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J Am Coll Cardiol, 2000; 35:1881-1889 © 2000 by the American College of Cardiology Foundation |

* Kosuyolu Heart and Research Hospital, Kosuyolu, Istanbul, Turkey
Cardiology Division, The University of Texas Health Center, Tyler, Texas, USA
Manuscript received September 27, 1999; revised manuscript received December 16, 1999, accepted February 21, 2000.
Reprint requests and correspondence: Dr. Ubeydullah Deligönül, Cardiology Division, UTHCT, 11937 US Highway 271, Tyler, TX 75708-3154
udeligon{at}uthct.edu
| Abstract |
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We analyzed the results of intravenous thrombolytic treatment under transesophageal echocardiographic (TEE) guidance in prosthetic valve thrombosis.
BACKGROUND
Thrombotic occlusion of prosthetic valves continues to be an uncommon but serious complication. Intravenous thrombolytic treatment has been proposed as an alternative to surgical intervention.
METHODS
In a four-year period, 32 symptomatic patients with prosthetic valve related thrombosis underwent 54 thrombolytic treatment sessions for the treatment of 36 distinct episodes. All patients had low international normalized ratio values at the presentation. Transesophageal echocardiography was performed at baseline and repeated after each thrombolytic treatment session (total 98 TEE examinations). Streptokinase was used as the initial agent with a repeat dose given within 24 h when necessary. Recurrent thrombosis was treated either with tissue plasminogen activator or urokinase.
RESULTS
The initial success after first dose was only 53% (17/32) but increased up to 88% (28/32) after repeated thrombolytic sessions upon documentation of suboptimal results on TEE examination (p < 0.01). In addition, four asymptomatic patients with large thrombi were also successfully treated with single infusion. The TEE characteristics of thrombus correlated with clinical presentation and response to lytics. Success was achieved with single lytic infusion in 40% of the obstructive thrombi as compared with 75% of the nonobstructive ones (p < 0.05). The success rates of lytic treatment were similar for mitral versus aortic valves, and for tilting disk versus bileaflet valves. Rapid (3 h) and slow (15 to 24 h) infusion of streptokinase resulted in similar success rates. However, major complications (three patients) occurred only in the rapid infusion group.
CONCLUSION
In patients with prosthetic valve thrombosis, intravenous slow infusion thrombolysis given in discrete, successive sessions guided by serial TEE and transthoracic echocardiography can be achieved with a low risk of complications and a high rate of success.
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In the present study, we analyzed the results in a consecutive series of patients with prosthetic heart valves in whom the thrombolytic treatment was administered in discrete, successive treatment sessions guided by serial TEE. The success and the complication rates were analyzed according to the echocardiographic and clinical characteristics of the patients.
| Methods |
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Echocardiographic criteria. The echocardiographic data used in this study were as follows: prosthetic valve thrombus was recognized as soft and homogeneous, mobile or fixed echo densities located at the valve occluder and/or valve struts. The largest diameter of the thrombus as well as the length of the mobile portion, if present, were measured. A diagnosis of pannus formation was made when fixed, bright echodense structures, sometimes containing focal calcific deposits, were present primarily along the valve ring with extension into the valve orifice. Patients with valve dysfunction due to pannus formation were not included in this series (four patients in the same time period, all confirmed at surgery).
Although different makes of mechanical valves will have different "normal gradient" ranges, we arbitrarily selected the cutoff points for valvular obstruction. These limits were largely based on the previously published values (40). Since we did not have a baseline recording for each valve, more specific cutoff points could not be determined. The limitation of the occluder movement was evaluated subjectively. A significant narrowing of the prosthesis was diagnosed when the Doppler mitral valve area was
1.5 cm2 and the mitral valve mean gradient was
10 mm Hg, or when the aortic mean gradient was
40 mm Hg.
Thrombolytic treatment.
Patients with obstructive thrombus, and those with nonobstructive thrombus, who either had a history of embolization or had a large thrombus mass (
10 mm base diameter and/or
5 mm mobile segment length) were accepted as candidates for thrombolysis. Patients with large thrombus were not excluded. Thrombolytic treatment was contraindicated in patients with bleeding tendency and in those with expanding or hemorrhagic cerebral infarcts.
Streptokinase (SK) was the initial agent infused in all patients. No loading dose of SK was used. In the early experience (15 patients), a total of 1.5 million units of SK was administered in 3 h. In subsequent patients, a slow infusion of 60,000 to 100,000 U/h for a total of 15 to 24 h was given (Table 2). When the persistence of thrombus was documented by repeated TEE, another infusion of 1.5 million units of SK was given. Urokinase (UK) or tissue plasminogen activator (tPA) (depending on the availability) was chosen for recurrent thrombus or in the case of failure of two subsequent SK sessions. The tPA dose was 100 mg (10-mg bolus followed by the infusion of the remaining amount in 5 h). The UK dose for each session was 1.5 million units given as a 15-h continuous infusion (100,000 U/h).
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75% reduction in largest diameter of the thrombus mass was achieved. For nonobstructive thrombi, a reduction by
75% in thrombus diameter or complete lysis of the mobile portion of the thrombus was required as criteria for complete success. The positive responses that were less than "completely successful" were accepted as partial success.
Heparin and warfarin treatment was started in patients with complete and partial success and heparin therapy was continued until an international normalized ratio (INR) of
2.5 was achieved.
Statistical analysis. Chi-square test and Students t test were utilized for the comparison of discrete and continuous variables, respectively. A p value of <0.05 was accepted as significant.
| Results |
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The symptoms at presentation (Table 1) of 36 distinct clinical episodes in 32 patients were mainly dyspnea (58%) and embolic events or transient ischemic attacks (36%). Interestingly, four patients reported muffling or cessation of their prosthetic valve sounds. The New York Heart Association (NYHA) functional class was III or greater in 50% of the episodes.
The number and the type of treatment sessions are also shown in Table 1. In the mitral position, 41 thrombolytic sessions (including 4 recurrent thrombus) were performed in 27 episodes in 23 patients. In aortic position 9 thrombolytic sessions were given for 7 episodes in 7 valves. The patient with both aortic and mitral valve thrombi was given SK in two successive sessions. The patient with tricuspid prosthesis previously had SK infusion at another institution and was presented with recurrence (14). Doppler hemodynamic measurements before and after the final session of thrombolytic treatment were listed in Table 2.
The outcome of thrombolytic treatment. According to the study definitions, four episodes resulted in partial success (Table 3). These were included in the complete success group for their small numbers. The initial rate of success after the first dose of SK in primary valvular thrombosis was only 53% (17/32), but increased up to 87.5% (28/32) after repeated thrombolytic sessions upon documentation of suboptimal results on TEE examination (p < 0.01). One additional thrombolytic session was administered in 17 episodes. A total of three thrombolytic sessions were necessary in only one patient, who had an unsuccessful result. In four patients with five episodes of recurrent thrombosis, a single dose was successful in two and two successive treatments were necessary in the remaining three. Of the three patients with no response to lytics, two were maintained on regimens of higher-dose oral anticoagulants and the third one underwent surgery.
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II, III and IV symptoms, respectively (p = NS). There was no difference in success rate for rapid as compared with slow infusion of SK (Table 4).
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Thrombolytic treatment in asymptomatic patients. There were two male and two female patients with mitral valve prostheses (three bileaflet, one tilting disk) who underwent successful thrombolysis for large, nonobstructive left atrial thrombi detected on routine examination (Table 1). The thrombi were mobile in two and fixed type in the remaining two. A single SK infusion session was successful in all four patients.
Left atrial mural thrombus associated with thrombosis of the mitral valve prosthesis. The left atrial mural thrombus persisted in six patients despite successful lysis of the thrombus associated with the prothesis itself. No systemic embolization was noted in this group.
Complications of thrombolytic treatment. The symptomatic and asymptomatic groups of patients combined for the analysis of complications. The complications of thrombolytic treatment were seen in 15% of the 40 total thrombotic episodes in 36 patients (Table 1). Major complications included death in one patient (2.8%), coronary embolization in one patient (2.8%) and cerebral embolization in one patient (2.8%). Both patients with embolization had large, fixed, obstructive thrombi on TEE. Death was due to cerebral bleeding in a patient with 10-day-old brain embolism with no evidence of hemorrhagic infarct on baseline computed tomographic (CT) scan. Minor bleeding was noted in three (8.3%) of the episodes. Of interest, all major complications occurred in the group that received the rapid infusion of SK as initial treatment. No complications occurred in four asymptomatic patients. No complications occurred as a result of TEE examinations.
| Discussion |
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Obstructive versus nonobstructive thrombus. Although the hemodynamic benefit of lysing an obstructive thrombus is obvious, the issue with nonobstructive prosthetic valve thrombus is somewhat controversial. Recently published guidelines by Lengyel et al. (30) proposed intensive anticoagulation, rather than thrombolysis, in patients with nonobstructive thrombi. Valvular thrombi without hemodynamic obstruction can be detected with higher accuracy by TEE (35) and may be seen in 15% to 18% of the patients in the early postoperative period following valve replacement (41). Despite the absence of hemodynamic embarrassment, nonobstructive prosthetic thrombi may not be totally benign. We and others showed that nonobstructive mobile prosthetic valve thrombi carried an increased risk of systemic embolization (35,41). In the current study, the thrombolytic treatment was not associated with increased embolic complications in this subset despite the more frequent initial presentation with embolic events. Similarly, a more recent study, again by Lengyel et al. (42), reported that the anticoagulant treatment failed in half of the patients with nonobstructive thrombi, while there was no failure or complication in the group treated with thrombolysis. Together these results bring strong support to extending the indications for thrombolytic treatment to patients with nonobstructive thrombi. Transesophageal echocardiography may show persistent residual thrombus (with embolic potential) following initial thrombolysis, even if the relief of hemodynamic obstruction is detected by other means. In our series, 9 of 25 (32%) obstructive thrombi were transformed into nonobstructive but large thrombi (4 of them gaining mobility) after the first SK dose and were treated successfully with additional infusion of the thrombolytic in all but one.
Thrombolysis results according to the valve type and location. Roudaut et al. (20) reported higher thrombolytic success rates for aortic than mitral prosthetic valves. Some authors suggested that the bileaflet valve thrombotic occlusions were more responsive to thrombolysis (20,23). An explanation for this was the potential for the flow obstruction by a smaller thrombus occupying the critical pivot point in a bileaflet valve as compared with a single disk valve. Our series, in contrast, did indicate similar success rates in both valve locations and valve types. This was true even when the success rates for each valve location and type were further stratified according to fixed or mobile, and obstructive or nonobstructive thrombus characteristics.
Thrombolysis results according to the clinical status. The thrombolytic success was achieved in equal proportion of patients who were in class II or less as compared with those who were in class III or greater. Hurrell et al. (29) recommended direct surgical treatment rather than thrombolytics for patients with class IV symptoms, because of a high medical mortality reported in some series. The ACC/AHA valve disease guidelines (39) also recommended surgical treatment in class IV patients except those who are nonsurgical candidates. Unfortunately, the surgical mortality is also highest in this group of patients (4,5). Recently published thrombolytic therapy guidelines (30) proposed the thrombolytic treatment as the treatment of choice for the "critically ill" patients in functional class III or IV, although the definition of "critically ill" may be quite variable. We believe that an individual approach based on the expected surgical mortality rate is necessary in patients with class IV symptoms. We suggest that, in the absence of cardiogenic shock, these patients may be treated in the intensive care unit by TEE-guided thrombolysis.
Systemic embolization and other complications. Due to the lack of a generally accepted standard regimen, various infusion protocols and thrombolytic doses were used in the previous studies (631), making a direct comparison of the results difficult. The rate of major events and minor bleeding in our study was within the previously reported range. The embolization rate of 5.7% (two patients) in our series compares favorably with previously reported single institution series (Table 6). Both embolic complications occurred in patients with fixed, obstructive thrombi who were given rapid thrombolytic infusions. In the recent thrombolytic treatment guidelines article (31), the presence of a large thrombus on the prosthetic valve or in the left atrium has been included in the relative contraindications based on one case report of embolism following a rapid (3-h) infusion of tPA (26). In a recent study by Manteiga et al. (31) 3 instances of embolization (33%) occurred in 10 patients with large left atrial thrombi who were given rapid infusion of SK (1.5 million units in 90 min). It appears that rapid thrombolytic infusion, especially in the presence of large thrombus, may increase the risk of embolization. Understanding the predictors of systemic embolism is important because this complication seems to be the Achilles heel of the thrombolytic treatment of prosthetic valve thrombosis. There are little data available on this subject. Reddy et al. (24) published the series with lowest embolization rate and suggested that advanced age and atrial fibrillation may be the risk factors for embolic complications. Roudaut et al. (20), however, found that class IV clinical status was the only predictor of embolic complications (and death). It is not known whether this was secondary to larger amounts of thrombi in these patients.
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| Conclusions |
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| References |
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