Matches in SemOpenAlex for { <https://semopenalex.org/work/W3208990930> ?p ?o ?g. }
Showing items 1 to 97 of
97
with 100 items per page.
- W3208990930 endingPage "615" @default.
- W3208990930 startingPage "608" @default.
- W3208990930 abstract "L’angiœdème héréditaire (AOH) est caractérisé par des poussées récidivantes d’œdèmes de localisations et de sévérité variables. Une altération de la qualité de vie des patients atteints d’AOH est décrite par plusieurs études. Nous avons étudié l’impact global de la maladie chez les patients suivis pour un AOH de type I, notamment son retentissement sur les activités de la vie quotidienne, la sphère émotionnelle et la qualité de vie. Un questionnaire a été distribué aux patients consultant pour un AOH de type I, recueillant les caractéristiques démographiques, les caractéristiques de la maladie, le retentissement sur la vie professionnelle, le score Hospital Anxiety And Depression (HAD), le score SF-36 et le questionnaire de handicap prioritaire McMaster Toronto Arthritis Patient Preference Disability Questionnaire (MACTAR). Les 33 patients inclus rapportaient en moyenne de 5,17 crises sur l’année précédente. Le stress était le principal facteur déclenchant. Un traitement de fond était rapporté par 58 % des patients, 72 % recevaient un traitement spécifique en cas de crise sévère. Un absentéisme pendant leurs études était rapporté 33 % des patients, et pendant leur travail par 34 %. Un patient souffrait de symptômes dépressifs et dix autres de symptômes anxieux d’après le questionnaire HAD. Les domaines les plus impactés sur le score SF-36 étaient la perception générale de la santé et de la vitalité. Le score moyen pour le MACTAR était faible. L’AOH a un retentissement encore important dans la vie quotidienne et affective des patients, malgré la disponibilité de traitements préventifs et curatifs des crises. Hereditary angioedema (HAE) is characterized by recurrent attacks of swelling of various locations and severity. An impaired quality of life of patients with HAE has been reported by several studies. We aimed at examining the overall impact of the disease in patients followed for type I HAE, particularly its impact on daily life activities, emotions and quality of life. A questionnaire was distributed to patients consulting for type I HAE, collecting demographics, disease characteristics, impact on professional life, Hospital Anxiety and Depression score (HAD), SF-36 score and the McMaster Toronto Arthritis Patient Preference Disability Questionnaire (MACTAR). The 33 patients included reported an average of 5.17 attacks over the last year. Stress was the main trigger A long-term treatment was reported by 58% of patients, 72% received specific treatment in the event of a serious attack. Sick days were reported by 33% of patients during their studies, and by 34% during work. One patient suffered from depressive symptoms and ten from anxious symptoms, according to the HAD score. The areas most impacted on the SF-36 score were general health and vitality. The mean score for MACTAR was low. HAE still has a significant impact on the daily and emotional lives of patients, despite the availability of prophylactic and crisis treatments." @default.
- W3208990930 created "2021-11-08" @default.
- W3208990930 creator A5013406612 @default.
- W3208990930 creator A5014020914 @default.
- W3208990930 creator A5016242138 @default.
- W3208990930 creator A5018314421 @default.
- W3208990930 creator A5018486655 @default.
- W3208990930 creator A5043602648 @default.
- W3208990930 creator A5043652725 @default.
- W3208990930 creator A5051759477 @default.
- W3208990930 creator A5054156769 @default.
- W3208990930 creator A5064938194 @default.
- W3208990930 date "2021-09-01" @default.
- W3208990930 modified "2023-10-14" @default.
- W3208990930 title "Impact de l’angiœdème héréditaire sur les activités de la vie quotidienne, la sphère émotionnelle et la qualité de vie des patients" @default.
- W3208990930 cites W1983267522 @default.
- W3208990930 cites W1984687020 @default.
- W3208990930 cites W1985540648 @default.
- W3208990930 cites W1996649492 @default.
- W3208990930 cites W2002576194 @default.
- W3208990930 cites W2012767544 @default.
- W3208990930 cites W2025941853 @default.
- W3208990930 cites W2031123437 @default.
- W3208990930 cites W2044194498 @default.
- W3208990930 cites W2067723030 @default.
- W3208990930 cites W2070603663 @default.
- W3208990930 cites W2081368903 @default.
- W3208990930 cites W2095224014 @default.
- W3208990930 cites W2098192722 @default.
- W3208990930 cites W2101571846 @default.
- W3208990930 cites W2106265177 @default.
- W3208990930 cites W2108265793 @default.
- W3208990930 cites W2126904741 @default.
- W3208990930 cites W2138027697 @default.
- W3208990930 cites W2163505092 @default.
- W3208990930 cites W2165383253 @default.
- W3208990930 cites W2166281097 @default.
- W3208990930 cites W2182789205 @default.
- W3208990930 cites W2318188974 @default.
- W3208990930 cites W2319286676 @default.
- W3208990930 cites W2577986790 @default.
- W3208990930 cites W2727587197 @default.
- W3208990930 cites W2788038611 @default.
- W3208990930 cites W2808815147 @default.
- W3208990930 cites W2900230874 @default.
- W3208990930 cites W2902818271 @default.
- W3208990930 cites W2905169675 @default.
- W3208990930 cites W3011482704 @default.
- W3208990930 doi "https://doi.org/10.1016/j.revmed.2021.05.013" @default.
- W3208990930 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/34158189" @default.
- W3208990930 hasPublicationYear "2021" @default.
- W3208990930 type Work @default.
- W3208990930 sameAs 3208990930 @default.
- W3208990930 citedByCount "3" @default.
- W3208990930 countsByYear W32089909302022 @default.
- W3208990930 countsByYear W32089909302023 @default.
- W3208990930 crossrefType "journal-article" @default.
- W3208990930 hasAuthorship W3208990930A5013406612 @default.
- W3208990930 hasAuthorship W3208990930A5014020914 @default.
- W3208990930 hasAuthorship W3208990930A5016242138 @default.
- W3208990930 hasAuthorship W3208990930A5018314421 @default.
- W3208990930 hasAuthorship W3208990930A5018486655 @default.
- W3208990930 hasAuthorship W3208990930A5043602648 @default.
- W3208990930 hasAuthorship W3208990930A5043652725 @default.
- W3208990930 hasAuthorship W3208990930A5051759477 @default.
- W3208990930 hasAuthorship W3208990930A5054156769 @default.
- W3208990930 hasAuthorship W3208990930A5064938194 @default.
- W3208990930 hasBestOaLocation W32089909301 @default.
- W3208990930 hasConcept C142362112 @default.
- W3208990930 hasConcept C15708023 @default.
- W3208990930 hasConcept C29456083 @default.
- W3208990930 hasConcept C71924100 @default.
- W3208990930 hasConceptScore W3208990930C142362112 @default.
- W3208990930 hasConceptScore W3208990930C15708023 @default.
- W3208990930 hasConceptScore W3208990930C29456083 @default.
- W3208990930 hasConceptScore W3208990930C71924100 @default.
- W3208990930 hasIssue "9" @default.
- W3208990930 hasLocation W32089909301 @default.
- W3208990930 hasOpenAccess W3208990930 @default.
- W3208990930 hasPrimaryLocation W32089909301 @default.
- W3208990930 hasRelatedWork W1995515455 @default.
- W3208990930 hasRelatedWork W1999344589 @default.
- W3208990930 hasRelatedWork W2039318446 @default.
- W3208990930 hasRelatedWork W2080531066 @default.
- W3208990930 hasRelatedWork W2748952813 @default.
- W3208990930 hasRelatedWork W2789448498 @default.
- W3208990930 hasRelatedWork W2899084033 @default.
- W3208990930 hasRelatedWork W3031052312 @default.
- W3208990930 hasRelatedWork W3032375762 @default.
- W3208990930 hasRelatedWork W3108674512 @default.
- W3208990930 hasVolume "42" @default.
- W3208990930 isParatext "false" @default.
- W3208990930 isRetracted "false" @default.
- W3208990930 magId "3208990930" @default.
- W3208990930 workType "article" @default.