A Large Case Series On Surgical Outcomes In Congenital Factor XIII Deficiency Patients In Iran

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Curriculum Vitae - European Medicines Agency

22 Dec 2020 Willebrand disease who are undergoing elective surgery: Reply. congenital thrombotic thrombocytopenic purpura. patient with factor XIII deficiency and recurrent pregnancy loss. pregnancy in type 2B von Willebrand disease: case report and literature patients with severe Factor X deficiency in Iran.

Women With Congenital Hypofibrinogenemia/Afibrinogenemia

by Y Zhang 2020 Cited by 3 107 children with congenital factor deficiencies (including hemophilia, FIB tectable FIB.16 A large Iranian cohort depicted clinical bleed-.

APPLICATION FOR THROMBOSIS VASCULAR TRAINING

Case Series on Surgical. Outcomes in Congenital FXIII Deficiency Patients in Iran. Bleeding and for Surgery in Patients with Congenital Fibrinogen Deficiency. XXVI ISTH abortions: a case report and review of literature. XXVI ISTH A Large-Scale Prospective Cohort Study on Factor XIII Deficiency in. Southeast of 

Review Series - Regione Lazio

26 Mar 2015 of coagulation factors fibrinogen, factor (F)II, FV, combined FV and FVIII, FVII, FX, FXI, FXIII, and congenital deficiency of case of severe bleeding or major surgery, higher prothrombin levels are have a high incidence (16%) in a series of 75 patients.47 Thrombotic Consanguineous marriage in Iran.

Evaluating for Suspected Child Abuse: Conditions That

25 Mar 2013 expensive and, in the case of young children with limited total blood The list of congenital and acquired bleeding disorders that could iciency, factor XIII and other factor deiciencies, thrombocytopenia, 9.1%.25 The largest series to date of patients' test results will fall below Factor XIII Deficiency.

VOLUME 35 - Carver College of Medicine - The University of

Results 59 - 1119 Asymmetric Bilateral Hip Dislocations: A Case Report and Historical Prenatal Ultrasound Diagnosis of Congenital Talipes Equinovarus in Health Literacy in Patients Seeking Orthopaedic Care: Results of the strength deficiency as compared to non-surgical treat- Iranian Journal of Orthopaedic.

www.SID.ir

by M Shamsizadehe 2016 Cited by 9 Factor XIII Deficiency Treated Prophylactically with Fibrogammin P® Allied Medical Sciences, Iran University of Medical Sciences, Tehran, Iran Congenital FXIIID is a rare but severe and bleeding episodes, most patients receive province has the largest population of patients Once a case referred.

Treatment of rare factor deficiencies other than hemophilia

24 Oct 2019 disease, RCDs are much less prevalent, ranging from 1 case ated by a complex series of cascade reactions involving different congenital factor deficiencies for whom no alternative, spe- study carried out on patients with FVII deficiency and over a large congenital factor XIII deficiency: clinical.

57 Annual Scientific and Standardization Committee Meeting

23 Jul 2011 products in surgical patients - Schulman S, Angeras, Bergqvist, Eriksson, Lassen, What to do in case of bleeding? associated with congenital fibrinogen deficiencies; plasma-derived Congenital coagulation factor XIII (FXIII) Fortunately in the last few years larger case series have been reported and.

The role of fibrinogen and fibrinogen concentrate in cardiac

by G Erdoes 2019 Cited by 21 cardiopulmonary bypass in patients and procedures with a high risk of bleeding appears to be a conditions, such as deficiencies of factor VIII, factor XIII and.

Inhibitors in Patients with Congenital Bleeding - CORE

Cited by 8 in particular on those developing in patients with congenital deficiency of coagulation factor V, factor VII, factor XI, and factor XIII. Issue Theme Alloantibodies and.

Hemophilia in Iran - Taylor & Francis Online

by A Dorgalaleh 2016 Cited by 32 Results and discussion: There are 5369 patients with HA and HB in Iran among which Conclusion: Although this study was performed in Iranian patients, the large XIII. Table 1 Number of patients with hemophilia in different parts of Iran​11 17 with common bleeding disorders had a severe degree of factor deficiency.

(NCCN) Breast Cancer Clinical Practice Guidelines

15 Jul 2020 Case Comprehensive Cancer Center/ Footnote ss added: In select patients with high-risk features Added to Breast Cancer Index treatment implications: Results BINV-13 l See Surgical Axillary Staging (BINV-D). p See Principles of Breast NCCN Task Force Report: Bone Health In Cancer Care.

Recombinant FXIII (rFXIII-A2) - Home - Thieme Connect

by M Carcao 2018 Cited by 14 surgery. Abstract. Recombinant factor XIII-A2 (rFXIII-A2) was in patients with congenital FXIII A-subunit deficiency. mentor™2 recessive coagulation disorder with a high risk of life-threa- this is particularly the case in Iran, which has the highest Here, we report the long-term safety and efficacy results 

Volume 1a - National Blood Authority

2 Jul 2011 Technical report on perioperative patient blood management surgery, is anaemia an independent risk factor for adverse outcomes? perioperative patient blood management Volume 1a. July 2011 xiii evidence relevant to both critical bleeding/massive transfusion and established iron deficiency.

Perioperative laboratory monitoring in congenital haemophilia

by DP Hart 2019 haemophilia patients with inhibitors undergoing surgery. This topic has also been​. 27 addressed in case studies and series, including a case 

Management of severe perioperative bleeding: guidelines

by SA Kozek-Langenecker 2017 Cited by 548 Rio Hortega, Valladolid, Spain (CA), Department of General Surgery, Lithuanian University of Health 1.11 Patients with congenital bleeding disorders intervention in the case of perioperative bleeding. 1C and factor XIII deficiency are predictive of bleeding same series of key clinical questions about the manage-.

Instructions for use 'Template Research Protocol' - Clinical Trials

5 Jul 2017 Rationale: Rare bleeding disorders (deficiency of fibrinogen, factor II, V, V&VIII, VII, X, XI, registered in comprehensive registries in Iran, Italy and the United In a case series of 13 patients 15% of patients had epistaxis, menorrhagia in females) and post-traumatic bleeding following surgery or delivery,.

Rare congenital bleeding disorders - Annals of Translational

23 Aug 2018 in 500,000 for factor VII up to one in 2,000,000 for factor XIII in the general population. Patients one case in 2 3 million for FII and FXIII deficiencies (the rarest) to In the case of abnormal results of the disorders and consanguinity are high (10). a series of 75 patients with FVII deficiency (37), but this.

Case Report Recurrent Hematomas following a Revision Total

by Y Takashima 2019 Arthroplasty in Acquired Coagulation Factor XIII Deficiency Department of Orthopaedic Surgery, Kobe University Graduate School of In this case report, we describe a patient with recurrent hematomas, 67g/L, but her coagulation test results remained within congenital or an acquired illness.

Inhibitors in Patients with Congenital Bleeding Disorders Other Than

in particular on those developing in patients with congenital deficiency of coagulation congenital FV deficiency and a high-titer (6 BU) inhibitor who fresh frozen plasma; FV, factor V; FVII, factor VII; FXI, factor XI; FXIII, factor XIII; ITI, bleeding during menstruation, but case series of women Results from a genotype-.

(1946 to present); Embase

3 Mar 2018 Management of a patient with factor XI deficiency with inhibitors undergoing cardiac surgery: A case report and review of the literature.

Management of Inherited Bleeding Disorders in Pregnancy

by GG No 2017 Aim for factor VIII/IX levels of at least 0.5 iu/ml to cover surgical or invasive woman who should be advised to report any increase in postpartum blood loss. P Patients with factor XI deficiency should be assessed for the presence of During pregnancy, increased intensity prophylaxis is required using factor XIII plasma.

SO2-D2.1.2 Priority List of COVID-19 Adverse events of

11 Jan 2021 From Aug 7 through Nov 13, 3 separate searches were run; yielding 3901 COVID cases); 1 case report of fatal outcome of a patient with common variable A large meta-analysis including 40 studies and 24,527 patients (Shao) Persistent hiccups in a patient with mild congenital factor V deficiency.

NMRC Annual Report 2003 - National Medical Research

Department of Experimental Surgery (SGH) Table 13: Commitments for CPRG by type of research, FY2003 Research outcomes have grown steadily since the inception of the IRG. The made in CELL, a prestigious US-based scientific journal of high impact factor Cancer patients with DPD deficiency were found to​.

New developments in the management of - CiteSeerX

by Z Fadoo 2013 Cited by 37 Abstract: Congenital Factor XIII (FXIII) deficiency is a rare, inherited, compound heterozygosity is observed.7 10 High rates of consanguineous A recent case-​series report at a tertiary care hospital in the region identified ten the severity of the disease in patients deficient in FXIII.24 26 presentation and outcome.

Read by TiTle - Karger Publishers

by PM Mannucci 2009 THROMbiN GeNeRaTiON iN CaSe OF FaCTOR Xi deFiCieNCy. M. Sassi, H. Patients and Methods: We included 13 patients with record of disorders of of Surgery and Orthopedics, Botucatu Medical School - UNESP, Sao Paulo Results: Fourty-one of these patients (27.5%) had associated high risk conditions​.

THYROID DISORDERS - Kementerian Kesihatan Malaysia

Patients with overt Graves' hyperthyroidism should be treated with any of the following where there is lack of access to a high-volume thyroid surgeon. Subacute MANAGEMENT OF THYROID DISORDERS. 13. Dr. Norasyikin A. Wahab on grey scale ultrasound in 100% of their case series (n=22).221 (​Level III).

Aspects on bleeding and transfusion in elective - GUPEA

by M Carling 2015 Results: An association was found between low fibrinogen concentration and large perioperative bleeding and RBC transfusion for scoliosis surgery patients Keywords: orthopaedic surgery, fibrinogen, factor XIII, surgical bleeding, In patients with a suspected congenital or acquired FXIII deficiency a low Iran., 2014.

A large case series on surgical outcomes in congenital factor

by M Naderi 2017 Cited by 3 A large case series on surgical outcomes in congenital factor. XIII deficiency patients in Iran J Thromb Haemost 2017; 15: 2300 5. Essentials.  

PDF-FA - Iranian Journal of Blood and Cancer

Clinical Trials: should contain patients' informed consent and the approval of the ethics Development in the management of congenital factor XIII deficiency with factor Hematopoietic stem cell transplantation results in Taleghani BMT center :​8 A case report of hypereosinophilic syndrome with FIP1L1-PDGFRA positive 

Scientific Programme Friday, 05. July 2019 Registration

5 Jul 2019 Platelet and Plasma Factor XIII Levels after Replacement Therapy in. Severe Congenital Factor XIII Deficiency: Origin of Platelets Factor XIII.

Congenital Bleeding Disorders amid the COVID-19 pandemic

This article reviews the current knowledges of congenital bleeding disorders factor XIII (FXIII) deficiency (2). previous haemostatic challenges (such as surgery, tooth Pooled results revealed that PT and D-Dimer patients with CBD from Iran was reported. a single case report from China has been published de-.

Approach to the Diagnosis and Management of Common

The evaluation of a patient presenting with bleeding symptoms riage, or surgery. A congenital bleeding disorder is often suspected when Postsurgical bleeding. 1 6. 28 toms reminiscent of severe hemophilia (e.g., in the case of Normal results can be seen with mild factor deficiencies, mild VWD, report (​USA).

INTRODUCTION AND OBJECTIVES - DiVA

by B Eslami 2013 CONGENITAL HEART DISEASE IN IRAN. Bahareh Eslami. All previously published papers were reproduced with permission from the publishers. Cover 

Abstracts from the 53rd European Society of Human - Nature

by R Maksimova 2020 E-P01.21. Recurrent congenital microcephaly: a case report genes, rather than hormone deficiency may effect the fate of pregnancy endothelial growth factor (​VEGF) during pregnancy as a possible least 1 in 13 patients, here we present the results of ana- Mazaheri's Medical Genetics lab Yazd, IRAN., Yazd, Iran,.

Immunoglobulin therapy for Myasthenia Gravis - Medical

Table 13 The functional or clinical categorical scales used to assess patients in Table 23 Adverse events in a case series receiving IVIg MG maintenance by the critical patient relevant outcomes in the key studies low doses or high doses of each therapy are compared, immunoglobulin is deficiency, active renal or.

Factor V Deficiency in Korean Patients - Journal of Korean

by YH Park 2016 Cited by 7 patients. Between January 1987 and December 2013, 10 case reports Life-​threatening bleeding episodes occurred in the peritoneal cavity Keywords: Factor V Deficiency; Republic of Korea; Treatment Outcome; sanguineous marriage are common (such as Iran and southern A total of 13 patients were identified.

Hemophilia, rodentophilia and humanity - DADUN

by J Hermida 2003 Cited by 8 Our results demonstrate at day 15 a mean reduction of Thrombosis Center, Department of Medical and Surgical Critical Care, University patients at high risk of bleeding or in patients over 75 years, if 2, PO Box 9600, 2300 RC Leiden, the Netherlands. Pattern of symptoms in 93 Iranian patients with severe factor XIII.

World report on vision - L'Organisation pour la Prévention de

This report makes the case that integrated people-centred eye care is the care intensive near vision activity (as a risk factor) and longer time spent premise that (i) the use of best corrected visual acuity overlooks a large Further studies report that patients who undergo cataract surgery in congenital glaucoma.

THE RARE COAGULATION DISORDERS - World Federation

by PHB Bolton-Maggs 2006 Cited by 15 The Treatment of Hemophilia series is intended to provide general information on the treatment Appendix 1: Clotting factor concentrates for rare bleeding disorders results, even in a severe coagulation disorder. Two large case series, one from deficiency in 35 Iranian patients. Br J. Haematol 1998; 103:​1067-9. 13.

Annex 4 Recommendations for the production, control and

Factor VIII. Blood coagulation factor VIII, deficient in patients with haemophilia A. Also called A (large-scale) process by which plasma is separated into individual conditions for patients or which results in, or prolongs, hospitalization or morbidity. of the blood, which are returned to the donor in a series of collection/.

EHA Scientific Conference on Bleeding Disorders, Barcelona

Results. Before surgery, patients showed significantly (p<0.005) higher PT ratio and higher fibrinogen Results. Overall considered, patients with congenital bleeding disorders showed XIII DEFICIENCY: IS THERE A ROLE FOR FACTOR XIII UPTAKE the whole case series, and of 4.6% in the series of patients with.

Congenital structural and functional fibrinogen disorders: a

23 Dec 2019 activated factor XIII.1 Fibrin, together with plate lets and red The first Polish case of dysfibrinogenemia, Fi brinogen the whole report, see Wypasek et al12). patients with severe fibrinogen deficiency have is common, for example, in Iran.4 As hypofibri thrombosis.13 In a large patient cohort, approx.

Lava Ahmed Talat Sharief (MBChB, MSc) July 2013 Submitted

Factor XIII (FXIII) deficiency is a rare bleeding disorder with an average frequency of case series have demonstrated an increase in the risk of miscarriage and among women and its associated reproductive outcomes using an electronic search on The frequency of bleeding in patients with congenital FXIII deficiency​.

Poster Presentation - Wiley Online Library

patients with mild FVII deficiency undergoing surgeries deficiency undergoing surgery or critical haemorrhage Results: The base-case assumptions yielded ICERs of factor VIII (FVIII) inhibitors are at high risk of congenital factor deficiencies who were followed up in severe factor XIII deficiency: a case report and.

Factor Deficiencies in Pregnancy - Hematology/Oncology Clinics

All patients with factor deficiencies should be registered with a hemophilia cular injections and surgery (eg, circumcision) should be delayed until the results are occurring in the uteroplacental bed.13 15 reported in a small Iranian series of 14 patients.27 congenital absence of prothrombin activity: case report.

2017 stroke in childhood - RCPCH

13 Heart Defects, Congenital/ 10 treatment outcome/or outcome assessment/ 64 (refer*3 or prevent* or treat* or management or surgical or medical or factor 8/or blood clotting factor 7/or blood clotting factor 7 deficiency/or blood clotting ischemic childhood stroke. Retrospective case series. 42 children with. AIS.

Scientific Programme Sunday, 12. July 2020 Plenary Session

12 Jul 2020 events in high-risk cardiovascular patients taking anticoagulant therapy with warfarin Inhibitor against Congenital Coagulation Factor XIII Deficiency: A Case Report Factor XII deficiency- a very rare coagulation disorder- case report Postoperative Outcomes in Cardiac Surgery: A Post-Hoc Analysis of 

Curriculum Vita

of Bleeding Episodes in Patients with Haemophilia and Inhibitors. Iran Red social factors on high prevalence of factor XIII deficiency in southeast Iran. Journal