Perianal Abscess Recurrence and Fistula Formation: Antibiotics Following Incision and Drainage Trial - (PARFAIT) A Vanguard Randomized Controlled Trial
试验速览
- 阶段
- 3 期
- 状态
- 已完成
- 入组人数
- 15
- 试验地点
- 6
- 主要终点
- Total number of participants accrued across all sites, per month
研究概览
简要总结
Most perianal abscesses (PA) result from an infection originating in anal crypts that extend into anal glands in the intersphincteric plane. Patients commonly present to the ER and usually require surgical intervention, which poses a burden on the healthcare system. If left undrained, a PA can expand into the adjacent tissues as well as progress to systemic infection. One of the major complications of PA are perianal fistulae; the creation of a tract between the anal canal and the perianal skin that is lined with granulation tissue or skin cells. Up to 1/3 of patients with a PA will develop a fistula; which occurs if a PA drains spontaneously through the perianal skin, and the infection becomes chronic. If this happens, surgical intervention is needed and abscesses may reoccur. Post incision and drainage (I&D) antibiotics in PA have been used to address complications but their use is still controversial and there are no specific recommendations on their use to prevent the formations of fistulae.
Recent findings from a systematic review (6 studies, N=817 patients) published in 2019 demonstrated that antibiotic use following I&D of PA was associated with a 36% lower odds of fistula formation, though the quality of the evidence was low.
As there are no established prophylactic treatments for fistulae, and because they are difficult to treat, further study of this simple intervention seems warranted. In this trial, adults with a PA requiring I&D will be randomly assigned to receive standard of care with antibiotics or standard of care without antibiotics after I&D. This trial will be conducted under the IMPACTS (Innovative, Multicentre, Patient-centred Approach to Clinical Trials in Surgery) program umbrella and will follow IMPACTS methodology. For the Vanguard trial, the aim is to determine the feasibility of conducting a definitive trial. Future outcomes of interest are incidence of fistula formation (defined as drainage of the perianal region at or after 2 months), need for re-intervention (i.e., any intervention on the perianal region), quality of life, healthcare utilization, healing time and mortality.
详细描述
The development of perianal abscesses is relatively common with an estimated incidence in the UK of 40 per 100,000 habitants (Canadian incidence unknown). It is uncertain if there is any benefit to using prophylactic antibiotics after incision and drainage of a perianal abscess in order to reduce the formation of fistulae, the need for re-intervention, health system costs, and healing time. Further research from high-quality RCTs is needed to establish a benefit, if any, for this practice.
Objectives: Before embarking on a definitive RCT, this pilot trial has five specific feasibility objectives:
- To assess our ability to accrue patients using the IMPACTS Program design platform at multiple institutions, over the course of one year.
- To assess our ability to adaptively randomize patients and deliver the randomized assignment using the IMPACTS Program design platform, over the course of one year.
- To assess our ability to collect complete data directly from participants (patients and clinicians) on: re-intervention, fistula formation, quality of life, and healing time over the course of one year.
- To examine our ability to carry out data linkages using the IMPACTS Program design platform over the course of one year.
- To estimate the incidence of fistula formation to inform the sample size calculation for the definitive trial.
Study design: This is a multicentre, pragmatic, open label, three-arm parallel-group Vanguard feasibility randomized controlled trial. Adult patients with perianal abscesses requiring incision and drainage will be randomized to receive standard of care with antibiotics or standard of care without antibiotics after incision and drainage. If feasibility is demonstrated during the pilot trial, we will plan to conduct a definitive trial. If there are only minimal changes to the protocol, we will include data from the pilot phase into the definitive trial analysis (i.e. a Vanguard design).
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Prevention
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Patients aged ≥18 years
- •Perianal abscess requiring incision and drainage
排除标准
- •Allergies or contraindications to amoxicillin + clavulanic acid, penicillin, ciprofloxacin, or metronidazole
- •Definite need to be on antibiotics at the treating clinicians' discretion
- •Immunosuppression such as: human immunodeficiency virus (HIV), chronic steroids treatment, current chemotherapy
- •Abscess associated with Inflammatory Bowel Disease (IBD)
- •Supralevator perianal abscess
- •Recurrent perianal abscesses within 5 years
- •Known rectal cancer diagnosis within 5 years
- •History of pelvic radiotherapy within 5 years
研究组 & 干预措施
Antibiotic 1 arm (amoxicillin + clavulanic acid)
Patients will undergo I&D of PA by the clinician as per standard of care. This may occur in the emergency department or operating room. Patients may or may not receive packing based on the clinician's standard practice and institutional routines.
Patients randomized to the antibiotic 1 arm will receive a prescription for amoxicillin + clavulanic acid (875 mg amoxicillin and 125 mg clavulanic acid BID) PO for 7 days. Otherwise, all participants will be treated identically according to the institution's standard practices.
干预措施: Antibiotic 1 arm (amoxicillin + clavulanic acid) (Drug)
Antibiotic 2 arm (ciprofloxacin + metronidazole)
Patients will undergo I&D of PA by the clinician as per standard of care. This may occur in the emergency department or operating room. Patients may or may not receive packing based on the clinician's standard practice and institutional routines.
Patients randomized to the antibiotic 2 arm will receive a prescription for ciprofloxacin + metronidazole (ciprofloxacin 500 mg and metronidazole 500 mg BID) PO for 7 days. Otherwise, all participants will be treated identically according to the institution's standard practices.
干预措施: Antibiotic 2 arm (ciprofloxacin + metronidazole) (Drug)
结局指标
主要结局
Total number of participants accrued across all sites, per month
时间窗: 1 year
Feasible if 3 or more patients accrued per month between all sites
Proportion of complete data collection for patient-reported outcome surveys, across all sites
时间窗: 1 year
Feasible if \>80% of data is collected
Estimation of fistula formation in three groups
时间窗: 1 year
Rate of fistula formation in the three groups
Proportion of participants who received the allocated intervention, across all sites
时间窗: 1 year
Feasible if \>90% of patients receive correct intervention
Proportion of successful data linkage of patient-reported outcome data with Institute of Clinical Evaluative Sciences dataset(s)
时间窗: 1 year
Feasible if linkage is possible in \>90% of patients
次要结局
未报告次要终点
研究者
Dr. Paul Karanicolas
Scientist and Associate Professor
Sunnybrook Health Sciences Centre