What You Need to Know About Skin Grafts and Donor Site Wounds
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Medical Policy
Medical Policy Joint Medical Policies are a source for BCBSM and BCN medical policy information only. These documents are not to be used to determine benefits or reimbursement. Please reference the appropriate certificate or contract for benefit information. This policy may be updated and is therefore subject to change. *Current Policy Effective Date: 5/1/21 (See policy history boxes for previous effective dates) Title: Composite Tissue Allotransplantation Description/Background Composite tissue allotransplantation refers to the transplantation of histologically different tissue that may include skin, connective tissue, blood vessels, muscle, bone, and nerve tissue. The procedure is also known as reconstructive transplantation. To date, primary applications of this type of transplantation have been of the hand and face (partial and full), although there are also reported cases of several other composite tissue allotransplantations, including that of the larynx, knee, and abdominal wall. The first successful partial face transplant was performed in France in 2005, and the first complete facial transplant was performed in Spain in 2010. In the United States, the first facial transplant was done in 2008 at the Cleveland Clinic; this was a near-total face transplant and included the midface, nose, and bone. The first hand transplant with short-term success occurred in 1998 in France. However, the patient failed to follow the immunosuppressive regimen, which led to graft failure and removal of the hand 29 months after transplantation. The -
Transplantation and Hepatic Pathology University of Pittsburgh Medical Center November, 2007
Resident Handbook Division of Transplantation and Hepatic Pathology University of Pittsburgh Medical Center November, 2007 For private use of residents only- not for public distribution Table of Contents Anatomic Transplantation Pathology Rotation Clinical Responsibilities of the Division ........................................................3 Categorizations of Specimens and Structure of Signout.................................3 Resident Responsibilities................................................................................4 Learning Resources.........................................................................................4 Transplantation Pathology on the World-Wide Web......................................4 Weekly Schedule ............................................................................................6 Staff Locations and Telephone Numbers........................................................7 Background Articles Landmarks in Transplantation ........................................................................8 Trends in Organ Donation and Transplantation US 1996-2005.....................18 Perspectives in Organ Preservation………....................................................26 Transplant Tolerance- Editorial……………………………………….…….36 Kidney Grading Systems Banff 2005 Update……………………….....................................................42 Banff 97 Components (I t v g etc.) ................................................................44 Readings Banff 05 Meeting Report………………………………………...................47 -
Msc Payment Schedule Index
MSC PAYMENT SCHEDULE INDEX SECTIONS (To go directly to the an applicable section of the Payment Schedule, click on the Section heading listed below) GENERAL PREAMBLE TO THE PAYMENT SCHEDULE .................................. 1 2. OUT-OF-OFFICE HOURS PREMIUMS ............................................................... 2 3. GENERAL SERVICES ......................................................................................... 3 4. DIAGNOSTIC AND SELECTED THERAPEUTIC PROCEDURES ...................... 4 5. CRITICAL CARE .................................................................................................. 5 6. EMERGENCY MEDICINE .................................................................................... 6 7. GENERAL PRACTICE ......................................................................................... 7 8. ANESTHESIA ...................................................................................................... 8 9. DERMATOLOGY ................................................................................................. 9 10. OPHTHALMOLOGY .......................................................................................... 10 11. OTOLARYNGOLOGY ........................................................................................ 11 12. GENERAL INTERNAL MEDICINE .................................................................... 12 13. CARDIOLOGY ................................................................................................... 13 14. CLINICAL IMMUNOLOGY AND ALLERGY -
Costal Cartilage Graft in Asian Rhinoplasty: Surgical Techniques Sarina Rajbhandari and Chuan-Hsiang Kao
Chapter Costal Cartilage Graft in Asian Rhinoplasty: Surgical Techniques Sarina Rajbhandari and Chuan-Hsiang Kao Abstract Asian rhinoplasty is one of the most difficult and challenging surgeries in facial plastic surgery. As many Asians desire a higher nasal bridge and a refined nasal tip, they undergo various augmentation procedures such as artificial implant grafting and filler injections. Autologous rib graft is a very versatile graft material that can be used to augment the nose, with lesser complications, if done precisely. In this chapter, we have discussed the steps of rib graft harvesting, carving and setting into the nose to form a new dorsal height. Keywords: rhinoplasty, costal cartilage, Asians, warping 1. Introduction Asian rhinoplasty is one of the most difficult and challenging surgeries in facial plastic surgery. In Asians, the most common complaints regarding appearance of the nose are a low dorsum and an unrefined tip. Thus, most Asian rhinoplasties include augmentation of the nasal dorsum using either autologous or artificial implant, and/or nasal tip surgery. Clients who have had augmentation rhinoplasty previously frequently opt for revision. Hence, when a client comes for augmenta- tion or Asian rhinoplasty, the surgeon has to confirm whether the client has had any rhinoplasty (or several rhinoplasties) earlier. Artificial nasal implants for augmentation are still in vogue, owing to their simplicity and efficiency, but they are accompanied by several major and minor complications. Revision surgeries for these complications include correcting nasal contour deformities and fix functional problems, and require a considerable amount of cartilage. Revision surgeries are more complex than primary Asian rhinoplasty as they require intricate reconstruc- tion and the framework might be deficient. -
Skin Grafts in Cutaneous Oncology* Enxertia De Pele Em Oncologia
RevABDV81N5.qxd 07.11.06 17:07 Page 465 465 Artigo de Revisão Enxertia de pele em oncologia cutânea* Skin grafts in cutaneous oncology* José Anselmo Lofêgo Filho1 Paula Dadalti2 Diogo Cotrim de Souza3 Paulo Roberto Cotrim de Souza4 Marcos Aurélio Leiros da Silva5 Cristina Maeda Takiya6 Resumo: Em oncologia cutânea depara-se freqüentemente com situações em que a confec- ção de um enxerto é uma boa alternativa para o fechamento do defeito cirúrgico. Conhecer aspectos referentes à integração e contração dos enxertos é fundamental para que os cirur- giões dermatológicos procedam de maneira a não contrariar princípios básicos do trans- plante de pele. Os autores fazem uma revisão da classificação e fisiologia dos enxertos de pele, acrescendo considerações cirúrgicas determinantes para o sucesso do procedimento. Palavras-chave: Neoplasias cutâneas; Transplante de pele; Transplante homólogo Abstract: In cutaneous oncology, there are many situations in which skin grafts could be a good alternative for closing surgical defect. Dermatological surgeons should have enough knowledge about graft integration and contraction in order to not contradict the basic prin- ciples of skin transplantation. The authors review skin graft classification and physiology and make some surgical considerations on successful procedures. Keywords: Skin neoplasms; Skin transplantation; Transplantation, homologous INTRODUÇÃO Enxerto é parte de um tecido vivo transplanta- tológica. São simples quando apresentam um único do de um lugar para outro no mesmo organismo ou tipo de tecido e compostos quando constituídos de em organismos distintos.1 Contudo, a utilização da dois ou mais tipos de tecidos. Em oncologia cutânea, terminologia enxerto para designar uma modalidade um enxerto composto é usado quando o defeito cirúrgica, apesar de errônea, tornou-se coloquial. -
Bone Grafting, Its Principle and Application: a Review
OSTEOLOGY AND RHEUMATOLOGY Open Journal PUBLISHERS Review Bone Grafting, Its Principle and Application: A Review Haben Fesseha, MVSc, DVM1*; Yohannes Fesseha, MD2 1Department of Veterinary Surgery and Diagnostic Imaging, School of Veterinary Medicine, Wolaita Sodo University, P. O. Box 138, Wolaita Sodo, Ethiopia 2College of Health Science, School of Medicine, Mekelle University, P. O. Box1871, Mekelle, Ethiopia *Corresponding author Haben Fesseha, MVSc, DVM Assistant Professor, Department of Veterinary Surgery and Diagnostic Imaging, School of Veterinary Medicine, Wolaita Sodo University, P. O. Box: 138, Wolaita Sodo, Ethiopia;; E-mail: [email protected] Article information Received: March 3rd, 2020; Revised: March 20th, 2020; Accepted: April 11th, 2020; Published: April 22nd, 2020 Cite this article Fesseha H, Fesseha Y. Bone grafting, its principle and application: A review. Osteol Rheumatol Open J. 2020; 1(1): 43-50. doi: 10.17140/ORHOJ-1-113 ABSTRACT Bone grafting is a surgical procedure that replaces missing bone through transferring bone cells from a donor to the recipient site and the graft could be from a patient’s own body, an artificial, synthetic, or natural substitute. Bone grafts and bone graft substitutes are indicated for a variety of orthopedic abnormalities such as comminuted fractures (due to car accidents, falling from a height or gunshot injury), delayed unions, non-unions, arthrodesis, osteomyelitis and congenital diseases (rickets, abnormal bone development) and are used to provide structural support and enhance bone healing. Autogenous, allogeneic, and artificial bone grafts are common types and sources of grafts and the advancement of allografts, synthetic bone grafts, and new operative techniques may have influenced the use of bone grafts in recent years. -
AMRITA HOSPITALS AMRITA AMRITA HOSPITALS HOSPITALS Kochi * Faridabad (Delhi NCR) Kochi * Faridabad (Delhi NCR)
AMRITA HOSPITALS HOSPITALS AMRITA AMRITA AMRITA HOSPITALS HOSPITALS Kochi * Faridabad (Delhi NCR) Kochi * Faridabad (Delhi NCR) A Comprehensive A Comprehensive Overview Overview A Comprehensive Overview AMRITA INSTITUTE OF MEDICAL SCIENCES AIMS Ponekkara P.O. Kochi, Kerala, India 682 041 Phone: (91) 484-2801234 Fax: (91) 484-2802020 email: [email protected] website: www.amritahospitals.org Copyright@2018 AMRITA HOSPITALS Kochi * Faridabad (Delhi-NCR) A COMPREHENSIVE OVERVIEW A Comprehensive Overview Copyright © 2018 by Amrita Institute of Medical Sciences All rights reserved. No portion of this book, except for brief review, may be reproduced, stored in a retrieval system, or transmitted in any form or by any means —electronic, mechanical, photocopying, recording, or otherwise without permission of the publisher. Published by: Amrita Vishwa Vidyapeetham Amrita Institute of Medical Sciences AIMS Ponekkara P.O. Kochi, Kerala 682041 India Phone: (91) 484-2801234 Fax: (91) 484-2802020 email: [email protected] website: www.amritahospitals.org June 2018 2018 ISBN 1-879410-38-9 Amrita Institute of Medical Sciences and Research Center Kochi, Kerala INDIA AMRITA HOSPITALS KOCHI * FARIDABAD (DELHI-NCR) A COMPREHENSIVE OVERVIEW 2018 Amrita Institute of Medical Sciences and Research Center Kochi, Kerala INDIA CONTENTS Mission Statement ......................................... 04 Message From The Director ......................... 05 Our Founder and Inspiration Sri Mata Amritanandamayi Devi .................. 06 Awards and Accreditations ......................... -
Clinical Considerations in Facial Transplantation
CLINICAL CONSIDERATIONS IN FACIAL TRANSPLANTATION by Anthony Renshaw A thesis submitted in fulfilment of the requirements of University College London for the degree of Doctor of Medicine January 2011 Department of Plastic and Reconstructive Surgery, Academic Division of Surgical & Interventional Sciences, University College London 1 Declaration I, Anthony Renshaw, confirm that the work presented in this thesis is my own. Where information has been derived from other sources, I confirm that this has been indicated in the thesis The copyright of this thesis rests with the author and no quotation from it or information derived from it may be published without the prior written consent of the author. …………………………………………………………. 2 Abstract Facial transplantation has emerged as the next step on the reconstructive ladder for severe facial disfigurement. Clinical issues surrounding facial tissue donation are examined, comprising pre-transplant facial vessel delineation; pre-operative aesthetic matching; and attitudes towards donation. An anatomical study of 200 consecutive facial and transverse facial vessels was performed using colour Doppler ultrasound. Facial vessels were measured at three landmarks and their branching pattern documented. The facial artery main branch was detected at the lower mandibular border in 99.5% of cases, the accompanying facial vein in 97.5%. The transverse facial artery was present in 75.5% of cases, the vein found in 58%. When the facial artery was undetectable, there was transverse facial artery dominance. When the facial vein was absent it was replaced with a transverse facial vein. This provides valuable pre-operative information regarding vessel status. A quantitative eleven- point skin tonal matching scheme is described using digital analysis of facial imagery. -
78581/2020/Estt-Ne Hr
105 78581/2020/ESTT-NE_HR 1| T a r i f f - AIMS 106 78581/2020/ESTT-NE_HR INDEX 1. General Information ( Section A) 3 i. Out Patient Department ii. Ambulance Charges 2. General Information ( Section B) 5 i. Bed charges ii. In patient Consultation fees iii. Billing Of Surgery Anesthesia and OT Charges iv. Billing Of Surgery /Procedure/ others 3. LAB 9 4. Outsouce Lab 16 5. Blood Bank 64 6. Imaging & Radiodiagnosis 65 7. Non – Invasive Lab 80 8. Anesthesia 82 9. Cardiology and Cardiac Surgery 84 10. Critical Care Services 89 11. Baby Care 91 12. Common Procedure 94 13 Dental 94 14 Dermatology 101 15 E N T 105 16 Gastroenterology 110 17 Maxillo Facial Surgery 113 18 Nephrology 116 19 Neuro Diagnostic Lab 118 20 Oncology 112 21 Ophthalmology 136 22 Orthopedies 142 23 OBS & Gynaecology 149 24 Physiotherapy 154 25 Respiratory Medicine 156 26 Surgery & Major Procedures i. General Surgery 158 ii. Pediatric Surgery 165 iii. PlasticSurgery 170 iv. Neuro Surgery 182 27 Urology 185 28 Interventional Radiology 192 29 Interventional Pain Management 194 30 Paediatric Cardiac Surgery 197 31 Bed Side Service Charges200 2| T a r i f f - AIMS 107 78581/2020/ESTT-NE_HRSection – A GENERAL INFORMATION OUT PATIENT DEPARTMENT OPD Consultations: Superspeciality OPD Consultation * Rs. 700 Specialty OPD Consultation** Rs. 400 to 800 Note: OPD Timing Monday- Saturday ( 8:00AM – 7:00PM) *Super specialty Departments – Cardiac Surgery, Cardiology, Neurology, Neurosurgery, Oncology, Respiratory Medicine, Urology, Plastic Surgery, Gastroenterology, Endocrinology, Paediatric -
Donor Handbook
DONOR Together against HANDBOOK blood cancer Charity No: 1150056 / SC046917 THERE ARE SURVIVORS BECAUSE THERE ARE LIFESAVERS DEAR POTENTIAL DONOR If you are reading this handbook you have very likely been asked to donate some of your FOREWORD 2 blood stem cells to someone in desperate need. Or maybe you are reading this because you are considering registering as a potential blood stem cell donor and want to find out more. WHY YOU ARE BEING CONTACTED 3 Whatever stage you are at, this handbook will help you to understand the process of blood How you are matched 4 stem cell donation and outline the support offered to you by the team at DKMS. Confirming you are a match 5 The DKMS organisation started in Germany in 1991 around one family’s search for a donor. Confirmatory Typing process at a glance 7 This search for potential donors still goes on today for every patient in need of a blood stem You have been selected 8 cell donation. DKMS has grown to become the largest international organisation to recruit donors. TWO WAYS TO DONATE BLOOD STEM CELLS 9 Today over 10 million potential donors have registered with DKMS and over 82,000 1. Peripheral Blood Stem Cell Collection 11 donations have taken place, to give people a second chance at life. New hope opens up for 2. Bone Marrow Collection 13 patients worldwide, as our international registry of donors expands both in size and ethnic diversity, meaning that currently 20 people per day get that second chance at life. FREQUENTLY ASKED QUESTIONS 15 Thank you for making the commitment to saving lives. -
Skin Grafting in the Dog Elroy C
Volume 19 | Issue 3 Article 1 1957 Skin Grafting in the Dog Elroy C. Jensen Iowa State College Follow this and additional works at: https://lib.dr.iastate.edu/iowastate_veterinarian Part of the Small or Companion Animal Medicine Commons, and the Veterinary Anatomy Commons Recommended Citation Jensen, Elroy C. (1957) "Skin Grafting in the Dog," Iowa State University Veterinarian: Vol. 19 : Iss. 3 , Article 1. Available at: https://lib.dr.iastate.edu/iowastate_veterinarian/vol19/iss3/1 This Article is brought to you for free and open access by the Journals at Iowa State University Digital Repository. It has been accepted for inclusion in Iowa State University Veterinarian by an authorized editor of Iowa State University Digital Repository. For more information, please contact [email protected]. SKIN GRAFTING In The Dog Elroy C. J,ensen, D.V.M. THERE are several histological factors the arm instead of from the forehead. which have made skin grafting pos This technique is now known as the Ital sible in man and animals. First, the com ian method of rhinoplasty. Free skin parative ease which epithelium can regen grafting started early in the 19th century erate is a factor. This new growth of tis by two charlatans which is related by sue occurs either from the periphery of a Baroni, the physi'Ologist, "A woman wound or it may result from proliferation named Gamba Curat, in order to show of the external root sheath of the hair the efficiency of an ointment she was sel follicles providing the dermis has not been ling, cut a piece of skin from her thigh completely destroyed. -
Role of Ia-Like Products of the Main Histocompatibility Complex in Conditioning Skin Allograft Survival in Man
Role of Ia-Like Products of the Main Histocompatibility Complex in Conditioning Skin Allograft Survival in Man J. Dausset, … , T. Meo, F. T. Rapaport J Clin Invest. 1979;63(5):893-901. https://doi.org/10.1172/JCI109389. Research Article This report correlates the survival time of 93 intrafamilial skin allografts performed under conditions of main histocompatibility complex (HLA) haploidentity with donor-recipient compatibility for products of the HLA-A, -B, -C, and - DR, as well as C3 proactivator, Glyoxalase I, and P loci located on the human 6th chromosome. Incompatibilities for HLA- A and -B (and to a lesser extent for HLA-C) and(or) for HLA-DR products exerted a strong influence upon the fate of skin allografts. When HLA-A and -B were considered alone, the most compatible group of grafts had a mean survival time of 15.8 d, as compared with 11.3 d for the most incompatible transplants. HLA-DR compatibility alone was associated with a mean survival time of 15.3 d, whereas HLA-DR-incompatible grafts had a mean survival time of 11.5 d. Incompatibilities for C3 proactivator, Glyoxalase I, and P did not have a significant effect upon graft survival. There was no evidence of an association between donor-recipient incompatibility at HLA-A, -B, or -C or at HLA-DR; such incompatibilities occurred independently of each other, in spite of the state of linkage disequilibrium known to exist between HLA-B and -DR. Incompatibilities for HLA-A, -B, and for HLA-DR exerted a potent additive effect upon graft survival.