Literature DB >> 20052750

Systemic AL amyloidosis with acquired factor X deficiency: A study of perioperative bleeding risk and treatment outcomes in 60 patients.

Carrie A Thompson1, Robert Kyle, Morie Gertz, John Heit, Rajiv Pruthi, Animesh Pardanani.   

Abstract

Systemic light-chain (AL) amyloidosis may be associated with acquired factor X (FX) deficiency and optimal management of this coagulopathy is unknown. We reviewed our experience with 60 patients with isolated FX deficiency (< or =50%) due to AL amyloidosis that underwent an invasive procedure between 1975 and 2007. They were classified as having severe (<10%; n = 6), moderate (10-25%; n = 15), or mild (26-50%; n = 39) FX deficiency. The patients underwent a total of 112 procedures, 19 (17%) of which were managed with periprocedural treatment with one or more hemostatic agents. There were complications in 14 (13%) procedures (bleeding = 12, thrombosis = 1, death = 1). Baseline FX level was not predictive of bleeding risk; the only association with postintervention bleeding was central venous catheter placement. However, bleeding complications were relatively infrequent, particularly in patients with mild or moderate FX deficiency undergoing nonvascular procedures. Activated recombinant factor VII might be considered in patients undergoing major surgical procedures, but further experience is needed. Optimal management of AL patients with FX deficiency undergoing invasive procedures remains to be determined. 2009 Wiley-Liss, Inc.

Entities:  

Mesh:

Substances:

Year:  2010        PMID: 20052750      PMCID: PMC2896569          DOI: 10.1002/ajh.21603

Source DB:  PubMed          Journal:  Am J Hematol        ISSN: 0361-8609            Impact factor:   10.047


  21 in total

Review 1.  Complications associated with the treatment of haemophiliacs with inhibitors.

Authors:  D Green
Journal:  Haemophilia       Date:  1999-09       Impact factor: 4.287

2.  Guidelines on the selection and use of therapeutic products to treat haemophilia and other hereditary bleeding disorders.

Authors: 
Journal:  Haemophilia       Date:  2003-01       Impact factor: 4.287

3.  Acquired factor X deficiency in patients with amyloid light-chain amyloidosis: incidence, bleeding manifestations, and response to high-dose chemotherapy.

Authors:  E B Choufani; V Sanchorawala; T Ernst; K Quillen; M Skinner; D G Wright; D C Seldin
Journal:  Blood       Date:  2001-03-15       Impact factor: 22.113

4.  Recombinant human factor VIIa in the management of amyloid-associated factor X deficiency.

Authors:  L Boggio; D Green
Journal:  Br J Haematol       Date:  2001-03       Impact factor: 6.998

5.  Bleeding symptoms and coagulation abnormalities in 337 patients with AL-amyloidosis.

Authors:  A D Mumford; J O'Donnell; J D Gillmore; R A Manning; P N Hawkins; M Laffan
Journal:  Br J Haematol       Date:  2000-08       Impact factor: 6.998

Review 6.  Continuous infusion of coagulation factors.

Authors:  A Batorova; U Martinowitz
Journal:  Haemophilia       Date:  2002-05       Impact factor: 4.287

7.  A prospective study of recombinant activated factor VII administered by continuous infusion to inhibitor patients undergoing elective major orthopaedic surgery: a pharmacokinetic and efficacy evaluation.

Authors:  Christopher A Ludlam; Mark P Smith; Massimo Morfini; Alessandro Gringeri; Elena Santagostino; Geoffrey F Savidge
Journal:  Br J Haematol       Date:  2003-03       Impact factor: 6.998

8.  Central venous access devices for paediatric patients with haemophilia: a single-institution experience.

Authors:  R Titapiwatanakun; C Moir; R K Pruthi; P L Stavlo; K A Schmidt; V Rodriguez
Journal:  Haemophilia       Date:  2009-01       Impact factor: 4.287

9.  Complications of central venous access devices in paediatric haemophilia patients.

Authors:  J A Domm; M G Hudson; R L Janco
Journal:  Haemophilia       Date:  2003-01       Impact factor: 4.287

Review 10.  Successful perioperative management of factor X deficiency associated with primary amyloidosis.

Authors:  Kazuaki Takabe; Peter R Holman; Kenneth D Herbst; Catherine A Glass; Michael Bouvet
Journal:  J Gastrointest Surg       Date:  2004 Mar-Apr       Impact factor: 3.452

View more
  20 in total

1.  Prolonged PT and aPTT in a patient with severe proteinuria.

Authors:  Irene Motta; Andrea Artoni; Margherita Migone De Amicis; Cinzia Hu; Maria Domenica Cappellini
Journal:  Intern Emerg Med       Date:  2013-08-09       Impact factor: 3.397

2.  Hemorrhage because of amyloid-related factor X deficiency after insertion of Tenckhoff catheter.

Authors:  G Harman; B B McCormick
Journal:  Perit Dial Int       Date:  2012 Sep-Oct       Impact factor: 1.756

3.  Factoring in the missing link.

Authors:  Nilay Sethi; Reza Sedighi Manesh; Adam Sperling; Scott C Bresler; Nathan T Connell; Lawrence M Tierney
Journal:  Am J Hematol       Date:  2016-08-22       Impact factor: 10.047

Review 4.  Prothrombin Complex Concentrates for Bleeding in the Perioperative Setting.

Authors:  Kamrouz Ghadimi; Jerrold H Levy; Ian J Welsby
Journal:  Anesth Analg       Date:  2016-05       Impact factor: 5.108

5.  Management of rare acquired bleeding disorders.

Authors:  Marzia Menegatti; Eugenia Biguzzi; Flora Peyvandi
Journal:  Hematology Am Soc Hematol Educ Program       Date:  2019-12-06

6.  Outcome of patients with severe AL amyloidosis and biopsy-proven renal involvement ineligible for bone marrow transplantation.

Authors:  Roberta Fenoglio; Simone Baldovino; Michela Ferro; Savino Sciascia; Gianluca Rabajoli; Giacomo Quattrocchio; Giulietta Beltrame; Carla Naretto; Daniela Rossi; Mirella Alpa; Antonella Barreca; Mario Giulio Papotti; Dario Roccatello
Journal:  J Nephrol       Date:  2020-05-29       Impact factor: 3.902

7.  The amyloidoses: clinical features, diagnosis and treatment.

Authors:  Kelty R Baker; Lawrence Rice
Journal:  Methodist Debakey Cardiovasc J       Date:  2012 Jul-Sep

8.  Coagulation and fibrinolytic features in AL amyloidosis with abnormal bleeding and usefulness of tranexamic acid.

Authors:  Masahisa Arahata; Hiroyuki Takamatsu; Eriko Morishita; Yasuko Kadohira; Shinya Yamada; Akitada Ichinose; Hidesaku Asakura
Journal:  Int J Hematol       Date:  2020-01-03       Impact factor: 2.490

9.  Systemic immunoglobulin light-chain amyloidosis presenting hematochezia as the initial symptom.

Authors:  Tetsuo Kon; Naoki Nakagawa; Fumitsugu Yoshikawa; Kazunao Haba; Nagako Kitagawa; Michihiro Izumi; Setsuo Kumazaki; Satoshi Ishida; Ryuichi Aikawa
Journal:  Clin J Gastroenterol       Date:  2016-06-18

10.  Factor X deficiency: an uncommon presentation of AL amyloidosis.

Authors:  Ajaydas T Manikkan
Journal:  Ups J Med Sci       Date:  2012-06-01       Impact factor: 2.384

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.