Retrospective study of a series of choanal atresia patients

Detalhes bibliográficos
Autor(a) principal: Manica, Denise
Data de Publicação: 2014
Outros Autores: Schweiger, Claudia, Netto, Cátia de Souza Saleh, Kuhl, Gabriel
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UFRGS
Texto Completo: http://hdl.handle.net/10183/198049
Resumo: Introduction Although it has been more than 250 years since the first description of choanal atresia (CA), there are still doubts about this abnormality. The differences between unilateral and bilateral forms are seldom discussed. Objectives Aggregate data from patients diagnosed with CA, grouping patients with unilateral and bilateral forms. Methods Retrospective study. Results Eighteen patients were included: 12 (66.6%) presented bilateral atresia, of which 77.8% were mixed bony-membranous type and 22.2% were pure bony type. From the 12 patients with bilateral atresia, 10 presented related malformations, 3 of whom had CHARGE syndrome (coloboma, heart defects, choanal atresia, retardation of growth and development, genitourinary problems, ear abnormalities). From the remaining 6 patients with unilateral atresia, only 2 showed malformations, 1 renal and 1 cardiac. All patients with unilateral atresia needed only 1 surgical procedure, and patients with the bilateral form needed amedian of 2.85 interventions (p ¼ 0.003). The median age of surgical procedure in the unilateral group was 6 years, ranging from 6 months to 18 years, and in the bilateral group was 25 days, ranging from 6 days to 6 years (p ¼ 0.003). The median interval between diagnosis and surgery was 9 months in the unilateral group, ranging from 1 month to 18 years, and in the bilateral group was 1 day, ranging from 1 day to 2 months (p ¼ 0.001). Discussion and Conclusions Success rates with the endoscopic approach vary from 62 to 100%. Nonetheless, most of these reports present results without considering the number of compromised sides. In our opinion, unilateral and bilateral cases involve distinct patients (taking into account the related malformations), have diverging clinical presentations, and show discrepant restenosis rates and therefore could be considered in different groups of analysis.
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spelling Manica, DeniseSchweiger, ClaudiaNetto, Cátia de Souza SalehKuhl, Gabriel2019-08-15T02:30:31Z20141809-4864http://hdl.handle.net/10183/198049001084127Introduction Although it has been more than 250 years since the first description of choanal atresia (CA), there are still doubts about this abnormality. The differences between unilateral and bilateral forms are seldom discussed. Objectives Aggregate data from patients diagnosed with CA, grouping patients with unilateral and bilateral forms. Methods Retrospective study. Results Eighteen patients were included: 12 (66.6%) presented bilateral atresia, of which 77.8% were mixed bony-membranous type and 22.2% were pure bony type. From the 12 patients with bilateral atresia, 10 presented related malformations, 3 of whom had CHARGE syndrome (coloboma, heart defects, choanal atresia, retardation of growth and development, genitourinary problems, ear abnormalities). From the remaining 6 patients with unilateral atresia, only 2 showed malformations, 1 renal and 1 cardiac. All patients with unilateral atresia needed only 1 surgical procedure, and patients with the bilateral form needed amedian of 2.85 interventions (p ¼ 0.003). The median age of surgical procedure in the unilateral group was 6 years, ranging from 6 months to 18 years, and in the bilateral group was 25 days, ranging from 6 days to 6 years (p ¼ 0.003). The median interval between diagnosis and surgery was 9 months in the unilateral group, ranging from 1 month to 18 years, and in the bilateral group was 1 day, ranging from 1 day to 2 months (p ¼ 0.001). Discussion and Conclusions Success rates with the endoscopic approach vary from 62 to 100%. Nonetheless, most of these reports present results without considering the number of compromised sides. In our opinion, unilateral and bilateral cases involve distinct patients (taking into account the related malformations), have diverging clinical presentations, and show discrepant restenosis rates and therefore could be considered in different groups of analysis.application/pdfengInternational archives of otorhinolaryngology. Vol. 18, n. 1 (jan. 2014), p. 2-5Atresia das cóanasEstudos retrospectivosAnormalidades congênitasSíndrome CHARGERespiração bucalNasofaringeCirurgiaCHARGE syndromeChoanal atresiaMouth breathingNasopharynxNose diseasesRetrospective study of a series of choanal atresia patientsinfo:eu-repo/semantics/articleinfo:eu-repo/semantics/otherinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UFRGSinstname:Universidade Federal do Rio Grande do Sul (UFRGS)instacron:UFRGSTEXT001084127.pdf.txt001084127.pdf.txtExtracted Texttext/plain15882http://www.lume.ufrgs.br/bitstream/10183/198049/2/001084127.pdf.txt09f4b4e6c1dd5d890d66732b32da282fMD52ORIGINAL001084127.pdfTexto completo (inglês)application/pdf199727http://www.lume.ufrgs.br/bitstream/10183/198049/1/001084127.pdfd44854114f8b5d84addd4e0618686cdcMD5110183/1980492023-11-29 04:26:55.348217oai:www.lume.ufrgs.br:10183/198049Repositório de PublicaçõesPUBhttps://lume.ufrgs.br/oai/requestopendoar:2023-11-29T06:26:55Repositório Institucional da UFRGS - Universidade Federal do Rio Grande do Sul (UFRGS)false
dc.title.pt_BR.fl_str_mv Retrospective study of a series of choanal atresia patients
title Retrospective study of a series of choanal atresia patients
spellingShingle Retrospective study of a series of choanal atresia patients
Manica, Denise
Atresia das cóanas
Estudos retrospectivos
Anormalidades congênitas
Síndrome CHARGE
Respiração bucal
Nasofaringe
Cirurgia
CHARGE syndrome
Choanal atresia
Mouth breathing
Nasopharynx
Nose diseases
title_short Retrospective study of a series of choanal atresia patients
title_full Retrospective study of a series of choanal atresia patients
title_fullStr Retrospective study of a series of choanal atresia patients
title_full_unstemmed Retrospective study of a series of choanal atresia patients
title_sort Retrospective study of a series of choanal atresia patients
author Manica, Denise
author_facet Manica, Denise
Schweiger, Claudia
Netto, Cátia de Souza Saleh
Kuhl, Gabriel
author_role author
author2 Schweiger, Claudia
Netto, Cátia de Souza Saleh
Kuhl, Gabriel
author2_role author
author
author
dc.contributor.author.fl_str_mv Manica, Denise
Schweiger, Claudia
Netto, Cátia de Souza Saleh
Kuhl, Gabriel
dc.subject.por.fl_str_mv Atresia das cóanas
Estudos retrospectivos
Anormalidades congênitas
Síndrome CHARGE
Respiração bucal
Nasofaringe
Cirurgia
topic Atresia das cóanas
Estudos retrospectivos
Anormalidades congênitas
Síndrome CHARGE
Respiração bucal
Nasofaringe
Cirurgia
CHARGE syndrome
Choanal atresia
Mouth breathing
Nasopharynx
Nose diseases
dc.subject.eng.fl_str_mv CHARGE syndrome
Choanal atresia
Mouth breathing
Nasopharynx
Nose diseases
description Introduction Although it has been more than 250 years since the first description of choanal atresia (CA), there are still doubts about this abnormality. The differences between unilateral and bilateral forms are seldom discussed. Objectives Aggregate data from patients diagnosed with CA, grouping patients with unilateral and bilateral forms. Methods Retrospective study. Results Eighteen patients were included: 12 (66.6%) presented bilateral atresia, of which 77.8% were mixed bony-membranous type and 22.2% were pure bony type. From the 12 patients with bilateral atresia, 10 presented related malformations, 3 of whom had CHARGE syndrome (coloboma, heart defects, choanal atresia, retardation of growth and development, genitourinary problems, ear abnormalities). From the remaining 6 patients with unilateral atresia, only 2 showed malformations, 1 renal and 1 cardiac. All patients with unilateral atresia needed only 1 surgical procedure, and patients with the bilateral form needed amedian of 2.85 interventions (p ¼ 0.003). The median age of surgical procedure in the unilateral group was 6 years, ranging from 6 months to 18 years, and in the bilateral group was 25 days, ranging from 6 days to 6 years (p ¼ 0.003). The median interval between diagnosis and surgery was 9 months in the unilateral group, ranging from 1 month to 18 years, and in the bilateral group was 1 day, ranging from 1 day to 2 months (p ¼ 0.001). Discussion and Conclusions Success rates with the endoscopic approach vary from 62 to 100%. Nonetheless, most of these reports present results without considering the number of compromised sides. In our opinion, unilateral and bilateral cases involve distinct patients (taking into account the related malformations), have diverging clinical presentations, and show discrepant restenosis rates and therefore could be considered in different groups of analysis.
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