A rabbit model for capsular contracture

Development and clinical implications

William P. Adams, M. Scott Haydon, Joseph Raniere, Suzanne Trott, Marisa Marques, Michael Feliciano, Jack B. Robinson, Liping Tang, Spencer A. Brown

Research output: Contribution to journalArticle

61 Citations (Scopus)

Abstract

BACKGROUND: Capsular contracture remains one of the most common complications involving aesthetic and reconstructive breast surgery; however, its cause, prevention, and treatment remain to be fully elucidated. Presently, there is no accurate and reproducible pathologic in vitro or in vivo model examining capsular contracture. The purpose of this study was to establish an effective pathologic capsular contracture animal model that mimics the formation of capsular contracture response in humans. METHODS: New Zealand White rabbits (n = 32) were subdivided into experimental (n = 16) and control groups (n = 16). Each subgroup underwent placement of smooth saline mini implants (30 cc) beneath the panniculus carnosus in the dorsal region of the back. In addition, the experimental group underwent instillation of fibrin glue into the implant pocket as a capsular contracture-inducing agent. Rabbits were euthanized from 2 to 8 weeks after the procedure. Before the animals were euthanized, each implant was serially inflated with saline and a pressure-volume curve was developed using a Stryker device to assess the degree of contracture. Representative capsule samples were collected and histologically examined. Normal and contracted human capsular tissue samples were also collected from patients undergoing breast implant revision and replacement procedures. Tissue samples were assessed histologically. RESULTS: Pressure-volume curves demonstrated a statistically significantly increased intracapsular pressure in the experimental group compared with the control group. The experimental subgroup had thicker, less transparent capsules than the control group. Histologic evaluation of the rabbit capsule was similar to that of the human capsule for the control and experimental subgroups. CONCLUSIONS: The authors conclude that pathologic capsular contracture can be reliably induced in the rabbit. This animal model provides the framework for future investigations testing the effects of various systemic or local agents on reduction of capsular contracture.

Original languageEnglish (US)
Pages (from-to)1214-1219
Number of pages6
JournalPlastic and Reconstructive Surgery
Volume117
Issue number4
DOIs
StatePublished - Apr 1 2006

Fingerprint

Contracture
Rabbits
Capsules
Pressure
Control Groups
Reconstructive Surgical Procedures
Animal Models
Breast Implants
Fibrin Tissue Adhesive
Esthetics
Breast
Equipment and Supplies

ASJC Scopus subject areas

  • Surgery

Cite this

Adams, W. P., Haydon, M. S., Raniere, J., Trott, S., Marques, M., Feliciano, M., ... Brown, S. A. (2006). A rabbit model for capsular contracture: Development and clinical implications. Plastic and Reconstructive Surgery, 117(4), 1214-1219. https://doi.org/10.1097/01.prs.0000208306.79104.18

A rabbit model for capsular contracture : Development and clinical implications. / Adams, William P.; Haydon, M. Scott; Raniere, Joseph; Trott, Suzanne; Marques, Marisa; Feliciano, Michael; Robinson, Jack B.; Tang, Liping; Brown, Spencer A.

In: Plastic and Reconstructive Surgery, Vol. 117, No. 4, 01.04.2006, p. 1214-1219.

Research output: Contribution to journalArticle

Adams, WP, Haydon, MS, Raniere, J, Trott, S, Marques, M, Feliciano, M, Robinson, JB, Tang, L & Brown, SA 2006, 'A rabbit model for capsular contracture: Development and clinical implications', Plastic and Reconstructive Surgery, vol. 117, no. 4, pp. 1214-1219. https://doi.org/10.1097/01.prs.0000208306.79104.18
Adams, William P. ; Haydon, M. Scott ; Raniere, Joseph ; Trott, Suzanne ; Marques, Marisa ; Feliciano, Michael ; Robinson, Jack B. ; Tang, Liping ; Brown, Spencer A. / A rabbit model for capsular contracture : Development and clinical implications. In: Plastic and Reconstructive Surgery. 2006 ; Vol. 117, No. 4. pp. 1214-1219.
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