ACG, ASGE release first quality indicators for capsule endoscopy, deep enteroscopy

September 27, 2022

2 min read

The authors report no relevant financial disclosures.

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The ACG and ASGE have released a joint guideline on comprehensive quality indicators for capsule endoscopy and deep enteroscopy in the diagnosis and management of small-bowel disease.

“Small-bowel capsule endoscopy (CE) and deep enteroscopy (DE) are both relatively new procedures that enable evaluation of the entire small bowel,” Jonathan A. Leighton, MD, FACG, a gastroenterologist at Mayo Clinic in Scottsdale, Arizona, and colleagues wrote in The American Journal of Gastroenterology and Gastrointestinal Endoscopy. “CE has revolutionized small-bowel assessment, particularly for suspected small-bowel bleeding. Currently, CE is a purely diagnostic test. DE is more invasive and complements CE with important therapeutic capabilities.”

Key takeaways from the joint ACG, ASGE guideline on quality indicators for capsule endoscopy and deep enteroscopy: 1.	 Frequency of demonstrating competency 2.	Frequency of generating a full report  3.	Frequency of detailing a management plan to patients

While both tests “have an important positive impact on the diagnosis and management of small-bowel diseases,” the authors wrote, “comprehensive quality indicators for CE and DE performance have been lacking, despite previous efforts to create individual quality metrics.”

Leighton and colleagues conducted a literature review and developed a list of proposed quality indicators applicable to preprocedure, intraprocedure and postprocedure periods for CE and DE using a modified RAND/University of California Los Angeles Appropriateness Method. Based on this method, an indicator was deemed appropriate when benefits outweigh any potential risk, regardless of cost.

The task force identified 13 quality indicators for CE/DE use, which are highlighted below.

Quality indicators for CE

During the preprocedure period, quality indicators include frequency of demonstrating competency, frequency of obtaining informed consent with specific discussion of associated risks and frequency of performing CE in a timely manner following an episode of overt, suspected small-bowel bleeding.

The quality indicator during the intraprocedure period is frequency of performing CE placement for patients with contraindications to swallowing the capsule or for patients at risk for gastric retention.

Postprocedure quality indicators include the frequency of performing photo documentation and documenting small-bowel transit time, the frequency of recommending an appropriate management plan based on CE findings, and the frequency of generating a complete report for all patients undergoing CE.

Quality indicators for DE

Like CE, frequency of demonstrating competency was also cited as a quality indicator in the preprocedure period of DE. Additional indicators during this time include frequency of performing DE for an indication that is documented and included in a standard list of appropriate indications, and frequency of discussing the management of anticoagulation and documenting the periprocedural anticoagulation plan.

During the intraprocedure period, quality indicators include frequency of marking the most distal point of advancement when indicated and frequency of characterizing and treating clinically significant lesions.

Frequency of generating a complete report and frequency of tracking DE complications and appropriate management are postprocedure quality indicators.

“The task force hoped to improve the quality performance of these relatively new small-bowel diagnostic techniques by compiling comprehensive recommendations of quality indicators for CE and DE procedures,” Leighton and colleagues concluded. “Incorporating the measures into clinical practice will improve standardization of these procedures, further increasing quality.”

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