SBIR-STTR Award

Bioadhesive/Mesh Constructs For Incisional Hernia Prevention
Award last edited on: 2/1/12

Sponsored Program
SBIR
Awarding Agency
NIH : NIGMS
Total Award Amount
$253,839
Award Phase
1
Solicitation Topic Code
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Principal Investigator
Jeffery Lawrence Dalsin

Company Information

Kensey Nash Corporation

735 Pennsylvania Drive
Exton, PA 19341
   (484) 713-2100
   info@kenseynash.com
   www.kenseynash.com
Location: Multiple
Congr. District: 06
County: Chester

Phase I

Contract Number: 1R43GM096527-01
Start Date: 9/30/11    Completed: 9/29/12
Phase I year
2011
Phase I Amount
$253,839
Bioadhesive/Mesh Constructs for Incisional Hernia Prevention. Although many surgical procedures are now performed using laparoscopic techniques, a large number of abdominal surgeries still require a laparotomy. From 2% to 23% of laparotomy closures result in herniation of the abdominal incision, and an estimated 400,000 incisional hernia repairs are performed annually in the US. This healthcare burden becomes significantly amplified when considering that recurrence rates after initial hernia repair typically range from 20% to 25%. Mean hospital costs for incisional hernia repair are estimated to be between $10K and $15K, for a total of $4-6 Billion annually. If introduction of a reliable method for prophylaxis resulted in even a 20% reduction in the incidence of incisional hernias, the savings in hospital costs alone would range from an estimated $800 Million to $1.2 Billion. Prevention of incisional hernias represents a significant unmet clinical need. Despite ongoing efforts to reduce the risk of herniation, the incidence of incisional hernias has remained relatively steady, and there is no consensus as to the best way to reduce this risk. Although no single approach has proven itself to be an effective hernia prevention strategy, the majority of studies indicate that risk reduction is possible through better surgical materials and techniques. The goal of this Phase I proposal is to establish the feasibility of reinforcing the traditional suture closure of laparotomies by placement of an adhesive-coated mesh in an on-lay position on the superficial fascia over the fascial incision. The adhesive coated meshes will be applied in a peel-and-stick manner over the continuous suture repair of the superficial fascia, thereby reinforcing this closure. The inspiration for the novel technology comes from the adhesive proteins secreted by marine mussels. Even in a wet, turbulent and saline environment, these adhesive proteins harden rapidly and enable marine mussels to anchor themselves to various surfaces. Nerites Corporation has developed a series of synthetic versions of these adhesive proteins that can take the form of a liquid that can be sprayed or painted onto tissue, or that can be cast into dry thin films or membranes that can be used alone or in conjunction with synthetic or biologic meshes or scaffolds. This Phase I project will evaluate several adhesive/mesh formulations and characterize them based the performance metrics of strength, resorption, and biocompatibility. Feasibility of the approach will be demonstrated in a rodent model of incisional hernia.

Public Health Relevance:
Prevention of incisional hernias represents a significant unmet clinical need. Apart from the significant impact on patients'outcome and quality of life, around $4 B is spent annually in the US on incisional hernia repairs. If introduction of a reliable method for prophylaxis reduced the incidence of incisional hernias by even 20%, the savings in hospital costs alone would range from an estimated $800 million to $1.2 billion dollars and around 80,000 patients would benefit.

Thesaurus Terms:
Abdomen;Abdominal;Address;Adhesives;Agarose;Animals;Antiheparin Factor;Approaches To Prevention;Assay;Bioassay;Biocompatible;Biologic Assays;Biological;Biological Assay;Blood Platelet Factor Iv;Blood Platelet Factor 4;Body Tissues;Breathing;Chemokine (C-X-C Motif) Ligand 4;Clinical;Clinical Trials;Consensus;Development;Devices;Drug Formulations;Environment;Esters;Ethyl Carbamate;Ethyl Urethan;Evaluation;Factor 4;Fascia;Filler;Film;Formulation;Funding;Goals;Healed;Health Care Costs;Health Costs;Healthcare;Healthcare Costs;Heparin Neutralizing Protein;Hernia;Histology;Hospital Costs;Hypodermis;In Vitro;Incidence;Inhalation;Inhaling;Laparotomy;Left;Liquid Substance;Lytotoxicity;Marines;Marketing;Membrane;Methods;Metric;Modeling;Muscle;Muscle Tissue;Mussels;Operative Procedures;Operative Surgical Procedures;Otomy;Outcome;Paint;Patients;Performance;Phase;Platelet Factor 4;Polymers;Position;Positioning Attribute;Post-Operative;Postoperative;Postoperative Period;Prevention;Prevention Measures;Prevention Approach;Prevention Strategy;Preventive Strategy;Prophylactic Treatment;Prophylaxis;Proteins;Qol;Quality Of Life;Recombinant Platelet Factor 4;Recurrence;Recurrent;Respiratory Aspiration;Respiratory Inspiration;Risk;Risk Reduction;Rodent Model;Safety;Saline;Saline Solution;Savings;Sepharose;Series;Shear Strength;Small Inducible Cytokine B4;Small Inducible Cytokine Subfamily B, Member 4;Sprague-Dawley Rats;Subcutaneous Tissue;Subcutis;Superficial Fascia;Surface;Surgical;Surgical Interventions;Surgical Procedure;Surgical Incisions;Surgical Sutures;Sutures;Techniques;Technology;Tela Subcutanea;Testing;Thick;Thickness;Time;Timeline;Tissues;Urethane;Adhesive Polymer;Animal Efficacy;Base;Biocompatibility;Biomaterial Compatibility;Clinical Investigation;Commercialization;Cytotoxicity;Cytotoxicity Test;Design;Designing;Developmental;Ethyl Ester Carbamic Acid;Experiment;Experimental Research;Experimental Study;Fluid;Gamma-Thromboglobulin;Gene Product;Healing;Health Care;In Vivo;Incision;Innovate;Innovation;Innovative;Inspiration;Interest;Liquid;Manufacturing Process;Meetings;Membrane Structure;Muscular;New Technology;Novel Technologies;Platelet Factor Iv;Repair;Repaired;Research Study;Scaffold;Scaffolding;Scale Up;Surgery;Surgery Material;Surgical Material

Phase II

Contract Number: ----------
Start Date: 00/00/00    Completed: 00/00/00
Phase II year
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Phase II Amount
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