• Tidak ada hasil yang ditemukan

Takayasu’s arteritis

Dalam dokumen A Comprehensive Guide for Clinicians (Halaman 136-139)

Another rare cause of aortopathy in pregnancy is Takayasu’s arteritis. Dissection is rare. Severe hyper- tension, arterial occlusions, and acute aortic regurgita- tion are more common. In the largest series, about 25%

of pregnancies resulted in fetal death .[ 50 ]

Conclusions

Aortopathies include a wide range of acquired, genetic, and congenital disorders, many of which have multisys- tem involvement. Prepregnancy counseling is manda- tory in women with a known or suspected aortopathy.

Th is should include a multidisciplinary discussion with appropriate genetic, cardiac, obstetric, anesthetic, and neonatal input. Although a diverse group of dis- eases, there are guiding principles that assist in mak- ing appropriate complex management plans that these patients require .

References

1. Huisman CM , Zwart JJ , Roos-Hesselink JW et al. Incidence and predictors of maternal

cardiovascular mortality and severe morbidity in the Netherlands: A prospective cohort study . PLoS ONE 2013 ; 8 : e56494 .

2. Cantwell R , Clutton-Brock T , Cooper G. Saving Mothers’ Lives . Reviewing maternal death to make motherhood safer 2006–2008. BJOG 2011 ; 118 ( Supp.1 ): 1 – 203 .

3. Mabie WC , DiSessa TG , Crocker LG , et al. A

longitudinal study of cardiac output in normal human pregnancy . Am J Obstet Gynecol 1994 ; 170 : 849–56 . 4. Robson SC , Hunter S , Boys RJ. et al. Serial study of

factors infl uencing changes in cardiac output during pregnancy . Am J Physiol 1989 ; 256 : H1060–5 .

5. Poppas A , Shroff SG , Korcarz CE et al. Serial assessment of the cardiovascular system in normal pregnancy.

Role of arterial compliance and pulsatile arterial load . Circulation 1997 ; 95 : 2407–15 .

6. Gutin LS , Merz AE , Bakalov VK et al. Parity and aortic dimensions in healthy women . Int J Cardiol 2013 ; 165 ( 2 ): 383–4 .

7. Campisi D , Cutolo M , Carruba G et al. Evidence for soluble and nuclear site I binding of estrogens in human aorta . Atherosclerosis 1993 ; 103 : 267–77 .

8. Wingrove CS , Garr E , Godsland IF et al.

17-beta-oestradiol enhances release of matrix metalloproteinase-2 from human vascular smooth muscle cells . Biochim Biophys Acta 1998 ; 1406 : 169–74 . 9. Manallo-Estrella P , Barker AE . Histopathologic

fi ndings in human aortic media associated with pregnancy . Arch Path 1967 ; 83 : 336–41 .

10. Pedowitz P , Perell A . Aneurysms complicated by pregnancy. I. Aneurysms of the aorta and its major branches . Am J Obstet Gynecol 1957 ; 73 ( 4 ): 720–35 . 11. Pyeritz RE . Disorders of fi brillins and

microfi brilogenesis: Marfan syndrome, MASS phenotype, contractural arachnodactyly and related conditions. In: Principles and Practice of Medical Genetics , 3rd edn. New York :  Churchill Livingstone ;  1996 .

12. Lind J , Wallenburg HC . Th e Marfan syndrome and pregnancy: A retrospective study in a Dutch

population . Eur J Obstet Gynecol Reprod Biol 2001 ; 98 ( 1 ): 28 – 35 .

13. Meijboom LJ , Drenthen W , Pieper PG et al. Obstetric complications in Marfan syndrome . Int J Cardiol 2006 ; 110 : 53–9 .

14. Pini R , Roman MJ , Kramer-Fox R et al. Mitral valve dimensions and motion in Marfan patients with and without mitral valve prolapse. Comparison to primary mitral valve prolapse and normal subjects . Circulation 1989 ; 80 : 915–24 .

15. Schnitker MA , Bayer CA . Dissection aneurysm of the aorta in young individuals, particularly in association with pregnancy . Ann Intern Med 1944 ; 29 : 486 – 511 . 16. Williams GM , Gott VL , Brawley RK. et al. Aortic

disease associated with pregnancy . J Vasc Surg 1988 ; 8 : 470–5 .

17. Hirst AE , Johns VJ , Kime SW . Dissecting aneurysm of the aorta: A review of 505 cases . Medicine (Baltimore) 1958 ; 37 : 217–79 .

18. Oskoui R , Lindsay J . Aortic dissection in women

< 40 years of age and the unimportance of pregnancy . Am J Cardiol 1994 ; 73 ( 11 ): 821–3 .

19. Meijboom LJ , Vos FE , Timmermans J et al.

Pregnancy and aortic root growth in the Marfan syndrome: A prospective study . Eur Heart J 2005 : 26 ( 9 ): 914–20 .

20. European Society of Gynecology (ESG) , Association for European Paediatric Cardiology (AEPC) , German Society for Gender Medicine (DGesGM) , et al. ESC Guidelines on the management of cardiovascular diseases during pregnancy: Th e Task Force on the Management of Cardiovascular Diseases during Pregnancy of the European Society of Cardiology (ESC) . Eur Heart J 2011 ; 32 : 3147–97 .

21. Hiratzka LF , Bakris GL , Beckman JA et al. 2010 ACCF/

AHA/AATS/ACR/ASA/SCA/SCAI/SIR/STS/SVM Guidelines for the diagnosis and management of patients with thoracic aortic disease. A Report of the American College of Cardiology Foundation/American Heart Association Task Force on Practice Guidelines, American Association for Th oracic Surgery, American College of Radiology, American Stroke Association, Society of Cardiovascular Anesthesiologists, Society for Cardiovascular Angiography and Interventions, Society of Interventional Radiology, Society of Th oracic Surgeons, and Society for Vascular Medicine . J Am Coll Cardiol 2010 ; 55 ( 14 ): e27–e129 .

22. Groenink M , Lohuis TAJ , Tijssen JGP et al.

Survival and complication free survival in Marfan syndrome: Implications of current guidelines . Heart 1999 ; 82 : 499 – 504 .

23. Silverman DI , Gray J , Roman MJ et al. Family history of severe cardiovascular disease in Marfan

Section 4: Antenatal Care: Specifi c Maternal Conditions

syndrome is associated with increased aortic diameter and decreased survival . J Am Coll Cardiol 1995 ; 26 ( 4 ): 1062–7 .

24. Immer FF , Bansi AG , Immer-Bansi AS. et al. Aortic dissection in pregnancy: Analysis of risk factors and outcome . Ann Th orac Surg 2003 ; 76 ( 1 ): 309–14 . 25. Williams A , Child A , Rowntree J et al. Marfan

syndrome: Successful pregnancy aft er aortic root and arch replacement . BJOG 2002 ; 109 ( 10 ): 1187–8 . 26. Shores J , Berger KR , Murphy EA et al. Progression

of aortic dilatation and the benefi t of long-term beta-adrenergic blockade in Marfan syndrome . N Engl J Med 1994 ; 330 ( 19 ): 1335–41 .

27. Groenink M , de Roos A , Mulder BJ et al. Changes in aortic distensibility and pulse wave velocity assessed with magnetic resonance imaging following beta-blocker therapy in the Marfan syndrome . Am J Cardiol 1998 ; 82 ( 2 ): 203–8 .

28. Gao L , Mao Q , Wen D et al. Th e eff ect of beta-blocker therapy on progressive aortic dilatation in children and adolescents with Marfan syndrome: A meta-analysis . Acta Paediatr 2011 ; 100 ( 9 ): e101–5 .

29. Groenink M , den Hartog AW , Franken R et al. Losartan reduces aortic dilatation rate in adults with Marfan syndrome: A randomized controlled trial . Eur Heart J 2013 ; 34 ( 45 ): 3491–500 .

30. Harton GL , Tsipouras P , Sisson ME. et al.

Preimplantation genetic testing for Marfan syndrome . Mol Hum Reprod 1996 ; 2 ( 9 ): 713–5 .

31. Regalado ES , Guo DC , Estrera AL et al. Acute aortic dissections with pregnancy in women with ACTA2 mutations . Am J Med Genet A 2014 ; 164 : 106–12 . 32. Rossiter JP , Repke JT , Morales AJ et al. A prospective

longitudinal evaluation of pregnancy in the Marfan syndrome . Am J Obstet Gynecol 1995 ; 173 ( 5 ): 1599–606 . 33. Zeebregts CJ , Schepens MA , Hameeteman TM et al.

Acute aortic dissection complicating pregnancy . Ann Th orac Surg 1997 ; 64 : 1345–8 .

34. Parry AJ , Westaby S . Cardiopulmonary bypass during pregnancy . Ann Th orac Surg 1996 ; 61 ( 6 ): 1865–9 . 35. Mahli A , Izdes S , Coskun D . Cardiac operations during

pregnancy: Review of factors infl uencing fetal outcome . Ann Th orac Surg 2000 ; 69 : 1622–6 .

36. Lacassie HJ , Millar S , Leithe LG et al. Dural ectasia: A likely cause of inadequate spinal anaesthesia in two parturients with Marfan syndrome . Br J Anaesth 2005 ; 94 ( 4 ): 500–4 . 37. Beauchesne LM , Connolly HM , Ammash NM et al.

Coarctation of the aorta: Outcome of pregnancy . J Am Coll Cardiol 2001 ; 38 ( 6 ): 1728–33 .

38. Stern HC , Locher D , Wallnofer K et al. Noninvasive assessment of coarctation of the aorta: Comparative

measurements by two-dimensional echocardiography, magnetic resonance, and angiography . Pediatr Cardiol 1991 ; 12 ( 1 ): 1 – 5 .

39. Stewart AB , Ahmed R , Travill CM et al. Coarctation of the aorta life and health 20–44 years aft er surgical repair . Br Heart J 1993 ; 69 ( 1 ): 65 – 70 .

40. Siu SC , Sermer M , Colman JM et al. Prospective multicenter study of pregnancy outcomes in women with heart disease . Circulation 2001 ; 104 ( 5 ): 515–21 . 41. Kupferminc MJ , Lessing JB , Jaff a A et al. Fetomaternal

blood fl ow measurements and management of combined coarctation and aneurysm of the thoracic aorta in pregnancy . Acta Obstet Gynecol Scand 1993 ; 72 ( 5 ): 398 – 402 .

42. Knyshov GV , Sitar LL , Glagola MD et al. Aortic aneurysms at the site of the repair of coarctation of the aorta: A review of 48 patients . Ann Th orac Surg 1996 ; 61 ( 3 ): 935–9 .

43. Rose V , Gold RJM , Lindsay G et al. A possible increase in the incidence of congenital heart defects among the off spring of aff ected parents . JACC 1985 ; 6 : 376–82 . 44. Cecconi M , Manfrin M , Moraca A et al. Aortic

dimensions in patients with bicuspid aortic valve without signifi cant valve dysfunction . Am J Cardiol 2005 ; 95 ( 2 ): 292–4 .

45. Oliver JM , Alonso-Gonzalez R , Gonzalez AE et al.

Risk of aortic root or ascending aorta complications in patients with bicuspid aortic valve with and without coarctation of the aorta . Am J Cardiol 2009 ; 104 ( 7 ): 1001–6 .

46. McKellar SH , MacDonald RJ , Michelena HI et al.

Frequency of cardiovascular events in women with a congenitally bicuspid aortic valve in a single community and eff ect of pregnancy on events . Am J Cardiol 2011 ; 107 : 96–9 .

47. Ostberg JE , Brookes JA , McCarthy C et al. A comparison of echocardiography and magnetic resonance imaging in cardiovascular screening of adults with Turner syndrome . J Clin Endocrinol Metab 2004 ; 89 ( 12 ): 5966–71 .

48. Hagman A , Loft A , Wennerholm UB et al. Obstetric and neonatal outcome aft er oocyte donation in 106 women with Turner syndrome: A Nordic cohort study . Hum Reprod 2013 ; 28 ( 6 ): 1598–609 .

49. Lurie S , Manor M , Hagay ZJ . Th e threat of type IV Ehlers-Danlos syndrome on maternal well-being during pregnancy: Early delivery may make the diff erence . J Obstet Gynaecol 1998 ; 18 ( 3 ): 245–8 . 50. Hauenstein E , Frank H , Bauer JS. et al. Takayasu’s

arteritis in pregnancy: Review of literature and discussion . J Perinat Med 2010 ; 38 : 55 – 62 .

Heart Disease and Pregnancy, 2nd edn. ed. Philip J. Steer and Michael A. Gatzoulis. Published by Cambridge University Press.

© Cambridge University Press 2016.

Chapter

Practical practice points

1. Severe valvular stenosis is poorly tolerated in pregnancy.

2. Rheumatic mitral stenosis is the leading cardiac cause of maternal death in the developing world.

3. Th e initial presentation of many women with rheumatic mitral stenosis occurs when pregnancy precipitates symptoms for the fi rst time.

4. Diuretics and beta-blockers are useful in medical management, but balloon mitral valvuloplasty has a high success rate and is the mainstay of treatment for severe mitral stenosis in pregnancy .

5. Bicuspid aortic valve is the commonest cause of aortic stenosis in women of childbearing age.

6. Preconception assessment is important to determine whether a woman with moderate or severe aortic stenosis is likely to tolerate pregnancy well, or whether she should undergo prepregnancy aortic valve replacement.

7. Th e severely stenotic bicuspid aortic valve in adulthood is oft en unsuitable for balloon valvotomy, so surgical aortic valve replacement may be necessary if a woman with severe aortic stenosis decompensates during pregnancy .

Dalam dokumen A Comprehensive Guide for Clinicians (Halaman 136-139)