15
FOCUS ISSUE: VALVULAR HEART DISEASE Year in Cardiology Series The Year in Valvular Heart Disease Shahbudin H. Rahimtoola, MB, FRCP, DSC (HON) Los Angeles, California Aortic Stenosis (AS) Reviews. The following reviews were published during the year: “Insights into degenerative aortic valve (AV) disease” (1) and “Genomics: The next step to elucidate the etiology of calcific aortic stenosis (AS)” (2). State-of-the-art papers. In 2008, Ross published “Trans- septal left heart catheterization: a 50 year odyssey” (3). Comment. Transseptal left heart catheterization, a pio- neering procedure, was developed by John Ross Jr. when he was a surgical intern on a research rotation. He changed his specialty and went on to become a distinguished figure in cardiovascular medicine. Another article published at this time is “Emerging Applications for Transseptal Catheterization: Old Tech- niques for New Procedures” (4). Grading of AS severity; inconsistencies of echocardio- graphic criteria. The consistency of 3 echocardiographic criteria for severe AS (aortic valve area [AVA] 1.0 m 2 [or 0.6 cm 2 /m 2 ], mean gradient [MG] 40 mm Hg or peak flow [V max ] 4 m/s) used in the Guidelines were evaluated in 3,483 echocardiographic studies performed in 2,427 patients with normal left ventricular (LV) systolic function and calculated AVA of 2 cm 2 performed from 1994 to 2004 (5). There were “clinically significant” differences (Fig. 1, Table 1). Comment. This important and useful study highlights inconsistencies in criteria for severe AS. An accompanying editorial (6) discusses the importance of this study and probable reasons for the differences. The problem may be the guidelines. In this study, it would have been better to have measured cardiac output (CO). The authors acknowl- edge that calculating stroke volume from echocardiography is “often difficult.” They assumed a CO of 6 l/min, heart rate of 80 beats/min, and a systolic ejection time of 0.33 s. (Also see Gutierrez-Chico et al. [10] cited below.) Increasing blood pressure (BP) affects measured AS severity. In 22 patients, BP was increased by handgrip or phenylephrine infusion from a mean of 99 8 mm Hg to 121 10 mm Hg (p 0.001) (7). The AVA decreased from 1.15 0.32 cm 2 to 1.09 0.33 cm 2 (p 0.02). Comment. Flow was not measured but was calculated. The clinical situation arises in patients with severe or borderline severe AS, low gradient, and hypertension. The clinical problem is as follows: To what level, by what method, and how rapidly should BP be lowered before the measurements are repeated? Cardiac multidetector computed tomography (MDCT) to assess the severity of AS. Forty consecutive patients scheduled for aortic valve replacement (AVR) had echocar- diography, MDCT, and coronary angiography within a time span of 1 week (8). The AVA as measured by MDCT and echocardiography was 0.87 0.22 cm 2 versus 0.81 0.20 cm 2 (p 0.01; r 0.77, and p 0.01, respectively). Mean difference was 0.06 0.15 cm 2 . The authors found that MDCT correctly identified 26 of 33 patients (79%) with coronary artery stenosis and overestimated 3 patients with 50% stenosis. Where is pressure recovery best measured? In a pulse duplicator with flow rates of 2 to 5 l/min and orifice areas between 0.32 and 2.85 cm 2 , pressure recovery data were best measured 5 cm above AV (9), assuming that AV is a circular orifice, proximal aorta is circular without sinuses or bends, and flow is axially symmetric. The measurement of AVA by RT3D. In 41 patients with AS, AVA was measured with the use of Gorlin’s equation, Hakki’s formula, Doppler continuity equation (CE), 2D Simpson’s volumetric method, and by the real-time 3-dimensional echocardiography (RT3D). Cardiac output was measured by the thermodilution technique (10). RT3D had the best linear association and absolute agreement with Gorlin’s method of all noninvasive methods (r 0.902; intraclass correlation coefficient of 0.846) (Fig. 2). RT3D underestimates AVA (95% confidence interval [CI]: 0.084 to 0.193) and also grades most efficiently the severity of AS as mild, moderate, or severe (weighted kappa 0.932). The use of receiver-operating characteristic curves showed the optimal cutoff point to consider severe AS “remains close to 1 cm 2 (1.06 cm 2 ).” From the Griffith Center, Division of Cardiovascular Medicine, Department of Medicine, LACUSC Medical Center, Keck School of Medicine at University of Southern California, Los Angeles, California. Dr. Rahimtoola has received honoraria for educational lectures from the American College of Cardiology Foundation; American College of Physicians; University of California Los Angeles; University of California Irvine; Cornell University; Creighton University; Thomas Jefferson Uni- versity; Cedars-Sinai Medical Center; Harvard Medical School; University of Wis- consin; University of Hawaii; Cardiologists Association of Hong Kong, China; ATS; St. Jude Medical; Carbomedics; Merck; Pfizer; and Edwards Life Sciences. This review covers articles published from July 2007 to June 2008. Manuscript received September 18, 2008; revised manuscript received January 21, 2009, accepted February 6, 2009. Journal of the American College of Cardiology Vol. 53, No. 20, 2009 © 2009 by the American College of Cardiology Foundation ISSN 0735-1097/09/$36.00 Published by Elsevier Inc. doi:10.1016/j.jacc.2009.02.023

The Year in Valvular Heart Disease · septal left heart catheterization: a 50 year odyssey” (3). Comment. Transseptal left heart catheterization, a pio-neering procedure, was developed

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    Journal of the American College of Cardiology Vol. 53, No. 20, 2009© 2009 by the American College of Cardiology Foundation ISSN 0735-1097/09/$36.00P

    FOCUS ISSUE: VALVULAR HEART DISEASE Year in Cardiology Series

    The Year in Valvular Heart Disease

    Shahbudin H. Rahimtoola, MB, FRCP, DSC (HON)

    Los Angeles, California

    ublished by Elsevier Inc. doi:10.1016/j.jacc.2009.02.023

    osIsp1f

    TbcmmCtsdta0MtwwWdbmoaTAHS3whGiutauo

    ortic Stenosis (AS)

    eviews. The following reviews were published during theear: “Insights into degenerative aortic valve (AV) disease”1) and “Genomics: The next step to elucidate the etiologyf calcific aortic stenosis (AS)” (2).tate-of-the-art papers. In 2008, Ross published “Trans-eptal left heart catheterization: a 50 year odyssey” (3).

    Comment. Transseptal left heart catheterization, a pio-eering procedure, was developed by John Ross Jr. when heas a surgical intern on a research rotation. He changed his

    pecialty and went on to become a distinguished figure inardiovascular medicine.

    Another article published at this time is “Emergingpplications for Transseptal Catheterization: Old Tech-iques for New Procedures” (4).rading of AS severity; inconsistencies of echocardio-

    raphic criteria. The consistency of 3 echocardiographicriteria for severe AS (aortic valve area [AVA] �1.0 m2 [or0.6 cm2/m2], mean gradient [MG] �40 mm Hg or peak

    ow [Vmax] �4 m/s) used in the Guidelines were evaluatedn 3,483 echocardiographic studies performed in 2,427atients with normal left ventricular (LV) systolic functionnd calculated AVA of �2 cm2 performed from 1994 to004 (5). There were “clinically significant” differences (Fig., Table 1).

    Comment. This important and useful study highlightsnconsistencies in criteria for severe AS. An accompanyingditorial (6) discusses the importance of this study androbable reasons for the differences. The problem may behe guidelines. In this study, it would have been better toave measured cardiac output (CO). The authors acknowl-dge that calculating stroke volume from echocardiographys “often difficult.” They assumed a CO of 6 l/min, heart rate

    rom the Griffith Center, Division of Cardiovascular Medicine, Department ofedicine, LAC�USC Medical Center, Keck School of Medicine at University of

    outhern California, Los Angeles, California. Dr. Rahimtoola has received honorariaor educational lectures from the American College of Cardiology Foundation;merican College of Physicians; University of California Los Angeles; University ofalifornia Irvine; Cornell University; Creighton University; Thomas Jefferson Uni-

    ersity; Cedars-Sinai Medical Center; Harvard Medical School; University of Wis-onsin; University of Hawaii; Cardiologists Association of Hong Kong, China; ATS;t. Jude Medical; Carbomedics; Merck; Pfizer; and Edwards Life Sciences. Thiseview covers articles published from July 2007 to June 2008.

    1Manuscript received September 18, 2008; revised manuscript received January 21,

    009, accepted February 6, 2009.

    f 80 beats/min, and a systolic ejection time of 0.33 s. (Alsoee Gutierrez-Chico et al. [10] cited below.)ncreasing blood pressure (BP) affects measured ASeverity. In 22 patients, BP was increased by handgrip orhenylephrine infusion from a mean of 99 � 8 mm Hg to21 � 10 mm Hg (p � 0.001) (7). The AVA decreasedrom 1.15 � 0.32 cm2 to 1.09 � 0.33 cm2 (p � 0.02).

    Comment. Flow was not measured but was calculated.he clinical situation arises in patients with severe ororderline severe AS, low gradient, and hypertension. Thelinical problem is as follows: To what level, by whatethod, and how rapidly should BP be lowered before theeasurements are repeated?ardiac multidetector computed tomography (MDCT)

    o assess the severity of AS. Forty consecutive patientscheduled for aortic valve replacement (AVR) had echocar-iography, MDCT, and coronary angiography within aime span of 1 week (8). The AVA as measured by MDCTnd echocardiography was 0.87 � 0.22 cm2 versus 0.81 �.20 cm2 (p � 0.01; r � 0.77, and p � 0.01, respectively).ean difference was 0.06 � 0.15 cm2. The authors found

    hat MDCT correctly identified 26 of 33 patients (79%)ith coronary artery stenosis and overestimated 3 patientsith �50% stenosis.here is pressure recovery best measured? In a pulse

    uplicator with flow rates of 2 to 5 l/min and orifice areasetween 0.32 and 2.85 cm2, pressure recovery data were besteasured 5 cm above AV (9), assuming that AV is a circular

    rifice, proximal aorta is circular without sinuses or bends,nd flow is axially symmetric.he measurement of AVA by RT3D. In 41 patients withS, AVA was measured with the use of Gorlin’s equation,akki’s formula, Doppler continuity equation (CE), 2D

    impson’s volumetric method, and by the real-time-dimensional echocardiography (RT3D). Cardiac outputas measured by the thermodilution technique (10). RT3Dad the best linear association and absolute agreement withorlin’s method of all noninvasive methods (r � 0.902;

    ntraclass correlation coefficient of 0.846) (Fig. 2). RT3Dnderestimates AVA (95% confidence interval [CI]: 0.084o 0.193) and also grades most efficiently the severity of ASs mild, moderate, or severe (weighted kappa � 0.932). These of receiver-operating characteristic curves showed theptimal cutoff point to consider severe AS “remains close to

    cm2 (1.06 cm2).”

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    Comment. AVA by Gorlin’s formula is very good if datapressures and CO) are both obtained and calculated ap-ropriately.ortic valve replacement (AVR). “LOW FLOW/LOW GRADI-

    NT” AS. A total of 217 consecutive patients in a Europeanulticenter Study with severe AS (AVA �1.0 cm2), low

    eft ventricular ejection fraction (LVEF) (�35%), and lowG (�30 mm Hg) underwent AVR. Operative mortality

    as 20% from 1990 to 1999 and 10% from 2000 to 200511). On multivariate analysis, very low MG and multivesseloronary artery disease (MVD) were predictors of excesserioperative mortality. In the subgroup who underwentobutamine stress echocardiography, on multivariate anal-sis, a lack of “contractile reserve” (odds ratio [OR]: 4.4;5% CI: 1.5 to 17.5; p � 0.03) and MVD (OR: 6.0; 95%I: 1.5 to 2.4, p � 0.01) were strong predictors of operativeortality. The 5-year survival was 49 � 4%. Lower MG,

    reater score on the European system for cardiac operativeisk evaluation (EuroSCORE), previous atrial fibrillation,nd MVD were identified as independent predictors ofverall long-term mortality (Fig. 3).

    Figure 1 Relationship of Valve Areas in Aortic Stenosis

    Aortic valve area from the Gorlin equation versus mean gradient (left) and peak floQuadrants are based on cut-off values for severe aortic stenosis as stated in theindicate consistent grading but not those in the upper right and lower left quadran

    ercentage of Patients Diagnosed With Severeortic Stenosis Depending on Whichchocardiographic Criterion Was Used

    Table 1Percentage of Patients Diagnosed With SevereAortic Stenosis Depending on WhichEchocardiographic Criterion Was Used

    GuidelinesRecommendations Parameter

    Patients WithSevere AS (%)

    ACC/AHA AVA �1.0 cm2 69

    ESC AVA/BSA �0.6 cm2/m2 76

    ACC/AHA (Otto) Vmax �4.0 m/s 45

    ACC/AHA � Pm �40 mm Hg 40

    eprinted, with permission, from Minners et al. (5).ACC/AHA � American College of Cardiology/American Heart Association; AS � aortic stenosis;

    nVA � aortic valve area; BSA � body surface area; ESC � European Society of Cardiology; � Pm�ean pressure gradient; Vmax � peak flow velocity.

    Comment. A diagnosis of hibernating myocardium wouldave been an important part of pre-operative testing (12).lso, it would be best to perform right heart catheterization

    o document cardiac index/stroke index were “low.”evere AS, normal LVEF, and low MG. A total of 215atients had isolated AS, normal sinus rhythm, and normalVEF. Patient characteristics and outcome in those withG �30 and �30 mm Hg (13) are shown in Table 2. The

    atients with MG �30 mm Hg had a lower referral to AVRnd a greater death rate both before and after AVR.

    Comment. This was a large study in which cardiacatheterization was performed. It documents in detail pa-ient characteristics and hemodynamics in the 2 subgroupsf patients.symptomatic patients with severe AS. Of 622 patientsho were initially asymptomatic between 1984 and 1995,nly 263 of 622 patients who subsequently had surgery athe authors’ institution are described. Of the 263 patients,66 had developed symptoms and 97 remained asymptom-tic (14); operative mortality in the 2 subgroups was 2% and%, respectively. In those who had symptoms or weresymptomatic, the survival of patients who underwenturgery was better than those who did not (Fig. 4).

    Comment. This study of asymptomatic patients has manyreas of concern, which have been described in detailreviously (15). These data are from highly selected pa-ients. 1) Of 694 patients in the database, 72 with moreevere AS had AVR initially, leaving 622 for follow-up16,17). 2) Although 352 patients had subsequent surgery,nly the 263 who had surgery at the authors’ institution areescribed. Moreover, the criteria for selecting patients forVR was not provided and were not pre-determined. Toetermine that AVR was better than no AVR, data are

    city (right). The predicted and fitted curves of the study population are shown.t guidelines. Data pairs positioned in the upper left and lower right quadrantsprinted, with permission, from Minners et al. (5).

    w velocurrents. Re

    eeded on baseline characteristics of operated versus non-

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    1896 Rahimtoola JACC Vol. 53, No. 20, 2009Year in Valvular Heart Disease May 19, 2009:1894–1908

    perated patients in both the symptomatic and asymptom-tic subgroups, characteristics that were not provided.he EuroSCORE overestimates operative mortality of

    alve surgery. A total of 1,299 patients had either isolatedalve surgery procedures or valve surgery plus coronaryrtery bypass graft surgery (CABG) (18). The observedortality in the 2 groups was 2.8% and 6.8%, respectively.ortality predicted by the New York model (19) was 3.4%

    nd 6.2%, respectively, which was much closer to the actualbserved mortality. Mortality predicted by the use of Eu-oSCORE (20,21) was 6.1% and 7.8%.

    A total of 731 patients with a EuroSCORE of 7 orreater underwent isolated AVR (22). A minimally invasivepproach was used in 469 (64.2%). The mean EuroSCOREas 9.7 (median 10); 731 patients had a EuroSCORE �7,f whom 332 had a EuroSCORE �10. The actual observedperative mortality was 7.8% and that predicted by logisticuroSCORE was 17.2%. Freedom from all-cause death

    including hospital mortality) was 72.4% at 5 years (Fig. 5).Comment. The EuroSCORE was first published in 1999

    Figure 2 Relationship of Aortic Valve Area by the Use of Gorlin

    Linear regression of the aortic valve areas by echocardiographic (echo) methods arepresents the regression line, 95% confidence intervals for the mean (interruptedrupted, outer bounds). Reprinted, with permission, from Gutierrez-Chico et al (10).

    20). It was based on a dataset of 13,302 patients, of whom E

    pproximately 60% were patients undergoing CABG, 30%ndergoing valve surgery, and 10% other surgical proce-ures. Cardiac surgery for valve disease is constantly im-roving; for example, New York State Cardiac Surgery datahow that hospital mortality from 2001 to 2003 was lowerhan from 1998 to 2000 (23).redictors of poorer survival after AVR. Of 3,049 pa-

    ients who underwent AVR for AS from 1991 to 2004,redictors of decreased survival (24) were severe LV hyper-rophy, severity of AS, use of smaller prosthesis, andentricular dysfunction.

    ortic Regurgitation (AR)

    re-operative LV end-systolic diameter index (ESDI)25 mm/m2 is a better predictor of outcomes than ESD50 mm. A total of 147 consecutive patients age 52 � 12

    ears underwent surgery for chronic severe AR for symp-oms in 107 (76.3%) and 40 (23.7%) for LV dysfunctionparameters” (25). The comparison of ESDI �25 mm to

    rmula to That by Noninvasive and Invasive Techniques

    ki’s formula (x-axis) with that by Gorlin’s equation (y-axis). Center line (yellow), inner bounds), and 95% confidence intervals for the individuals (red, inter-2-dimensional; 3D � 3-dimensional.

    ’s Fo

    nd Hakyellow2D �

    SD �50 mm showed that the use of ESDI better

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    dentified symptomatic patients, asymptomatic patientsith LV dysfunction, patients with worse LVEF after

    urgery, and overall rate of mortality.linical outcome in asymptomatic patients with AR. A

    otal of 251 patients were enrolled from 1991 to 2003 andollowed until their death or 2006, whichever came first.he patients were 60 � 17 years of age with a diastoliclood pressure of 71 � 12 mm Hg which, in the severe ARroup, was 64 � 13 mm Hg. A history of hypertension wasresent in 49% (26). A total of 93 patients were categorizeds severe AR on the basis of regurgitant volume �60l/beat or effective regurgitant orifice �30 mm2 from

    Figure 3 5-Year Survival in Patients With Low Gradient Aortic S

    5-year survival after aortic valve replacement in patients with low gradient severe apresence of multivessel coronary artery disease (MVD) (left) and mean aortic valv

    atient Characteristicsith Low and High Gradients

    Table 2 Patient CharacteristicsWith Low and High Gradients

    Mean Gradient

    p Value30 mm Hg

    n 47 168 —

    Age (yrs) 79 � 9 76 � 10 0.20

    Hypertension 43 (91%) 107 (64%) 0.0004

    LVEDVI (ml/m2) 47 � 9 56 � 12 �0.0001

    LVEF 0.62 � 0.09 0.65 � 0.09 0.03

    SV index (ml/beats/m2) 37 � 12 41 � 11 0.002

    Cardiac output (l/min) 4.4 � 1.1 5.2 � 1.3 0.0001

    SVR (dyne·cm·s�5) 2,163 � 754 1,879 � 528 0.05

    AVA (cm2) 0.85 � 0.19 0.68 � 0.17 �0.0001

    AVA (cm2/m2) 0.46 � 0.09 0.37 � 0.09 �0.0001

    AV mean gradient (mm Hg) 23 � 5 50 � 15 �0.0001

    Coronary artery disease 36 (76%) 138 (82%) 0.58

    Death before AVR 9 (19%) 16 (9.5%) 0.05

    AVR 15 (33%) 97 (58%) 0.01

    Death after AVR 4 (27%) 5 (5%) —

    ata from Barasch et al. (13).AV � aortic valve; AVR � aortic valve replacement; LVEDVI � left ventricular end-diastolic

    polume index; LVEF � left ventricular ejection fraction; SV � stroke volume; SVR � systemicascular index; other abbreviations as in Table 1.

    oppler echocardiographic studies. When severe AR versusild AR was compared, 10-year survival was lower (69 �

    % vs. 92 � 4%, p � 0.05) and cardiac events (cardiac death,eart failure, and new atrial fibrillation) were higher (63 � 8%s. 21 � 8%, p � 0.0001). Patients with moderate AR showedno significant reduction of cardiac events after surgery (p �.92),” but patients with severe AR had a reduction inardiac events: linearized yearly rates were 11.2% “underedical management” and 2.3% with surgery (p � 0.002).Comment. There are many concerns with this type of

    atural history study (15). For example: 1) At entry into thetudy, patients were in their 60s and 70s, but there is nonformation about lipid profile and the percent of patientsho on entry had coronary arteriography and significantlybstructive coronary artery disease (CAD). Did none haveAD at entry? Ten years later, when patients were in their0s and 80s, did none develop or have progression of CADhat could have led to heart failure, atrial fibrillation, oreath? 2) What was “medical management”? How effectiveas it in controlling abnormalities?Other concerns include the following: 1) Likely, the

    0-year survival in the moderate group was not significantlyower than in the severe group (75 � 6% vs. 69 � 9%); the

    value was not provided. This finding adds to the possi-ility that AR was not the cause of the event(s). 2) Theiastolic blood pressure was 64 � 13 mm Hg. Thus, ARas not severe in many patients. The American Society ofchocardiography (27,28) recommends: a) 3 quantitative

    riteria to define severity of AR. The severity of AR wasudged by only 1 of 2 quantitative criteria—why not both?

    as there discordance between the 2 criteria? What abouthe third criterion? b) Correction of LV dimensions andolumes for body size. These measurements were not

    sis

    tenosis according to the pre-operativeient (right). Reprinted, with permission, from Levy et al. (11).

    teno

    ortic se grad

    resented, which also raises concerns about the severity of

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    1898 Rahimtoola JACC Vol. 53, No. 20, 2009Year in Valvular Heart Disease May 19, 2009:1894–1908

    R. 3) Cardiac surgery was stated to be performed in 80 of1 patients for AR, but 11 had surgery for physician and/oratient preference, 11 for “aortic aneurysm,” and an un-nown number “for LV enlargement,” which was unde-ned. In chronic severe AR, LV had to have been enlargedt baseline and the amount of additional increase of LVize/volume to warrant AVR was not described.

    icuspid Aortic Valve (BAV)

    symptomatic patients with BAV; low event rate at 20ears. A total of 212 asymptomatic residents of Olmstedounty, Minnesota, with BAV, 65% male, ages 32 � 20

    ears between 1980 and 1999, with LVEF 0.63 � 0.05 and

    Figure 4 Survival in Asymptomatic Patients With Severe Aortic

    Survival of “all patients” diagnosed with asymptomatic severe aortic stenosis.Reprinted, with permission, from Brown et al. (14). AVR � aortic valve replacemen

    Figure 5 Survival After Aortic Valve Replacement in Older Patie

    Survival of “high-risk” patients with severe aortic stenosis after traditional surgical

    bsent or mild AS and/or AR were followed for up to 20ears (29). The AV degeneration was subjectively scored foralcification, thickening, and mobility reduction (0 to 3 forach). Events at 20 years are shown in Table 3. Independentredictors for cardiovascular events were age �50 yearsOR: 3.0; 95% CI: 1.5 to 5.7; p � 0.01); valve degeneration atiagnosis (OR: 2.4; 95% CI: 1.2 to 4.5; p � 0.016) (Fig. 6)ith �70% events at 10 years; and baseline ascending aorta40 mm for surgery for aortic dilation (OR: 10.8; 95% CI:

    .8 to 77.3; p � 0.01).ortic dilation has distinct patterns. Thoracic aorticorphology in 64 patients with BAV was determined at 10

    evels with the use of computed tomographic angiography or

    osis

    � symptoms.

    t High Risk

    valve replacement. Reprinted, with permission, from Grossi et al. (22).

    Sten

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    agnetic resonance angiography (30). Patients in the dif-erent clusters needed different surgical techniques of aorticurgery (Fig. 7).

    Comment. Patients with BAV may need surgery for thealve, the aorta, or both. It is important to evaluate andeasure the ascending aorta at the annulus, sinuses, and

    inotubular junction, at the largest size in the whole of thescending aorta and in the arch of the aorta because it helpso determine the need for surgery on the aorta and also theurgical procedure that will need to be done.ong-term survival after the Bentall procedure. A totalf 206 patients underwent composite aortic root replace-ent (i.e., button-Bentall procedure). Hospital mortalityas 2.9%, stroke rate was 1.9% (31); risk factors for these

    vents were clot or atheroma (p � 0.02) and age �65 yearsp � 0.05). Follow-up ranged from 5 to 18 years; 5- and0-year survival rates were 93% and 89%, respectively.

    0-Year Outcomes in Patientsith Bicuspid Aortic Valve (Age 32 � 10 Years)

    Table 3 20-Year Outcomes in PatientsWith Bicuspid Aortic Valve (Age 32 � 10 Years)

    Incidence of Outcomes (%)

    Death 10 � 3

    Heart failure 7 � 2

    New cardiac symptoms 26 � 4

    Cardiovascular medical events 33 � 5

    Aortic valve surgery 24 � 4

    Ascending aortic surgery 5 � 2

    Any cardiovascular surgery 27 � 4

    Aortic dissection None

    Total cardiovascular (medical or surgical) events 42 � 5

    eprinted, with permission, from Michelena et al. (29).

    Figure 6 Bicuspid Aortic Valve: Long-Term Outcome in Asympto

    Bicuspid aortic valve: incidence of aortic valve surgery (left) and of medical eventsration (blue; score �3). Medical events included cardiac death, heart failure, newMichelena et al. (29).

    itral Regurgitation (MR)

    ole of imaging. O’Gara et al. (32) provide a useful andmportant description of the role of echocardiographic/

    oppler imaging, including the importance of segmentalnatomy in chronic “degenerative” MR.ardiovascular magnetic resonance (CMR) of mitral

    alve (MV) prolapse. CMR performed in 16 patients had100% sensitivity and 100% specificity compared with these of transesophageal echocardiography (TTE) for the-mm threshold for leaflet excursion into the left atrium33). It was found that CMR showed larger and longerndexed posterior leaflet and larger index mitral annulariameters. Late gadolinium enhancement (LGE) wasresent in 94% in the MV and mitral annulus and in theapillary muscles in 10 of 16 patients (63%), which isuggestive of fibrosis and which was associated with theresence of complex ventricular arrhythmias.

    Comment. This was a study with a small number ofatients. There was no information on coronary arterio-raphic findings in the patients with LGE in the papillaryuscle. The etiology of LGE was not clear. The presence ofGE may be a clue to another etiological factor of MVrolapse. Additional studies of CMR in MV prolapse areeeded, especially in those with complex ventricular ar-hythmias.

    reater operative mortality for MV surgery in youngeromen. Of 24,977 patients (49% women) in the Society ofhoracic Surgeons (STS) database (34), the operative mortal-

    ty in women was 3.9% versus 2.4% for men. The incidence ofll comorbidities also was greater. The adjusted female/male

    ic Patients

    t) in those with early valve deterioration (red; score �3) or no early valve deterio-vascular symptoms, stroke, and endocarditis. Reprinted, with permission, from

    mat

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    1900 Rahimtoola JACC Vol. 53, No. 20, 2009Year in Valvular Heart Disease May 19, 2009:1894–1908

    R for hospital mortality in the group ages 40 to 49 years was.56 (95% CI: 1.31 to 5.01; p � 0.0058) and in those ages 50o 59 years was 1.95 (95% CI: 1.32 to 2.89; p � 0.0009).

    months is optimal timing for echocardiography/oppler for MR after myocardial infarction. From base-

    ine to 1 year, LV end-diastolic volume index increased from6 � 15 ml/m2 to 63 � 19 ml/m2 (p � 0.0001) (35); araded increase depending on MR at 3 months at whichime the incidence of no MR was 21%, mild MR 32%, andoderate/severe MR 60% (p � 0.008). By multivariate

    Figure 7 Bicuspid Aortic Valve:Computed Tomography of the Aorta

    Three-dimensional computed tomographic angiographic reconstruction of apatient with bicuspid aortic valve. Ten sections (A to J) at which the aorticdiameter was measured are shown. In cluster I, 8 patients (13%) had involve-ment of aortic root (A to C). In cluster II, 9 (14%) had involvement of the tubu-lar portion of the ascending aorta (D and E). In cluster III, 18 (28%) hadinvolvement of the tubular portion of the ascending aorta and transverse aorticarch aortic proximal and distal to takeoff of the innominate artery (E to G). Incluster IV, 29 (45%) had diffuse involvement of the aortic root, ascendingaorta, and proximal aortic arch. Clusters I and IV, both of which involved theaortic root involvement, accounted for 73% of the patients. Reprinted, with per-mission, from Fazel et al. (30).

    nalysis, MR at 3 months but not at baseline was indepen- R

    ently associated with increased hospitalization and death atmedian follow-up of 1,226 days.urability of mitral valve repair (MVrep). A total of 348

    atients had MVrep and “the classic techniques described byarpentier and others were used” (36). Hospital mortalityas 1.6%. Survival at 5 and 10 years was 93 � 1.5% and0.1 � 3.7%, respectively (Fig. 8). Survival was identical inhose with Barlow’s disease and in fibroelastic deficiency.o patient was lost to follow-up. The mean number of

    ollow-up echocardiograms was 4.6 (range 2 to 16). At 1onth, 98.7% of patients had no or trivial MR (0/4 to 1/4);

    n Barlow’s disease, it was 97.1%, and in fibroelastic defi-iency, it was 99.8%. The incidence of failing repair (free-om from MR grade �2/4) was 82.2 � 3.7% at 5 years and4.9 � 5.6% at 10 years (Table 4). At baseline, atrialbrillation was present in 22%.At most recent follow-up, patients in New York Heart

    ssociation (NYHA) functional classes I, II, III, and IV were5%, 19%, 5%, and 1%, respectively. Warfarin anticoagulationas given to 35% of patients. Freedom from thromboembolic

    vents and/or anticoagulation-related bleeding was 93.5 �.5% at 5 years and 86.7 � 2.7% at 10 years.

    Comment. Flameng et al. (36) have once again presentedareful, detailed results of MVrep. Follow-up includedrequent echocardiograms, and results are reported as recur-ences of MR and not as reoperation rates, which is aovable target. This study has important implications for

    ype of MVrep, MV repair versus replacement, and also forndications of surgery in the asymptomatic patient. To beoted, data on the pre-operative NYHA functional classesnd MR severity were not provided.

    utcomes after MVrep are similar to mitral valve re-lacement (MVR). From 1985 to 2005, a total of 3,286atients underwent primary operation for “degenerative” MR37). Hospital mortality in 3,051 patients with MVrep was.26% and for 235 patients with MVR was 2.1% (p � 0.001).atients undergoing MVR were older (70 � 12 years vs. 57 �3 years) and had more complex valve pathology, symptoms,nd LV dysfunction. In propensity-matched patients, survivalas similar (p � 0.8) (i.e., at 5 years 86% vs. 83%, at 10 years3% vs. 62%, and at 15 years 43% vs. 48%). Freedom fromeoperation also was similar (p � 0.6) for MVrep at 5 and 10ears was 95% and for MVR was 95 and 92%, respectively.

    Comment. David (38), in discussing this article, statedhat a subsequent analysis of his own data in propensity-atched patients confirmed the aforementioned findings.eoperation after MVrep. From January 1980 to January005, a total of 4,024 patients in the same institution as theforementioned study had MVrep for “degenerative” diseaseausing MR, and 188 (4.7%) underwent reoperation forecurrent MR (39). Reoperation for procedure-relatedroblems occurred early (median 19 days) in 96 patientsnd, for valve-related problems, occurred later (median 5.4ears) in 109 patients (p � 0.0001). Mitral valve replace-ent was performed in 64% and repeat MVrep in 36%.

    epeat MVrep was performed in 65% of recent reopera-

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    1901JACC Vol. 53, No. 20, 2009 RahimtoolaMay 19, 2009:1894–1908 Year in Valvular Heart Disease

    ions. After re-repair at 10 years, the incidence of seconde-repair was 7% and survival was 62%.

    ricuspid Regurgitation (TR)

    he incidence of TR in patients with constrictive peri-arditis. TR was present in 185 of 261 (71%) patients whoad pericardiectomy (40); TR was moderate to severe in 5420%). Previous cardiac surgery and radiation were the causen 34 (63%) and 15 (28%), respectively. Moderate-to-severeR versus none-to-mild TR was associated with a greaterperative mortality (13% vs. 4.3%; p � 0.019); however,xcluding those cases caused by radiation, operative mortal-ty was similar. Five-year survival was poorer in those with

    oderate-to-severe TR at 47% versus 87% in those withild TR. Tricuspid valve repair had no significant impact

    n late survival.

    nfective Endocarditis (IE)

    igh mortality of dialysis patients undergoing valveurgery. A total of 1,862 valvular procedures were recordedn dialysis patients with IE in the STS database. Points weressigned for operative mortality risks (Table 5) (41). Thebserved mortality increased from 7.1% to 76% as risk scoreoints increased from 0 to 10� (Table 6).

    Figure 8 Recurrence of MR After Valve Repair

    Linearized curves for recurrence of mitral regurgitation (MR) �2/4 after mitral valvrisk factors are nonuse of annuloplasty ring, nonuse of sliding plasty, or performanmission, from Flameng et al. (36).

    inearized Recurrence Rate% Per Year) for Recurrent MR >2/4

    Table 4 Linearized Recurrence Rate(% Per Year) for Recurrent MR >2/4

    All Patients FED Barlow

    Overall 3.2 2.6 6.0

    Without surgical risk 2.4 2.2 2.9

    With surgical risk 4.7 3.6 14.9

    urgical risk indicates the nonuse of annuloplasty ring, nonuse of sliding plasty, or performance of

    hordal shortening. Reprinted, with permission, from Flameng et al. (36).MR � mitral regurgitation; FED � fibroelastic deficiency.

    (

    Comment. In 50% of the patients, the risks ranged from3% to 60%.omograft valve not superior to conventional prosthesis.f 127 consecutive patients, 54 (43%) were treated with

    ortic homograft and 73 (57%) with conventional prosthesis42). Homografts were inserted in 41 of 63 (65%) patientsho had an annular abscess. Between the 2 types ofrostheses, hospital mortality was not significantly different11% vs. 8%, p � 0.6). By multivariate analysis, prostheticalve IE was associated with greater mortality (OR: 12.5;5% CI: 1.4 to 114.2; p � 0.001). The 10-year survival freef end point (IE recurrence, noninfective prostheses dys-unction, or long-term cardiovascular mortality) was 44 �0% and was not significantly different between the 2 typesf prostheses (p � 0.2).

    Comment. Studies are needed to better define patientsho need a homograft. Should a homograft be necessarynly in those with an abscess and/or with persistent sepsis?

    ir in those with fibroelastic disease (left) and Barlow’s disease (right). Surgicalchordal shortening and for patients not having these factors. Reprinted, with per-

    isk Scores for Mortality With Surgery inatients With Infective Endocarditis on Dialysis

    Table 5 Risk Scores for Mortality With Surgery inPatients With Infective Endocarditis on Dialysis

    Variable Point

    Salvage status/cardiogenic shock 3

    Double valve surgery 3

    Age �60 yrs 2

    Mitral valve only surgery 2

    BSA �2.1 m2 2

    Female sex 1

    Active endocarditis type 1

    Arrhythmia 1

    otal risk score determined by summing all points. Reprinted, with permission, from Rankin et al.

    e repace of

    41).Abbreviations as in Table 1.

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    1902 Rahimtoola JACC Vol. 53, No. 20, 2009Year in Valvular Heart Disease May 19, 2009:1894–1908

    ranscatheter Valve Therapy

    osition statement for transcatheter valve implanta-ion. In 2008, the European Association of Cardio-horacic Surgery, the European Society of Cardiology, and

    he European Association of Percutaneous Cardiovascularnterventions (43) published a position statement on trans-atheter valve implantation.ndovascular resection of human aortic valves in situ. Per-

    utaneous resection of the diseased native valve before theew valve is percutaneously implanted was performed in 10uman cadavers (44).ransarterial AV implantation. Percutaneous transfemo-

    al AV implantation was performed in 50 high-risk severelyymptomatic patients by use of the Cribier-Edwards 23-nd 26-mm expandable valves (Edwards Lifesciences Inc.,rvine, California). Mortality at 30 days was 12% in patientsn whom the logistic EuroSCORE was 28% (45). Thereas a learning curve, and procedural success increased from6% to 96% (Fig. 9). Valve area measured from echocardio-rams increased from 0.6 � 0.2 cm2 to 1.7 � 0.4 cm2.aravalvular regurgitation was mild, LVEF increased (p �.001), and functional class improved (p � 0.0001).

    Comment. Retrograde implantation is a significant ad-ance. The current model of the Edwards SAPIEN valveses the bovine pericardium with THERMA FIX, which inhe PERIMOUNT valve for traditional surgical AVR has aow rate of structural valve deterioration out to 15 to 20ears (46). The SAPIEN valve was successfully delivered in7 of 54 (87%) patients, the 30-day mortality was 7.4%, andhe major adverse cardiac rate was 16.7% (47).

    Concern exists regarding the severity of AR after percu-aneous valve insertion. In an earlier multicenter study withhe Cribier-Edwards valve the incidence of 3�/4� AR wascommon” (48). In this study, echocardiographic/Dopplerriteria for severity of AR were not quantitative as isecommended by the American Society of Echocardiogra-hy. Left ventricular and femoral artery tracings raise

    bserved Mortality With Surgery by Risk Scoren Patients With Infective Endocarditis on Dialysis

    Table 6 Observed Mortality With Surgery by Risk Scorein Patients With Infective Endocarditis on Dialysis

    Risk Score No. of Patients Mean Observed Mortality (%)

    0 85 7.1

    1 158 7.6

    2 206 12.6

    3 330 16.7

    4 298 22.8

    5 235 26.4

    6 204 34.3

    7 117 41.9

    8 67 59.7

    9 30 50.0

    10� 25 76.0

    eprinted, with permission, from Rankin et al. (41).

    oncerns as discussed in Figure 10 (49).

    Percutaneous AV implantation was performed with the usef a second-generation CoreValve 21-F catheter in 50 patientsnd 18-F third-generation catheter in 36 patients (CoreValvenc., Irvine, California). The logistic EuroSCORE was 21.7 �2.6%, and 83% of patients were in NYHA functionallasses III and IV. In 6 patients, misplacement of the valveesulted in conversion to surgical AVR and, in 2 patients,alcified AV could not be crossed. Procedural success was4% (50). The 30-day mortality was 12%, and the incidencef death, stroke, and myocardial infarction was 22%.

    Comment. The CoreValve System seems to have a lot ofetal, appears bulky, and currently has only a 21-mm

    ioprosthesis. It utilizes porcine pericardium whose rate ofVD is not known. Also, there was a high rate of proceduralilation after valve implantation (28% of 76 valve implan-ations) (51). The valve area post-procedure was not pro-ided.

    The 21-F CoreValve System (CoreValve, Paris, France)as inserted under femoro-femoral cardiopulmonary bypass

    upport in 10 high-risk patients (estimated mortality deter-ined by a EuroSCORE of 32% for surgical AVR) (52).he 30-day and 3-month mortalities were 20% and 30%,

    espectively. The AVA increased from 0.57 � 0.19 cm2 to.2 � 0.35 cm2 (p � 0.0001), and the median NYHAunctional class improved from III to II (p � 0.01).

    Comment. Post-procedure the mean valve area was only.2 cm2!A total of 66 consecutive patients age �70 years with

    evere symptomatic AS were reported (53). Of 39 patients withEuroSCORE �20%, AVA was 0.6 � 0.2 cm2 (0.4 � 0.1

    m2/m2), MG was 47 � 14 mm Hg, and LVEF was 0.52 �.15. Pulmonary artery hypertension �60 mm Hg wasresent in 9% of patients who were considered at high risk

    Figure 9 Learning Curve ofPercutaneous Aortic Valve Replacement

    Survival was better (p � 0.09) for the second 25 patients when compared withthe first 25 patients after percutaneous aortic valve replacement. Reprinted,with permission, from Webb et al. (45).

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    r inoperable for surgery. Twelve received percutaneousAPIEN valves (Edwards LifeSciences, Inc.). A total of 27ad contraindications to percutaneous valve and received aariety of therapies. In the 12 who had the percutaneousalve replacement, hospital mortality was 25%. A total of 31atients had surgical AVR. In 27, the EuroSCORE was20%, and 4 were considered at high risk for percutaneousVR. The hospital mortality was 4%.re endovascular valved stents suitable for all

    atients? Thirty-five patients with severe AS who werecheduled for AVR were studied. A braided nitinol self-xpanded stent from Laboratories Perouse (Ivry-le-Temple,rance) that was used was calibrated for implantation insidecircular orifice with a 20-mm diameter and was implanted

    n a triangular or an elliptical orifice with a circumferencedentical to the circular orifice (54). In tricuspid AV, thehape of the stent deployment was circular (68%), triangular21%), or elliptic (11%). In bicuspid AV, elliptical deploy-ent was present in 79%. The incidence of gaps between

    he stent external surface and the AV, in tricuspid andicuspid AV, was 58% and 43%, respectively (p � 0.49).

    Comment. The high incidence of gaps is of concern.ransapical aortic valve implantation (TAP-AVI). TheAP-AVI with the use of an Edwards SAPIEN valve

    Edwards Lifesciences) was performed in 59 consecutiveatients ages 81 � 6 years with an average EuroSCORE forredicted mortality of 27 � 14%. The TAP-AVI wasuccessfully performed in 53 patients; 4 required earlyonversion to sternotomy (55). The 30-day mortality was3.6%. Actuarial survival at 110 � 77 days was 75.7 � 5.9%Fig. 11).

    A TAP-AVI in 40 patients with the use of thedwards SAPIEN valve (Edwards Lifesciences) waserformed in 40 high-risk patients; 35 were successfully

    Figure 10 Aortic Valve Gradients WithPercutaneous Valve Replacement

    “Transaortic gradients” before and after percutaneous aortic valve replace-ment. The pressure scale is not included. In the pre-procedure tracing (left),LV systolic pressure is off scale. The post-procedure tracings (right) show nodelay from LV to FA (is “FA” from ascending aorta?), and the pulse pressure isvery wide, raising concern about severity of AR. FA � femoral artery; LV � leftventricle. Reprinted, with permission, from Webb (49).

    eated (56). The 30-day death rate was 17.5%, and in-

    ospital death rate was 22.5%. The AVA increased from 0.620.13 cm2 to 1.61 � 0.37 cm2 (p � 0.0001). Actuarial

    urvival was 81.8 � 6.2% at 1 month and 71.7 � 7.7% at 3onths (Fig. 12).Comment. An in-hospital death rate that is greater than

    he 30-day mortality implies that some patients had diedfter 30 days and not yet been discharged from the hospitalfter surgery.alve-in-a-valve procedure. The CoreValve System wassed in an 80-year-old man with severe AR in a degeneratedioprosthetic valve. The logistic EuroSCORE was 36%57). After 1 year, the patient was asymptomatic with goodalve-in-a-valve prosthetic function.

    Comment. The suitability of EuroSCORE for estimatingortality after valve surgery has been questioned (please see

    he previous section, “Aortic Stenosis”).mportance of echocardiography in percutaneous aorticalve implantation (PAVI). Fifty consecutive patientsere deemed suitable for PAVI by the use of TTE, and 37

    74%) also underwent TEE (59). The authors used TTE toetermine annular dimension and to guide correct deviceizing. Using TEE, they were able to successfully guideevice implantation in 97%, and TEE also was useful in theetection and treatment of “significant” paravalvular AR.he authors concluded that echocardiography has an “im-ortant role in case selection, in guiding device placement,nd in detecting complications” of PAVI.valuation of aortic root by multislice computed tomog-

    aphy. The use of multislice computed tomography pro-ides information in 2 different views of aortic annulus andts shape (59). It also provides information on the distancerom the annulus to the coronary ostia.ntraventricular conduction abnormalities and the needor permanent pacemaker implantation. Forty consecu-ive patients who had PAVI were studied (60). Left bundle

    Figure 11 Survival After Transapical AorticValve Replacement: Multicenter Experience

    Survival at 110 � 77 days after transapical minimally invasive aortic valvereplacement, a multicenter experience. Reprinted, with permission, fromWalther et al. (55). pts � patients.

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    1904 Rahimtoola JACC Vol. 53, No. 20, 2009Year in Valvular Heart Disease May 19, 2009:1894–1908

    ranch block (BBB) was present in 15% before PAV and5% after PAVI (p � 0.0001). Two patients with right BBBecame dependent on a pacemaker. Temporary and perma-ent pacemakers were needed in 20% and 18%, respectively.Of 123 patients with PAVI, 2 patients (1.6%) required

    acemaker implantation because of pre-existing intermit-ent bradycardia, 7 (5.7%) developed complete heart blocknd needed permanent pacemakers (61), and 4 (3.3%)eveloped left BBB.hanges in MR with the Mitra Clip. In the Mitra Clip,VEREST-1 (Endovascular Valve Edge-to-Edge Re-air) study, MR was evaluated in a central echocardio-raphic laboratory (62). Comparing pre-procedure vol-mes to 6-month post-procedure volumes, the authorsound that mean regurgitant volume had decreased from0.3 to 27.5 ml (change �22.8 ml; p � 0.0001),egurgitant fraction from 44.6% to 28.9% (change15.7%; p � 0.0001), color flow grade from 3.4 to 1.8

    change �1.6; p � 0.0001), and pulmonary vein flowrom 2.8 to 1.8 (change �1.0; p � 0.0018).

    rosthetic Heart Valve (PHV)

    uidelines for reporting mortality and morbidity. Up-ated Guidelines from the American Association for Tho-acic Surgery, The Society of Thoracic Surgeons, and Theuropean Association for Cardio-Thoracic Surgery wereublished in 2008 (63).troke after cardiac valve operation. In 2,808 patients,ges 63 � 15 years, the incidence of stroke was 2.2 %; thencidence after AVR plus MVR was 5.4%, and valve �ABG was 3.6% (64). Brain imaging, which was positive in4% of patients, showed ischemic stroke. Multivariateredictors of stroke were calcified ascending aorta, LVEF

    Figure 12 Survival After Transapical AorticValve Replacement: U.S Experience

    Survival after trans-left ventricular apex aortic valve replacement; U.S. feasibil-ity study. Error bars at 1 standard error. Reprinted, with permission, fromSvensson et al. (56).

    0.30, diabetes, age �70 years, and bypass time �120 min. H

    ospital mortality in those patients with stroke was 24%ersus 4.6%; 5-year survival was 54%, which was lower thanhose without stroke (p � 0.001) (Fig. 13).Low-dose” oral anticoagulation is better than the con-entional dose in patients with mechanical PHV: finaleport. In ESCAT II (Early Self-Controlled Anticoagula-ion Trial), a prospective randomized trial, the authorsvaluated “low-dose” international normalized ratio of 1.8o 2.8 for AVR and 2.5 to 3.5 for MVR compared with theonventional international normalized ratio range of 2.5 to.5 (65). The authors’ findings were similar to those in theirreliminary report (66).

    Comment. The authors claim their preliminary report in005 led to the lower dose recommendation by the Amer-can College of Cardiology/American Heart Association

    uidelines in 2006, which is an incorrect claim. After theirreliminary report, it was pointed out that their low doseas similar to the American College of Cardiology/merican Heart Association recommendation in 1998 (66),hich preceded the preliminary report of the authors by 7ears (1998 vs. 2005).

    ood 25-year outcome after AVR with Medtronic-HallHV. In this study, 816 patients had AVR, and follow-upas 99.6% complete (67). Survival at 25 years was 24.9%.here were no mechanical failures. Older age, female sex,

    nd associated CABG was associated with lower survival.inearized rates of thromboembolic complications,arfarin-related bleeding, and IE were 1.5%, 0.7%, and.16% per patient year, respectively; at follow-up, 79% weren NYHA functional classes I and II.

    Comment. The patients’ conditions at baseline were notresented. Their comorbid conditions, which are very im-ortant factors in determining patient outcomes, weremphasized in 1988 (68).

    reater mortality with bioprosthesis in patients ages 50o 70 years. From 1991 to 2000, 1,100 patients ages 50 to0 years had isolated AVR � CABG. Of these, 510 had St.ude Medical mechanical and 257 Carpentier-Edwardsioprostheses model numbers 2625 (first-generation por-ine valve), 2700 (standard Perimount pericardial valve),nd 2800 (reduced-sewing ring version of the 2700 valve)69). Data were analyzed in 440 patients matched 1:1 onlyy age, sex, CABG, and valve size in 220 patients in eachroup, mechanical and bioprosthesis. The “perioperative”ortality was much greater in the bioprosthetic group (5.5%

    s. 1.8%, p � 0.04), who also had longer cross-clamp andardiopulmonary bypass time (p � 0.03) and, on average,ere 0.9 years older. Follow-up was 92% complete; forechanical valve, it averaged 8.6 years and for bioprosthesis

    .2 years. The unadjusted 5- and 10-year survival for theechanical group was 87% (95% CI: 83% to 92%) and 68%

    95% CI: 62% to 76%), respectively, and for the biopros-hesis group it was 72% (95% CI: 66% to 78%) and 50%95% CI: 52% to 58%, p � 0.01) for both. Survival foratched groups and total groups was “virtually identical.”

    emorrhagic complications necessitating hospitalization

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    1905JACC Vol. 53, No. 20, 2009 RahimtoolaMay 19, 2009:1894–1908 Year in Valvular Heart Disease

    ere greater in the mechanical group (15% vs. 7%, p �.01). Freedom from reoperation was similar in the 2roups.

    Comment. This area of investigation is an important one,ut this study has the following concerns regarding itsonclusions: 1) The VA randomized trial had shown aetter survival after 10 years with Bjork-Shiley (Delron ringalve) compared with the porcine valve largely because ofVD and its complications that were observed with theorcine valve only in those �65 years of age (70). Thus,ost patients in the present study were at risk for SVD with

    ioprosthesis and, thus, at risk for greater mortality.2) It was shown in 1988 that survival after valve replace-ent was importantly determined by the patient’s comorbid

    onditions (68). The incidence of lipid abnormalities, hy-ertension, and the percent who had pre-operative coronaryrteriography were not presented. In the VA randomizedrial, approximately 60% of late deaths after AVR were notelated to the prosthesis; the cause(s) of death had beenetermined by a blinded committee (70). In the presenttudy, matching was performed for only 4 baseline charac-eristics. The much greater operative mortality and longerypass and cross-clamp time indicate that those in theioprosthesis group were at greater risk.ole of AVR in septuagenarian’s quality of life (QOL).

    total of 160 septuagenarians underwent AVR, withABG in 18.8% (71). “Global” hospital mortality was 8.8%.t follow-up (mean 3.4 � 2.8 years), 121 were still alive and

    Figure 13 Survival After Stroke in Patients After Valve Surgery

    Unadjusted survival with or without stroke after valve surgery. Reprinted, with perm

    nswered the Medical Outcomes Study Short-Form 36 t

    ealth Survey QOL questionnaire. Importantly, meanOL scores on each of the 7 Short-Form 36 scales were

    ignificantly greater in the patients who underwent surgeryhan in the general Italian matched population; only the 8thcale (vitality domain) was not statistically significantlyreater (Fig. 14).

    Comment. A previous study in octogenarians also hadimilar data with regard to QOL scores (72); it had alsohown marked improvement in patients’ functional class.hus, most septuagenarians and octogenarians undergoing

    raditional surgical AVR have a very good QOL and shouldot be denied AVR simply because of age.ncreased mortality with composite AV and root replace-

    ent (CVG). From 1986 to 2004, 122,971 patients inhe U.K. Heart Valve Registry were identified (73). Theperative mortality with CVG was greater than withVR alone during the entire time period. Excludingperative mortality, the 15-year survival in both groupsas similar.Comment. In the STS database of 409,904 valve proce-

    ures, the operative mortality for AVR was 5.7% and ofVG, when there was no aortic root pathology, was 9.5%

    23).Note. Procedures that require root reconstruction with-

    ut root pathology include use of stentless valves, ho-ografts (allografts), and pulmonary autografts (Ross

    rinciple). The incidence of SVD with use of theserostheses is of considerable interest (see the following

    , from Filosoufi et al. (64).

    ission

    ext).

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    1906 Rahimtoola JACC Vol. 53, No. 20, 2009Year in Valvular Heart Disease May 19, 2009:1894–1908

    he use of SVD in stentless PHV, homografts, andutografts. TORONTO STENTLESS PORCINE VALVE (SPV). From991 to 2004, 357 patients received the Toronto SPV; thereere 2 operative deaths. The 12-year survival was 64 � 4%

    74). The freedom from SVD at 12 years was 69 � 4%; 52 �% for patients younger than 65 years of age, and 85 � 4%or patients �65 years of age (p � 0.002). The authorstated the TSPV has provided “. . .suboptimal durability,articularly in patients less than 65 years of age. We now usehis valve mostly in older patients who have a small aorticnnulus.”

    Comment. This statement from Tirone David, arguablythe father of the stentless valve,” is a powerful one.

    A total of 57 patients underwent reoperation for SVD (47ith Toronto SPV; 10 with Medtronic Free-style). Oper-

    tive mortality was 11%; for redo AVR �1 year aftertentless valve implantation versus �1 year was 67% versus% (p � 0.03) (75). The authors stated that “[R]eoperationfter stentless AVR is a challenging procedure that fre-uently requires aortic root replacement.”

    Comment. Reoperation within 1 year after AVR isssociated with an extremely high mortality.ryolife O’Brien SPV. A total of 185 patients had AVRith the Cryolife O’Brien from 1994 to 2004 (76). Hospitalortality was 5.4%. Actuarial survival at 5 and 10 years was

    8% and 40%, respectively. Freedom from SVD at 5 and 10ears was 91% and 44%, respectively.

    Comment. This study reports a very high rate of SVD andf mortality.omografts (allografts). A total of 200 consecutive pa-

    ients underwent subcoronary AVR (77). Operative mortal-ty was 1.5%. Minimum follow-up was 20 years, and

    aximum was 30 years. At 10, 15, 20, and 25 years, survival

    Figure 14 Quality of Life After ValveReplacement in Septuagenarians

    Eight quality-of-life measures after traditional surgical aortic valve replacementwith bileaflet prosthesis in patients �70 years (mean age 73 � 33 years) inItalian patients compared with Italian subjects matched for age and sex.Reprinted, with permission, from Vicchio et al. (71).

    as 80.8 � 2.8%, 67.8 � 3.4%, 57.0 � 3.6%, and 52.0 �

    .2%, respectively, and freedom from reoperation for anyeason was 86.5 � 2.6%, 70.0 � 3.8%, 40.3 � 5.1%, and6.0 � 5.4%, respectively.

    Comment. Patients’ age not given; data are from aegional center (pediatric and adult patients) and a chil-ren’s hospital.omografts and autografts. A total of 169 consecutive

    atients with congenital AV disease ages 16 to 55 years weretudied; 63 received an autograft at age 29 � 9 years and06 at age 38 � 10 years received homografts (78). Hospitalortality was 3.2%. The 13-year survival for autograft

    ersus allografts recipients was 94.6 � 2.1% versus 92.7 �.3% (p � 0.45), respectively. At 13 years, freedom fromeoperation for SVD was 63.4 � 9.6% for autografts and8.8 � 6.3% for homografts (p � 0.44).

    Comment. The rates of reoperation for SVD of bothHVs are high.

    eprint requests and correspondence: Dr. Shahbudin H. Ra-imtoola, University of Southern California, 2025 Zonal Avenue,NH 7131, Los Angeles, California 90033. E-mail: rahimtoo@

    sc.edu.

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    ey Words: valve stenosis/regurgitation y percutaneous valve y

    rosthetic heart.

    The Year in Valvular Heart DiseaseAortic Stenosis (AS)ReviewsState-of-the-art papersGrading of AS severity; inconsistencies of echocardio-graphic criteriaIncreasing blood pressure (BP) affects measured AS severityCardiac multidetector computed tomography (MDCT) to assess the severity of ASWhere is pressure recovery best measuredThe measurement of AVA by RT3DAortic valve replacement (AVR)“LOW FLOW/LOW GRADI-ENT” AS

    Severe AS, normal LVEF, and low MGAsymptomatic patients with severe ASThe EuroSCORE overestimates operative mortality of valve surgeryPredictors of poorer survival after AVR

    Aortic Regurgitation (AR)Pre-operative LV end-systolic diameter index (ESDI) 25 mm/m2 is a better predictor of outcomes than ESD >50 mmClinical outcome in asymptomatic patients with AR

    Bicuspid Aortic Valve (BAV)Asymptomatic patients with BAV; low event rate at 20 yearsAortic dilation has distinct patternsLong-term survival after the Bentall procedure

    Mitral Regurgitation (MR)Role of imagingCardiovascular magnetic resonance (CMR) of mitral valve (MV) prolapseGreater operative mortality for MV surgery in younger women3 months is optimal timing for echocardiography/Doppler for MR after myocardial infarctionDurability of mitral valve repair (MVrep)Outcomes after MVrep are similar to mitral valve re-placement (MVR)Reoperation after MVrep

    Tricuspid Regurgitation (TR)The incidence of TR in patients with constrictive peri-carditis

    Infective Endocarditis (IE)High mortality of dialysis patients undergoing valve surgeryHomograft valve not superior to conventional prosthesis

    Transcatheter Valve TherapyPosition statement for transcatheter valve implanta-tionEndovascular resection of human aortic valves in situTransarterial AV implantationAre endovascular valved stents suitable for all patients?Transapical aortic valve implantation (TAP-AVI)Valve-in-a-valve procedureImportance of echocardiography in percutaneous aortic valve implantation (PAVI)Evaluation of aortic root by multislice computed tomog-raphyIntraventricular conduction abnormalities and the need for permanent pacemaker implantationChanges in MR with the Mitra Clip

    Prosthetic Heart Valve (PHV)Guidelines for reporting mortality and morbidityStroke after cardiac valve operation“Low-dose” oral anticoagulation is better than the con-ventional dose in patients with mechanical PHV: final reportGood 25-year outcome after AVR with Medtronic-Hall PHVGreater mortality with bioprosthesis in patients ages 50 to 70 yearsRole of AVR in septuagenarian's quality of life (QOL)Increased mortality with composite AV and root replace-ment (CVG)The use of SVD in stentless PHV, homografts, and autograftsTORONTO STENTLESS PORCINE VALVE (SPV)

    Cryolife O'Brien SPVHomografts (allografts)Homografts and autografts

    REFERENCES