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Published in: World Journal of Surgery 12/2011

01-12-2011

General Surgery in Patients With a Bleeding Diathesis: How We Do It

Authors: Kamal R. Aryal, D. Wiseman, Ajith K. Siriwardena, Paula H. B. Bolton-Maggs, Charles R. M. Hay, James Hill

Published in: World Journal of Surgery | Issue 12/2011

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Abstract

Background

This study was undertaken to assess perioperative management, postoperative complications, and the adequacy of perioperative plasma factor levels in a regional hemophilia center.

Methods

A total of 113 consecutive patients (75 men, 38 women; median age 48 years, range 18–86 years) with bleeding disorders undergoing general surgical and endoscopic procedures (144 procedures: 15 urgent, 129 elective) were reviewed. The episodes were identified from a prospectively collected database at a regional hemophilia center from 1998 to the end of 2008. In all, 46% of the surgical patients had hemophilia A, 38% had von Willebrand disease, 6% had hemophilia B, 5% had factor XI deficiency, and 4% had other disorders.

Results

Procedures carried out were endoscopic in 40%, minor in 25%, and intermediate and major in 35%. There were two postoperative deaths, both in patients undergoing urgent major procedures. Postoperative complications occurred after 7.6% (4.0% hemorrhagic, 3.6% nonhemorrhagic) of the procedures. Four of six patients with postoperative hemorrhage required further operative intervention. The median dose of clotting factor for Hemophilia A patients was 2240 U for endoscopic procedures, 7500 U for minor procedures, and 23,500 U for intermediate/major procedures. In hemophiliacs, the mean preoperative plasma factor level attained was 129 IU/dl (SD 16) in patients who developed postoperative hemorrhagic complications and 125 IU/dl (SD 37) in those who did not have bleeding, indicating that in no case was hemorrhage attributable to inadequate factor replacement.

Conclusions

General surgical and endoscopic procedures can be performed with low morbidity and mortality rates when there is appropriate factor replacement and good support from the hemophilia team.
Literature
2.
go back to reference Pool JG, Hershgold EJ, Pappenhagen AR (1964) High potency antihaemophilic factor concentrate prepared from cryoglobulin precipitate. Nature 203:312PubMedCrossRef Pool JG, Hershgold EJ, Pappenhagen AR (1964) High potency antihaemophilic factor concentrate prepared from cryoglobulin precipitate. Nature 203:312PubMedCrossRef
3.
go back to reference Krieger JN, Hilgartner MW, Redo SF (1977) Surgery in patients with congenital disorders of blood coagulation. Ann Surg 185:290–294PubMedCrossRef Krieger JN, Hilgartner MW, Redo SF (1977) Surgery in patients with congenital disorders of blood coagulation. Ann Surg 185:290–294PubMedCrossRef
4.
go back to reference Brown B, Steed DL, Webster MW et al (1986) General surgery in adult haemophiliacs. Surgery 99:154–159PubMed Brown B, Steed DL, Webster MW et al (1986) General surgery in adult haemophiliacs. Surgery 99:154–159PubMed
5.
go back to reference Anscombe AR (1970) Surgery in haemophilia and allied disorders. Ann R Coll Surg Engl 47:125–138PubMed Anscombe AR (1970) Surgery in haemophilia and allied disorders. Ann R Coll Surg Engl 47:125–138PubMed
6.
go back to reference Rudowski W (1981) Major surgery in haemophilia. Ann R Coll Surg Engl 65:111–117 Rudowski W (1981) Major surgery in haemophilia. Ann R Coll Surg Engl 65:111–117
7.
go back to reference Sadler JE (1994) A revised classification of von Willebrand disease for the subcommittee on von Willebrand factor of the scientific and standardization committee of the international society on thrombosis and haemostasis. Thromb Haemost 71:520–525PubMed Sadler JE (1994) A revised classification of von Willebrand disease for the subcommittee on von Willebrand factor of the scientific and standardization committee of the international society on thrombosis and haemostasis. Thromb Haemost 71:520–525PubMed
8.
go back to reference Sadler JE, Budde U, Eikenboom JC et al (2006) Update on the pathophysiology and classification of von Willebrand disease: a report of the Subcommittee on von Willebrand Factor. J Thromb Haemost 4:2103–2114PubMedCrossRef Sadler JE, Budde U, Eikenboom JC et al (2006) Update on the pathophysiology and classification of von Willebrand disease: a report of the Subcommittee on von Willebrand Factor. J Thromb Haemost 4:2103–2114PubMedCrossRef
9.
go back to reference National Heart Lung and Blood Institute (2007) The diagnosis, evaluation and management of von Willebrand disease. NIH publication no. 08–5832. NHLBI, Bethesda, MD National Heart Lung and Blood Institute (2007) The diagnosis, evaluation and management of von Willebrand disease. NIH publication no. 08–5832. NHLBI, Bethesda, MD
10.
go back to reference Hermans C, Altisent C, Batorova A et al (2009) Replacement therapy for invasive procedures in patients with haemophilia: literature review, European survey and recommendations. Haemophilia 15:639–658PubMedCrossRef Hermans C, Altisent C, Batorova A et al (2009) Replacement therapy for invasive procedures in patients with haemophilia: literature review, European survey and recommendations. Haemophilia 15:639–658PubMedCrossRef
11.
go back to reference British United Provident Association (1989) Schedule of procedures. BUPA, London British United Provident Association (1989) Schedule of procedures. BUPA, London
12.
go back to reference Lavelle J, Davies MG et al (1992) A review of the nature and activity of a general surgical service in Ireland. Ir J Med Sci 161:127–130PubMedCrossRef Lavelle J, Davies MG et al (1992) A review of the nature and activity of a general surgical service in Ireland. Ir J Med Sci 161:127–130PubMedCrossRef
13.
go back to reference Jones SM, Collins CD (1990) Caseload or workload? Scoring complexity of operative procedures as a means of analysing workload. BMJ 301:324–325PubMedCrossRef Jones SM, Collins CD (1990) Caseload or workload? Scoring complexity of operative procedures as a means of analysing workload. BMJ 301:324–325PubMedCrossRef
14.
go back to reference Srivastava A (2004) Dose and response in haemophilia: optimisation of factor replacement therapy. Br J Haematol 127:12–25PubMedCrossRef Srivastava A (2004) Dose and response in haemophilia: optimisation of factor replacement therapy. Br J Haematol 127:12–25PubMedCrossRef
15.
go back to reference Bastounis E, Pikoulis E, Leppaniemi A et al (2000) General surgery in haemophiliac patients. Postgrad Med J 76:494–495PubMedCrossRef Bastounis E, Pikoulis E, Leppaniemi A et al (2000) General surgery in haemophiliac patients. Postgrad Med J 76:494–495PubMedCrossRef
16.
go back to reference Batarova A, Martinowitz U (2000) Intermittent injections vs continuous infusion of factor VIII in haemophilia patients undergoing major surgery. Br J Haematol 110:715–720CrossRef Batarova A, Martinowitz U (2000) Intermittent injections vs continuous infusion of factor VIII in haemophilia patients undergoing major surgery. Br J Haematol 110:715–720CrossRef
17.
go back to reference Dingli D, Gastineau DA, Gilchrist GS et al (2002) Continuous factor VIII infusion therapy in patients with haemophilia A undergoing surgical procedures with plasma-derived or recombinant factor VIII concentrates. Haemophilia 8:629–634PubMedCrossRef Dingli D, Gastineau DA, Gilchrist GS et al (2002) Continuous factor VIII infusion therapy in patients with haemophilia A undergoing surgical procedures with plasma-derived or recombinant factor VIII concentrates. Haemophilia 8:629–634PubMedCrossRef
18.
go back to reference Ragni MV, Pasi Kj, White GC et al (2002) Use of recombinant factor IX in subjects with haemophilia B undergoing surgery. Haemophilia 8:91–97PubMedCrossRef Ragni MV, Pasi Kj, White GC et al (2002) Use of recombinant factor IX in subjects with haemophilia B undergoing surgery. Haemophilia 8:91–97PubMedCrossRef
19.
go back to reference Srivastava A, Chandy M, Sunderaj GD et al (1998) Low-dose intermittent factor replacement for post-operative haemostasis in haemophilia. Haemophilia 4:799–801PubMedCrossRef Srivastava A, Chandy M, Sunderaj GD et al (1998) Low-dose intermittent factor replacement for post-operative haemostasis in haemophilia. Haemophilia 4:799–801PubMedCrossRef
20.
go back to reference Kasper CK, Boylen L, Ewing NP et al (1985) Haematologic management of haemophilia A for surgery. JAMA 253:1279–1283PubMedCrossRef Kasper CK, Boylen L, Ewing NP et al (1985) Haematologic management of haemophilia A for surgery. JAMA 253:1279–1283PubMedCrossRef
21.
go back to reference Ihasz M, Hung CM, Regoly-Merei J et al (1997) Complications of laparoscopic cholecystectomy in Hungary: a multicentre study of 13,833 patients. Eur J Surg 163:267–274PubMed Ihasz M, Hung CM, Regoly-Merei J et al (1997) Complications of laparoscopic cholecystectomy in Hungary: a multicentre study of 13,833 patients. Eur J Surg 163:267–274PubMed
22.
go back to reference Cohen AT, Wagner MB, Mohamed MS (1997) Risk factors for bleeding in major abdominal surgery using heparin thromboprophylaxis. Am J Surg 174:1–5PubMedCrossRef Cohen AT, Wagner MB, Mohamed MS (1997) Risk factors for bleeding in major abdominal surgery using heparin thromboprophylaxis. Am J Surg 174:1–5PubMedCrossRef
Metadata
Title
General Surgery in Patients With a Bleeding Diathesis: How We Do It
Authors
Kamal R. Aryal
D. Wiseman
Ajith K. Siriwardena
Paula H. B. Bolton-Maggs
Charles R. M. Hay
James Hill
Publication date
01-12-2011
Publisher
Springer-Verlag
Published in
World Journal of Surgery / Issue 12/2011
Print ISSN: 0364-2313
Electronic ISSN: 1432-2323
DOI
https://doi.org/10.1007/s00268-011-1265-6

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