{"id":15411,"date":"2023-10-19T17:06:46","date_gmt":"2023-10-19T15:06:46","guid":{"rendered":"https:\/\/francelyme.fr\/site\/?p=15411"},"modified":"2023-10-19T23:01:42","modified_gmt":"2023-10-19T21:01:42","slug":"en-belgique-luniversite-de-gand-chiffre-le-cout-de-la-maladie-de-lyme-persistante-a-plus-de-40-000-e-par-an-et-par-malade","status":"publish","type":"post","link":"https:\/\/francelyme.fr\/site\/en-belgique-luniversite-de-gand-chiffre-le-cout-de-la-maladie-de-lyme-persistante-a-plus-de-40-000-e-par-an-et-par-malade\/","title":{"rendered":"En Belgique, l\u2019universit\u00e9 de Gand chiffre le co\u00fbt de la maladie de Lyme persistante \u00e0 plus de 40 000 \u20ac par an et par malade"},"content":{"rendered":"
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L\u2019Universit\u00e9 de Gand, en Belgique, a chiffr\u00e9 le co\u00fbt de la maladie de Lyme pour les patients atteints de la forme persistante, dans un article publi\u00e9 il y a quelques mois.<\/p>\n\n\n\n

Une partie des patients atteints de borr\u00e9liose de Lyme (LB) pr\u00e9sentent des sympt\u00f4mes persistants \u00e0 long terme, m\u00eame apr\u00e8s le traitement antibiotique recommand\u00e9. Les auteurs utilisent l\u2019acronyme anglais PTLDS pour d\u00e9signer ce syndrome de la maladie de Lyme post-traitement, que l\u2019on appelle \u00e9galement forme persistante de Lyme, ou Lyme long.<\/p>\n\n\n\n

Les auteurs soulignent qu\u2019il n’existe actuellement pas de consensus sur les orientations en mati\u00e8re de diagnostic et de traitement. Par cons\u00e9quent, les patients souffrent et restent \u00e0 la recherche de r\u00e9ponses, ce qui a un impact n\u00e9gatif sur leur qualit\u00e9 de vie et sur les d\u00e9penses de sant\u00e9. Pourtant, les donn\u00e9es \u00e9conomiques sur la PTLDS restent rares.<\/p>\n\n\n\n

Des patients atteints de PTLDS (187 au total) avec un diagnostic confirm\u00e9 de LB ont \u00e9t\u00e9 recrut\u00e9s par une organisation de patients. Les patients ont rempli un questionnaire autod\u00e9clar\u00e9 sur l’utilisation des soins de sant\u00e9 li\u00e9s \u00e0 la maladie, l’absence de travail et le ch\u00f4mage. Les co\u00fbts unitaires (ann\u00e9e de r\u00e9f\u00e9rence 2018) ont \u00e9t\u00e9 obtenus \u00e0 partir de bases de donn\u00e9es nationales et de la litt\u00e9rature publi\u00e9e. Les co\u00fbts moyens et les intervalles d’incertitude ont \u00e9t\u00e9 calcul\u00e9s, et les donn\u00e9es ont \u00e9t\u00e9 extrapol\u00e9es \u00e0 la population belge.<\/p>\n\n\n\n

Les r\u00e9sultats sont tr\u00e8s int\u00e9ressants :<\/p>\n\n\n\n

– les co\u00fbts directs s’\u00e9l\u00e8vent en moyenne \u00e0 4 618 \u20ac par an et par patient, dont la moiti\u00e9 sont des d\u00e9penses \u00e0 la charge du patient (ce qui fait plus de 2 300 \u20ac par an et par patient),
– et les co\u00fbts indirects s’\u00e9l\u00e8vent en moyenne \u00e0 36 081 \u20ac par an et par patient !<\/p>\n\n\n\n

Ce qui donne ce total proprement hallucinant pour la soci\u00e9t\u00e9 belge et les patients : 40 699 \u20ac par an et par patient !!<\/p>\n\n\n\n

En France, nous estimons qu\u2019il y a au minimum de 300 000 malades porteurs de Lyme long.<\/p>\n\n\n\n

Les co\u00fbts de cette maladie en France seraient ainsi, selon ce chiffrage, sup\u00e9rieurs \u00e0 12 milliards d\u2019euros par an total. C\u2019est un chiffre tout \u00e0 fait plausible.<\/p>\n\n\n\n

Et c\u2019est un co\u00fbt consid\u00e9rable pour la soci\u00e9t\u00e9 fran\u00e7aise ! Peu de maladies co\u00fbtent aussi cher \u00e0 la collectivit\u00e9 dans notre pays, il est grand temps que les \u00e9conomistes s\u2019y int\u00e9ressent, et que les autorit\u00e9s sanitaires et sociales s\u2019en occupent s\u00e9rieusement.<\/p>\n\n\n\n

Pour en savoir plus : https:\/\/biblio.ugent.be\/publication\/01GWP4X9G0P1DZ06MA6XZVF9RR<\/a><\/p>\n

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