Implementation of CRP Point of Care Testing in Primary Care to Improve Antibiotic Targeting in Respiratory Illness (ICAT)
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 2,606
- 试验地点
- 1
- 主要终点
- Proportion of patients aged 1 to 65 years, consulting for ARI, who are prescribed antibiotics in the two study arms
研究概览
简要总结
The proposed study will monitor and evaluate a quality improvement project - the introduction of commercially available lateral flow CRP tests with international regulatory approval, as a routine care service to improve the management of patients with acute respiratory infection (ARI) and reduce unnecessary antibiotic prescribing. No research staff will be present, and to minimise disruption and alteration of routine care, a waiver of written patient informed consent will be requested from the relevant ethical review boards, in accordance with the 2016 WHO/CIOMS International Guidance for Health-related Research Involving Humans8. Instead, patients in intervention clusters will be provided with information concerning how the test can assist healthcare workers in identifying when antibiotics are required, after which they will be free to refuse its use.
The test selected for use in the study is the Actim® CRP test from Medix Biochemica (Finland; ISO certification ISO13485:2016). The test is a simple lateral flow device that uses capillary blood, obtained through a finger/heel puncture. The test provides a semi-quantitative indication of whether CRP concentrations are <10mg/L, between 10-40mg/L, between 40-80mg/L, or above 80mg/L, in under 5 minutes with minimal training requirements. The test has been approved by the European regulatory body (CE-marking) as well as in 13 other countries around the world (including Switzerland, Norway, Iceland, Israel and Thailand) and has been validated for accuracy in previous publications.9,10 Our own research group has also confirmed the tests' accuracy in both laboratory and field environments, including their thermos-stability in a tropical climate (see annex). Neither Medix Biochemica nor any of its distributors, have had involvement with the design of the evaluation and our group has no conflict of interest with respect to the choice of the test.
Main research question: Can point of care CRP tests introduced in routine primary healthcare reduce prescription of antibiotics for patients with acute respiratory infections, outside of the research context?
Brief description of the intervention: The implementation of CRP point of care tests will be conducted at commune health centres (CHCs), the primary access point for public health services in Vietnam (CHC details are described in the Location section below). Prior to introduction of the tests, an educational session will be provided for local healthcare workers in both intervention and control arms about the role of antibiotics and AMR. After randomization, further training will be provided for healthcare workers in the intervention CHCs as to the use of CRP testing to guide antibiotic prescribing decisions. In the intervention CHCs, healthcare workers will be trained on the use and interpretation of CRP testing in ARI (detailed in section 5.4). Educational materials will also be developed for patients and care-givers regarding the value of CRP testing.
Description of the population to be studied: This study will be conducted in the general population of Nam Dinh, a rural province in northern Vietnam. The test will be provided at CHCs and recommended for use in patients presenting with a chief complaint of ARI.
详细描述
STUDY PROCEDURES
- Screening and Recruitment - A list of potential CHCs will be compiled by province-level officials, and those meeting eligibility criteria will be invited to take part. CHCs will be randomly allocated to intervention or routine care arms using a computer-generated random allocation procedure.
If baseline variability in antibiotic prescribing practices is identified from reviewing retrospective routine records, high and low prescription centres will be stratified.
In the intervention CHCs, patients with ARIs will be provided leaflets with information about CRP testing, antibiotics and AMR. Healthcare workers will then decide whether to use a CRP test as part of routine care of patients with ARI. Patients' autonomy will be respected and as with any medical procedure this test can be declined. In the control CHCs patients will be provided with an information leaflet regarding the need for rational use of antibiotics in ARIs but with no mention of CRP testing. 2. Clinical assessment - All patients will have a medical history taken and will be examined as per normal practice. In the control arm, local guidelines and WHO IMCI recommendations will guide treatment. In the intervention arm, doctors can choose to use CRP test results in addition to existing guidelines. 3. General training and education - Healthcare worker training - Before the study sites (CHCs) are randomized, an overview of the study will be presented to all local healthcare workers and provide education about the role of antibiotics, antimicrobial resistance and identification of clinical signs of severity as well as good clinical practice (GCP) for research.
Patient education - Educational materials will be developed for patients and care-givers regarding antibiotic use and AMR. These will be available to patients presenting with ARIs in both arms, with additional information regarding the CRP tests added to the intervention group leaflets. 4. Intervention - CRP test - The ACTIM CRP Rapid Test (Medix, Biochemica) will be made available to the healthcare workers at the CHCs for use in patients in the target population.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 1 Year 至 64 Years(Child, Adult)
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Patients aged from 1 to under 65 years old
- •First consultation with an acute respiratory infection diagnosed by the healthcare worker with at least 1 focal sign or symptom*
- •Symptoms lasting less than 7 days * Focal signs and symptoms: (1) cough, (2) rhinitis (sneezing, nasal congestion, or runny nose), (3) pharyngitis (sore throat), (4) shortness of breath, (5) wheezing, (6) chest pain, or (7) auscultation abnormalities.
排除标准
- •Patients requiring referral to a higher level facility based on the healthcare worker's clinical assessment
- •immunosuppressed patients (known HIV, long term steroid use)
- •those with a suspicion of tuberculosis or a non-respiratory tract illness
结局指标
主要结局
Proportion of patients aged 1 to 65 years, consulting for ARI, who are prescribed antibiotics in the two study arms
时间窗: Through study completion, the proportion of 1 year
次要结局
- The proportion of patients that consulted with ARI in the preceding year.(Before the 1st recruitment)
- Prescription rates for ARI patients in the preceding year.(Before the 1st recruitment)
- Proportion of patients indicated CRP test according to diagnosis, age, gender(Through study completion, the data of 1 year)
- Proportion of patients receiving an antibiotic prescription by diagnosis, age, season, recorded fever, sex(Through study completion, the proportion of 1 year)
- Proportion of patients prescribed an antibiotic in the intervention arm with: a. CRP < 10 mg/L b. CRP from 10mg/L to 40mg/L c. CRP > 40mg/L(Through study completion, the proportion of 1 year)
- Proportion of patients receiving an antibiotic with the denominator being: a. All attendances b. All non-routine attendances(Through study completion, the proportion of 1 year)
- The proportion of patients referred to a higher level facility at the initial consultation by checking the e-database of health insurance (HI) reimbursement(Through study completion, the proportion of 1 year)
- Proportion of patients in whom the test is indicated who re-attend the health facility within a 30 days period, and whether antibiotics were prescribed comparing intervention CHCs and controls(Through study completion, the proportion of 1 year)
- Proportion of patients in whom the test is indicated hospitalised within a 30 day period (excluding patients referred at consultation)(30 days after the last recruitment)
- Qualitatively measure the usability and acceptability of CRP test among healthcare workers(After finishing the recruitment, organize the structured interviews, ask about 1 year of study implementation)
- Measure of cost-effectiveness(Through study completion, estimate the cost-effectiveness of the intervention for 1 year)
- the proportion of patients in whom use of the test was recommended that received the test.(Through study completion, the proportion of 1 year)
