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Can you lower your rate of return to the operating room or hospital due to complications?
At Ethicon our goal is to provide products and support that help to improve patient outcomes. In pre-clinical testing Ethicon products have been shown to outperform the competitor for these risk factors that are common considerations in colorectal procedures.
Ethicon Colorectal Solutions
At Ethicon, we are the market leader in products supporting colorectal surgeries.2 We offer the most comprehensive portfolio to support surgeon’s colorectal surgery needs.3
Providing Colorectal Professional Education Programs and Resources
The J&J Institute offers learning opportunities for surgeons performing colorectal procedures on the safe and efficacious usage of Ethicon devices to improve patient outcomes. These experiences include in-person courses, digital learning and hands-on practice led by distinguished faculty.
Fielding and Supporting Research Studies and Evidence Generation
At Ethicon our goal is to optimize patient outcomes through generating and analyzing real world evidence, preclinical and clinical studies. For example, a recent pre-clinical study showed – ECHELON CIRCULAR Powered Stapler combined with CONTOUR Curved Cutter Stapler and ECHELON FLEX GST System produced significantly fewer leaks at the staple line in colon tissue.4
Utilizing Digital Technology to Help Advance Patient Outcomes
At J&J Medical Devices we strive to bring new technologies to the market to improve patient outcomes. Currently in the U.S. only C-SATS is offered. C-SATS was developed to harness the power of surgical video analytics, expert feedback and peer review, to help surgeons of all levels track performance and continuously refine their skills.
Featured Colorectal Products
ECHELON CIRCULAR™ Powered Stapler
The ECHELON Circular Powered Stapler reduces leaks by 61% at the staple line without compromising perfusion compared to the Medtronic DST Series™ EEA™ Stapler.*
ECHELON FLEX™ GST System
The ECHELON FLEX GST System‡ delivered 2.3X less slippage on colon compared to Endo GIA™ with Tri-Staple™ Technology.¥
Advanced Bipolar Energy - ENSEAL®
59% less bleeding at the distal tip with ENSEAL X1 Large Jaw compared to LigaSure Impact™.† Vessels sealed at a 90º angle using ENSEAL G2 Articulating Tissue Sealers were shown to be up to 51% stronger than vessels sealed at a 45º angle¶
Plus Antibacterial Sutures
28% reduction in surgical site infection risk with the use of triclosan-coated sutures demonstrated in a meta-analysis.§1
Support Tools to Help Surgeons with their Patients
Ethicon provides resources to help with patient education. They include a patients websites on Colon cancer, diverticulitis and IBD; and a Shared Decision Making guide that provides for an interactive conversation between the patient and surgeon. The discussion guide outlines information about a colectomy procedure. The goal is to drive better outcomes and patient satisfaction through better awareness, understanding and involvement.
Providing help in the coding for medical reimbursement of colectomies and anastomoses.
Addressing Risk Factors Associated with Surgical Site Infection
Three globally recognized health authorities now recommend the use of triclosan-coated sutures for surgical site infection prevention - The CDC, WHO and ACS/SIS. Four types of triclosan-coated sutures are available in the Ethicon portfolio: PDS® Plus, Coated VICRYL® Plus, MONOCRYL® Plus, and STRATAFIX™ Symmetric PDS™ Plus Knotless Tissue Control Device
Operating Room Safety
Across the world, Ethicon is elevating clinician Operating Room Safety through education, partnerships and products. Some examples include our MEGADYNE™ Smoke Evacuation Pencils and support program, and our MEGADYNE™ MegaSoft™ Universal Reusable Plus Patient Return Electrode.
* Benchtop testing in porcine tissue ≤30mmHg (26mmHg average pressure experienced during intra-operative leak test), comparing Ethicon ECHELON CIRCULAR™ Powered Stapler CDH25P to Medtronic DST Series™ EEA™ Stapler EEA2535 (p<0.001) and preclinical perfusion model, in which perfusion was not significantly different between devices.
† Preclinical test of distal tip bleeding in thick porcine mesentery base; ENSEAL® vs. Impact-LF4318 (p=0.001).
‡ System components include ECHELON FLEX™ Powered Plus Stapler and ECHELON™ ENDOPATH Reloads with Gripping Surface Technology
§ 21 RCTs, 6462 patients, 95% CI: (14, 40%), P < 0.001. All triclosan-coated sutures in these RCTs were Ethicon Plus Antibacterial Sutures (Monocryl Plus, Vicryl Plus and PDS Plus), barbed sutures were not included.
¶ ENSEAL® devices tested in a benchtop study on 5-7mm porcine carotid arteries. With NSLG2C35A devices, median burst pressures were 51% higher for vessels sealed at a 90° angle compared to vessels sealed at a 45° angle (p=0.0007). With NSLG2S35A devices, mean burst pressures were 29% higher for vessels sealed at a 90° angle compared to vessels sealed at a 45° angle (p=0.001).
β Based on benchtop metrology and porcine comparative studies vs. legacy HARMONIC® and LigaSure™ Maryland devices.
¥. Benchtop testing in porcine colon ranging in width from 28mm to 36mm, and in thickness from 1.5mm to 2.5mm. Mean tissue slippage GST45 with Blue reload (1.69mm), Tri-Staple45 with Purple reload (2.12mm), p=0.022.
1. de Jonge SW, Atema JJ, Solomkin JS, Boermeester MA. Meta-analysis and trial sequential analysis of triclosan-coated sutures for the prevention of surgical site infection. Brit J Surg. 2017;ePub-DOI: 10.1002/bjs.10445
2. Ethicon 2017 procedure spotlight data
3. Comparing product lines of major manufacturers
4. Benchtop testing in porcine colon compared the rate of staple line leak failure at ≤30mmHg, compared Ethicon CDH29P/CS40B/CR40B to Ethicon CDH29A/CS40B/CR40B, n=30 ea p=0.029. Leak rate at ≤30mmHg was selected based on a preclinical study that measured the intraluminal pressure associated with an intra-operative leak test by surgeons (n=31). Average selected pressure was 26 +/-1.8 mmHg.
SURGICEL Essential Product Information
SURGICEL® Absorbable Hemostat (oxidized regenerated cellulose) is used adjunctively in surgical procedures to assist in the control of capillary, venous, and small arterial hemorrhage when ligation or other conventional methods of control are impractical or ineffective. SURGICEL® ORIGINAL, SURGICEL® FIBRILLAR™, SURGICEL® NU-KNIT®, and SURGICEL® SNoW™ Absorbable Hemostats can be cut to size for use in endoscopic procedures.
Use only as much SURGICEL® Absorbable Hemostat as is necessary for hemostasis, holding it firmly in place until bleeding stops. Remove any excess before surgical closure in order to facilitate absorption and minimize the possibility of foreign body reaction.
In urological procedures, minimal amounts of SURGICEL® Absorbable Hemostat should be used and care must be exercised to prevent plugging of the urethra, ureter, or a catheter by dislodged portions of the product.
Since absorption of SURGICEL® Absorbable Hemostat could be prevented in chemically cauterized areas, its use should not be preceded by application of silver nitrate or any other escharotic chemicals.
If SURGICEL® Absorbable Hemostat is used temporarily to line the cavity of large open wounds, it should be placed so as not to overlap the skin edges. It should also be removed from open wounds by forceps or by irrigation with sterile water or saline solution after bleeding has stopped.
Precautions should be taken in otorhinolaryngologic surgery to assure that none of the material is aspirated by the patient. (Examples: controlling hemorrhage after tonsillectomy and controlling epistaxis.)
Care should be taken not to apply SURGICEL® Absorbable Hemostat too tightly when it is used as a wrap during vascular surgery (see Adverse Reactions section of the complete product package insert).
• ADVERSE EVENTS
“Encapsulation” of fluid and foreign body reactions have been reported.
There have been reports of stenotic effect when SURGICEL® Absorbable Hemostat has been applied as a wrap during vascular surgery.
Paralysis and nerve damage have been reported when SURGICEL® Absorbable Hemostat was used around, in, or in proximity to foramina in bone, areas of bony confine, the spinal cord, and/or the optic nerve and chiasm.
Blindness has been reported in connection with surgical repair of a lacerated left frontal lobe when SURGICEL® Absorbable Hemostat was placed in the anterior cranial fossa.
Possible prolongation of drainage in cholecystectomies and difficulty passing urine per urethra after prostatectomy have been reported.
For more information, please consult your doctor or for product quality and technical questions, call 1-800-795-0012. For complete product information including indications, contraindications, warnings, precautions, and adverse reactions, please reference the individual product package inserts.