Standardised Drug Provocation Testing in Perioperative Hypersensitivity
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 50
- 试验地点
- 2
- 主要终点
- Hypersensitivity during DPT
研究概览
简要总结
The goal of this clinical trial is to evaluate the safety and outcome of systematic drug provocation testing with anaesthetics at therapeutic doses in adult patients undergoing diagnostic work-up for perioperative hypersensitivity.
详细描述
Perioperative hypersensitivity reactions (POH) pose a risk for major morbidity and mortality in the perioperative period. After resolution of the initial reaction it is crucial to determine the culprit drug to allow safe anaesthetics for future procedures.However this is not easy, as many drugs are administered near simultaneously and both anaesthesia and surgery may provoke or mask many of the symptoms of a hypersensitivity reaction. Conventional testing seems to offer good predictive value based on the low incidence of POH in subsequent re-exposures after negative work-up. Despite negative work-up anaesthetists often chose not to re-administer an neuromuscular blocking agent (NMBA) used in the index reaction, especially if no other culprit was found. This introduces an important bias as this group (no culprit found, NMBA not re-exposed) might be at the highest risk of containing false negatives as NMBA are the most frequent cause of POH in our region.The same remark can be made regarding earlier attempts by our group and others at establishing the negative predictive value (NPV) of conventional testing through retrospective analysis of subsequent re-exposures.To truly establish the NPV for conventional testing and thus the need for DPT, a prospective approach is needed where all patients are challenged with index drugs after negative conventional testing.
Adult patients that are referred for diagnostic work-up for POH will be included if they have a clinical history fitting with POH.
All patients will first receive a full diagnostic work-up for all index products consisting of in vivo (skin tests) and in vitro (specific IgE and -for drugs in which it is available- basophil activation tests). Clinical reactions (both index reactions and any reactions during DPT) will be classified according to the National Audit Program (NAP-6) classification which separates non-fatal POH in 4 grades:
- NAP 1 (only cutaneous/mucosal signs)
- NAP 2 (circulatory or respiratory symptoms which don't require treatment)
- NAP 3 (circulatory or respiratory symptoms which require treatment or potential airway compromise)
- NAP 4 (fulfilling indications for cardiopulmonary resuscitation)
Skin tests will be performed at the allergology day clinic following the protocols of the French Society for Anaesthesia and Intensive Care and the French Society of Allergology. Based on these results we make a distinction between patients with an identified culprit and those without an identified culprit.
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Diagnostic
- 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
- 是
入选标准
- •patients consulting the allergology department of the Antwerp University hospital medical with a history consistent with perioperative hypersensitivity
- •Indication for diagnostic work-up as determined at an interdisciplinary meeting between allergologists and anaesthetists
- •willing to sign separate informed consent forms for both general anaesthesia and the Drug Provocation Test.
排除标准
- •patient refusal
- •incomplete diagnostic work-up
- •history inconsistent with perioperative hypersensitivity
结局指标
主要结局
Hypersensitivity during DPT
时间窗: 1 hour
Prevalence of hypersensitivity during direct provocation for drugs that tested negatively in conventional tests.
次要结局
- Severe reactions during DPT(1 hour)
- Adverse events during DPT(1 hour)
- Sensitivity of conventional tests(1 hour)
