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| Name | Class |
|---|---|
| Orthopaedic Trauma Association | OTHER |
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Enhancing Wound Perfusion in High-Risk Lower Extremity Orthopaedic Surgery: A Feasibility Study on Nitropaste Using Intraoperative SPY Imaging.
Tissue perfusion is a critical determinant of wound healing, particularly in lower extremity surgery where wound necrosis, dehiscence, and infection can result in limb loss. Despite current advances in wound therapy, rates of wound complications for certain lower extremity incisions remain high. Thus, there remains a critical need to identify agents that may potentially augment wound healing in orthopaedic surgery.
Nitropaste has been successfully used in plastic surgery to enhance perfusion and reduce flap necrosis, but its role in orthopaedic surgery is under-explored. In a meta-analysis of 6947 patients from 3 randomized controlled trials (RCTs) and 2 retrospective studies found that the use of nitropaste was associated with 0.23 odds [0.10-0.53, 95% confidence interval] of reduced mastectomy flap failure. Preliminary data from the investigator's institution involving 18 patients who received intraoperative nitropaste showed no adverse hypotensive effects, though wound complications occurred in three cases. Laser Assisted Indocyanine Green (LA-ICG) provides real-time, quantitative perfusion measurements, making it an ideal tool to evaluate the efficacy of nitropaste. Therefore, The purpose of this study is to evaluate the effects of nitropaste on immediate tissue perfusion and wound complications in high-risk lower extremity orthopaedic incisions using LA-ICG. Additionally, the investigators will assess the safety of single-dose nitropaste in these patients. The investigators hypothesize that intraoperative nitropaste application will significantly improve tissue perfusion, which in turn would be associated with reduced wound complications, with minimal adverse effects.
Aim 1: To evaluate the effect of nitropaste on immediate tissue perfusion in lower extremity orthopaedic incisions using LA-ICG.
Aim 2: To assess trial feasibility and ability to identify wound complications for a future large-scale trial.
Aim 3: To assess the safety of nitropaste in lower extremity orthopaedic surgeries.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Nitropaste | Experimental | All patients enrolled in this study will receive a baseline perfusion measurement with the LA-ICG system. This will occur after wound closure. Subsequently, all patients will receive a single dose of nitropaste intraoperatively and a final LA-ICG tissue perfusion measurement. |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Nitroglycerin Ointment 2% | Drug | Patients will have pre- and post-nitropaste tissue perfusion measurement with the LA-ICG system. |
|
| Measure | Description | Time Frame |
|---|---|---|
| Absolute fluorescence unit (AFU) | raw fluorescence measurement | Intraoperative measurement |
| Relative fluorescence unit (RFU) | Will be calculated as a ratio of the mean fluorescence measure to the mean "normal" measurement. The mean "normal" measurement will be defined as the maximal signal intensity in a region outside of the wound area. | Intraoperative measurement |
| mean incision perfusion (MIP) | the mean fluorescence of 10 points adjacent to the incision. | Intraoperative measurement |
| mean perfusion impairment (MPI) | the difference between mean of each pair of points on each side of the incision. | Intraoperative measurement |
| Measure | Description | Time Frame |
|---|---|---|
| Number of Participants with Wound dehiscence | participants with wound dehiscence (when two edges of a wound separate) | From surgery to 3 months post-operation |
| Number of participants with Wound necrosis |
| Measure | Description | Time Frame |
|---|---|---|
| recruitment rate | Patients recruited into the study per time and per patients approached | From study start to final recruitment approximately 8 months |
| retention rate | Percent patient follow-up at 3 months postoperative |
Inclusion Criteria:
Adults aged 18 years or older.
Undergoing surgery for one of the following procedures:
English-speaking
Able to provide informed consent during preoperative clinic visit, in the preoperative nursing area, or on inpatient units.
Exclusion Criteria:
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| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Henry T Shu, MD | Contact | 2408050284 | hshu5@jhmi.edu | |
| Babar Shafiq, MD, MSPT | Contact | 4432877847 | bshafiq2@jhmi.edu |
| Name | Affiliation | Role |
|---|---|---|
| Henry T Shu, MD | Johns Hopkins University | Study Director |
| Babar Shafi, MD, MSPT | Johns Hopkins University | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| The Johns Hopkins Hospital | Baltimore | Maryland | 21201 | United States |
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 27826472 | Background | Sanniec K, Teotia S, Amirlak B. Management of Tissue Ischemia in Mastectomy Skin Flaps: Algorithm Integrating SPY Angiography and Topical Nitroglycerin. Plast Reconstr Surg Glob Open. 2016 Oct 6;4(10):e1075. doi: 10.1097/GOX.0000000000001075. eCollection 2016 Oct. |
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No sharing will occur to protect patient Protected Health Information (PHI)
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This study is a single-arm open-label prospective clinical trial with no randomization or placebo. All patients will serve as own controls for LA-ICG fluorescence measurement. This study is considered a Phase I feasibility study, or a Stage 2a Development study under the IDEAL Framework
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participants with any death of peri-incisional skin
| From surgery to 3 months post-operation |
| Number of participants with Superficial infection | participants with any wound infection that is treated only with oral antibiotics | From surgery to 3 months post-operation |
| Number of participants with Deep infection | Any wound infection that requires surgical management | From surgery to 3 months post-operation |
| From study start to 3 months after final patient is recruited |
| Johns Hopkins Bayview Medical Center | Baltimore | Maryland | 21224 | United States |
|
| ID | Term |
|---|---|
| D000092463 | Tibial Plateau Fractures |
| D064386 | Ankle Fractures |
| D013529 | Surgical Wound Dehiscence |
| D014946 | Wound Infection |
| ID | Term |
|---|---|
| D000092443 | Knee Fractures |
| D050723 | Fractures, Bone |
| D014947 | Wounds and Injuries |
| D013978 | Tibial Fractures |
| D007718 | Knee Injuries |
| D007869 | Leg Injuries |
| D016512 | Ankle Injuries |
| D011183 | Postoperative Complications |
| D010335 | Pathologic Processes |
| D013568 | Pathological Conditions, Signs and Symptoms |
| D007239 | Infections |
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