Læknablaðið - 01.01.2015, Blaðsíða 34
34 LÆKNAblaðið 2015/101
Valdar heimildir
1. www.hagstofa.is/Pages/95?NewsID=5028 - desember
2014.
3. Pursnani S, Korley F, Gopaul R, Kanade P, Chandra
N, Shaw RE, et al. Percutaneous coronary intervention
versus optimal medical therapy in stable coronary
artery disease: a systematic review and meta-analysis of
randomized clinical trials. Circ Cardiovasc Interv 2012; 5:
476-90.
5. Blaha MJ, Martin SS. How do statins work?: changing
paradigms with implications for statin allocation. J Am
Coll Cardiol 2013; 62: 2392-4.
6. Montalescot G, Sechtem U, Achenbach S, Andreotti F,
Arden C, Budaj A, et al. 2013 ESC guidelines on the
management of stable coronary artery disease: the Task
Force on the management of stable coronary artery
disease of the European Society of Cardiology. Eur Heart
J 2013; 34: 2949-3003.
8. Gibbons RJ, Chatterjee K, Daley J, Douglas JS, Fihn SD,
Gardin JM, et al. ACC/AHA/ACP-ASIM guidelines for
the management of patients with chronic stable angina: a
report of the American College of Cardiology/American
Heart Association Task Force on Practice Guidelines
(Committee on Management of Patients With Chronic
Stable Angina). J Am Coll Cardiol 1999; 33: 2092-197.
10. Henderson RA, O'Flynn N, Guideline Development
Group: Management of stable angina: summary of NICE
guidance. Heart 2012; 98: 500-7.
11. Hjalmarson A, Goldstein S, Fagerberg B, Wedel H,
Waagstein F, Kjekshus J, et al. Effects of controlled-
release metoprolol on total mortality, hospitalizations,
and well-being in patients with heart failure: the
Metoprolol CR/XL Randomized Intervention Trial in
congestive heart failure (MERIT-HF). MERIT-HF Study
Group JAMA 2000; 283: 1295-302.
12. Bangalore S, Steg PG, Bhatt DL. beta-Blocker use for
patients with or at risk for coronary artery disease--reply.
JAMA 2013; 309: 439-40.
16. Nissen SE, Tuzcu EM, Libby P, Thompson PD, Ghali
M, Garza D, et al. Effect of antihypertensive agents on
cardiovascular events in patients with coronary disease
and normal blood pressure: the CAMELOT study: a
randomized controlled trial. JAMA 2004; 292: 2217-25.
23. Baigent C, Blackwell L, Emberson J, Holland LE, Reith
C, Bhala N, et al. Efficacy and safety of more intensive
lowering of LDL cholesterol: a meta-analysis of data from
170,000 participants in 26 randomised trials. Lancet 2010;
376: 1670-81.
25. Randomised trial of cholesterol lowering in 4444
patients with coronary heart disease: the Scandinavian
Simvastatin Survival Study (4S). Lancet 1994; 344: 1383-9.
26. Libby P: Mechanisms of acute coronary syndromes and
their implications for therapy. N Engl J Med 2013; 368:
2004-13.
28. Oddsson SJ, Sigurdsson MI, Helgadottir S, Sigurjonsson
H, Viktorsson S, Arnorsson T, et al. Lower mortality
following coronary arterial revascularization in patients
taking statins. Scand Cardiovasc J 2012; 46: 353-8.
31. Stone NJ, Robinson J, Lichtenstein AH, Merz CN, Blum
CB, Eckel RH, et al. 2013 ACC/AHA Guideline on the
Treatment of Blood Cholesterol to Reduce Atherosclerotic
Cardiovascular Risk in Adults: A Report of the American
College of Cardiology/American Heart Association Task
Force on Practice Guidelines. Circulation 2014; 129 (25
Suppl 2): S1-45.
32. Nielsen SF, Nordestgaard BG, Bojesen SE. Statin use and
reduced cancer-related mortality. N Engl J Med 2012; 367:
1792-802.
37. Keaney JF Jr, Curfman GD, Jarcho JA. A pragmatic view
of the new cholesterol treatment guidelines. N Engl J
Med 2014; 370: 275-8.
40. Perk J, De Backer G, Gohlke H, Graham I, Reiner Z,
Verschuren WM, et al. European guidelines on cardiovas-
cular disease prevention in clinical practice (version
2012) : the fifth joint task force of the European society
of cardiology and other societies on cardiovascular
disease prevention in clinical practice (constituted by
representatives of nine societies and by invited experts).
Int J Behav Med 2012; 19: 403-88.
41. Yusuf S, Zhao F, Mehta SR, Chrolavicius S, Tognoni
G, Fox KK. Clopidogrel in Unstable Angina to Prevent
Recurrent Events Trial Investigators. Effects of clopidog-
rel in addition to aspirin in patients with acute coronary
syndromes without ST-segment elevation. N Engl J Med
2001; 345: 494-502.
44. Lahoute C, Herbin O, Mallat Z, Tedgui A: Adaptive
immunity in atherosclerosis: mechanisms and future
therapeutic targets. Nat Rev Cardiol 2011; 8: 348-58.
45. Roberts R, Stewart AF: 9p21 and the genetic revolution
for coronary artery disease. Clin Chem 2012; 58: 104-12.
47. Danielsen R, Eyjolfsson K, Sigurdsson AF, Jonmundsson
EH. Árangur kransæðavíkkunaraðgerða á Íslandi 1987-
1998. Læknablaðið 2000; 86: 241-249.
49. ucr.uu.se/swedeheart/ - júní 2014.
53. Ciabattoni G, Ujang S, Sritara P, Andreotti F, Davies G,
Simonetti BM, et al. Aspirin, but not heparin, suppresses
the transient increase in thromboxane biosynthesis asso-
ciated with cardiac catheterization or coronary angio-
plasty. J Am Coll Cardiol 1993, 21: 1377-81.
54. Mehta SR, Yusuf S, Peters RJ, Bertrand ME, Lewis
BS, Natarajan MK, et al. Effects of pretreatment with
clopidogrel and aspirin followed by long-term therapy
in patients undergoing percutaneous coronary interven-
tion: the PCI-CURE study. Lancet 2001; 358: 527-33.
55. Danielsen R. Kransæðavíkkun eða segaleysandi meðferð
við bráðri kransæðastíflu. Læknablaðið 2000; 86: 237-8.
56. Steg PG, James SK, Atar D, Badano LP, Blomstrom-
Lundqvist C, Borger MA, et al. ESC Guidelines for the
management of acute myocardial infarction in patients
presenting with ST-segment elevation. Eur Heart J 2012;
33: 2569-619.
58. Wald DS, Morris JK, Wald NJ, Chase AJ, Edwards RJ,
Hughes LO, et al. Randomized trial of preventive angio-
plasty in myocardial infarction. N Engl J Med 2013; 369:
1115-23.
60. Hamm CW, Bassand JP, Agewall S, Bax J, Boersma E,
Bueno H, et al. ESC Guidelines for the management of
acute coronary syndromes in patients presenting without
persistent ST-segment elevation: The Task Force for the
management of acute coronary syndromes (ACS) in pati-
ents presenting without persistent ST-segment elevation
of the European Society of Cardiology (ESC). Eur Heart J
2011; 32: 2999-3054.
63. Sigurjonsson H, Helgadottir S, Oddsson SJ, Sigurdsson
MI, Geirsson A, Arnorsson T, et al. Árangur kransæðahjá-
veituaðgerða á Íslandi 2002-2006. Læknablaðið 2012; 98:
451-6.
65. Danielsen R, Eyjólfsson K. Samanburður á árangri og
fylgikvillum kransæðavíkkana hjá konum og körlum.
Læknablaðið 2003; 89: 759-64.
67. Danielsen R, Eyjolfsson K. Frumárangur kransæðavíkk-
ana hjá sjúklingum með sykursýki á Íslandi. Læknablaðið
2004, 90: 227-32.
68. Abizaid A, Costa MA, Centemero M, Abizaid AS,
Legrand VM, et al. Clinical and economic impact of
diabetes mellitus on percutaneous and surgical treatment
of multivessel coronary disease patients: insights from
the Arterial Revascularization Therapy Study (ARTS)
trial. Circulation 2001; 104: 533-8.
69. Erbel R, Haude M, Hopp HW, Franzen D, Rupprecht HJ,
Heublein B, et al. Coronary-artery stenting compared
with balloon angioplasty for restenosis after initial
balloon angioplasty. Restenosis Stent Study Group. N
Engl J Med 1998; 339: 1672-8.
71. Banning AP, Westaby S, Morice MC, Kappetein AP,
Mohr FW, Berti S, et al. Diabetic and nondiabetic patients
with left main and/or 3-vessel coronary artery disease:
comparison of outcomes with cardiac surgery and pacli-
taxel-eluting stents. J Am Coll Cardiol 2010; 55: 1067-75.
72. Long-term results of prospective randomised study of
coronary artery bypass surgery in stable angina pectoris.
European Coronary Surgery Study Group. Lancet 1982;
2: 1173-80.
73. Serruys PW, Onuma Y, Garg S, Vranckx P, De Bruyne B,
Morice MC, et al. 5-year clinical outcomes of the ARTS
II (Arterial Revascularization Therapies Study II) of the
sirolimus-eluting stent in the treatment of patients with
multivessel de novo coronary artery lesions. J Am Coll
Cardiol 2010; 55: 1093-101.
Heimildalistinn er birtur í heild sinni á heimasíðu blaðsins
Y f i R l i T
30 daga.121,122 Mest er þó áhættan hjá sjúklingum með alvarlegan
kransæðasjúkdóm og þeim sem koma til aðgerðar í losti vegna
bráðs hjartadreps.121,125
Lifun og forspárþættir
Rannsóknir á árangri kransæðahjáveituaðgerða hafa flestar beinst
að 30 daga dánartíðni (skurðdauða) fremur en langtímalifun. Þó
eru nokkrar rannsóknir sem sérstaklega hafa beinst að afdrifum
þessara sjúklinga til lengri tíma.126 Í bandarískri rannsókn reyndist
heildarlifun 5 árum eftir kransæðahjáveitu 86%,127 sem er heldur
lakari árangur en í íslenskri rannsókn þar sem 5 ára heildarlifun
var 90% (mynd 7).128 Sterkustu forspárþættir dauða innan 30 daga
frá aðgerð eru skert útfallsbrot, langur aðgerðartími, bráðaaðgerð,
langur legutími á gjörgæslu, óstöðug hjartaöng, sykursýki og
háþrýstingur.129 Í íslenskri rannsókn sem tók til sjúklinga eldri
en 75 ára voru mikilvægustu forspárþættir dauða innan 30 daga
insúlínháð sykursýki og alvarleg nýrnabilun.130 Í sömu rannsókn
reyndist lifun einu ári frá aðgerð vera 92%.
lokaorð
Árangur meðferðar við kransæðasjúkdómi hefur stórbatnað á
síðustu áratugum. Þessa þróun má rekja til ýmissa framfara, ekki
síst notkun statína, öflugri blóðflöguhemjandi lyfja og framfara
í kransæðavíkkunum, sérstaklega notkun nýrri stoðneta. Auk
þess hefur árangur hjáveituaðgerða batnað og eftirmeðferð er
markvissari. Nýjungar í meðferð hafa einnig fækkað fylgikvillum
og aukið lífsgæði sjúklinga, ekki síst í hópi aldraðra. Forvarnir og
bætt lýðheilsa eiga þó stærstan þátt í lækkandi dánartíðni krans-
æðasjúkdóms. Samvinna ýmissa sérgreina er lykilatriði að bættum
árangri, ekki síst náið samstarf hjartalækna, hjartaskurðlækna og
svæfinga- og gjörgæslulækna. Ekki má heldur gleyma hlutverki
heilsugæslulækna og fjölmargra annarra heilbrigðisstétta í for-
varnastarfi og eftirmeðferð, en öflugar forvarnir eru lykilatriði í að
koma frekari böndum á þetta umfangsmikla heilsufarsvandamál.