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The Impact of Device Innovation on Clinical Outcomes in Expander-based Breast Reconstruction.
Momeni, Arash; Li, Alexander Y; Tsai, Jacqueline; Wan, Derrick; Karin, Mardi R; Wapnir, Irene L.
Affiliation
  • Momeni A; Division of Plastic and Reconstructive Surgery, Stanford University School of Medicine, Stanford, Calif.
  • Li AY; Division of Plastic and Reconstructive Surgery, Hagey Laboratory for Pediatric Regenerative Medicine, Stanford University School of Medicine, Stanford, Calif.
  • Tsai J; Division of Plastic and Reconstructive Surgery, Stanford University School of Medicine, Stanford, Calif.
  • Wan D; Division of General Surgery, Stanford University School of Medicine, Palo Alto, Calif.
  • Karin MR; Division of Plastic and Reconstructive Surgery, Stanford University School of Medicine, Stanford, Calif.
  • Wapnir IL; Division of Plastic and Reconstructive Surgery, Hagey Laboratory for Pediatric Regenerative Medicine, Stanford University School of Medicine, Stanford, Calif.
Plast Reconstr Surg Glob Open ; 7(12): e2524, 2019 Dec.
Article in En | MEDLINE | ID: mdl-32537287
ABSTRACT
Staged expander-based breast reconstruction represents the most common reconstructive modality in the United States. The introduction of a novel tissue expander with an integrated drain (Sientra AlloX2) holds promise to further improve clinical outcomes.

METHODS:

Patients who underwent immediate expander-based pre-pectoral breast reconstruction were identified. Two cohorts were created, that is, patients who underwent placement of a conventional tissue expander [133MX (Allergan)] (Group 1) versus AlloX2 (Sientra) (Group 2). The study endpoint was successful completion of expansion with the objective being to investigate differences in outcome following expander placement.

RESULTS:

Fifty-eight patients underwent 99 breast reconstructions [Group 1 N = 24 (40 breasts) versus Group 2 N = 34 (59 breast)]. No differences were noted for age (P = 0.586), BMI (P = 0.109), history of radiation (P = 0.377), adjuvant radiotherapy (P = 1.00), and overall complication rate (P = 0.141). A significantly longer time to drain removal was noted in Group 1 (P < 0.001). All patients with postoperative infection in Group 1 required surgical treatment versus successful washout of the peri-prosthetic space via the AlloX2 drain port in 3 of 5 patients in Group 2 (P = 0.196). Furthermore, both cases of seroma in Group 1 required image-guided drainage versus in-office drainage via the AlloX2 drain port in 1 patient in Group 2 (P =0.333).

CONCLUSION:

The unique feature of the AlloX2 provides surgeons easy access to the peri-prosthetic space without altering any of the other characteristics of a tissue expander. This resulted in a reduced time to drain removal and facilitated management of postoperative seroma and infection.

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Prognostic_studies Language: En Journal: Plast Reconstr Surg Glob Open Year: 2019 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Prognostic_studies Language: En Journal: Plast Reconstr Surg Glob Open Year: 2019 Document type: Article