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TGF-ß1 and CD68 immunoexpression in capsules formed by textured implants with and without mesh coverage: a study on female rats
Berger, Ralf; Ribas Filho, Jurandir Marcondes; Souza, Marcelo Augusto de; Paula, Pedro Henrique de; Doubek, João Gabriel Cavazzani; Pires, Rafael de Castro e Souza; Nassif, Paulo Afonso Nunes; Silva, Eduardo Nascimento.
  • Berger, Ralf; Faculdade Evangélica Mackenzie. Postgraduate Program in Principles of Surgery. Curitiba. BR
  • Ribas Filho, Jurandir Marcondes; Faculdade Evangélica Mackenzie. Postgraduate Program in Principles of Surgery. Curitiba. BR
  • Souza, Marcelo Augusto de; Universidade Estadual de Ponta Grossa. Ponta Grossa. BR
  • Paula, Pedro Henrique de; Universidade Estadual de Ponta Grossa. Ponta Grossa. BR
  • Doubek, João Gabriel Cavazzani; Faculdade Evangélica Mackenzie. Curitiba. BR
  • Pires, Rafael de Castro e Souza; Universidade Estadual de Ponta Grossa. Regional University Hospital of Campos Gerais. Curitiba. BR
  • Nassif, Paulo Afonso Nunes; Faculdade Evangélica Mackenzie. Curitiba. BR
  • Silva, Eduardo Nascimento; Universidade Estadual de Ponta Grossa. Ponta Grossa. BR
Acta cir. bras ; 37(2): e370201, 2022. tab, graf, ilus
Article in English | LILACS, VETINDEX | ID: biblio-1374072
ABSTRACT

Purpose:

To evaluate fibrosis formation and number of macrophages in capsules formed around textured implants without and with mesh coverage.

Methods:

Fibrosis was analyzed through transforming growth factor-beta 1 (TGF-ß1) immunomarker expression and the number of macrophages through CD68 percentage of cells in magnified field. Sixty female Wistar rats were distributed into two groups of 30 rats (unmeshed and meshed). Each group was then subdivided into two subgroups for postoperative evaluation after 30 and 90 days. The p value was adjusted by Bonferroni lower than 0.012.

Results:

No difference was observed in fibrosis between meshed and unmeshed groups (30 days p = 0.436; 90 days p = 0.079) and from 30 to 90 days in the unmeshed group (p = 0.426). The meshed group showed higher fibrosis on the 90th day (p = 0.001). The number of macrophages was similar between groups without and with mesh coverage (30 days p = 0.218; 90 days p = 0.044), and similar between subgroups 30 and 90 days (unmeshed p = 0.085; meshed p = 0.059).

Conclusions:

In the meshed group, fibrosis formation was higher at 90 days and the mesh-covered implants produced capsules similar to microtextured ones when analyzing macrophages. Due to these characteristics, mesh coating did not seem to significantly affect the local fibrosis formation.

Subject(s)


Full text: Available Index: LILACS (Americas) Main subject: Surgical Mesh / Fibrosis / Antigens, CD / Breast Implants / Breast Implantation / Transforming Growth Factor beta1 Limits: Animals Language: English Journal: Acta cir. bras Year: 2022 Type: Article Institution/Affiliation country: Faculdade Evangélica Mackenzie/BR / Universidade Estadual de Ponta Grossa/BR

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Full text: Available Index: LILACS (Americas) Main subject: Surgical Mesh / Fibrosis / Antigens, CD / Breast Implants / Breast Implantation / Transforming Growth Factor beta1 Limits: Animals Language: English Journal: Acta cir. bras Year: 2022 Type: Article Institution/Affiliation country: Faculdade Evangélica Mackenzie/BR / Universidade Estadual de Ponta Grossa/BR