IPBronch Review
🩺 Clinical Context
In the era of “Choosing Wisely” and value-based care, the routine practice of ordering pre-procedural pathology or laboratory testing (e.g., coagulation panels, CBCs) for patients undergoing bronchoscopy is increasingly scrutinized. This study addresses the clinical utility, economic burden, and environmental impact of these “routine” orders. For the interventional pulmonologist, the core question is whether these tests—often performed reflexively—actually alter management or patient safety outcomes, or if they represent low-value care that contributes to hospital waste and unnecessary patient anxiety.
📊 Methodological Strengths & Weaknesses
- Strengths:
- Multidimensional Analysis: The study uniquely bridges clinical utility with administrative and environmental metrics (cost and carbon footprint), providing a holistic view of hospital waste.
- Real-world Application: By evaluating “routine” orders, the study captures the gap between evidence-based guidelines and actual clinical practice patterns.
- Weaknesses:
- Retrospective Design: The study is inherently limited by its observational nature, which may not fully account for the “defensive medicine” rationale behind ordering these tests in complex, comorbid populations.
- Generalizability: The economic and environmental impact calculations are highly dependent on the specific hospital system’s cost structures and supply chain, which may not be universally applicable.
- Selection Bias: The study may not adequately capture the subset of patients with occult coagulopathy or hematologic disorders where these tests did provide actionable data, potentially underestimating the utility in high-risk cohorts.
💡 Takeaway for Fellows
- Challenge the “Routine” Order: As an IP fellow, you are the gatekeeper of the procedural suite. Stop reflexively ordering coagulation panels or CBCs for every bronchoscopy. Use the American College of Chest Physicians (ACCP) guidelines: testing should be driven by clinical history (e.g., known liver disease, anticoagulation use, or bleeding diathesis) rather than institutional habit.
- The “Hidden” Cost: Recognize that every order has a downstream cost—not just in dollars, but in environmental impact (reagents, plastic waste, energy consumption). Reducing low-value testing is a tangible way to improve your hospital’s sustainability.
- Clinical Judgment Over Protocol: If a patient has a normal history and physical, the pre-test probability of a clinically significant abnormality that would change your procedural plan is negligible. Reserve testing for patients where the result will fundamentally change your management (e.g., holding anticoagulation or delaying the procedure).
- Advocacy: Use these findings to update your institution’s electronic health record (EHR) order sets. Removing “routine” pre-procedural panels from default order sets is the most effective way to reduce low-value care.
Original Abstract
Background:
Routine preprocedural pathology testing is no longer recommended for minor and intermediate-risk elective procedures. British Thoracic Society guidelines advise hemoglobin, platelet count, and coagulation studies only in patients with risk factors for bleeding. Despite this, such tests are commonly ordered without a clear clinical indication before bronchoscopic procedures, incurring unnecessary financial and environmental costs.
Methods:
We conducted a retrospective review of outpatient bronchoscopic procedures over a 12-month period at an Australian tertiary hospital. Preprocedural pathology testing was defined as any test ordered at bronchoscopy referral or repeated within 6 weeks before the procedure. We evaluated the impact on clinical management and complication rate. Financial cost was estimated using Australian Medical Benefits Schedule (MBS) prices, and environmental impact via carbon dioxide equivalent (CO2e) emissions.
Results:
A total of 436 bronchoscopic procedures were performed, with all with preprocedural pathology testing. Abnormal results occurred in 8.3% of cases, but only 4.0% led to clinical intervention—all in patients with established risk factors. No interventions were required for patients without risk factors, and no procedures were delayed or cancelled. There was no correlation between abnormal blood test results and adverse outcomes. Routine testing cost AUD 30,441.20 (19,548.12 USD) and produced an estimated carbon footprint of 103.2 kg CO2e.
Conclusion:
Routine pathology testing before bronchoscopic procedures offers limited value, with most results not influencing management. Clinically significant abnormalities occurred only in patients with established risk factors, supporting a targeted approach. Given the significant financial and environmental costs, transitioning to selective, evidence-based testing is essential to optimize resource use and improve sustainability.