Urologic surgery has advanced with new technologies to allow less invasive management of common afflictions such as kidney stones, these procedures are notoriously painful as the ureter must be dilated to accommodate any instruments, and a ureteral stent is often left following surgery to allow for adequate healing. Unfortunately, stents are poorly tolerated by a significant number of patients, with up to 100% complaining of bothersome pain and 10% of patients with unplanned healthcare visits. Further complicating kidney stone management is the frequency of concurrent chronic kidney disease (CKD) or acute kidney injury (AKI) that prohibits many patients from taking NSAIDs which limits pain management options. There is now a push to treat these patients with multimodal analgesia to provide better care and reduce opioid use. Suzetrigine is a new a first-in-class selective inhibitor of the NaV1.8 sodium channel that functions as a non-opioid analgesic developed to treat acute pain and neuropathic pain. This study assesses the addition of suzetrigine to standard-of-care multimodal analgesia. We hypothesize a demonstrated decrease in opioid use, decrease Emergency Room visits within 30 days, decrease the number of unplanned care encounters.
Urologic surgery has advanced with new technologies to allow less invasive management of common afflictions such as kidney stones, these procedures are notoriously painful as the ureter must be dilated to accommodate any instruments, and a ureteral stent is often left following surgery to allow for adequate healing. Unfortunately, stents are poorly tolerated by a significant number of patients, with up to 100% complaining of bothersome pain and 10% of patients with unplanned healthcare visits. Further complicating kidney stone management is the frequency of concurrent chronic kidney disease (CKD) or acute kidney injury (AKI) that prohibits many patients from taking NSAIDs which limits pain management options. There is now a push to treat these patients with multimodal analgesia to provide better care and reduce opioid use. Suzetrigine is a new a first-in-class selective inhibitor of the NaV1.8 sodium channel that functions as a non-opioid analgesic developed to treat acute pain and neuropathic pain. This study assesses the addition of suzetrigine to standard-of-care multimodal analgesia. We hypothesize a demonstrated decrease in opioid use, decrease Emergency Room visits within 30 days, decrease the number of unplanned care encounters. This prospective open-label interventional single-center study will compare 30-day postoperative patient reported outcomes and pain medication use between a pre-implementation cohort of patients managed with standard-of-care multimodal analgesia after ureteroscopy with a post-implementation cohort of patient with this regimen and addition of suzetrigine. The primary outcome will be opioid usage after discharge with standard of care multimodal analgesia (historical control) vs opioid usage after discharge with suzetrigine included with the standard of care multimodal analgesia regimen (intervention). Secondary outcomes will include unplanned care encounters within 30 days (Emergency Room, unplanned clinic visits) and surveyed patient reported outcomes measured on a post-operative survey including PROMIS (Patient-Reported Outcomes Measurement Information System) questions as well as an end of study administration of WISQOL (The Wisconsin Stone Quality of Life Questionnaire). The study will be conducted within a single academic institution including the primary hospital (Brigham and Women's Hospital) and satellite sites (Brigham and Women's Faulkner Hospital).
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
100
multimodal analgesia regimen
suzetrigine with multimodal analgesia regimen
Brigham and Women's Hospital
Boston, Massachusetts, United States
Brigham and Women's Faulkner Hospital
Boston, Massachusetts, United States
Post-discharge opioid consumption (MME)
assessed at post-operative visit
Time frame: 1-2 weeks
Post-discharge opioid consumption (MME)
assessed at 30 days after surgery
Time frame: 30 days
Rate of unplanned care encounters
Emergency Room visits
Time frame: 30 days
patient reported outcomes: pain score
measured on a 0 to 10 analog scale on post-operative survey
Time frame: 2 weeks
patient reported outcomes: pain score
measured on a 0 to 10 analog scale on post-operative survey
Time frame: 30 days
patient reported outcomes: PROMIS composite score
total score where each of the following is rated from 0 to 4 then aggregated into a total value: 1. How much did pain interfere with your day-to-day activities? 2. How much did pain interfere with work around the home? 3. How much did pain interfere with your ability to participate in social activities? 4. How much did pain interfere with your household chores? 5. How much did pain interfere with things you usually do for fun? 6. How much did pain interfere with your enjoyment of social activities?
Time frame: 2 weeks
patient reported outcomes: PROMIS composite score
total score where each of the following is rated from 0 to 4 then aggregated into a total value: 1. How much did pain interfere with your day-to-day activities? 2. How much did pain interfere with work around the home? 3. How much did pain interfere with your ability to participate in social activities? 4. How much did pain interfere with your household chores? 5. How much did pain interfere with things you usually do for fun? 6. How much did pain interfere with your enjoyment of social activities?
Time frame: 30 days
patient reported outcomes (PROMIS) pain interfere with your day-to-day activities
rated from 0 to 4
Time frame: 2 weeks
patient reported outcomes (PROMIS) pain interfere with your day-to-day activities
rated from 0 to 4
Time frame: 30 days
patient reported outcomes (PROMIS) pain interfere with work around the home
rated from 0 to 4
Time frame: 2 weeks
patient reported outcomes (PROMIS) pain interfere with work around the home
rated from 0 to 4
Time frame: 30 days
patient reported outcomes (PROMIS) pain interfere with your ability to participate in social activities
rated from 0 to 4
Time frame: 2 weeks
patient reported outcomes (PROMIS) pain interfere with your ability to participate in social activities
rated from 0 to 4
Time frame: 30 days
patient reported outcomes (PROMIS) pain interfere with your household chores
rated from 0 to 4
Time frame: 2 weeks
patient reported outcomes (PROMIS) pain interfere with your household chores
rated from 0 to 4
Time frame: 30 days
patient reported outcomes (PROMIS) pain interfere with things you usually do for fun
rated from 0 to 4
Time frame: 2 weeks
patient reported outcomes (PROMIS) pain interfere with things you usually do for fun
rated from 0 to 4
Time frame: 30 days
patient reported outcomes (PROMIS) pain interfere with your enjoyment of social activities
rated from 0 to 4
Time frame: 2 weeks
patient reported outcomes (PROMIS) pain interfere with your enjoyment of social activities
rated from 0 to 4
Time frame: 30 days
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