Value of risk scores in the decision to palliate patients with ruptured abdominal aortic aneurysm

Author:

,Sweeting M J1ORCID,Ulug P2,Roy J3,Hultgren R3,Indrakusuma R4ORCID,Balm R4,Thompson M M5,Hinchliffe R J6,Thompson S G1,Powell J T2,Balm R7,Koelemay M J W7,Idu M M7,Kox C7,Legemate D A7,Huisman L C7,Willems M C M7,Reekers J A7,van Delden O M7,van Lienden K P7,Hoornweg L L7,Reimerink J J7,van Beek S C7,Vahl A C8,Leijdekkers V J8,Bosma J8,Montauban van Swijndregt A D8,de Vries C8,van der Hulst V P M8,Peringa J8,Blomjous J G A M8,Visser M J T8,van der Heijden F H W M8,Wisselink W9,Hoksbergen A W J9,Blankensteijn J D9,Visser M T J9,Coveliers H M E9,Nederhoed J H9,van den Berg F G9,van der Meijs B B9,van den Oever M L P9,Lely R J9,Meijerink M R9,Westra I9,Voorwinde A10,Ultee J M10,van Nieuwenhuizen R C10,Dwars B J11,Nagy T O M11,Tolenaar P12,Wiersema A M12,Lawson J A13,van Aken P J13,Stigter A A13,van den Broek T A A14,Vos G A14,Mulder W15,Strating R P15,Nio D16,Akkersdijk G J M16,van der Elst A16,van Exter P17,Desgranges P18,Becquemin J-P18,Allaire E18,Cochennec F18,Marzelle J18,Louis N18,Schneider J18,Majewski M18,Castier Y19,Leseche G19,Francis F19,Steinmetz E20,Berne J-P20,Favier C20,Haulon S21,Koussa M21,Azzaoui R21,Piervito D21,Alimi Y22,Boufi M22,Hartung O22,Cerquetta P22,Amabile P23,Piquet P23,Penard J23,Demasi M23,Alric P24,Cannaud L24,Berthet J-P24,Julia P25,Fabiani J-N25,Alsac J M25,Gouny P26,Badra A26,Braesco J26,Favre J-P27,Albertini J-N27,Martinez R28,Hassen-Khodja R29,Batt M29,Jean E29,Sosa M29,Declemy S29,Destrieux-Garnier L30,Lermusiaux P31,Feugier P31,Powell J T32,Ashleigh R33,Gomes M34,Greenhalgh R M35,Grieve R34,Hinchliffe R36,Sweeting M37,Thompson M M36,Thompson S G37,Ulug P38,Cheshire N J39,Boyle J R40,Serracino-Inglott F41,Smyth J V41,Thompson M M36,Hinchliffe R J36,Bell R42,Wilson N43,Bown M44,Dennis M44,Davis M45,Ashleigh R33,Howell S46,Wyatt M G47,Valenti D48,Bachoo P49,Walker P50,Mac- Sweeney S51,Davies J N52,Rittoo D53,Parvin S D53,Yusuf W54,Nice C55,Chetter I56,Howard A57,Chong P58,Bhat R59,Gordon A60,Lane I60,Hobbs S61,Pillay W62,Rowlands T63,El-Tahir A63,Asquith J64,Cavanagh S65,Dubois L66,Forbes T L66,Hultgren R67,Roy J67,Zommorodi S67,Lindquist Liljeqvist M67,Siika A67,Nilsson O67,Garcia Värild A67, , ,

Affiliation:

1. Department of Public Health and Primary Care, University of Cambridge, Cambridge, UK

2. Vascular Surgery Research Group, Imperial College London, London, UK

3. Department of Molecular Medicine and Surgery, Karolinska Institute, Stockholm, Sweden

4. Department of Vascular Surgery, Academic Medical Centre, Amsterdam, The Netherlands

5. Stanford School of Medicine, Stanford, California, USA

6. Bristol Centre for Surgical Research, University of Bristol, Bristol, UK

7. Academic Medical Centre, Amsterdam, The Netherlands

8. Onze LieveVrouwe Gasthuis, Amsterdam, The Netherlands

9. VU University Medical Centre, Amsterdam, The Netherlands

10. Sint Lucas Andreas Ziekenhuis, Amsterdam, The Netherlands

11. Slotervaartziekenhuis, Amsterdam, The Netherlands

12. Boven IJ Ziekenhuis, Amsterdam, The Netherlands

13. Ziekenhuis Amstelland, Amsterdam, The Netherlands

14. Waterlandziekenhuis, Purmerend, The Netherlands

15. Zaans Medisch Centrum, Zaandam, The Netherlands

16. Spaarne Ziekenhuis, Hoofddorp, The Netherlands

17. Regional ambulance services

18. Centre Hospitalier Universitaire (CHU) Henri Mondor, Créteil, France

19. CHU Bichat, Paris, France

20. CHU Dijon, Dijon, France

21. Centre Hospitalier Régional Universitaire (CHRU) Lille, Lille, France

22. Hôpital Nord Marseille, Marseille, France

23. CHUMarseille, Marseille, France

24. CHU Montpellier, Montpellier, France

25. CHU Hôpital Européen Georges-Pompidou, Paris, France

26. CHU Brest, Brest, France

27. CHU Saint Etienne, Saint Etienne, France

28. CHRU Tours, Tours, France

29. CHU Nice, Nice, France

30. Centre Hospitalier Régional Annecy, Annecy, France

31. CHU Lyon, Lyon, France

32. Chair; Imperial College London, London, UK

33. University Hospital of South Manchester, Manchester, UK

34. London School of Hygiene and Tropical Medicine, London, UK

35. Imperial College London, London, UK

36. St George's Hospital, London, UK

37. University of Cambridge, Cambridge, UK

38. ImperialCollege London, London, UK

39. Imperial College Healthcare NHS Trust, London, UK

40. Addenbrooke's Hospital, Cambridge, UK

41. Manchester Royal Infirmary, Manchester, UK

42. Guy's and St Thomas’ Hospital, London, UK

43. Kent and Canterbury Hospital, Canterbury, UK

44. Leicester Royal Infirmary, Leicester, UK

45. Royal Free Hospital, London, UK

46. Leeds General Infirmary, Leeds, UK

47. Freeman Hospital, Newcastle upon Tyne, UK

48. King's College Hospital, London, UK

49. Aberdeen Royal Infirmary, Aberdeen, UK

50. JamesCook University Hospital, Middlesbrough, UK

51. Queen's Medical Centre, Nottingham, UK

52. Royal Cornwall Hospital, Truro, UK

53. Royal BournemouthHospital, Bournemouth, UK

54. Royal Sussex County Hospital, Brighton, UK

55. Queen Elizabeth Hospital, Gateshead, UK

56. Hull Royal Infirmary, Hull, UK

57. Colchester General Hospital, Colchester, UK

58. Frimley Park Hospital, Frimley, UK

59. Ninewells Hospital, Dundee, UK

60. University Hospital of Wales, Cardiff, UK

61. New Cross Hospital, Wolverhampton, UK

62. Doncaster Royal Infirmary, Doncaster, UK

63. Royal Derby Hospital, Derby, UK

64. University Hospital of North Staffordshire, Stoke-on-Trent, UK

65. York Hospital, York, UK

66. London Health Sciences Centre, University of Western Ontario, London, Ontario, Canada

67. Karolinska Institute, Stockholm, Sweden

Abstract

Abstract Background The aim of this study was to develop a 48-h mortality risk score, which included morphology data, for patients with ruptured abdominal aortic aneurysm presenting to an emergency department, and to assess its predictive accuracy and clinical effectiveness in triaging patients to immediate aneurysm repair, transfer or palliative care. Methods Data from patients in the IMPROVE (Immediate Management of the Patient With Ruptured Aneurysm: Open Versus Endovascular Repair) randomized trial were used to develop the risk score. Variables considered included age, sex, haemodynamic markers and aortic morphology. Backwards selection was used to identify relevant predictors. Predictive performance was assessed using calibration plots and the C-statistic. Validation of the newly developed and other previously published scores was conducted in four external populations. The net benefit of treating patients based on a risk threshold compared with treating none was quantified. Results Data from 536 patients in the IMPROVE trial were included. The final variables retained were age, sex, haemoglobin level, serum creatinine level, systolic BP, aortic neck length and angle, and acute myocardial ischaemia. The discrimination of the score for 48-h mortality in the IMPROVE data was reasonable (C-statistic 0·710, 95 per cent c.i. 0·659 to 0·760), but varied in external populations (from 0·652 to 0·761). The new score outperformed other published risk scores in some, but not all, populations. An 8 (95 per cent c.i. 5 to 11) per cent improvement in the C-statistic was estimated compared with using age alone. Conclusion The assessed risk scores did not have sufficient accuracy to enable potentially life-saving decisions to be made regarding intervention. Focus should therefore shift to offering repair to more patients and reducing non-intervention rates, while respecting the wishes of the patient and family.

Funder

UK National Institute for Health Research (NIHR) Health Technology Assessment (HTA) programme

Publisher

Oxford University Press (OUP)

Subject

Surgery

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