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.