注射用聚丙烯酰胺水凝胶取出术后乳房畸形的处理:200例7年回顾性研究

Management of Breast Deformity After Removal of Injectable Polyacrylamide Hydrogel: Retrospective Study of 200 Cases for 7 Years.

作者信息

Chen Baoguo, Song Huifeng

机构信息

The first hospital affiliated to the People's Literative Army Hospital, 51#, Fucheng Road, Haidian District, 100048, Beijing, China.

出版信息

Aesthetic Plast Surg. 2016 Aug;40(4):482-91. doi: 10.1007/s00266-016-0646-5. Epub 2016 Jun 1.

Abstract

BACKGROUND

Polyacrylamide hydrogel (PAAG), once used as an injection for breast augmentation, has been banned in the medical field for cosmetic purposes for more than 10 years in China. But a large number of breasts have characteristic deformities due to the gel's feature of erosion. Our aim is to explore a retrospective study on PAAG's long-term effects on women, ensuing breast deformity and the strategy for breast plasticity after removing the gel in our center from 2007 to 2014.

METHODS

From 2007 to 2014, 200 patients, whose breasts were injected with PAAG, underwent the operation to remove the injectable material. Complications were summarized. Ultrasound or MRI was performed before the operation to disclose the general distribution of the gel and the muscle and gland infiltration. According to the gel distribution, muscle and gland infiltration, infection, gel residue, and other factors, the patients were treated, respectively, with or without prosthesis implantation surgery after the removal of the gel. According to the decision about whether or when to undergo prosthesis implantation, the patients were classified into three types: group I-prosthesis implantation at the first stage, group II-prosthesis implantation at the second stage, and group III-only removing the material without prosthesis implantation. The scores of the BREAST-Q program were used to evaluate the preoperative and postoperative differences.

RESULTS

Seventy-seven patients underwent prosthesis implantation at the first stage and 61 patients were operated on by placing the prosthesis at the second stage. A total of 62 patients only underwent the PAAG removal operation. By BREAST-Q evaluation, changes are summarized in Tables 1, 2, and 3 between mean preoperative scores and mean postoperative scores through categories of satisfaction with appearance of breasts, psychosocial wellbeing, sexual wellbeing, and physical wellbeing, in which all categories were presented with statistical significance (p < 0.001). Table 1 Patient demographics General patient data Number Number of patients 200 Age range 25-48 Follow-up period 6-12 months Injection material  Domestic material 84 (42 %)  Imported material 93 (46.5 %)  Domestic + imported 23 (11.5 %) Injection site  Regular hospital 47 (23.5 %)  Clinics 153 (76.5 %) Complication  Inflammation 10 (2 %)  Pain 75 (37.5 %)  Induration 155 (77.5 %)  Shift 50 (25 %)  Deformation 17 (8.5 %)  Bilateral asymmetry 48 (24 %)  Deposition milk 2 (1 %)  Psychological fear 150 (75 %)  Systemic symptoms 34 (17 %)  Single complication 25 (16.97 %)  Two or more complications 160 (80 %)  Preoperative aspiration 48 (24 %) Table 2 Group I-changes in mean preoperative scores and mean postoperative scores Category Preoperatively (n = 77) Postoperatively (n = 77) p Satisfaction with appearance of breasts 18.8 ± 16.2 81.6 ± 13.1 <0.001 Psychosocial wellbeing 39.5 ± 20.2 84.5 ± 19.3 <0.001 Sexual wellbeing 38.7 ± 23.1 77.2 ± 20.5 <0.001 Physical wellbeing 42.4 ± 16.3 81.7 ± 10.5 <0.001 Table 3 Group II-changes in mean preoperative scores and mean postoperative scores Category Preoperatively (n = 61) Postoperatively (n = 61) p Satisfaction with appearance of breasts 19.6 ± 15.3 82.5 ± 11.1 <0.001 Psychosocial wellbeing 38.9 ± 19.3 83.6 ± 20.1 <0.001 Sexual wellbeing 37.6 ± 22.4 79.3 ± 20.4 <0.001 Physical wellbeing 41.3 ± 15.1 82.2 ± 9.9 <0.001 CONCLUSIONS: Timely removal is critical for women who have received the PAAG removal operation. However, the surgery may destroy the shape of the breast. It is recommended that preoperative communication and local tissue condition are guidelines for surgeons to choose conservative or aggressive surgery. A balance must be maintained between removing the gel as much as possible and retaining soft tissue to reshape breasts.

LEVEL OF EVIDENCE IV

This journal requires that authors assign a level of evidence to each article. For a full description of these Evidence-Based Medicine ratings, please refer to the Table of Contents or the online Instructions to Authors www.springer.com/00266 .

摘要

背景

聚丙烯酰胺水凝胶(PAAG)曾作为隆胸注射材料使用,在中国已被禁止用于医疗美容领域10多年。但由于该凝胶具有侵蚀性,大量隆胸者出现了乳房畸形。我们的目的是对2007年至2014年期间在本中心接受PAAG隆胸的女性进行回顾性研究,探讨PAAG对女性的长期影响、随之而来的乳房畸形以及取出凝胶后的乳房塑形策略。

方法

2007年至2014年,200例曾注射PAAG隆胸的患者接受了注射材料取出手术。总结并发症情况。术前进行超声或磁共振成像(MRI)检查,以了解凝胶的总体分布以及肌肉和腺体浸润情况。根据凝胶分布、肌肉和腺体浸润、感染、凝胶残留等因素,在取出凝胶后,对患者分别进行或不进行假体植入手术。根据是否进行或何时进行假体植入的决定,将患者分为三类:I组——一期假体植入;II组——二期假体植入;III组——仅取出材料不进行假体植入。采用BREAST-Q评分系统评估术前和术后差异。

结果

77例患者一期进行了假体植入,6例患者二期进行了假体植入手术。共有62例患者仅接受了PAAG取出手术。通过BREAST-Q评估,术前平均得分与术后平均得分在乳房外观满意度、心理幸福感、性健康和身体健康等方面的变化总结于表1、表2和表3中,所有类别均具有统计学意义(p<0.001)。表1患者人口统计学资料一般患者数据患者数量200年龄范围25 - 48岁随访时间6 - 12个月注射材料国产材料84(42%)进口材料93(46.5%)国产+进口23(11.5%)注射部位正规医院47(23.5%)诊所153(76.5%)并发症炎症10(2%)疼痛75(37.5%)硬结硬155(77.5%)移位50(25%)变形17(8.5%)双侧不对称48(24%)积乳2(1%)心理恐惧150(75%)全身症状34(17%)单一并发症25(16.97%)两种或更多并发症160(80%)术前抽吸48(24%)表2 I组术前平均得分与术后平均得分变化类别术前(n = 77)术后(n = 77)p乳房外观满意度18.8±16.2 81.6±13.1<0.001心理幸福感39.5±20.2 84.5±19.3<0.001性健康38.7±23.1 77.2±20.5<0.001身体健康42.4±16.3 81.7±10.5<0.001表3 II组术前平均得分与术后平均得分变化类别术前(n = 61)术后(n = 61)p乳房外观满意度19.6±15.3 82.5±11.1<0.001心理幸福感38.9±19.3 83.6±20.1<0.001性健康37.6±22.4 79.3±20.4<0.001身体健康41.3±15.1 82.2±9.9<0.001结论:对于接受PAAG取出手术的女性,及时取出至关重要。然而,手术可能会破坏乳房形状。建议术前沟通和局部组织状况是外科医生选择保守或积极手术的指导原则。必须在尽可能多地取出凝胶与保留软组织以重塑乳房之间保持平衡。

证据水平IV:本刊要求作者为每篇文章指定证据水平。有关这些循证医学评级的完整描述,请参阅目录或在线作者指南www.springer.com/00266

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