lung function was significantly lower among those affected by MI (reduction of -4·3% 95% CI -8·0 to -0·5, p = 0·028) up to the age of 18 years. A greater prevalence of &lt;i>Pseudomonas aeruginosa&lt;/i> colonization was observed in the MI group (79·1% (272/344) versus 64·5% (2818/4367); p &lt; 0·0001). Survival was significantly worse in the MI group, and the results of the Cox regression model revealed that the impact of MI on mortality was significant after controlling for other risk factors (HR = 1·84, 95% CI 1·50-2·25, p &lt; 0·0001).&lt;h4>Interpretation&lt;/h4>CF individuals affected by MI had more severe and earlier declines in lung function, slower rates of weight and height gain, and lower survival rates. These findings underscore the importance of early identification and tailored management strategies for this high-risk subgroup.&lt;h4>Funding&lt;/h4>None.</pubmed_abstract><journal>Lancet regional health. Americas</journal><pagination>101099</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12435481</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>The significant impact of meconium ileus on clinical outcomes among Brazilian individuals with cystic fibrosis-a retrospective analysis of a patient registry.</pubmed_title><pmcid>PMC12435481</pmcid><pubmed_authors>Dalcin PT</pubmed_authors><pubmed_authors>Gurmini J</pubmed_authors><pubmed_authors>Valente SE</pubmed_authors><pubmed_authors>Perez MF</pubmed_authors><pubmed_authors>Santana MA</pubmed_authors><pubmed_authors>Souza EL</pubmed_authors><pubmed_authors>Goncalves CM</pubmed_authors><pubmed_authors>Prado LJ</pubmed_authors><pubmed_authors>Costa LD</pubmed_authors><pubmed_authors>Castro-E-Silva C</pubmed_authors><pubmed_authors>Veras TN</pubmed_authors><pubmed_authors>da Silva-Filho LVRF</pubmed_authors><pubmed_authors>Fonseca ACC</pubmed_authors><pubmed_authors>Belchior G</pubmed_authors><pubmed_authors>Knabben AS</pubmed_authors><pubmed_authors>Brazilian CF Registry Contributors Team</pubmed_authors><pubmed_authors>Oliveira RF</pubmed_authors><pubmed_authors>Steinhaus C</pubmed_authors><pubmed_authors>Martins VC</pubmed_authors><pubmed_authors>Ferrao DM</pubmed_authors><pubmed_authors>Nishi MP</pubmed_authors><pubmed_authors>Araujo-Filho EM</pubmed_authors><pubmed_authors>Fernandes MI</pubmed_authors><pubmed_authors>Adde FV</pubmed_authors><pubmed_authors>Piacentini-Filho E</pubmed_authors><pubmed_authors>Yamamoto FW</pubmed_authors><pubmed_authors>Bezerra PG</pubmed_authors><pubmed_authors>Silva EP</pubmed_authors><pubmed_authors>Tanaka SO</pubmed_authors><pubmed_authors>Melotti RC</pubmed_authors><pubmed_authors>Mota LR</pubmed_authors><pubmed_authors>Duarte MC</pubmed_authors><pubmed_authors>Epifanio M</pubmed_authors><pubmed_authors>Sousa MA</pubmed_authors><pubmed_authors>Riedi CA</pubmed_authors><pubmed_authors>Fuccio MB</pubmed_authors><pubmed_authors>Rached S</pubmed_authors><pubmed_authors>Oliveira DV</pubmed_authors><pubmed_authors>Garcia RV</pubmed_authors><pubmed_authors>Vergara AA</pubmed_authors><pubmed_authors>Procianoy EF</pubmed_authors><pubmed_authors>Ribeiro AF</pubmed_authors><pubmed_authors>Cartaxo CG</pubmed_authors><pubmed_authors>Britto MC</pubmed_authors><pubmed_authors>Moura KV</pubmed_authors><pubmed_authors>Oliveira KI</pubmed_authors><pubmed_authors>Andries LC</pubmed_authors><pubmed_authors>Borgli DS</pubmed_authors><pubmed_authors>Goncalves MM</pubmed_authors><pubmed_authors>Malini FB</pubmed_authors><pubmed_authors>Foletto GM</pubmed_authors><pubmed_authors>Figueiredo MR</pubmed_authors><pubmed_authors>Nakaie CM</pubmed_authors><pubmed_authors>Fernandes FF</pubmed_authors><pubmed_authors>Paes AT</pubmed_authors><pubmed_authors>Dantas VM</pubmed_authors><pubmed_authors>Haidar DM</pubmed_authors><pubmed_authors>Goya A</pubmed_authors><pubmed_authors>Ziegler B</pubmed_authors><pubmed_authors>Velloso-Monte LF</pubmed_authors><pubmed_authors>Augustin AE</pubmed_authors><pubmed_authors>Canan MG</pubmed_authors><pubmed_authors>Chong-E-Silva DC</pubmed_authors><pubmed_authors>Sad I</pubmed_authors><pubmed_authors>Chiba SM</pubmed_authors><pubmed_authors>Kussek PC</pubmed_authors><pubmed_authors>Soriano Freire NC</pubmed_authors><pubmed_authors>Melo SF</pubmed_authors><pubmed_authors>Guimaraes EV</pubmed_authors><pubmed_authors>Pessoa BP</pubmed_authors><pubmed_authors>Fischer GB</pubmed_authors><pubmed_authors>Moreira ME</pubmed_authors><pubmed_authors>De-Sillos MD</pubmed_authors><pubmed_authors>Rodrigues MT</pubmed_authors><pubmed_authors>Pinto LA</pubmed_authors><pubmed_authors>Coelho LS</pubmed_authors><pubmed_authors>Marostica PJ</pubmed_authors><pubmed_authors>Folescu TW</pubmed_authors><pubmed_authors>Castro VA</pubmed_authors><pubmed_authors>Damaceno N</pubmed_authors><pubmed_authors>Meneses DG</pubmed_authors></additional><is_claimable>false</is_claimable><name>The significant impact of meconium ileus on clinical outcomes among Brazilian individuals with cystic fibrosis-a retrospective analysis of a patient registry.</name><description>&lt;h4>Background&lt;/h4>Meconium ileus (MI) is one of the earliest manifestations of cystic fibrosis (CF), affecting 15-20% of individuals. The impact of MI on health outcomes has yet to be elucidated and may vary based on the amount of health care resources. The aim of this study was to investigate the clinical impact of MI on outcomes among Brazilian CF individuals using data from the Brazilian Cystic Fibrosis Patient Registry.&lt;h4>Methods&lt;/h4>This retrospective cohort study included data from individuals with CF from 53 reference centres in Brazil. Data from individuals with a history of MI during the neonatal period were compared to those of the non-MI individuals. Demographic data, genotype, lung function, nutritional data, microbiological data and survival data were compared between groups. The impact of MI on lung function and anthropometric outcomes was evaluated using mixed effects models after adjusting for age. Individual survival data were analyzed by Kaplan-Meier curves, log-rank tests and Cox proportional hazards models.&lt;h4>Findings&lt;/h4>Among the 5128 individuals included in the registry, 369 (7·2%) were diagnosed with MI at birth. The occurrence of MI was associated with an earlier diagnosis of CF but a lower mean Z score for weight (-0·32, 95% CI -0·46 to -0·18, p &lt; 0·0001) and height (-0·28 95% CI -0·40 to -0·15, p &lt; 0·0001). Lung function was significantly lower among those affected by MI (reduction of -4·3% 95% CI -8·0 to -0·5, p = 0·028) up to the age of 18 years. A greater prevalence of &lt;i>Pseudomonas aeruginosa&lt;/i> colonization was observed in the MI group (79·1% (272/344) versus 64·5% (2818/4367); p &lt; 0·0001). Survival was significantly worse in the MI group, and the results of the Cox regression model revealed that the impact of MI on mortality was significant after controlling for other risk factors (HR = 1·84, 95% CI 1·50-2·25, p &lt; 0·0001).&lt;h4>Interpretation&lt;/h4>CF individuals affected by MI had more severe and earlier declines in lung function, slower rates of weight and height gain, and lower survival rates. These findings underscore the importance of early identification and tailored management strategies for this high-risk subgroup.&lt;h4>Funding&lt;/h4>None.</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Jun</publication><modification>2026-06-01T06:20:50.404Z</modification><creation>2026-04-08T09:44:03.134Z</creation></dates><accession>S-EPMC12435481</accession><cross_references><pubmed>40959767</pubmed><doi>10.1016/j.lana.2025.101099</doi></cross_references></HashMap>