Wednesday, January 17, 2024

ESRD confers a 7-fold risk of major adverse limb events in patients undergoing percutaneous vascular interventions

Association between End-Stage Renal Disease and Major Adverse Limb Events after Peripheral Vascular Intervention


Clinical question

Does End-Stage Renal Disease predict major adverse limb events post-peripheral vascular intervention?

Take away point

End-stage renal disease gives patients a more than 7-fold risk of below-knee amputation after percutaneous vascular intervention compared to patients without End-stage renal disease.

Reference 

Association between End-Stage Renal Disease and Major Adverse Limb Events after Peripheral Vascular Intervention. Babore, Y et al. Journal of Vascular Interventional Radiology 2023 Sep 9:S1051-0443(23)00655-3. doi: 10.1016/j.jvir.2023.06.042.

https://www.jvir.org/article/S1051-0443(23)00655-3/fulltext

Study design

This was a retrospective, observational, propensity score matched cohort study

Funding Source

No funding listed

Setting

Academic, University of Pennsylvania

Figure


Kaplan-Meier curves comparing patients with and without end-stage renal disease (ESRD) with 95% CIs. (a) Major adverse limb event (MALE) (P = .0001, log-rank test); (b) major amputation (P < .0001, log-rank test); (c) above-knee amputation (AKA) (P = .02, log-rank test); (d) below- knee amputation (BKA) (P < .0002, log-rank test); (e) bypass reintervention (P = .75, log-rank test); (f) percutaneous vascular intervention (PVI) reintervention (P = .2, log-rank test).

Summary

Peripheral arterial disease affects over 200 million people worldwide. Patients with peripheral arterial disease who underwent amputation above the ankle have a one-year mortality of 50% and 3-year mortality of 70%. End-stage renal disease is a known risk factor for poorer outcomes of revascularization, with higher risks of major adverse limb events and major amputations. However, robust assessment of the effect of end-stage renal disease on major adverse limb events after percutaneous vascular interventions is lacking. The recent BEST-CLI trial comparing endovascular therapy and surgical bypass among patients with critical limb ischemia, could not assess the effects given that only 11% of the included patient population had end-stage renal disease.

This paper seeks to assess how end-stage renal disease affect percutaneous vascular interventions, leading to higher complications and major adverse limb events (defined as reintervention or major amputation). The researchers gathered information from one institution where they reviewed patient records, institutional and clinic data systems to find patients who underwent tibial percutaneous vascular intervention for critical limb ischemia (Rutherford Category 4-6). The patients with end-stage renal disease were defined as a glomerular filtration rate of <15 mL/min/1.73 m2 or need for long-term kidney replacement therapy to live. Ultimately, the study included 350 patients, 88 of whom had end-stage renal disease.

Propensity score matching was used to define a contemporaneous control population against the population of interest with end-stage renal disease. Kaplan-Meier modeling was performed for comparisons from the time of the percutaneous vascular intervention to the primary study endpoint of major adverse limb events. Cox proportional hazards models were also used to estimate hazard ratios and the significance of the effect for each variable of interest (medication therapy, comorbid factors such as HgbA1c, hypertension, interventions performed, and limb events).

Ultimately, Kaplan-Meier estimates revealed a significant difference in mean times to major adverse limb events (P = 0.0001), as well as estimated duration without major adverse limb events at 6, 12, and 24 months. There were also significant differences in mean times to major amputation (P < .0001), above knee amputation (P = .02), and below knee amputation (P = .0002) between the end-stage renal disease group and the control group. Most importantly, patients with end-stage renal disease were associated with a 7-fold increase in major amputations and the effect was primarily driven by below knee amputations since these patients tend to have more distal disease involvement.

Commentary

This study highlighted peripheral arterial disease, an important disease state that impacts a large patient population. Several modifiable and nonmodifiable risk factors associated with the disease were known. And risk stratification using these factors is crucial for individualized treatment planning and outcome prediction. It was clear by the analyses that end-stage renal disease severely impacts not just the initial pathogenesis of peripheral arterial disease, but the procedural outcomes and complications. Also interesting was the fact that the effects were mostly driven by below knee amputations, which tend to confer a better quality of life and lower mortality compared to above knee amputations.

To further expand on the clinical knowledge in the context of end-stage renal disease and percutaneous vascular interventions, a wider patient population and different treatment approaches would be beneficial. The authors had also found some potential inconsistencies with other major trials and medical foundations. One example was that “higher HbA1c level was the only independent predictor of above knee amputations and was found to confer lower risk.” “Cox proportional hazards analysis revealed a 2-fold increase in the risk of MALE in patients on anticoagulant therapy” was the second example. These seemingly counterintuitive findings may be due to the design of the current study and will require further investigation to clarify.

Ultimately, this paper provided critical clinical value in the evaluation of patients with end-stage renal disease and peripheral arterial disease. Closer follow-up is warranted in patients with end-stage renal disease who underwent percutaneous vascular interventions and new treatment strategies are necessary to decrease their risks of major adverse limb events.

Post Author

Christopher Loiselle, MS, OMSIV
Lincoln Memorial University-DeBusk College of Osteopathic Medicine
Twitter Handle: @Caloiselle

Monday, January 8, 2024

Percutaneous cholecystoenteric anastomosis for non-surgical patients with indwelling chole tube

A Pilot Study of Percutaneous Cholecystoenteric Anastomosis: A New Option for High-Risk Patients with Symptomatic Gallstones


Clinical Question

Is percutaneous cholecystoenteric anastomosis creation via lumen-apposing metal stent safe and effective in patients with indwelling cholecystostomy tubes who are otherwise high-risk for surgical interventions?

Take Away Point

Cholecystoenteric anastomosis creation via stent placement demonstrated 100% technical success rate with a mean follow-up time of 15 months and 86% clinical success rate with subsequent removal of indwelling cholecystostomy tubes within 36 days.

Reference

Barragan C, Alshehri H, Marom G, Glazer Y, Swanstrom L, Shlomovitz E. A pilot study of percutaneous cholecystoenteric anastomosis: A new option for high-risk patients with symptomatic gallstones. Journal of Vascular and Interventional Radiology. 2023;35:74-79. doi:10.1016/j.jvir.2023.09.025

Link to article

Study Design

Retrospective and observational study consisting of 14 patients

Funding Source

No reported funding

Setting

Academic, University Health Network, Toronto, Canada
Academic, The Hebrew University of Jerusalem, Jerusalem
Public and Private, Institut de Chirurgie guidée par l’Image, Strasbourg, France

Figure



Summary

Acute calculus cholecystitis is a very common pathology in the United States, leading to over 200,000 cases of admissions annually. While laparoscopic cholecystectomy remains the gold standard, patients who are poor surgical candidates generally receive alternative management such as percutaneous cholecystostomy tube placement. However, these options expose patients to risks and complications in the long-term including infection, pain and tube dislodgement along with impairment in their quality of life.

The authors of this paper studied the safety and effectiveness of percutaneous cholecystoenteric anastomosis creation. They performed a retrospective analysis consisting of fourteen patients (10 male and 4 female) with indwelling cholecystostomy tubes, all of whom were high risk for surgery or percutaneous stone removal procedure. Technical success was defined as stent placement across the percutaneously created cholecystoduodenal anastomosis, while clinical success was defined as successful removal of any cholecystostomy drain after stent placement.

The results of the study demonstrated 100% technical success rate with a mean follow-up time of 15 months. Axios stents (Boston Scientific, Marlborough, Massachusetts) were utilized in 12/14 patients. Clinical success rate was 86% with a mean duration to cholecystostomy tube removal of 36 days (9 of whom had their tubes removed within 30 days). The remainder two patients included one death secondary to comorbid cardiac medical history and one lost to follow-up. The study reported no device-related adverse events.

This data demonstrated highly favorable results of percutaneous cholecystoenteric anastomosis creation using lumen-apposing metal stent. The advantages of this technique include no requirement for general anesthesia or endoscopy, improvement in quality of life, and prevention of tube-related complications (occlusion, tube dislodgement, pain, etc). The drawbacks include reliance on 2-dimensional representation of a 3-dimensional structure for puncture guidance and reliance on the pre-existing cholecystostomy tube access, and potential malpositioned stent across the cholecystoenteric tract.

The first limitation of the study is the evolving nature of the technique. Secondly, there is limited long-term data on the effects of stent placement across a cholecystoenteric anastomosis. Lastly, combination of this technique with existing gallstone management strategies remain unstudied.

Commentary

Percutaneous cholecystoenteric anastomosis creation with lumen-apposing metal stent is a novel technique that shows promising data in improving quality of life for high-risk patients with indwelling cholecystostomy tubes. However, more data is still needed, particularly on the generalizability of the procedure, long-term effects of the procedure, and comparative advantages to existing gallstone management strategies. This pilot study has laid the groundwork for future larger, multi-centered, preferably randomized comparative studies and may revolutionize gallstone management in high-risk non-surgical patients.

Post author

Naeem Patel, DO
Radiology Resident, PGY4
Department of Radiology, Interventional Radiology Division
Hartford Hospital, Hartford, CT
@Naeemp7Patel

Wednesday, January 3, 2024

Hydrogel augmentation for refractory chronic low back pain, does it work?

Hydrogel Augmentation of the Lumbar Intervertebral Disc: An Early Feasibility Study of a Treatment for Discogenic Low Back Pain


Clinical question


Is hydrogel augmentation a safe and effective treatment for chronic low back pain that is refractory to medical management?

Take away point


This early feasibility study with 20 patients experiencing chronic low back pain due to degenerative disc disease refractory to conventional management demonstrated the effectiveness of hydrogel augmentation in pain reduction and function improvement. Two serious adverse events of implant migration required transforaminal endoscopic removal.

Reference


Hydrogel Augmentation of the Lumbar Intervertebral Disc: An Early Feasibility Study of a Treatment for Discogenic Low Back Pain. Beall DP M.D. et al. Journal of Vascular and Interventional Radiology, Volume 35, Issue 1, 51-58.

Click here for abstract

Study design


The study was a prospective, nonrandomized, single-arm, single center study


Funding Source


ReGelTec, Baltimore, Maryland


Setting


Ceduil Medical Center, Barranquilla, Colombia


Figure



Figure 1(a) Lateral fluoroscopic image showing injection of contrast medium (black arrowheads) through 22-gauge needles (white arrowheads) into the L3–4 and L4–5 discs. (b) Lateral fluoroscopic image 2 weeks later showed a pattern of hydrogel after injection into the same discs. Note that the pattern of hydrogel distribution was similar to that of the contrast medium injected during discography 2 weeks earlier.




Figure 2 Box plots demonstrated the numerical rating scale (NRS) pain scores obtained at baseline, 1 month, 3 months, and 6 months for the patient’s (a) back pain and their (b) leg pain. Significance of post hoc Bonferroni-adjusted Wilcoxon signed rank tests were shown between baseline and follow-up visits. Data showed a 5.2-point reduction in back pain and a 3.4-point reduction in leg pain at the 6-month follow-up time point.

Summary


Low back pain is the leading cause of disability worldwide and is most often caused by degenerative disc disease. Originally, this was treated with replacement of the nucleus pulposus tissue to combat lost intradiscal tissue. Hydrogel materials have been investigated due to its similarity to the native nucleus pulposus tissue and its ability to form a continuous implant over time without cracks or fissures. The hydrogel combination of polyvinyl alcohol, polyethylene glycol, polyvinyl pyrrolidone, and barium sulfate was developed. The addition of polyethylene glycol allowed the preparation to liquify when heated to 65 °C and be injected through a smaller, 17-gauge needle, providing an ideal minimally invasive treatment approach.

The authors of the study performed a prospective, single arm, single center, clinical trial to evaluate the safety and effectiveness of hydrogel augmentation for refractory chronic low back pain due to degenerative disc disease. 20 patients met the inclusion criteria of clinical and imaging evidence of disc generation at 1 or 2 vertebral levels, disability present for at least 12 weeks, refractory to conventional medical management, and modified Pfirrmann levels II-VI on MR imaging. A complete safety assessment one month after treatment was performed by a safety committee to determine if patient recruitment should continue.

The hydrogel augmentation procedure was successfully performed in 20 patients at 29 total lumbar levels. The hydrogel was placed in the center of the disc with an injected volume ranging from 1.5 to 3.1 mL. Patients were assessed using a numerical rating scale for back and lower limb pain, and an Oswestry disability index for function at their baseline and follow-ups at 1 month, 3 months, and 6 months. There was a statistically significant reduction in back and lower leg pain, along with a statistically significant improvement in function.

18 total adverse events were noted in 12 of the 20 patients. 13 were of mild-moderate severity and not related to the device or procedure. One patient died from a pulmonary thromboembolism attributable to cardiorespiratory factors and unrelated to the study device or procedure. Two patients experienced persistent pain post procedure and were found to have hydrogel extrusion. These were resolved with endoscopic removal and both patients had pain scores of 0 at the 6-month follow-up.

The first limitation of this study is the small study population, with 19 patients who completed the 6 month follow up and 1 patient lost to follow up. This limitation is inherent to an early feasibility study. The next limitation is the lack of comparison arms. Future studies should compare hydrogel with continued non-surgical management, epidural steroid injections, and/or spinal fusion. The last limitation is the involvement of a single treatment site, which limits the generalizability to other interventionalists and locations.

Commentary


This study demonstrated that hydrogel augmentation can successfully treat refractory chronic low back pain caused by degenerative disc disease. Two serious adverse events of hydrogel migration were noted and required endoscopic removal. There were no persistently symptomatic adverse events 6 months post treatment. Determining risk factors associated with hydrogel migration and developing techniques that can minimize this serious adverse event are critical to improve the safety profile of the procedure. Comparisons with current treatment options including medical management, steroid or epidural injections, and spine fusion in blinded, randomized control trials are necessary to delineate the role of hydrogel augmentation in the treatment algorithm of chronic refractory low back pain. Hydrogel augmentation, when validated in larger multi-center trials with comparison arms, may revolutionize degenerative disc disease treatment by providing a minimally invasive intervention early in the disease course.



Post Author

Anthony M. Camargo, BA
MD candidate, Class of 2025
University of Massachusetts Chan Medical School
@anthonymcamargo