Beck D E
Department of Colorectal Surgery, Ochsner Clinic, New Orleans, LA, USA.
Eur J Surg Suppl. 1997(577):49-55.
To evaluate, the safety and efficacy of Seprafilm, a novel bioresorbable membrane of chemically modified hyaluronic acid and carboxymethylcellulose, in preventing and reducing postoperative adhesion formation.
Randomized, controlled, blinded, prospective multicenter study.
Major academic surgical centers.
183 (treatment, n = 91; control, n = 92) patients with ulcerative colitis or familial polyposis.
Restorative proctocolectomy and ileal J-pouch anastomosis with diverting ileostomy followed by second-stage laparoscopy for ileostomy closure and direct visual assessment of the peritoneal cavity. Before abdominal closure in treated patients, Seprafilm, averaging 406.9 cm2 per patient, was applied without suturing between the midline incision and underlying tissues and organs.
Determination of the incidence, extent (mean percentage of midline incision associated with adhesions), severity (grade 1, least severe; grade 2, moderately severe; grade 3, very severe), and distribution of adhesions.
In 175 (treatment, n = 90) evaluable patients, Seprafilm significantly reduced the incidence (49% and 94%, respectively, p < 0.0001), extent (23% and 63%, respectively, p < 0.0001), and severity (15% versus 58% grade 3 severity, respectively, p < 0.0001) of postoperative adhesions. Seprafilm decreased the rate of adhesion formation by nearly 50%. More than half (51%) of Seprafilm recipients were adhesion-free, versus only 6% of untreated patients. Thus treated patients were eight times more likely to be free of adhesions than untreated controls. The incidence of incisional adhesions associated with the omentum, small bowel, left sidewall, bladder, ileostomy, and stomach was significantly reduced in the Seprafilm patients. Effects on vital signs and laboratory parameters were comparable in the two groups and were attributable to the operative procedure, concomitant therapy, or comorbid disease. All reported adverse events were associated with the surgical procedure and/or comorbid disease and did not differ significantly between the two groups (p > 0.05).
Seprafilm is safe and significantly reduces the incidence, extent, and severity of postoperative adhesions to the midline incision compared with no treatment, the current standard of surgical care.
评估一种新型的化学修饰透明质酸和羧甲基纤维素生物可吸收膜Seprafilm在预防和减少术后粘连形成方面的安全性和有效性。
随机、对照、双盲、前瞻性多中心研究。
主要学术外科中心。
183例(治疗组,n = 91;对照组,n = 92)溃疡性结肠炎或家族性息肉病患者。
行保留直肠结肠切除术和回肠J形袋吻合术并做转流性回肠造口术,随后二期行腹腔镜回肠造口关闭术并直接观察腹膜腔。在接受治疗的患者腹部关闭前,应用Seprafilm,平均每位患者使用面积为406.9平方厘米,不缝合,置于中线切口与下方组织和器官之间。
确定粘连的发生率、范围(与粘连相关的中线切口平均百分比)、严重程度(1级为最轻微;2级为中度严重;3级为非常严重)以及粘连的分布情况。
在175例(治疗组,n = 90)可评估患者中,Seprafilm显著降低了术后粘连的发生率(分别为49%和94%,p < 0.0001)、范围(分别为23%和63%,p < 0.0001)以及严重程度(3级严重程度分别为15%和58%,p < 0.0001)。Seprafilm使粘连形成率降低了近50%。超过一半(51%)接受Seprafilm治疗的患者无粘连,而未治疗患者中这一比例仅为6%。因此,接受治疗的患者无粘连的可能性是未治疗对照组的8倍。Seprafilm组患者与大网膜、小肠、左侧腹壁、膀胱、回肠造口和胃相关的切口粘连发生率显著降低。两组对生命体征和实验室参数的影响相当,且归因于手术操作、伴随治疗或合并疾病。所有报告的不良事件均与手术操作和/或合并疾病相关,两组之间无显著差异(p > 0.05)。
与目前手术治疗的标准即不进行治疗相比,Seprafilm安全且能显著降低中线切口术后粘连的发生率、范围和严重程度。