Pancreatic Islet Cell Transplantation Annual Review Date: 01/26/2021 - Autologous Last Revised Date: 01/26/2021 - Allogeneic
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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 -
Rapidly Growing Epstein-Barr Virus-Associated Pulmonary Lymphoma After Heart Transplantation
Eur Respir J., 1994, 7, 612–616 Copyright ERS Journals Ltd 1994 DOI: 10.1183/09031936.94.07030612 European Respiratory Journal Printed in UK - all rights reserved ISSN 0903 - 1936 CASE REPORT Rapidly growing Epstein-Barr virus-associated pulmonary lymphoma after heart transplantation M. Schwend*, M. Tiemann**, H.H. Kreipe**, M.R. Parwaresch**, E.G. Kraatz+, G. Herrmann++, R.P. Spielmann$, J. Barth* Rapidly growing Epstein-Barr virus-associated pulmonary lymphoma after heart trans- Dept of *Internal Medicine, **Hemato- plantation. M. Schwend, M. Tiemann, H.H. Kreipe, M.R. Parwaresch, E.G. Kraatz, G. pathology, +Cardiovascular Surgery, Herrmann, R.P. Spielmann, J. Barth. ERS Journals Ltd 1994. ++Cardiology, and $Radiographic Diagnostics, ABSTRACT: There is strong evidence to show an association of Epstein-Barr virus Christian-Albrechts-University of Kiel, Kiel, Germany. (EBV) infection with the development of post-transplant lymphoproliferative dis- ease. We report the rapid development of a malignant lymphoma in a heart trans- Correspondence: J. Barth plant recipient, which occurred within less than eight weeks. I. Medizinische Universitätsklinik The diagnosis of this malignant high grade B-cell lymphoma was established by Schittenhelmstr. 12 open lung biopsy, and classified as centroblastic lymphoma of polymorphic subtype. D-24105 Kiel Immunohistochemically, the lymphoma showed reactivity with the B-cell markers Germany L-26 (CD20) and Ki-B5 and with the activation marker Ber-H2 (CD30). Furthermore, an expression of the bcl-2 oncoprotein was detected. Monoclonal JH gene rearrange- Keywords: Epstein-Barr virus ment was demonstrated by polymerase chain reaction (PCR), indicating monoclonal heart transplantation pulmonary lymphoma proliferation of B-blasts. -
MSBCBS Prior Authorization List: Codes to Be Deleted 9/27/10
MSBCBS Prior Authorization List: Codes to be Deleted 9/27/10 FOREHEAD FLAP WITH PRESERVATION OF VASCULAR PEDICLE (EG, AXIAL PATTERN 1 15731 FLAP) ABLATION, CRYOSURGICAL, OF FIBROADENOMA, INCLUDING ULTRASOUND 2 19105 GUIDANCE, EACH FIBROADENOMA COMPUTER-ASSISTED SURGICAL NAVIGATIONAL PROCEDURE FOR MUSCULOSKELETAL PROCEDURES, IMAGE-LESS (LIST SEPARATELY IN ADDITION TO CODE FOR PRIMARY 3 20985 PROCEDURE) 4 21125 AUGMENTATION, MANDIBULAR BODY OR ANGLE; PROSTHETIC MATERIAL AUGMENTATION, MANDIBULAR BODY OR ANGLE; WITH BONE GRAFT, ONLAY OR 5 21127 INTERPOSITIONAL (INCLUDES OBTAINING AUTOGRAFT) 6 21137 REDUCTION FOREHEAD; CONTOURING ONLY REDUCTION FOREHEAD; CONTOURING AND APPLICATION OF PROSTHETIC MATERIAL 7 21138 OR BONE GRAFT (INCLUDES OBTAINING AUTOGRAFT) REDUCTION FOREHEAD; CONTOURING AND SETBACK OF ANTERIOR FRONTAL SINUS 8 21139 WALL 9 21210 GRAFT, BONE; NASAL, MAXILLARY AND MALAR AREAS (INCLUDES OBTAINING GRAFT) 10 21215 GRAFT, BONE; MANDIBLE (INCLUDES OBTAINING GRAFT) ARTHROPLASTY, TEMPOROMANDIBULAR JOINT, WITH OR WITHOUT AUTOGRAFT 11 21240 (INCLUDES OBTAINING GRAFT) 12 21740 RECONSTRUCTIVE REPAIR OF PECTUS EXCAVATUM OR CARINATUM; OPEN RECONSTRUCTION REPAIR OF PECTUS EXCAVATUM OR CARINATUM; MINIMALLY 13 21742 INVASIVE APPROACH (NUSS PROCEDURE), WITHOUT THORACOSCOPY RECONSTRUCTIVE REPAIR OF PECTUS EXCAVATUM OR CARINATUM; MINIMALLY 14 21743 INVASIVE APPROACH (NUSS PROCEDURE), WITH THORACOSCOPY EXTRACORPOREAL SHOCK WAVE, HIGH ENERGY, PERFORMED BY A PHYSICIAN, REQUIRING ANESTHESIA OTHER THAN LOCAL, INCLUDING ULTRASOUND GUIDANCE, 15 28890 INVOLVING -
CIBMTR Scientific Working Committee Research Portfolio July 1, 2018
CIBMTR Scientific July 1, Working Committee 2018 Research Portfolio Milwaukee Campus Minneapolis Campus Medical College of Wisconsin National Marrow Donor Program/ 9200 W Wisconsin Ave, Suite Be The Match – 500 N 5th St C5500 Minneapolis, MN 55401-9959 USA Milwaukee, WI 53226 USA (763) 406-5800 (414) 805-0700 cibmtr.org CIBMTR Scientific Working Committee Research Portfolio: July 1, 2018 TABLE OF CONTENTS 1.0 OVERVIEW .................................................................................................................................................................. 1 1.1 Membership ........................................................................................................................................................... 2 1.2 Leadership .............................................................................................................................................................. 2 1.3 Productivity ............................................................................................................................................................ 3 1.4 How to Get Involved ............................................................................................................................................ 3 2.0 ACUTE LEUKEMIA WORKING COMMITTEE .................................................................................................. 6 2.1 Leadership ............................................................................................................................................................. -
Value of Donor–Specific Anti–HLA Antibody Monitoring And
CLINICAL RESEARCH www.jasn.org Value of Donor–Specific Anti–HLA Antibody Monitoring and Characterization for Risk Stratification of Kidney Allograft Loss † †‡ | Denis Viglietti,* Alexandre Loupy, Dewi Vernerey,§ Carol Bentlejewski, Clément Gosset,¶ † † †‡ Olivier Aubert, Jean-Paul Duong van Huyen,** Xavier Jouven, Christophe Legendre, † | † Denis Glotz,* Adriana Zeevi, and Carmen Lefaucheur* Departments of *Nephrology and Kidney Transplantation and ¶Pathology, Saint Louis Hospital and Departments of ‡Kidney Transplantation and **Pathology, Necker Hospital, Assistance Publique Hôpitaux de Paris, Paris, France; †Paris Translational Research Center for Organ Transplantation, Institut National de la Santé et de la Recherche Médicale, UMR-S970, Paris, France; §Methodology Unit (EA 3181) CHRU de Besançon, France; and |University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania ABSTRACT The diagnosis system for allograft loss lacks accurate individual risk stratification on the basis of donor– specific anti–HLA antibody (anti-HLA DSA) characterization. We investigated whether systematic moni- toring of DSA with extensive characterization increases performance in predicting kidney allograft loss. This prospective study included 851 kidney recipients transplanted between 2008 and 2010 who were systematically screened for DSA at transplant, 1 and 2 years post-transplant, and the time of post– transplant clinical events. We assessed DSA characteristics and performed systematic allograft biopsies at the time of post–transplant serum evaluation. At transplant, 110 (12.9%) patients had DSAs; post- transplant screening identified 186 (21.9%) DSA-positive patients. Post–transplant DSA monitoring im- proved the prediction of allograft loss when added to a model that included traditional determinants of allograft loss (increase in c statisticfrom0.67;95%confidence interval [95% CI], 0.62 to 0.73 to 0.72; 95% CI, 0.67 to 0.77). -
Time Course of Immune Recovery and Viral Reactivation Following Hematopoietic Stem Cell Transplantation
CLINICAL ARTICLES Cellular Therapy and Transplantation (CTT). Vol.5, No.4 (17), 2016 doi: 10.18620/ctt-1866-8836-2016-5-4-32-43 Submitted:02 November 2016, accepted: 09 December 2016 Time course of immune recovery and viral reactivation following hematopoietic stem cell transplantation 1Olga S. Pankratova, 2Alexei B. Chukhlovin 1Tampere University Hospital, Tampere, Finland 2R. Gorbacheva Memorial Research Institute of Children Oncology, Hematology and Transplantation, The St. Petersburg State I. Pavlov Medical University CD8+ cells specific for cytomegalovirus (CMV), or Ep- Summary stein-Barr virus (EBV) rapidly expand in cases of CMV or EBV activation. Total depletion of innate and adaptive immune cell pop- ulations occurs after intensive chemotherapy and he- Despite recovery of absolute B-cell counts by day 30 matopoietic stem cell transplantation (HSCT) then fol- post-HSCT, their functions, i.e., antigen-specific anti- lowed by gradual recovery of immune populations, due body production, are reduced for months and years after to progenitors derived from donor hematopoietic cells HSCT, due to slow restoration of mature immune cell which differentiate to myeloid and lymphoid lineages. populations, thus resemling normal evolution of B cell Time dynamics of immune reconstitution and differen- hierarchy in human organism. tial maturation of distinct immune populations is only partially evaluated, especially, at early terms post-trans- Reactivation of herpesviruses (mostly, CMV, EBV and plant. E.g., innate immunity is restored within 1st month Herpes Simplex) is a known feature of immune de- after HSCT, due to rapid reconstitution of granulocytes, ficiency. Timing of maximal herpesvirus incidence monocytes, and natural killer (NK) cells. -
Comprehensive Review of the Role of Rituximab in Pediatric Cardiac Transplantation
Central Journal of Pharmacology & Clinical Toxicology Review Research *Corresponding author Alfred Asante-Korang, Division of Cardiology, Johns Hopkins All Children’s Hospital, 601 5th Street South, Saint Comprehensive Review of the Petersburg, Florida 33701, Tel: 1-727-767-4772; Email: [email protected] Submitted: 22 June 2020 Role of Rituximab in Pediatric Accepted: 07 July 2020 Published: 10 July 2020 Cardiac Transplantation ISSN: 2333-7079 Copyright Amy L. Kiskaddon1 and Alfred-Asante Korang2* © 2020 Kiskaddon AL, et al. 1Department of Pharmacy, Johns Hopkins All Children’s Hospital, USA OPEN ACCESS 2Division of Cardiology, Johns Hopkins All Children’s Hospital, USA Keywords • Rituximab Abstract • Pediatric cardiac transplantation Rituximab is a chimeric anti-CD20 monoclonal antibody approved for the treatment of CD20 positive B cell malignancies. In the transplant context, rituximab has been used to prevent and treat antibody-mediated allograft rejection, minimize systemic toxicities secondary to chemotherapy, treat autoimmune anemias, and as a strategy for managing post-transplant lymphoproliferative disorders (PTLD). However, information in the pediatric cardiac transplant patient population is limited. This review summarizes the use of rituximab in the pediatric cardiac transplant population. ABBREVIATIONS polyangiitis, and pemphigus vulgaris. Generally, a rituximab dose of 375 mg/m2 weekly, depending on the indication it is utilized ADCC: Antibody-Dependent Cell Mediated Cytotoxicity; AIC: for, and has minimal reported side effects -
Chapter 118: Transplantation-Related Malignancies
CHAPTER 118 — REFERENCES 1. Bhatia S, Ramsay NK, Steinbuch M, et al. Malignant neoplasms following 30. Ellis NA, Huo D, Yildiz O, et al. MDM2 SNP309 and TP53 Arg72Pro in- bone marrow transplantation. Blood 1996;87:3633–3639. teract to alter therapy-related acute myeloid leukemia susceptibility. Blood 2. Witherspoon RP, Fisher LD, Schoch G, et al. Secondary cancers after bone 2008;112:741–749. marrow transplantation for leukemia or aplastic anemia. N Engl J Med 31. Casorelli I, Offman J, Mele L, et al. Drug treatment in the development 1989;321:784–789. of mismatch repair defective acute leukemia and myelodysplastic syndrome. 3. Curtis RE, Rowlings PA, Deeg HJ, et al. Solid cancers after bone marrow DNA Repair (Amst) 2003;2:547–559. transplantation. N Engl J Med 1997;336:897–904. 32. Seedhouse CH, Das-Gupta EP, Russell NH. Methylation of the hMLH1 4. Krishnan A, Bhatia S, Slovak ML, et al. Predictors of therapy-related leuke- promoter and its association with microsatellite instability in acute myeloid mia and myelodysplasia following autologous transplantation for lymphoma: leukemia. Leukemia 2003;17:83–88. an assessment of risk factors. Blood 2000;95:1588–1593. 33. Seedhouse C, Faulkner R, Ashraf N, et al. Polymorphisms in genes involved 5. Rowlings PA, Curtis RE, Passweg JR, et al. Increased incidence of Hodg- in homologous recombination repair interact to increase the risk of develop- kin’s disease after allogeneic bone marrow transplantation. J Clin Oncol ing acute myeloid leukemia. Clin Cancer Res 2004;10:2675–2680. 1999;17:3122–3127. 34. Matullo G, Palli D, Peluso M, et al. -
Autotransplantation of the Third Molar: a Therapeutic Alternative to the Rehabilitation of a Missing Tooth: a Scoping Review
bioengineering Review Autotransplantation of the Third Molar: A Therapeutic Alternative to the Rehabilitation of a Missing Tooth: A Scoping Review Mario Dioguardi 1,* , Cristian Quarta 1 , Diego Sovereto 1, Giuseppe Troiano 1 , Michele Melillo 1, Michele Di Cosola 1, Angela Pia Cazzolla 1 , Luigi Laino 2 and Lorenzo Lo Muzio 1 1 Department of Clinical and Experimental Medicine, University of Foggia, Via Rovelli 50, 71122 Foggia, Italy; [email protected] (C.Q.); [email protected] (D.S.); [email protected] (G.T.); [email protected] (M.M.); [email protected] (M.D.C.); [email protected] (A.P.C.); [email protected] (L.L.M.) 2 Multidisciplinary Department of Medical-Surgical and Odontostomatological Specialties, University of Campania “Luigi Vanvitelli”, 80121 Naples, Italy; [email protected] * Correspondence: [email protected] Abstract: Introduction: Tooth autotransplantation is the repositioning of an erupted, partially erupted, or non-erupted autologous tooth from one site to another within the same individual. Several factors influence the success rate of the autotransplant, such as the stage of root development, the morphology of the tooth, the surgical procedure selected, the extraoral time, the shape of the recipient socket, the vascularity of the recipient bed, and the vitality of the cells of the periodontal ligament. The aim of this scoping review was to provide the most up-to-date information and data on the clinical principles of the third-molar autograft and thus provide clinical considerations for its success. Citation: Dioguardi, M.; Quarta, C.; Materials and methods: This review was conducted based on PRISMA-ScR (Preferred Reporting Sovereto, D.; Troiano, G.; Melillo, M.; Items for Systematic reviews and Meta-Analyses extension for Scoping Reviews). -
A Nationwide Analysis of Kidney Autotransplantation
A Nationwide Analysis of Kidney Autotransplantation ZHOBIN MOGHADAMYEGHANEH, M.D., MARK H. HANNA, M.D., REZA FAZLALIZADEH, M.D., YOSHITSUGU OBI, M.D., PH.D., CLARENCE E. FOSTER, M.D., MICHAEL J. STAMOS, M.D., HIROHITO ICHII, M.D., PH.D. From the Department of Surgery, University of California, Irvine, School of Medicine, Orange, California There are limited data regarding outcomes of patients underwent kidney autotransplantation. This study aims to investigate outcomes of such patients. The nationwide inpatient sample database was used to identify patients underwent kidney autotransplantation during 2002 to 2012. Multivariate analyses using logistic regression were performed to investigate morbidity predictors. A total of 817 patients underwent kidney autotransplantation from 2002 to 2012. The most common indication of surgery was renal artery pathology (22.7%) followed by ureter pathology (17%). Overall, 97.7 per cent of operations were performed in urban teaching hospitals. The number of procedures from 2008 to 2012 were significantly higher compared with the number of them from 2002 to 2007 (473 vs 345, P < 0.01). The overall mortality and morbidity of patients were 1.3 and 46.2 per cent, respectively. The most common postoperative complications were transplanted kidney failure (10.7%) followed by hemorrhagic complications (9.7%). Obesity [adjusted odds ratio (AOR): 9.62, P < 0.01], fluid and electrolyte disorders (AOR: 3.67, P < 0.01), and preoperative chronic kidney disease (AOR: 1.80, P 5 0.03) were predictors of morbidity in patients. In conclusion, Kidney autotransplantation is associated with low mortality but a high morbidity rate. The most common indications of kidney autotransplantation are renal artery and ureter pathologies, respectively. -
Outpatient Immunosuppressive Drugs Under Medicare
Outpatient Immunosuppressive Drugs Under Medicare July 1991 OTA-H-452 NTIS order #PB92-117720 Recommended Citation: U.S. Congress, Office of Technology Assessment, Outpatient Immunosuppressive Drugs Under Medicare, OTA-H-452 (Washington, DC: U.S. Government Printing Office, Septem- ber 1991). For sale by the U.S. Government Printing Office Superintendent of Documents, Mail Stop: SSOP, Washington, DC 20402-9328” ISBN 0-16 -035315-7 Foreword Of all the astonishing achievements of modern medicine, the ability to successfully transplant a living organ from one human being to another is perhaps one of the most awesome. Immunosuppressive drugs are one of the spectrum of technological advances that have made organ transplants an everyday phenomenon. At the same time, however, transplant recipients’ needs for these drugs have presented Medicare with a continuing policy dilemma, because Medicare does not usually pay for outpatient prescription drugs. In 1984, the year after cyclosporine made its debut onto the health care market, OTA reported to Congress on the likely benefits of the drug for Medicare kidney transplant recipients. The present report, requested by the Senate Committee on Finance in the wake of the repeal of the Medicare Catastrophic Coverage Act, examines Medicare’s current immunosuppressive drug coverage dilemma and the policy tradeoffs it entails for the 1990s. OTA reports would not be possible without the assistance and input of a wide variety of individuals from both the public and the private sectors. OTA staff and contractors gratefully acknowledge the contributions of the many people who provided data, clarified facts, presented views, and reviewed the drafts of this report. -
Xenotransplantation of Ovarian Tissue Into Male
XENOTRANSPLANTATION OF OVARIAN TISSUE INTO MALE IMMUNODEFICIENT MICE by HUGO JOSE HERNANDEZ FONSECA (Under the direction of BENJAMÍN G. BRACKETT) ABSTRACT A male immunodeficient mouse model for transplantation of ovarian tissue was investigated. Bovine and human ovarian tissues were surgically placed either under the kidney capsule or in the subcutaneous spaces of male non obese diabetic (NOD) severe combined immunodeficient (SCID) mice. Time intervals required for development of growing follicles were determined for neonatal and adult bovine ovarian tissue grafts. This interval was much shorter (P <0.01) in adult tissue than in one-week-old calf tissue, i.e. 55 vs 124 days. The increase in the proportion of growing follicles was coincidental with a decrease in the proportion of resting follicles. This increment in the growing follicle populations took place abruptly and was significant by 55 days and by 124 days after transplantation in the adult cow and calf ovarian grafts, respectively. Recovery of oocytes from bovine ovarian grafts was successful. Several immature oocytes were recovered and evidence of maturation in one oocyte was obtained after 24 hours of in vitro maturation. Treatment of host mice with an FSH:LH preparation increased follicular development but did not enhance oocyte recovery rates. Human ovarian tissue grafted under the kidney capsule of intact male NOD SCID mice showed a greater proportion of growing follicles than similar grafts transplanted to the kidney of castrated hosts and to the subcutaneous space of intact hosts. However, no differences in follicular growth and development were detected between the intact/ kidney capsule and the castrated / subcutaneous groups.