Karl Storz endoscope - Best practices

Endoscope selection and handling

  • Choose the smallest possible diameter endoscope that is compatible with the target anatomy (typically 1.9–3.0 mm for mice and rats).

  • Use rigid scopes for straight-line access (gastroscopy, laparoscopy) and fiberscopes for curved pathways (colon, trachea).

  • Always inspect optics and light cable before use for clarity, cleanliness, and alignment.

Sterility and aseptic technique

  • Autoclave or disinfect all reusable instruments; use sterile sheaths if necessary.

  • Prepare the surgical site using standard antiseptic techniques (iodine or chlorhexidine scrub).

  • Perform procedures in a dedicated clean workspace to minimize infection risk.

Tissue protection and insufflation

  • Use gentle insufflation (CO₂ via endo-arthroflator) for laparoscopy, keeping pressures appropriate for rodent physiology (commonly ≤5 mmHg in mice).

  • Avoid excessive suction or irrigation volume to prevent mucosal trauma.

  • Keep procedures short and efficient to reduce anesthetic burden.

Pre-procedural preparation

  • Confirm animal eligibility: Use healthy, age- and weight-matched rodents; exclude animals showing signs of illness or stress.

  • Pre-anesthetic checks: Ensure hydration, record baseline weights, and apply ophthalmic ointment to protect corneas under anesthesia.

  • Fasting if applicable: For GI procedures, follow species-specific fasting guidelines to reduce stomach contents.

  • Use proper anesthesia and temperature control: Maintain stable anesthesia and prevent hypothermia with a regulated warming surface.

Instrumentation and setup

  • Select the correct endoscope type and size:
    • Use rigid endoscopes (1.9–3.0 mm) for linear access (stomach, colon, abdominal cavity).

    • Use fiberscopes or semi-flexible scopes for curved anatomical regions where maneuverability is essential.

  • Inspect optics before use: Ensure clarity of lenses or fiber bundles, and verify functionality of light and camera connections.

  • Sterilize all instruments: Autoclave rigid instruments or apply high-level disinfection for flexible scopes; use sterile drapes or sheaths as needed.

  • Test and calibrate auxiliary systems: Adjust the light source, camera focus, and insufflation or irrigation settings before beginning.

Animal positioning and scope insertion

  • Stabilize the animal: Use a secure but gentle restraint method (surgical platform or padded holders) that avoids restricting respiration.

  • Insert scope gently:
    • Lubricate the scope tip if necessary

    • Advance slowly under visual guidance to avoid trauma or perforation

  • Use insufflation judiciously: For laparoscopy, maintain low intra-abdominal pressure (≤5 mmHg) to avoid vascular or respiratory compromise.

  • Control irrigation and suction: Use gentle, pulsed flushing to maintain visibility and avoid tissue injury.

Intervention and imaging

  • Optimize image parameters:
    • Adjust brightness, white balance, and zoom prior to insertion.

    -Re-focus frequently, especially in curved or fluid-filled environments.

  • Preserve a clear field of view:
    • Flush blood or debris intermittently.

    • Use controlled suction to clear fluid without collapsing tissues.

  • Use working channels for precision:
    • Introduce instruments (biopsy forceps, injection needles) slowly and under direct visualization.

    • Monitor instrument path at all times to avoid off-target effects or damage.

  • Enhance image quality in fiberscopic systems:
    • Apply honeycomb artifact suppression filters to reduce the characteristic grid pattern from discrete fiber elements.

    • In live imaging, temporal or spatial averaging helps reduce noise while preserving resolution.

    • When possible, select fiberscopes with high fiber count and well-aligned coherent bundles to minimize inherent artifact visibility.

Fluorescence imaging (optional)

  • Use appropriate filters and sources: Select far-red fluorophores compatible with the far-red channel (ICG) and match light intensity to imaging goals.

  • Prevent photobleaching: Minimize LED exposure time and intensity; capture essential data in brief, focused intervals.

  • Clean optics: Eliminate background fluorescence by ensuring lenses, scopes, and covers are free of residue.