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17 - Blood disorders

from Section 5 - Other disorders

Published online by Cambridge University Press:  19 October 2009

M. Joanne Douglas
Affiliation:
Department of Anesthesia, BC Women's Hospital, Vancouver, Canada
Penny Ballem
Affiliation:
Clinical Professor, Department of Medicine, School of Hematology, Faculty of Medicine, University of British Columbia, Victoria, BC, Canada
David R. Gambling
Affiliation:
University of California, San Diego
M. Joanne Douglas
Affiliation:
University of British Columbia, Vancouver
Robert S. F. McKay
Affiliation:
University of Kansas
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Summary

Background

Normal hematological indices during pregnancy

Multiple changes occur to the hematological system during pregnancy as outlined in Table 17.1. It is essential that the clinician be familiar with these in order to determine what is normal and what is abnormal when reviewing laboratory results in the pregnant woman.

Hematological testing during pregnancy

A routine, complete blood count during early pregnancy (first trimester) is important to identify common, preexisting hematological disorders that may impact on the pregnancy. In the uncomplicated pregnancy, a repeat blood count in the third trimester is done to assess the hematocrit in preparation for delivery.

Coagulation screening is performed only:

  • to investigate a significant bleeding history

  • to follow factor levels in patients with established disorders

  • during acute peripartum complications such as preeclampsia, massive hemorrhage or disseminated intravascular coagulation (DIC)

  • to monitor anticoagulation therapy.

Screening assays include platelets, prothrombin time (PT), activated partial thromboplastin time (aPTT), and fibrinogen (see Table 17.2). The subjective nature of the bleeding time as a measure of platelet function and its established lack of sensitivity and specificity as a predictor of clinical bleeding, has precluded its usefulness.

Currently, several centers use thromboelastography (TEG) to detect the risk of clinical bleeding; however, the sensitivity and specificity of this test remain unproven. Another point of care instrument, the platelet function analyzer (PFA-100®), is thought to represent an “in vitro” bleeding time.

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Publisher: Cambridge University Press
Print publication year: 2008

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References

Hytten, F.Blood volume changes in normal pregnancy. Clin. Haematol. 1985; 14: 601–12.Google Scholar
Bentley, D. P.Iron metabolism and anaemia in pregnancy. Clin. Haematol. 1985; 14: 613–28.Google Scholar
Lockitch, G.Handbook of Diagnostic Biochemistry and Hematology in Normal Pregnancy. Boca Raton: CRC Press, 1993.
Letzky, E. Hematologic disorders. In Barron, W. M. & Lindheimer, M. D. (eds.), Medical Disorders During Pregnancy, 2nd edn. St. Louis:Mosby-Year Book Inc 1995.
Pitkin, R. M. & Witte, D. L.Platelet and leukocyte counts in pregnancy. J.A.M.A. 1979; 242: 2696–8.Google Scholar
Ballem, P. J. Diagnosis and management of thrombocytopenia in obstetrical syndromes. In Sacher, R. A. & Brecher, M. (eds.), Obstetrical Transfusion Practice. Bethesda, MD: American Association of Blood Banks, 1993.
Tygart, S. G., McRoyan, D. K., Spinnato, J. A.et al. Longitudinal study of platelet indices during normal pregnancy. Am. J. Obstet. Gynecol. 1986; 154: 883.Google Scholar
Sejeny, S. A., Eastham, R. D. & Baker, S. R.Platelet counts during pregnancy. J. Clin. Pathol. 1975; 28: 812.Google Scholar
Sill, P. R., Lind, T. & Walker, W.Platelet values during normal pregnancy. Br. J. Obstet. Gynaecol. 1985; 92: 480.CrossRefGoogle Scholar
Singer, C. R. J., Walker, J. J., Cameron, A.et al. Platelet studies in normal pregnancy and pregnancy-induced hypertension. Clin. Lab. Haematol. 1986; 8: 27.Google Scholar
Boehlen, F., Hohfeld, P., Extermann, P., Perneger, T. V. & Moerloose, P.Platelet count at term pregnancy: a reappraisal of the threshold. Obstet. Gynecol. 2000; 95: 29–33.Google Scholar
Sainio, S., Kekomaki, R., Riikonen, S. & Teramo, K.Maternal thrombocytopenia at term: a population-based study. Acta Obstet. Gynaecol. Scand. 2000; 79: 744–9.Google Scholar
Fay, R. A., Hughes, A. O. & Farron, N. T.Platelets in pregnancy; hyperdestruction in pregnancy. Obstet. Gynecol. 1983; 61: 238.Google Scholar
Gerbasi, F. R., Bottoms, S., Farag, A.et al. Increased intravascular coagulation associated with pregnancy. Obstet. Gynecol. 1990; 75: 385.Google Scholar
Hellgren, M.Hemostasis during normal pregnancy and puerperium. Sem. Thromb. Hemost. 2003; 29: 125–30.CrossRefGoogle Scholar
Bolton-Maggs, P. H. B., Perry, D. J., Chalmers, E. A.et al. The rare coagulation disorders – review with guidelines for management from the United Kingdom Haemophilia Centre Doctors' Organization. Haemophilia 2004; 10: 593–628.Google Scholar
Ahmed, S., Russo, L. A., Siddiqui, A. K.et al. Prolonged activated partial thromboplastin time in pregnancy: a brief report. Am. J. Med. Sci. 2004; 327: 123–6.Google Scholar
Rodgers, C. R. P. & Levin, J.A critical reappraisal of the bleeding time. Semin. Thromb. Hemost. 1990; 16: 1–20.CrossRefGoogle Scholar
Lind, S. E.The bleeding time does not predict surgical bleeding. Blood 1991; 77: 2547–52.Google Scholar
Mallett, S. V. & Cox, D. J. A.Thromboelastography. Br. J. Anaesth. 1992; 69: 307.CrossRefGoogle Scholar
Douglas, M. J. The use of neuraxial anesthesia in parturients with thrombocytopenia: what is an adequate platelet count? In Halpern, S. H. & Douglas, M. J. (eds.), Evidence-Based Obstetric Anesthesia. Massachusetts: BMJ Books, Blackwell Publishing, 2005.
Pepkowitz, S. H. Autologous blood donation and obstetric transfusion practice. In Sacher, R. A. & Brecher, M. E. (eds.), Obstetric Transfusion Practice. Bethesda, MD: American Association of Blood Banks, 1993, pp. 77–94.
Grange, C., Douglas, M. J.Adams, T. J.et al. Haemodilution for caesarean section. Am. J. Obstet. Gynecol. 1998; 178: 156–60.Google Scholar
Karalapillai, D. & Popham, P.Recombinant factor VIIa in massive postpartum hemorrhage. A review. Int. J. Obstet. Anesth. 2007; 16: 29–34.Google Scholar
Ahonen, J. & Jokela, R.Recombinant factor VIIa for life-threatening post-partum haemorrhage. Br. J. Anaesth. 2005; 94: 592–5.CrossRefGoogle Scholar
Abshire, T. & Kenet, G.Recombinant factor VIIa: review of efficacy, dosing regimens and safety in patients with congenital and acquired factor VII or IX inhibitors. J. Thromb. Haemost. 2004; 2: 899–909.CrossRefGoogle Scholar
Owen, H. G. & Brecher, M. E. Therapeutic apheresis of the pregnant patient. In Sacher, R. A. & Brecher, M. E. (eds.), Obstetric Transfusion Practice. Bethesda, MD: American Association of Blood Banks, 1993, pp. 95–115.
Kashiwagi, M., Breymann, C., Huch, R. & Huch, A.Hypertension in a pregnancy with renal anemia after recombinant human erythropoietin (rhEPO) therapy. Arch. Gynecol. Obstet. 2002; 267: 54–6.Google Scholar
Rappaport, V. J., Velazquez, M. & Williams, K.Hemoglobinopathies in pregnancy. Obstet. Gynecol. Clin. N. Am. 2004; 31: 287–317.Google Scholar
ACOG Practice Bulletin. Clinical Management Guidelines for Obstetrician-Gynecologists. Number 64. Hemoglobinopathies in pregnancy. Obstet. Gynecol. 2005; 106: 203–10.
Savona-Ventura, C. & Bonello, F.Beta-thalassemia syndromes and pregnancy. Obstet. Gynecol. Surv. 1994; 49: 129–37.Google Scholar
Singounas, E. G., Sakas, D. E., Hadley, D. M.et al. Paraplegia in a pregnant thalassemic woman due to extramedullary hematopoiesis: successful management with transfusions. Surg. Neurol. 1991; 36: 210–15.Google Scholar
Sheiner, E., Levy, A., Yerushalmi, R. & Katz, M.Beta-thalassemia minor during pregnancy. Obstet. Gynecol. 2004; 103: 1273–7.CrossRefGoogle Scholar
Waters, J. H., Lukauskiene, E. & Anderson, M. E.Intraoperative blood salvage during cesarean delivery in a patient with β-thalassemia intermedia. Anesth. Analg. 2003; 97: 1808–9.CrossRefGoogle Scholar
Hassell, K.Pregnancy and sickle cell disease. Hematol. Oncol. Clin. North Am. 2005; 19: 903–16.Google Scholar
Embury, S. H.The not-so-simple process of sickle cell vasoocclusion. Microcirculation 2004; 11: 101–13.Google Scholar
Serjeant, G. R., Loy, Look L., Crowther, M., Hambleton, I. R. & Thane, M.Outcome of pregnancy in homozygous sickle cell disease. Obstet. Gynecol. 2004; 103: 1278–85.CrossRefGoogle Scholar
Vichinsky, E. P., Haberkern, C. M., Neumayr, L.et al. A comparison of conservative and aggressive transfusion regimens in the perioperative management of sickle cell disease. N. Engl. J. Med. 1995; 333: 206–13.Google Scholar
Wanko, S. O. & Telen, M. J.Transfusion management in sickle cell disease. Hematology-Oncology Clin. N. Am. 2005; 19: 803–26.Google Scholar
Koshy, M. & Burd, L.Management of pregnancy in sickle cell syndromes. Hematol. Oncol. Clin. North Am. 1991; 5: 585–96.Google Scholar
Enk, A., Visschers, G., Jansen, W. & Statius Van Eps, L. W.Maternal death due to sickle cell chronic lung disease. Br. J. Obstet. Gynaecol. 1992; 99: 162–3.Google Scholar
Firth, P. G. & Head, C. A.Sickle cell disease and anesthesia. Anesthesiology 2004; 101: 766–85.Google Scholar
Finer, P., Blair, J. & Rowe, P.Epidural analgesia in the management of labor pain and sickle cell crisis – a case report. Anesthesiology 1988; 68: 799–800.Google Scholar
Faron, G., Corbisier, C., Tecco, L. & Vokaer, A.First sickle cell crisis triggered by induction of labor in a primigravida. Eur. J. Obstet. Gynecol. Reprod. Biol. 2001; 94: 304–6.Google Scholar
Kuczkowski, K. M.Labour-induced sickle cell crisis in a previously asymptomatic parturient with sickle cell disease. (letter)Anaesthesia 2003; 58: 1044–5.Google Scholar
Pattison, J., Harrop-Griffiths, A. W., Whitlock, J. E. & Roberts, J. D.Caesarean section in a patient with haemoglobin SC disease and a phaeochromocytoma. Anaesthesia 1990; 45: 958–9.Google Scholar
Edwards, R.Anaesthesia for caesarean section in haemoglobin SC disease complicated by eclampsia. A case report. Br. J. Anaesth. 1973; 45: 757–8.CrossRefGoogle Scholar
Koshy, M., Weiner, S. J., Miller, S. T.et al. Surgery and anesthesia in sickle cell disease. Blood 1995; 86: 3676–84.Google Scholar
The Anaesthesia Advisory Committee to the Chief Coroner of Ontario. Intraoperative death during caesarian section in a patient with sickle-cell trait. Can. J. Anaesth. 1987; 34: 67–9.
Tsen, L. C. & Cherayil, G.Sickle cell-induced peripheral neuropathy following spinal anesthesia for cesarean delivery. Anesthesiology 2001; 95: 1298–9.Google Scholar
Chiron, B., Laffon, M., Ferrandiere, M. & Pittet, J-F.Postdural puncture headache in a parturient with sickle cell disease: use of an epidural colloid patch. Can. J. Anesth. 2003; 50: 812–14.Google Scholar
Donnelly, J. D., Cooley, S. M., O'Connell, M. P., Murphy, J. F. & Keane, D. P.Pheochromocytoma, sickle cell disease and pregnancy: a case report. J. Mat. Fet. Neonatal Med. 2003; 14: 353–5.CrossRefGoogle Scholar
Bolton-Maggs, P. H. B.Hereditary spherocytosis; new guidelines. Arch. Dis. Child. 2004; 89: 809–12.Google Scholar
Ho-Yen, D. O.Hereditary spherocytosis presenting in pregnancy. Acta Haemat. 1984; 72: 29–33.CrossRefGoogle Scholar
Karnak, D., Beder, S., Kayacan, O. & Berk, O.Postoperative pulmonary embolism in a young female accompanying with Factor V Leiden mutation and hereditary spherocytosis. J. Thromb. Thrombolysis 2004; 17: 213–17.Google Scholar
Pajor, A., Lehoczky, D. & Szakacs, Z.Pregnancy and hereditary spherocytosis. Report of 8 patients and a review. Arch. Gynecol. Obstet. 1993; 253: 37–41.Google Scholar
Maberry, M. C., Mason, R. A., Cunningham, F. G. & Pritchard, J. A.Pregnancy complicated by hereditary spherocytosis. Obstet. Gynecol. 1992; 79: 735–8.Google Scholar
Phupong, V., Sareepapong, W. & Witoonpanich, P.Evans syndrome and pregnancy: a case report. B.J.O.G. 2004; 111: 274–6.Google Scholar
Kumar, R., Advani, A. R., Sharan, J., Basharutallah, M. S. & Al-Lumai, A. S.Pregnancy induced hemolytic anemia: an unexplained entity. Ann. Hematol. 2001; 80: 623–6.Google Scholar
Ball, S. E.The modern management of severe aplastic anemia. Br. J. Haematol. 2000; 110: 41–53.CrossRefGoogle Scholar
Tichelli, A., Socie, G., Marsh, J.et al. Outcome of pregnancy and disease course among women with aplastic anemia treated with immunosuppression. Ann. Intern. Med. 2002; 137: 164–72.Google Scholar
Baker, R. I., Manoharan, A., Luca, E. & Begley, C. G.Pure red cell aplasia of pregnancy: a distinct clinical entity. Br. J. Haematol. 1993; 85: 619–22.CrossRefGoogle Scholar
Perry, C. P. & Harris, R. E.Successful management of pregnancy-induced pancytopenia. Obstet. Gynecol. 1977; 50: 732–4.Google Scholar
Fleming, A. F.Hypoplastic anaemia in pregnancy. J. Obstet. Gynaecol. Br. Commonw. 1968; 75: 138–41.Google Scholar
Collins, D. J., Rosenthal, D. S., Goldstein, D. P. & Moloney, W. C.Aplastic anemia in pregnancy. Obstet. Gynecol. 1972; 39: 884–6.Google Scholar
Cohen, E., Ilan, Y., Gillis, S., Dann, E. J. & Rachmilewitz, E. A.Recurrent transient bone marrow hypoplasia associated with pregnancy. Acta Haematol. 1993; 89: 32–4.CrossRefGoogle Scholar
Aggio, M. C. & Zunini, C.Reversible pure red-cell aplasia in pregnancy. (Letter)N. Engl. J. Med. 1977; 297: 221–2.Google Scholar
Leong, K. W., Teh, A., Bosco, J. J. & Lim, J.Successful pregnancy following aplastic anemia. Post. Grad. Med. J. 1995; 71: 625–7.Google Scholar
Deka, D., Malhotra, N., Sinha, A.et al. Pregnancy associated aplastic anemia: maternal and fetal outcome. J. Obstet. Gynaecol. Res. 2003; 29: 67–72.Google Scholar
Choudhry, V. P., Gupta, S., Gupta, M., Kashyap, R. & Saxena, R.Pregnancy associated aplastic anemia – a series of 10 cases with review of the literature. Hematology 2002; 7: 233–8.Google Scholar
Knispel, J. W., Lynch, V. A. & Viele, B. D.Aplastic anemia in pregnancy: a case report, review of the literature, and a re-evaluation of management. Obstet. Gynecol. Surv. 1976; 31: 523–8.Google Scholar
Aitchison, R. G. M., Marsh, J. C. W., Hows, J. M., Russell, N. H. & Gordon-Smith, E. C.Pregnancy associated aplastic anaemia: a report of five cases and review of current management. Br. J. Haematol. 1989; 73: 541–5.CrossRefGoogle Scholar
Ang, H. Y. & Linn, Y. C.A case of aplastic anaemia in pregnancy. Aust. N.Z. J. Obstet. Gynaecol. 1999; 39: 102–5.Google Scholar
Djaldetti, M., Blay, A., Bergman, M., Salman, H. & Bessler, H.Pure red cell aplasia – a rare disease with multiple causes. Biomedicine & Pharmacotherapy 2003; 57: 326–32.Google Scholar
Makino, Y., Nagano, M., Tamura, K. & Kawarabayashi, T.Pregnancy complicated with pure red cell aplasia: a case report. J. Perinat. Med. 2003; 31: 530–4.Google Scholar
Setzen, R. & Guidozzi, F.Fanconi's anaemia in pregnancy. A case report. S. Afr. Med. J. 1990; 78: 691.Google Scholar
Dalle, J. H., Huot, C., Duval, M.et al. Successful pregnancies after bone marrow transplantation for Fanconi anemia. Bone Marrow Transplantation 2004; 34: 1099–100.Google Scholar
Halperin, D. S. & Freedman, M. H.Diamond-Blackfan anemia: etiology, pathophysiology, and treatment. Am. J. Pediatr. Hematol. Oncol. 1989; 11: 380–94.Google Scholar
Rijhsinghani, A. & Wiechert, R. J.Diamond-Blackfan anemia in pregnancy. Obstet. Gynecol. 1994; 83: 827–9.Google Scholar
Alter, B. P., Kumar, M., Lockart, L. L., Sprinz, P. G. & Rowe, R. F.Pregnancy in bone marrow failure syndromes: Diamond-Blackfan anaemia and Shwachman-Diamond syndrome. Br. J. Haematol. 1999; 107: 49–54.CrossRefGoogle Scholar
Barton Rogers, B., Bloom, S. L. & Buchanan, G. R.Autosomal dominantly inherited Diamond-Blackfan anemia resulting in nonimmune hydrops. Obstet. Gynecol. 1997; 89: 805–7.CrossRefGoogle Scholar
Orfal, K. A., Ohene-Abuakwa, Y. & Ball, S. E.Diamond-Blackfan anaemia in the UK: clinical and genetic heterogeneity. Br. J. Haematol. 2004; 125: 243–52.Google Scholar
Meyers, G. & Parker, C. J.Management issues in paroxysmal nocturnal hemoglobinuria. Int. J. Hematol. 2003; 77: 125–32.Google Scholar
Frakes, J. T., Burmeister, R. E. & Giliberti, J. J.Pregnancy in a patient with paroxysmal nocturnal hemoglobinuria. Obstet. Gynecol. 1976; 47: 22S–24S.Google Scholar
Hurd, W. W., Miodovnik, M. & Stys, S. J.Pregnancy associated with paroxysmal nocturnal hemoglobinuria. Obstet. Gynecol. 1982; 60: 742–6.Google Scholar
Spencer, J. A. D.Paroxysmal nocturnal haemoglobinuria in pregnancy: case report. Br. J. Obstet. Gynaecol. 1980; 87: 246–8.CrossRefGoogle Scholar
Bjorge, L., Ernst, P. & Haram, K. O.Paroxysmal nocturnal hemoglobinuria in pregnancy. Acta Obstet. Gynecol. Scand. 2003; 82: 1067–71.Google Scholar
Barton, J. R., Shaver, D. C. & Sibai, B. M.Successive pregnancies complicated by idiopathic sideroblastic anemia. Am. J. Obstet. Gynecol. 1992; 166: 576–7.Google Scholar
Impey, L., Greenwood, C., Taylor, D. & Wainscoat, J.Recurrent acquired sideroblastic anemia in a twin pregnancy. J. Mat. Fet. Med. 2000; 9: 248–9.Google Scholar
Bruce, D. L. & Koepke, J. A.Anesthetic management of patients with bone-marrow failure. Anesth. Analg. 1972; 51: 597.Google Scholar
Wong, A. Y. C., Chan, R. S. N. & Irwin, M. G.Anesthetic management of cesarean delivery in a patient with hypoplastic anemia and severe pre-eclampsia. Can. J. Anesth. 2004; 51: 923–7.Google Scholar
Hara, K., Saito, Y., Morimoto, N., Sakura, S. & Kosaka., Y.Anaesthetic management of caesarean section in a patient with myelodysplastic syndrome. Can. J. Anaesth. 1998; 45: 157–63.Google Scholar
Stocche, R. M., Garcia, L. V. & Klamt, J. G.Labor analgesia in a patient with paroxysmal nocturnal hemoglobinuria with thrombocytopenia. Reg. Anesth. Pain Med. 2001; 26: 79–82.Google Scholar
Kjaer, K., Comerford, M. & Gadalla, F.General anesethesia for cesarean delivery in a patient with paroxysmal nocturnal hemoglobinuria and thrombocytopenia. Anesth. Analg. 2004; 98: 1471–2.CrossRefGoogle Scholar
Paech, M. J. & Pavy, T. J. G.Management of a parturient with paroxysmal nocturnal hemoglobinuria. Int. J. Obstet. Anesth. 2004; 13: 188–91.Google Scholar
Harrison, C.Pregnancy and its management in the Philadelphia negative myeloproliferative diseases. Br. J. Haematol. 2005; 129: 293–306.CrossRefGoogle Scholar
Burrows, R. F.Platelet disorders in pregnancy. Curr. Opin. Obstet. Gynecol. 2001; 13: 115–19.Google Scholar
Harrison, C. N.Essential thrombocythaemia: challenges and evidence-based management. Br. J. Haematol. 2005; 130: 153–65.CrossRefGoogle Scholar
Vadher, B. D., Machin, S. J., Patterson, K. G., Sukhu, C. & Walker, H.Life-threatening thrombotic and haemorrhagic problems associated with silent myeloproliferative disorders. Br. J. Haematol. 1993; 85: 213–16.CrossRefGoogle Scholar
Schafer, A. I.Essential thrombocythemia. Prog. Hemost. Thromb. 1991; 10: 69–96.Google Scholar
Katz, L. E., Goyert, G. L., Bloom, R. E.et al. Essential thrombocytosis in pregnancy: is pharmacologic therapy indicated? (letter) J. Mat. Fetal Med. 1994; 3: 193.CrossRefGoogle Scholar
Bangerter, M., Guthner, C., Beneke, H.et al. Pregnancy in essential thrombocythaemia: treatment and outcome of 17 pregnancies. Eur. J. Haematol. 2000; 65: 165–9.Google Scholar
Randi, M. L., Barbone, E., Rossi, C. & Girolami, A.Essential thrombocythemia and pregnancy: a report of six normal pregnancies in five untreated patients. Obstet. Gynecol. 1994; 83: 915–17.CrossRefGoogle Scholar
Spivak, J. L.Polycythemia vera: myths, mechanisms, and management. Blood 2002; 100: 4272–90.Google Scholar
Terek, M. C., Ozkinay, E., Zekioglu, O.et al. Acute leukemia in pregnancy with ovarian metastasis: a case report and review of the literature. Int. J. Gynecol. Cancer 2003; 13: 904–8.Google Scholar
Caligiuri, M. A. & Mayer, R. J.Pregnancy and leukemia. Semin. Oncol. 1989; 16: 388–96.Google Scholar
Zuazu, J., Julia, A., Sierra, J.et al. Pregnancy outcome in hematologic malignancies. Cancer 1991; 67: 703–9.Google Scholar
Celo, J. S., Kim, H. C., Houlihan, C.et al. Acute promyelocytic leukemia in pregnancy: all-trans retinoic acid as a newer therapeutic option. Obstet. Gynecol. 1994; 83: 808–11.Google Scholar
Doll, D. C., Ringenberg, Q. S. & Yarbro, J. W.Management of cancer during pregnancy. Arch. Intern. Med. 1988; 148: 2058–64.Google Scholar
Pejovic, T. & Schwartz, P. E.Leukemias. Clin. Obstet. Gynecol. 2002; 45: 866–78.Google Scholar
Mubarak, A. A. S., Kakil, I. R., Awidi, A.et al. Normal outcome of pregnancy in chronic myeloid leukemia treated with interferon-α in 1st trimester: report of 3 cases and review of the literature. Am. J. Hematol. 2002; 69: 115–18.Google Scholar
Taylor, U. B., Bardeguez, A. D., Iglesias, N. & Gascon, P.Idiopathic myelofibrosis in pregnancy: a case report and review of the literature. Am. J. Obstet. Gynecol. 1991; 167: 38–9.Google Scholar
Ward, F. T. & Weiss, R. B.Lymphoma and pregnancy. Semin. Oncol. 1989; 16: 397–409.Google Scholar
Gobbi, P. G., Attardo-Parinello, G., Danesino, M.et al. Hodgkin's disease and pregnancy. Haematologica 1984; 69: 336–41.Google Scholar
Klezl, Z., Krbec, M., Gregora, E. & Stritesky, J.Rare presentation of non-Hodgkin lymphoma of the thoracolumbar spine in pregnancy with 7 years' survival. Arc. Orthop. Trauma Surg. 2002; 122: 308–10.Google Scholar
Dasan, J., Littleford, J., McRae, K., Farine, D. & Winton, T.Mediastinal tumour in a pregnant patient presenting as acute cardiorespiratory compromise. Int. J. Obstet. Anesth. 2002; 11: 52–6.Google Scholar
Szokol, J. W., Alspach, D., Mehta, M. K., Parilla, B. V. & Liptay, M. J.Intermittent airway obstruction and superior vena cava syndrome in a patient with undiagnosed mediastinal mass after cesarean delivery. Anesth. Analg. 2003; 97: 883–4.CrossRefGoogle Scholar
Malee, M. P.Multiple myeloma in pregnancy: a case report. Obstet. Gynecol. 1990; 75: 513–15.Google Scholar
Caudle, M. R., Dodd, S. & Solomon, A.Multiple myeloma in pregnancy: a case report. Obstet. Gynecol. 1990; 75: 516–18.Google Scholar
Pajor, A., Kelemen, E., Mohos, Z., Hambach, J. & Varadi, G.Multiple myeloma in pregnancy. Int. J. Gynaecol. Obstet. 1991; 35: 341–2.Google Scholar
Maglione, A., Giorgio, Di G., Petruzelli, F. & Longo, Pia M.Multiple myeloma diagnosed during early pregnancy: a case report. Eur. J. Obstet. Gynecol. Reprod. Biol. 2003; 111: 214–15.Google Scholar
Forthman, C. L., Ponce, B. A. & Mankin, H. J.Multiple myeloma with a pathologic fracture during pregnancy. J. Bone Joint Surg. 2004; 86-A: 1284–8.Google Scholar
Cheung, V. Y. T., Bocking, A. D., Hollomby, D., Gagnon, R. & Walton, J.Waldenström hypergammaglobulinemic purpura and pregnancy. Obstet. Gynecol. 1993; 82: 685–7.Google Scholar
Lowenwirt, I., Dadic, P. & Krishnamurthy, V.Essential thrombocythemia and epidural analgesia in the parturient: does thromboelastography help?Reg. Anesth. 1996; 21: 525–8.Google Scholar
Garci-Ferreira, J., Hernandez-Palazon, J., Garcia-Candel, A. & Verdu-Martinez, T.Subarachnoid block in a patient with essential thrombocytopenia. (letter)Anesth. Analg. 2005; 101: 800.Google Scholar
Hosoi, S., Adachi, T., Hara, T.et al. Pulmonary embolism after minor surgery in a patient with low-risk thrombocythemia. J. Anesth. 2004; 18: 146.Google Scholar
Ulrich, B. & Krelenbuhl, G.Complication after artery catheterization: digital gangrene in a patient with myeloproliferative disease with thrombocytosis. (letter)Anesth. Analg. 2000; 91: 767–8.CrossRefGoogle Scholar
Rehfeldt, K. H. & Sanders, M. S.Digital gangrene after radial artery catheterization in a patient with thrombocytosis. Anesth. Analg. 2000; 90: 45–6.CrossRefGoogle Scholar
Coleman, A. J. & Sliom, C. M.Polycythaemic hypoxaemia and general anaesthesia. A case report. Br. J. Anaesth. 1966; 38: 653–5.CrossRefGoogle Scholar
Schmitt, H. J., Becke, K. & Neidhardt, B.Epidural anesthesia for cesarean delivery in a patient with polycythemia rubra vera and preeclampsia. Anesth. Analg. 2001; 92: 1535–7.CrossRefGoogle Scholar
Spencer, J., Gadalla, F., Wagner, W. & Blake, J.Caesarean section in a diabetic patient with a recent myocardial infarction. Can. J. Anaesth. 1994; 41: 516–18.Google Scholar
Bucklin, B. A., Tinker, J. H. & Smith, C. V. Clinical dilemma: a patient with postdural puncture headache and acute leukemia. Anesth. Analg. 1999; 88: 166–8.Google Scholar
Lipton, J. H., Derzko, C., Fyles, G., Meharchand, J. & Messner, H. A.Pregnancy after BMT: three case reports. Bone Marrow Transplantation 1993; 11: 415–18.Google Scholar
Stein, R. A., Messino, M. J. & Hessel, E. A., 2nd. Anaesthetic implications for bone marrow transplant recipients. Can. J. Anaesth. 1990; 37: 571–8.Google Scholar
Salooja, N., Szydio, R. M., Socie, G.et al. Pregnancy outcomes after peripheral blood or bone marrow transplantation: a retrospective survey. Lancet 2001; 358: 271–6.Google Scholar
Scott, D. B. & Hibberd, B. M.Serious non-fatal complications associated with extradural block in obstetric practice. Br. J. Anaesth. 1990; 64: 537–41.CrossRefGoogle Scholar
Crawford, J. S.Some maternal complications of epidural analgesia for labour. Anaesthesia 1985; 40: 1219–25.Google Scholar
Loo, C. C., Dahlgren, G. & Irestedt, L. Neurological complications in obstetric regional anaesthesia. Int. J. Obstet. Anesth. 2000; 9: 99–124.Google Scholar
British Committee for Standards in Haematology General Haematology Task Force. Guidelines for the investigation and management of idiopathic thrombocytopenic purpura in adults, children and in pregnancy. Br. J. Haematol. 2003; 120: 574–96.
Louden, K. A., Pipkin, Broughton F., Heptinstall, S.et al. A longitudinal study of platelet behaviour and thromboxane production in whole blood in normal pregnancy and the puerperium. Br. J. Obstet. Gynaecol. 1990; 97: 1108–14.CrossRefGoogle Scholar
Harker, L. A. & Slichter, S. J.The bleeding time as a screening test for evaluation of platelet function. N. Engl. J. Med. 1972; 287: 155–9.Google Scholar
Burrows, R. F. & Kelton, J. G.Incidentally detected thrombocytopenia in healthy mothers and their infants. N. Engl. J. Med. 1988; 319: 142–5.Google Scholar
Anteby, E. & Shalev, O.Clinical relevance of gestational thrombocytopenia of < 100,000/µl. Am. J. Hematol. 1994; 47: 118–22.Google Scholar
Rolbin, S. H., Abbot, D., Musclow, E.et al. Epidural anesthesia in pregnant patients with low platelet counts. Obstet. Gynecol. 1988; 71: 918–20.Google Scholar
Rasmus, K. T., Rottman, R. L., Kotelko, D. M.et al. Unrecognized thrombocytopenia and regional anesthesia in parturients: a retrospective review. Obstet. Gynecol. 1989; 73: 943–6.Google Scholar
Burrows, R. F. & Kelton, J. G.Thrombocytopenia at delivery. A prospective survey of 6715 deliveries. Am. J. Obstet. Gynecol. 1990; 162: 731–4.Google Scholar
Ballem, P. J., Segal, G. M., Stratton, J. R.et al. Mechanisms of thrombocytopenia in chronic autoimmune thrombocytopenic purpura. Evidence of both impaired platelet production and increased platelet clearance. J. Clin. Invest. 1987; 80: 33–40.CrossRefGoogle Scholar
Cines, D. B. & Blanchette, B. S.Immune thrombocytopenic purpura. N. Engl. J. Med. 2002; 346: 995–1008.Google Scholar
Paidas, M. J., Haut, M. J. & Lockwood, C. J.Platelet disorders in pregnancy: implications for mother and fetus. Mt. Sinai J. Med. 1994; 61: 389–403.Google Scholar
Cines, D. B., Dusak, B., Tomaski, A., Mennuti, M. & Schreiber, A. D.Immune thrombocytopenic purpura and pregnancy. N. Engl. J. Med. 1982; 306: 826–31.Google Scholar
Burrows, R. F. & Kelton, J. G.Low fetal risks in pregnancies associated with idiopathic thrombocytopenic purpura. Am. J. Obstet. Gynecol. 1990; 163: 1147–50.Google Scholar
Cook, R. L., Miller, R. C., Katz, V. L. & Cefalo, R. C.Immune thrombocytopenic purpura in pregnancy: a reappraisal of management. Obstet. Gynecol. 1991; 78: 578–83.Google Scholar
Samuels, P., Bussel, J. B., Braitman, L. E.et al. Estimation of the risk of thrombocytopenia in the offspring of pregnant women with presumed immune thrombocytopenic purpura. N. Engl. J. Med. 1990; 323: 229–35.Google Scholar
Drachman, J. G.Inherited thrombocytopenia: when a low platelet count does not mean ITP. Blood 2004; 103: 290–8.Google Scholar
Rocca, B., Bellacosa, A., Cristofaro, R.et al. Wiskott-Aldrich syndrome: report of an autosomal dominant variant. Blood 1996; 87: 4538–43.Google Scholar
Parolini, O., Ressmann, G., Haas, O. A.et al. X-linked Wiskott-Aldrich syndrome in a girl. New Engl. J. Med. 1998; 338: 291–5.Google Scholar
Mandelbrot, L., Schlienger, I., Bongain, A.et al. Thrombocytopenia in pregnant women infected with human immunodeficiency virus: maternal and neonatal outcome. Am. J. Obstet. Gynecol. 1994; 171: 252–7.Google Scholar
Kam, P. C. A., Thompson, S. A. & Liew, A. C. S.Thrombocytopenia in the parturient. Anaesthesia 2004; 59: 255–64.Google Scholar
Horlocker, T. T., Wedel, D. J., Benzon, H.et al. Regional anesthesia in the anticoagulated patient: defining the risks (the second ASRA Consensus Conference on Neuraxial Anesthesia and Anticoagulation). Reg. Anesth. Pain Med. 2003; 28: 172–97.Google Scholar
Peng., T. C., Kickler, T. S., Bell, W. R. & Haller, E.Obstetric complications in a patient with Bernard-Soulier syndrome. Am. J. Obstet. Gynecol. 1991; 165: 425–6.Google Scholar
Saade, G., Homsi, R. & Seoud, M.Bernard-Soulier syndrome in pregnancy: a report of four pregnancies in one patient, and review of the literature. Eur. J. Obstet. Gynecol. Reprod. Biol. 1991; 40: 149–52.Google Scholar
Kriplani, A., Singh, Malhotra B., Sowbernika, R. & Choudhry, Prakash V.Successful pregnancy outcome in Bernard-Soulier syndrome. J. Obstet. Gynaecol. Res. 2005; 31: 52–6.Google Scholar
Fujimori, K., Ohto, H., Honda, S. & Sato, A.Antepartum diagnosis of fetal intracranial hemorrhage due to maternal Bernard-Soulier syndrome. Obstet. Gynecol. 1999; 94: 817–19.Google Scholar
Seri, M., Pecci, A., Bari, Di F.et al. MYH9-related disease. May-Hegglin anomaly, Sebastian syndrome, Fechtner syndrome, and Epstein syndrome are not distinct entities but represent a variable expression of a single illness. Medicine 2003; 82: 203–15.Google Scholar
Toren, A., Rozenfeld-Granot, G., Heath, K. E.et al. MYH9 spectrum of autosomal-dominant giant platelet syndromes: unexpected association with fibulin-1 variant-D inactivation. Am. J. Hematol. 2003; 74: 254–62.Google Scholar
Fukada, Y., Yasumizu, T., Sumino, E. & Hoshi, K.A pregnancy complicated with Fechtner syndrome: a case report. J. Exp. Med. 2000; 191: 183–6.Google Scholar
Chabane, H., Gallais, Y., Pathier, D., Tchernia, G. & Gaussem, P.Delivery management in a woman with thrombocytopenia of the May-Hegglin anomaly type. Eur. J. Obstet. Gynecol. Reprod. Biol. 2001; 99: 124–5.Google Scholar
Nelson, L. H., Dewan, D. M. & Mandell, G. L.Obstetric and anesthetic considerations in the May-Hegglin anomaly. A case report. J. Reprod. Med. 1993; 38: 311–13.Google Scholar
Kotelko, D. M.Anaesthesia for caesarean delivery in a patient with May-Hegglin anomaly. Can. J. Anaesth. 1989; 36: 328–30.Google Scholar
Duff, P. & Jackson, M. T.Pregnancy complicated by rhesus sensitization and the May-Hegglin anomaly. Obstet. Gynecol. 1985; 65: 7S-10S.Google Scholar
Siddiqui, T., Lammert, N., Danier, P. & Luke, M.Immune thrombocytopenia and May-Hegglin anomaly during pregnancy. J. Florida M. A. 1991; 78: 88–91.Google Scholar
Chatwani, A., Bruder, N., Shapiro, T. & Reece, E. A.May-Hegglin anomaly: a rare case of maternal thrombocytopenia in pregnancy. Am. J. Obstet. Gynecol. 1992; 166: 143–4.Google Scholar
Takashima, T., Maeda, H., Koyanagi, T., Nishimura, J. & Nakano, H.Prenatal diagnosis and obstetrical management of May-Hegglin anomaly: a case report. Fetal Diagn. Ther. 1992; 7: 186–9.Google Scholar
Gunay-Aygun, M., Huizing, M. & Gahl, W. A.Molecular defects that affect platelet dense granules. Semin. Thromb. Hemost. 2004; 30: 537–47.CrossRefGoogle Scholar
Price, F. V., Legro, R. S., Watt-Morse, M. & Kaplan, S. S.Chediak-Higashi syndrome in pregnancy. Obstet. Gynecol. 1992; 79: 804–6.Google Scholar
Sherer, D. M. & Lerner, R.Glanzmann's thrombasthenia in pregnancy: a case and review of the literature. Am. J. Perinatol. 1999; 16: 297–301.CrossRefGoogle Scholar
Ito, K., Yoshida, H., Hatoyama, H.et al. Antibody removal therapy used successfully at delivery of a pregnant patient with Glanzmann's thrombasthenia and multiple anti-platelet antibodies. Vox Sang. 1991; 61: 40–6.Google Scholar
Poon, M-C, d'Oiron, R., Hann, I.et al. Use of recombinant Factor VIIa (NovoSeven®) in patients with Glanzmann thrombasthenia. Semin. Hematol. 2001; 38: 21–5.Google Scholar
Kale, A., Bayhan, G., Yalinkaya, A. & Yayla, M.The use of recombinant factor VIIa in a primigravida with Glanzmann's thrombasthenia during delivery. J. Perinat. Med. 2004; 32: 456–8.Google Scholar
Monte, S. & Lyons, G.Peripartum management of patient with Glanzmann's thrombasthenia using Thrombelastograph®. Br. J. Anaesth. 2002; 88: 734–8.CrossRefGoogle Scholar
Thouli, E., Hay, C. R. M., O'Gorman, P. & Makris, M.Acquired Glanzmann's thrombasthenia without thrombocytopenia: a severe acquired autoimmune bleeding disorder. Br. J. Haematol. 2004: 127: 209–13.Google Scholar
Rao, A. K. & Holmsen, H.Congenital disorders of platelet function. Sem. Hematol. 1986; 23: 102–18.Google Scholar
Wax, J. R., Rosengren, S., Spector, E., Gainey, A. J. & Ingardia, C. J.DNA diagnosis and management of Hermansky-Pudlak syndrome in pregnancy. Am. J. Perinatol. 2001; 18: 159–61.CrossRefGoogle Scholar
Laskey, A. L. & Tobias, J. D.Anesthetic implications of the grey platelet syndrome. Can. J. Anesth. 2000; 47: 1224–9.Google Scholar
Edozien, L. C. & Mayers, F. N.Platelet storage pool deficiency in pregnancy. Br. J. Clin. Pract. 1995; 49: 220.Google Scholar
Thurlow, J. A. & Waterhouse, P.Patient-controlled analgesia in labour using remifentanil in two parturients with platelet abnormalities. Br. J. Anaesth. 2000; 84: 411–13.CrossRefGoogle Scholar
Weiner, C. P.Thrombotic microangiopathy in pregnancy and the postpartum period. Sem. Hematol. 1987; 24: 119–29.Google Scholar
Weinstein, L.Preeclampsia/eclampsia with hemolysis, elevated liver enzymes, and thrombocytopenia. Obstet. Gynecol. 1985; 66: 657–60.Google Scholar
Sibai, B. M., Taslimi, M. M., El-Nazer, A.et al. Maternal-perinatal outcome associated with the syndrome of hemolysis, elevated liver enzymes, and low platelets in severe preeclampsia-eclampsia. Am. J. Obstet. Gynecol. 1986; 155: 501–9.Google Scholar
Sibai, B. M., Ramadan, M. K., Usta, I.et al. Maternal morbidity and mortality in 442 pregnancies with hemolysis, elevated liver enzymes, and low platelets (HELLP syndrome). Am. J. Obstet. Gynecol. 1993; 169: 1000–6.Google Scholar
Sibai, B. M., Ramadan, M. K., Chari, R. S. & Friedman, S. A.Pregnancies complicated by HELLP syndrome (hemolysis, elevated liver enzymes, and low platelets): subsequent pregnancy outcome and long-term prognosis. Am. J. Obstet. Gynecol. 1995; 172: 125–9.Google Scholar
Martin, J. N., Blake, P. G., Perry, K. G.et al. The natural history of HELLP syndrome: patterns of disease progression and regression. Am. J. Obstet. Gynecol. 1991; 164: 1500–13.Google Scholar
Martin, J. N., Blake, P. G., Lowry, S. L.et al. Pregnancy complicated by preeclampsia-eclampsia with the syndrome of hemolysis, elevated liver enzymes, and low platelet count: how rapid is postpartum recovery?Obstet. Gynecol. 1990; 76: 737–41.CrossRefGoogle Scholar
Roberts, W. E., Perry, K. G., Woods, J. B.et al. The intrapartum platelet count in patients with HELLP (hemolysis, elevated liver enzymes, and low platelets) syndrome: is it predictive of later hemorrhagic complications?Am. J. Obstet. Gynecol. 1994; 171: 799–804.Google Scholar
Rose, C. H., Thigpen, B. D., Bofill, J. A.et al. Obstetric implications of antepartum corticosteroid therapy for HELLP syndrome. Obstet. Gynecol. 2005; 104: 1011–14.CrossRefGoogle Scholar
Ramanathan, J., Sibai, B. M., Vu, T. & Chauhan, D.Correlation between bleeding times and platelet counts in women with preeclampsia undergoing cesarean section. Anesthesiology 1989; 71: 188–91.Google Scholar
Schindler, M., Gatt, S., Isert, P., Morgans, D. & Cheung, A.Thrombocytopenia and platelet functional defects in pre-eclampsia: implications for regional anaesthesia. Anaesth. Intensive Care 1990; 18: 169–74.Google Scholar
Whitta, R. K. S., Cox, D. J. A. & Mallett., S. V.Thromboelastography reveals two causes of haemorrhage in HELLP syndrome. Br. J. Anaesth. 1995; 74: 464–8.CrossRefGoogle Scholar
Ramanathan, J., Khalil, M., Sibai, B. M. & Chauhan, D.Anesthetic management of the syndrome of hemolysis, elevated liver enzymes, and low platelet count (HELLP) in severe preeclampsia. A retrospective study. Reg. Anesth. 1988; 13: 20–4.Google Scholar
Crosby, E. T.Obstetrical anaesthesia for patients with the syndrome of haemolysis, elevated liver enzymes and low platelets. Can. J. Anaesth. 1991; 38: 227–33.Google Scholar
Elliott, M. D. & Nichols, W. L.Thrombotic thrombocytopenic purpura and hemolytic uremic syndrome. Mayo Clin. Proc. 2001; 76: 1154–62.Google Scholar
George, J. N.The association of pregnancy with thrombotic thrombocytopenic purpura-hemolytic uremic syndrome. Curr. Opin. Hematol. 2003; 10: 339–44.Google Scholar
McMinn, J. R. & George, J. N.Evaluation of women with clinically suspected thrombotic thrombocytopenic purpura-hemolytic uremic syndrome. J. Clin. Apheresis 2001; 16: 202–9.Google Scholar
Hayward, C. P., Sutton, D. M., Carter, W. H. Jr.et al. Treatment outcomes in patients with adult thrombotic thrombocytopenic purpura-hemolytic uremic syndrome. Arch. Intern. Med. 1994; 154: 982–7.Google Scholar
Vesely, S. K., George, J. N., Lammie, B.et al. ADAMTS13 activity in thrombotic thrombocytopenic pupura-hemolytic uremic syndrome: relation to presenting features and clinical outcomes in a prospective cohort of 142 patients. Blood 2003; 101: 60–8.Google Scholar
Pivalizza, E. G.Anesthetic management of a patient with thrombotic thrombocytopenic purpura. Anesth. Analg. 1994; 79: 1203–5.Google Scholar
Fesenmeier, M. F., Coppage, K. H., Lambers, D. S., Barton, J. R. & Sibai, B. M.Acute fatty liver of pregnancy in 3 tertiary care centers. Am. J. Obstet. Gynecol. 2005; 192: 1416–19.Google Scholar
Castro, M. S., Fassett, M. J., Reynolds, T. B., Shaw, K. J. & Goodwin, T. M.Reversible peripartum liver failure: a new perspective on the diagnosis, treatment, and cause of acute fatty liver of pregnancy, based on 28 consecutive cases. Am. J. Obstet. Gynecol. 1999; 181: 389–95.Google Scholar
Anday, E. K. & Cohen, A.Liver disease associated with pregnancy. Ann. Clin. Lab. Sci. 1990; 20: 233–8.Google Scholar
Samuels, P. & Cohen, A. W.Pregnancies complicated by liver disease and liver dysfunction. Obstet. Gynecol. Clin. N. Am. 1992; 19: 745–63.Google Scholar
Mammen, E. B.Sticky platelet syndrome. Sem. Thromb. Hemost. 1999; 25: 361–5.CrossRefGoogle Scholar
Begbie, M. E., Wallace, G. M. F. & Shovlin, C. L.Hereditary haemorrhagic telangiectasia (Osler-Weber-Rendu syndrome): a view from the 21st century. Postgrad. Med. J. 2003; 79: 18–24.Google Scholar
Swinburne, A. J., Fedullo, A. J., Gangemi, R.et al. Hereditary telangiectasia and multiple pulmonary arteriovenous fistulas: clinical deterioration during pregnancy. Chest 1986; 89: 459–60.Google Scholar
Bevelaqua, F. A., Ordorica, S. A., Lefleur, R. & Young, B.Osler-Weber-Rendu disease. Diagnosis and management of spontaneous hemothorax during pregnancy. N.Y. State J. Med. 1992; 12: 551–2.Google Scholar
Chao, H-S., Chern, M-S., Chen, Y-C. & Chang, S-C.Recurrence of pulmonary arteriovenous malformations in a female with hereditary hemorrhagic telangiectasia. Am. J. Med. Sci. 2004; 327: 294–8.Google Scholar
Gershon, A. S., Faughnan, M. E., Chon, K. S.et al. Transcatheter embolotherapy of maternal pulmonary arteriovenous malformations during pregnancy. Chest 2001; 119: 470–7.Google Scholar
Waring, P. H., Shaw, D. B. & Brumfield, C. G.Anesthetic management of a parturient with Osler-Weber-Rendu syndrome and rheumatic heart disease. Anesth. Analg. 1990; 71: 96–9.Google Scholar
Livneh, A., Langevitz, P., Morag, B., Catania, A. & Pras, M.Functionally reversible hepatic arteriovenous fistulas during pregnancy in patients with hereditary hemorrhagic telangiectasia. S. Med. J. 1988; 81: 1047–9.Google Scholar
Berde, C., Willis, D. C. & Sandberg, E. C.Pregnancy in women with pseudoxanthoma elasticum. Obstet. Gynecol. Surv. 1983; 38: 339–44.Google Scholar
Lao, T. T., Walters, B. N. J. & Swiet, M.Pseudoxanthoma elasticum and pregnancy. Two case reports. Br. J. Obstet. Gynaecol. 1984; 91: 1049–50.CrossRefGoogle Scholar
Viljoen, D. L., Beatty, S. & Beighton, P.The obstetric and gynaecological implications of pseudoxanthoma elasticum. Br. J. Obstet. Gynaecol. 1987; 94: 884–8.CrossRefGoogle Scholar
Bercovitch, L., Lerous, T., Terry, S. & Weinstock, M. A.Pregnancy and obstetrical outcomes in pseudoxanthoma elasticum. Br. J. Dermatol. 2004; 151: 1011–18.CrossRefGoogle Scholar
Koizumi, M., Hagino, D., Fukuyama, C.et al. Schönlein-Henoch purpura during pregnancy: case report and review of the literature. J. Obstet. Gynaecol. Res. 2004; 30: 37–41.Google Scholar
Cummins, D. L., Mimouni, D., Rencic, A., Douba, D. J. & Nousari, C. H.Henoch-Schönlein purpura in pregnancy. Br. J. Dermatol. 2003; 149: 128–5.Google Scholar
Douglas, M. J., Gunka, V. B. & Dadelszen, P.Anesthesia for the parturient with pseudoxanthoma elasticum. Int. J. Obstet. Anesth. 2002; 12: 45–7.Google Scholar
Youngs, P. J., Sice, P. & Harvey, P.Labour analgesia and pseudoxanthoma elasticum (PXE). Int. J. Obstet. Anesth. 2003; 12: 48–50.Google Scholar
Levitt, M. W. D. & Collison, J. M.Difficult endotracheal intubation in a patient with pseudoxanthoma elasticum. Anaesth. Intensive Care 1982; 10: 62–4.Google Scholar
Peyvandi, F. & Mannuci, P. M.Rare coagulation disorders. Thromb. Haemost. 1999; 82: 1207–14.CrossRefGoogle Scholar
Kadir, R. A.Women and inherited bleeding disorders: pregnancy and delivery. Semin. Hematol. 1999; 36: 28–35.Google Scholar
Kasper, C. K.Hereditary plasma clotting factor disorders and their management. Haemophilia 2000; 6: 13–27.Google Scholar
Strong, J.Bleeding disorders in pregnancy. Curr. Obstet. Gynaecol. 2003; 13: 1–6.Google Scholar
Haverkate, F. & Samama, M.Familial dysfibrinogenemia and thrombophilia. Report on a study of the SSC subcommittee on fibrinogen. Thromb. Haemost. 1995; 73: 151.Google Scholar
Inamoto, Y. & Terao, T.First report of case of congenital afibrinogenemia with successful delivery. Am. J. Obstet. Gynecol. 1985; 153: 803–4.Google Scholar
Goodwin, T. M.Congenital hypofibrinogenemia in pregnancy. Obstet. Gynecol. Surv. 1989; 44: 157–61.Google Scholar
Girolami, A., Scarano, L., Saggiorato, G.et al. Congenital deficiencies and abnormalities of prothrombin. Blood Coagul. Fibrinolysis 1998; 9: 557–69.Google Scholar
Catanzarite, V. A., Novotny, W. F., Cousins, L. M. & Schneider, J. M.Pregnancies in a patient with congenital absence of prothrombin activity: case report. Am. J. Perinatol. 1997; 14: 135–8.CrossRefGoogle Scholar
Girolami, A., Scandellari, R., Lombardi, A. M.et al. Pregnancy and oral contraceptives in factor V deficiency: a study of 22 patients (five homozygotes and 17 heterozygotes) and review of the literature. Haemophilia 2005; 11: 26–30.Google Scholar
O'Connell, M. P., Eogan, M., Murphy, K. M.et al. Solvent-detergent plasma as replacement therapy in a pregnant patient with factor V deficiency. J. Mat. Fet. Neonat. Med. 2004; 16: 69–70.Google Scholar
Perry, D. J.Factor VII deficiency. Br. J. Haematol. 2002; 118: 689–700.Google Scholar
Giansily-Blaizot, M., Biron-Andreani, D., Aguilar-Martinez, P.et al. Inherited factor VII deficiency and surgery: clinical data are the best criteria to predict the risk of bleeding. Br. J. Haematol. 2002; 117: 172–5.Google Scholar
Perry, M. G., Herrmann, F. H., Schulman, I. S.et al. Thrombosis in inherited factor VII deficiency. J. Thromb. Haemost. 2002; 1: 2153–8.Google Scholar
Rizk, D. E. E., Castella, A., Shaheen, H. & Deb, P.Factor VII deficiency detected during pregnancy: a case report. Am. J. Perinatol. 1999; 16: 223–6.CrossRefGoogle Scholar
Pehlivanov, B., Milchev, N. & Kroumov, G.Factor VII deficiency and its treatment in delivery with recombinant factor VII. Eur. J. Obstet. Gynecol. Reprod. Biol. 2004; 116: 237–8.Google Scholar
Eskandari, N., Feldman, N. & Greenspoon, J. S.Factor VII deficiency in pregnancy treated with recombinant factor VIIa. Obstet. Gynecol. 2002; 99: 935–7.Google Scholar
Jimenez-Yuste, V., Villar, A., Morado, M.et al. Continuous infusion of recombinant activated factor VII during caesarean section delivery in a patient with congenital factor VII deficiency. Haemophilia 2000; 6: 588–90.Google Scholar
Lee, J-W.Von Willebrand disease, hemophilia A and B, and other factor deficiencies. Int. Anesth. Clin. 2004; 42: 59–71.Google Scholar
Gill, Cox J.Diagnosis and treatment of von Willebrand disease. Hematol. Oncol. Clin. N. Am. 2004; 18: 1277–99.Google Scholar
Kadir, R. A., Lee, C. A., Sabin, C. A., Pollard, D. & Economides, D. L.Pregnancy in women with von Willebrand's disease or factor XI deficiency. Br. J. Obstet. Gynaecol. 1998; 105: 314–21.CrossRefGoogle Scholar
Kasper, C. K.Hemophilia of Georgia, U.S.A. Protocols for the treatment of haemophilia and von Willebrand disease. Haemophilia 2000; 6: 84–93.Google Scholar
Mannucci, P. M.Treatment of von Willebrand's disease. N. Engl. J. Med. 2004; 35: 683–94.Google Scholar
Giangrande, P. L. F.Management of pregnancy in carriers of haemophilia. Haemophilia 1998; 4: 779–84.Google Scholar
Dhar, P., Abramovitz, S., DiMichele, D., Gibb, C. B. & Gadalla, F.Management of pregnancy in a patient with severe haemophilia A. Br. J. Anaesth. 2003; 91: 432–5.CrossRefGoogle Scholar
Russell, Z., Riconda, D., Pollack, L., O'Leary, T. D. & Carlan, S. J. Thrombosis in a pregnant hemophilia A carrier after intrapartum recombinant factor VIII. Obstet. Gynecol. 2005; 105: 875–6.CrossRefGoogle Scholar
Fukada, Y., Shima, T., Kawashima, S., Hirata, S. & Hoshi, K.Heterozygous hemophilia developed during pregnancy. J. Obstet. Gynaecol. Res. 2005; 31: 50–1.Google Scholar
Briet, E., Reisner, H. M. & Blatt, P. M.Factor IX levels during pregnancy in a woman with hemophilia B. Haemostasis 1982; 11: 87–9.Google Scholar
Guy, G. P., Baxi, L. V., Hurlet-Jensen, A.et al. An unusual complication in a gravida with factor IX deficiency: case report with review of the literature. Obstet. Gynecol. 1992; 80: 502–5.Google Scholar
Yang, M. Y. & Ragni, M. V.Clinical manifestations and management of labor and delivery in women with factor IX deficiency. Haemophilia 2004; 10: 483–90.Google Scholar
Romagnolo, C., Burati, S., Ciaffoni, S.et al. Severe factor X deficiency in pregnancy: case report and review of the literature. Haemophilia 2004; 10: 665–8.Google Scholar
Brody, J. I. & Finch, S. C.Improvement of factor X deficiency during pregnancy. N. Engl. J. Med. 1960; 263: 996–9.Google Scholar
Konje, J. C., Murphy, P., Chazal, R., Davidson, A. & Taylor, D.Severe factor X deficiency and successful pregnancy. Br. J. Obstet. Gynaecol. 1994; 101: 910–11.CrossRefGoogle Scholar
Kumar, M. & Mehta, P.Congenital coagulopathies and pregnancy: report of four pregnancies in a factor X-deficient woman. Am. J. Hematol. 1994; 46: 241–4.Google Scholar
Hurria, K., Castellone, D., Peerschke, E. I. B. & Asch, A.Factor X deficiency and pregnancy. Lab. Med. 2003; 34: 302–3.Google Scholar
Bofill, J. A., Young, R. A. & Perry, K. G.Successful pregnancy in a woman with severe factor X deficiency. Obstet. Gynecol. 1996; 88: 723.CrossRefGoogle Scholar
Connelly, N. F. & Brull, S. J.Anesthetic management of a patient with Factor XI deficiency and Factor XI inhibitor undergoing a cesarean section. Anesth. Analg. 1993; 76: 1365–6.CrossRefGoogle Scholar
Salomon, O., Steilberg, D. M., Tamarin, I., Zivelin, A. & Seligsohn, U.Plasma replacement therapy during labor is not mandatory for women with severe factor XI deficiency. Blood Coagul. Fibrinolysis 2005; 16: 37–41.Google Scholar
David, A. L., Paterson-Brown, S. & Letsky, E. A.Factor XI deficiency presenting in pregnancy: diagnosis and management. B. J. O. G. 2002; 109: 840–3.Google Scholar
Pauer, H-U., Burfeind, P., Kostering, H., Emons, G. & Hinney, B.Factor XII deficiency is strongly associated with primary recurrent abortions. Fertil. Steril. 2003; 80: 590–4.CrossRefGoogle Scholar
Girolami, A., Randi, M. L., Gavasso, S., Lombardi, A. M. & Spiezia, F.The occasional venous thromboses seen in patients with severe (homozygous) FXII deficiency are probably due to associated risk factors: a study of prevalence in 21 patients and review of the literature. J. Thromb. Thrombolysis 2004; 17: 139–43.Google Scholar
Burrows, R. F., Fay, J. G. & Burrows, E. A.Bleeding risk and reproductive capacity among patients with factor XIII deficiency: a case presentation and review of the literature. Obstet. Gynecol. Surv. 2000; 55: 103–8.Google Scholar
Inbal, A. & Muszbek, L.Coagulation factor deficiencies and pregnancy loss. Semin. Thromb. Hemost. 2003; 29: 171–4.CrossRefGoogle Scholar
Shetty, S., Madkaikar, M., Nair, S.et al. Combined factor V and VIII deficiency in Indian population. Haemophilia 2000; 6: 504–7.Google Scholar
McMahon, M. J. & James, A. H.Combined deficiency of factors II, VII, IX, and X (Borgschulte-Grigsby deficiency) in pregnancy. Obstet. Gynecol. 2001; 97: 806–8.Google Scholar
Cohen, S., Daitch, J. S., Amar, D. & Goldiner, P. L.Epidural analgesia for labor and delivery in a patient with von Willebrand's disease. Reg. Anesth. 1989; 14: 95–7.Google Scholar
Milaskiewicz, R. M., Holdcroft, A. & Letsky, E.Epidural anaesthesia and von Willebrand's disease. Anaesthesia 1990; 45: 462.Google Scholar
Cohen, S. & Zada, Y.Neuraxial block for von Willebrand's disease. (letter)Anaesthesia 2001; 56: 397.Google Scholar
Jones, B. P., Bell, E. A. & Mohammed, M.Epidural labor analgesia in parturient with von Willebrand's disease type IIA and severe preeclampsia. Anesthesiology 1999; 90: 1219–20.Google Scholar
Hepner, D. L & Tsen, L. C.Severe thrombocytopenia, type 2B von Willebrand disease and pregnancy. Anesthesiology 2004; 101: 1465–7.Google Scholar
Inwood, M. J. & Meltzer, D. B.The female carrier of haemophilia – a problem for the anaesthetist. Can. Anaesth. Soc. J. 1978; 25: 266.Google Scholar
Paidas, M. J., De-Hui, W. K., Langhoff-Roos, J. & Arkel, Y. S.Inherited thrombophilias and adverse pregnancy outcome: screening and management. Sem. Perinatol. 2005; 29: 150–63.Google Scholar
Jordaan, D-J., Shoon, M. G. & Badenhorst, P. N.Thrombophilia screening in pregnancy. Obstet. Gynecol. Surv. 2005; 60: 394–404.Google Scholar
Confidential Enquiry into Maternal and Child Health. Why Mothers Die 2000–2002. London: RCOG Press. 2004.
Greer, I. A. & Nelson-Piercy, C.Low-molecular-weight heparins for thromboprophylaxis and treatment of venous thromboembolism in pregnancy: a systematic review of safety and efficacy. Blood 2005; 106: 401–7.Google Scholar
Selm, M., Kanhai, H. H. H. & Gravenhorst, J. B.Maternal hydrops syndrome: a review. Obstet. Gynecol. Surv. 1991; 46: 785–8.Google Scholar
Vidaeff, A. C., Pschirrer, E. R., Mastrobattista, J. M.et al. Mirror syndrome. A case report. J. Reprod. Med. 2002; 47: 770–4.Google Scholar
Mizrahi-Arnaud, A., Wilkins Haug, L., Marshall, A. & Silva, V.Maternal mirror syndrome after in utero aortic valve dilation. A case report. Fetal Diagn. Ther. 2006; 21: 439–43.Google Scholar

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  • Blood disorders
    • By M. Joanne Douglas, Department of Anesthesia, BC Women's Hospital, Vancouver, Canada, Penny Ballem, Clinical Professor, Department of Medicine, School of Hematology, Faculty of Medicine, University of British Columbia, Victoria, BC, Canada
  • Edited by David R. Gambling, University of California, San Diego, M. Joanne Douglas, University of British Columbia, Vancouver, Robert S. F. McKay, University of Kansas
  • Book: Obstetric Anesthesia and Uncommon Disorders
  • Online publication: 19 October 2009
  • Chapter DOI: https://doi.org/10.1017/CBO9780511544552.018
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  • Blood disorders
    • By M. Joanne Douglas, Department of Anesthesia, BC Women's Hospital, Vancouver, Canada, Penny Ballem, Clinical Professor, Department of Medicine, School of Hematology, Faculty of Medicine, University of British Columbia, Victoria, BC, Canada
  • Edited by David R. Gambling, University of California, San Diego, M. Joanne Douglas, University of British Columbia, Vancouver, Robert S. F. McKay, University of Kansas
  • Book: Obstetric Anesthesia and Uncommon Disorders
  • Online publication: 19 October 2009
  • Chapter DOI: https://doi.org/10.1017/CBO9780511544552.018
Available formats
×

Save book to Google Drive

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Google Drive.

  • Blood disorders
    • By M. Joanne Douglas, Department of Anesthesia, BC Women's Hospital, Vancouver, Canada, Penny Ballem, Clinical Professor, Department of Medicine, School of Hematology, Faculty of Medicine, University of British Columbia, Victoria, BC, Canada
  • Edited by David R. Gambling, University of California, San Diego, M. Joanne Douglas, University of British Columbia, Vancouver, Robert S. F. McKay, University of Kansas
  • Book: Obstetric Anesthesia and Uncommon Disorders
  • Online publication: 19 October 2009
  • Chapter DOI: https://doi.org/10.1017/CBO9780511544552.018
Available formats
×