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Index of deterioration of patients with mechanical prosthetic heart valve thrombosis
The Cardiothoracic Surgeon volume 28, Article number: 23 (2020)
Mechanical prosthetic heart valves are known for their durability; however, a malfunctioning prosthesis can deteriorate rapidly to become a life-threatening complication. Our aim was to calculate a numerical index to express the rate of clinical deterioration of patients presenting with a mechanical prosthetic heart valve thrombosis (PVT), called the index of deterioration (ID), and to evaluate its usefulness in predicting hospital outcomes.
The median ID and range were (0.43, 0.03-3) NYHA class/day. A higher ID was significantly related to early development of PVT after native valve replacement, younger age, female gender, pregnancy, non-compliance to oral anticoagulation (OAC), low LVEF%, high mean pressure gradient across a mitral prosthesis, raised serum creatinine, and SGOT on admission (P < 0.05). Independent predictors were early presentation after native valve replacement, female gender, and non-compliance to OAC (P < 0.05).
ID correlated positively with the need for urgent/emergency surgery, and the durations of cardiopulmonary bypass, postoperative mechanical ventilation, and positive inotropes. ID correlated negatively with the postoperative LVEF% (P < 0.05). Median ID of the 21 mortalities (0.75, 0.1-3) was > 2.1 times that of survivors (0.35: 0.03−2; P = 0.002), and the median ID of the 29 cases with postoperative complications (0.5, 0.1-1.5) was 2.5 times that of the 39 uneventful cases (0.2, 0.03-2; P = 0.011). The ID significantly predicted both mortality (odds ratio 3.87; 1.33-1.29; P = 0.013) and mortality and hospital complications (odds ratio 4.77; 1.49-15.2; P = 0.008). The respective discriminating abilities were AUC 0.734 (0.616-0.852; P = 0.002) and 0.724 (0.61-0.835; P < 0.001). EuroScore II correlated positively with ID (r = 0.571; P < 0.001) but showed better discriminative abilities.
The simple index of deterioration was useful in monitoring deterioration and predicting hospital progression and outcomes in patients presenting with PVT.
In our experience, mitral valve repair is not always feasible in the young rheumatic population and valve replacement with a mechanical valve is preferred over the use of a bioprosthesis, which is likely to degenerate over time and require reintervention . Although mechanical valves have long term durability, yet the incidence of malfunction is not negligible (0.1-6%) and mechanical prosthetic valve thrombosis (PVT) is one of those serious complications, where patients often deteriorate rapidly, compromising management outcomes. The aim of this study was to express the rate by which those patients deteriorate clinically by a simple numerical index and to test its value in monitoring hospital progression and predicting outcomes of surgery.
This prospective study included 86 patients with PVT who were operated upon in our hospital between January 2016 and October 2019. Written informed consent was obtained from all participants in this study. Inclusion criteria were patients of both sexes presenting with symptoms and or signs suggesting PVT that was documented by transthoracic as well as transesophageal echocardiography on hospital admission. We have excluded cases with recurrent PVT as well as the subset of patients who presented within a short period (1-2 weeks) of the development of mild symptoms (NYHA class I or II), had a small thrombus on echocardiography (< 1 cm) and who responded positively after a short period (1-2 days) of continuous IV heparinotherapy or fibrinolytic therapy.
History intake included date of native valve replacement type and size of implanted prosthesis and any history of valve or anticoagulant related complications. We suggested that every prosthesis is doomed to become malfunctioning 1 day or another and hence, the period that elapsed between the date of implantation of the prosthesis and the appearance of the signs and or symptoms suggesting PVT was recorded in months and was called the latent period of malfunction (LPM). The usually much shorter period that follows afterward and till the patient is reoperated was recorded in days and it was called the manifest period of malfunction (MPM). The patient’s medications were reviewed, especially his compliance to oral anticoagulation therapy (OAC). Non-compliance was defined as a patient skipping > 2 successive doses, changing dose, stopping intake, or shifting to another anticoagulation regimen, without cardiological consultation. In order to calculate the index of deterioration (ID), we assigned the numbers 1, 2, 3, and 4 to the patient’s NYHA class I, II, III, and IV respectively. The change in NYHA class for a particular patient (delta NYHA) was calculated by subtracting the baseline numerical NYHA class value before the event form the numerical NYHA class value of the patient at presentation. The patient’s ID was then calculated by dividing the delta NYHA by the duration of the MPM in days.
Once admitted, all patients benefited from routine preoperative preparation. Female patients were assessed for their pregnancy state and pregnant cases received immediate obstetric evaluation. Based on the clinical and echocardiographic findings, the timing of surgery was decided by the attending surgeon. Surgery was performed through median sternotomy under cardiopulmonary bypass, moderate hypothermia, and antegrade cold blood cardioplegia. The prosthesis was inspected, with the primary intention to be replaced by a mechanical prosthesis in most of the cases. The use of a bioprosthesis or limited thrombectomy was left to the personal surgeon’s judgment and patient preference. Operative survivors were transported to the ICU and managed routinely till discharge.
Qualitative variables were presented as numbers and percentages, and the significance of their association was tested by chi-square or Fisher’s exact test, as indicated. Shapiro-Wilk test showed a significant deviation of normality and calculated ID scores were hence expressed as medians and range. The significance of their association was tested by Spearman’s correlation rank test and groups were compared by Mann and Whitney test or Kruskal and Wallace test, as indicated.
To evaluate the discriminative ability of ID, we have calculated EuroScore II for our patients and both scores were subjected to the receiver-operating characteristic analyses, calculating the area under the curve (AUC) for hospital mortality as well as both hospital mortality and complications. In addition, univariate logistic regression analyses were run to evaluate the predicted probability of ID and EuroScore or hospital mortality as well as model calibration by the Hosmer-Lemeshow test for the lack of “goodness of fit.”
In order to detect the independent preoperative predictors of clinical deterioration (ID), variables that were significantly related to ID on univariate analysis were introduced in a multiple linear regression model. The dependent variable was the normalized values of ID, calculated by the 2 steps approach described by Templeton GF, which involves ranking cases followed by normalization of ranks with the inverse distribution function using fractional rank, mean, and standard deviation . Normality was then rechecked by the Shapiro-Wilk test. All tests were bilateral, and a P value of 5% was the limit of statistical significance. The analysis was performed by the statistical package software IBM-SPSS version 25 (IBM Corp, Chicago, IL, USA).
Table 1 shows the patients demographics. The median age was 49 (16-74) years, with a female predominance and a majority of patients having a single mechanical bileaflet prosthesis implanted in the mitral position (67 cases, 78%). The main presenting symptom was dyspnea and palpitation and 96.5% of cases presented with NYHA class III or IV. Two-thirds of patients were not compliant to OAC regimen on admission, including all the 16 pregnant cases included in our study. Eight of those cases (75%) reduced their recommended warfarin dose or completely stopped the intake for fear of warfarin-related embryopathy. The other 4 cases were shifted to inadequate heparin therapy by their attending obstetrician, without cardiological consultation. There was a statistically significant negative correlation between the index of deterioration and the time elapsed between native valve replacement and LPM (Fig. 1). The earlier the patient developed the malfunction, the faster he deteriorated (r = −0.489; P < 0.001).
Table 2 shows selected operative and postoperative outcomes. Only 2 patients were operated upon electively after presenting with progressive dyspnea and echocardiographic data showing a small thrombus, 60 and 180 months after mitral valve replacement with a SJ bileaflet mechanical prosthesis. The 2 patients were operated upon after failure to improve from a brief 2-days trial of heparin therapy followed by fibrinolytic therapy. Out of the 91 implanted prostheses, 86 were malfunctioning (94.5%), 80% of which were replaced with a bileaflet mechanical prosthesis. The use of a bioprosthesis was limited to the 16 cases (18.6%) who either preferred to avoid the life-long OAC regimen, as well as those patients having a history of repeated non-compliance to OAC. On the other hand, management was limited to thrombectomy and careful cleaning of the valve housing in one case presenting with a small recent thrombus and a low INR of 1.4 on admission. Unfortunately, the patient died postoperatively from persistent low cardiac output, with an apparently well-functioning prosthesis on transesophageal echocardiography. Our overall hospital mortality was high (21%) and 29 patients had non-fatal in-hospital complications (33.7%). A total of 49 complications were recorded in those cases including significant postoperative bleeding in 8 patients (16.3%), which necessitated reoperation in 2 cases (4%), prolonged mechanical ventilation in 7 cases (14.3%), need for reintubation in 4 cases (8.2%), temporary heart block in 6 cases (12.2%), low cardiac output in 5 cases (10.2%), cerebrovascular stroke in 2 cases (4%), septic shock in 2 cases (4%), multiorgan failure in 2 cases (4%), and acute renal failure necessitating dialysis in another case (2%). Ten adverse fetal outcomes were recorded among the 16 pregnant patients (20.4%), included 4 cases of abortion (8.2%), and 6 fetal losses (12.2%).
Table 3 shows the ID values for patients’ subgroups and their correlation with the patients’ demographics, associated risk factors, and hospital outcomes. Younger age on admission, female gender, pregnancy, and non-compliance to OAC were all significantly associated with a high ID. A high ID significantly correlated with increased mean pressure gradient across a malfunctioning mitral prosthesis, need for urgent or emergency surgery, and prolonged durations of cardiopulmonary bypass, postoperative mechanical ventilation, and inotropic support. A high ID was significantly associated with hospital mortality as well as the development of complications among survivors.
Table 3 also shows the calculated EuroScore II values that nearly followed the same pathway as the ID, with a statistically significant positive correlation between both indices (r = 0.571; P < 0.001; Fig. 2). EuroScore II correlated negatively with LPM and MPM and positively with NYHA class at presentation as well as the need for emergency surgery. A high EuroScore II was also significantly related to mortality and to the development of complications among hospital survivors. Unlike the index of deterioration, EuroScore II did not significantly correlate with the patient’s demographics at presentation, namely, age, gender, pregnancy status, and non-compliance to OAC.
Preoperative variables that were statistically significant on univariate analysis were introduced in a linear regression model to detect the independent preoperative predictors of ID, using the normalized ID as the dependent variable. The mean normalized ID + standard deviation was 0.56 + 0.48, the normalized ID of mortalities (0.82 + 0.33) was significantly higher than that calculated for survivors (0.5 + 0.49; P = 0.003). Out of the nine statistically significant variables shown in Table 3, only six were introduced in the model, namely, age on admission, gender, pregnancy state, non-compliance to OAC, mean pressure gradient across the prosthesis, and LPM. Both NYHA class and MPM were excluded for the high co-linearity due to their use in the direct calculation of the dependent variable itself. The urgency of the operation was not used for being the result rather than being the predictor of the deterioration. The model significantly explained ID, R2 = 0.33; P < 0,001. The independent predictors of high ID were female gender (B = 0.236: 0.042-0.43; P = 0.018), non-compliance to OAC (0.215, 0.031-0.4; P = 0.023), and early presentation of PVT as indicated by a short latent period of malfunction (−0.003: −0.004 to −0.002; P < 0.001).
Table 4 shows variables that were significantly related to hospital mortalities in univariate analysis. In order to detect the independent preoperative predictors of mortality variables that were statistically significant on univariate analysis were introduced in a logistic regression model. The model predicted mortality (sensitivity 96.4%, specificity 57.1%, and Negelkerke R square 0.577; P < 0.001); data fitted the model (Hosmer-Lemeshow test; P = 0.7) and the only independent predictor was low LVEF% on admission (odds ratio 0.85, 0.75-0.96; P = 0.008). The model was not improved by the introduction of either ID or EuroScore or both and none of them significantly predicted mortality.
Although our observed 21% hospital mortality was nearly triple that expected by EuroScore II (mean, 7.3%, median, 6.7%, range, 1.69-26.5, and 95% interval of confidence of median, 4-84-6.89); P < 0.001, yet the discriminative ability of the later (AUC 0.799, 0.69-0.9; P < 0.001) was better than that calculated with ID (AUC 0.734, 0.62-0.75; P = 0.002), as shown in Fig. 3. Univariate logistic regression analysis showed that both scores significantly predicted mortality but the EuroScore odds ratio 1.35 (1.13-1.61); P = 0.001 and Hosmer and Lemeshow test; P = 0.345; demonstrated more accurate predictive ability than those calculated for ID: odds ratio, 3.87 (1.3-11.3); P = 0.013; and Hosmer and Lemeshow test P = 0.07. As shown in Fig. 4, better discriminative ability for hospital mortality and complications was also recorded with EuroScore II (AUC 0.799: 0.69-0.9; P < 0.001) than with ID (AUC 0.734, 0.62-0.85; P < 0.002). Univariate logistic regression analysis showed that both scores significantly predicted mortality but the EuroScore odds ratio 1.36 (1.15-1.62); P < 0.001 and Hosmer and Lemeshow test; P = 0.08; demonstrated more accurate predictive ability than that calculated for ID: odds ratio, 3.87 (1.5-15.2); P = 0.008; and Hosmer and Lemeshow test P = 0.05.
Every foreign material implanted in the circulation invites thrombosis and hence, PVT is expected to remain an inherent complication of heart valve replacement. Put it another way, every mechanical prosthesis is assumed to develop PVT 1 day or another, which is why we have termed the period extending from the implantation of the prosthesis and till the development of the signs and/or the symptoms suggesting PVT as the latent period of malfunction (LPM). In a study that included 680 consecutive patients undergoing mechanical mitral valve replacement, routine transesophageal echocardiography performed at day 9 identified thrombus in as much as 9.4% of patients. Although 97% of those patients were successfully managed by anticoagulant therapy, yet 2 cases of PVT needed intervention .
Pathologically, the formation of a thrombus on the prosthetic structures reduces the effective orifice area and increases the trans-valvular gradient, producing a variety of symptoms starting from progressive shortness of breath and palpitation and up to a fulminating congestive heart failure. In addition, the hemodynamic disturbance involves the creation of areas of turbulence that increases shear stress and endothelial injury, and adjacent areas of stasis that increases blood coagulability (both inviting more thrombosis ) and can generate thromboembolic events [5, 6].
There are several mechanisms by which PVT occur, varying from a fast process commencing early after implantation, to the generation of vegetation during the process of endocarditis or the formation of thrombi with the slow ingrowth of a fibrotic pannus over the years [5, 7]. Blackstone and Kirklin have shown that prosthetic valve-related adverse outcomes are not only dependent upon the underlying pathology but also on the timing of presentation . In consequence, we expected that the different pace of those mechanisms will be reflected on the pattern of clinical presentation, especially the length of the period that starts with the patient developing symptoms and/or signs suggesting PVT and ends by reoperation: the manifest period of malfunction (MPM). We expected that the number of NYHA classes the patient loses during this period will objectively reflect the ongoing pathology and, hopefully, may be useful in predicting hospital outcomes. We can easily note that the operative risk of a patient who progresses slowly to reach NYHA class IV over a relatively long period of time is in many times different from another NYHA class IV patient whose prosthesis was catastrophically obstructed by a large thrombus. In fact, the importance of both deterioration in NYHA class and the rate by which it occurs was previously noted by Husebey and colleagues who suggested that advanced NYHA functional class and need for emergency (rapid rate of progression) have to be treated separately . Our suggested ID overcomes this separation as it expresses both the size of deterioration (advancement in NYHA class) and its rate (MPM) in a single numerical value.
The annual rate of PVT is estimated to be between 0.1 and 5.7%, with higher rates being observed in the early perioperative period [10, 11], with prosthesis implanted in the mitral and tricuspid position [5, 12], in association with sub-therapeutic anticoagulation [11,12,13,14,15] or interruption of oral anticoagulants for anticipated non-cardiac surgery  or during pregnancy [15, 17]. Predominance of female gender was reported in 2 large series [8, 11]. Blackstone and Kirklin identified female gender as the only risk factor that was significantly associated with acute prosthetic thrombosis .
In our study, the median LPM that extended up to 30 years after native valve replacement was as early as 44.6 months, 85% of thrombosed prostheses were implanted in the mitral position, 60% of patients were females and two-thirds of cases had a positive history of non-compliance to OAC. Comparable results noting the timing of presentation (39+ 42 months), 85% female predominance, 85% mechanical prosthesis implanted in the mitral position, and 26% non-compliance to OAC were reported by Durrleman and colleagues . Our 61.6% rate of non-compliance is even higher than the 45% rate reported by Buttard and colleagues  but can be attributed to our series including 16 non-compliant pregnant patients. In fact, the ID was able to identify every one of those risk factors, being significantly higher in those patients who were older, of female gender, pregnant, having a history of non-compliance to OAC, or who developed PVT early after native valve replacement, compared to the other patients who were privileged by the absence of those risk factors. In concordance to others, the female gender [8, 11], early PVT after native valve replacement [11, 12], and non-compliance to OAC [11,12,13, 17] were associated with worsening of outcomes and those were the factors that independently predicted a high ID in our study. In practice, a female presenting with PVT is expected to deteriorate 2 times faster than a male companion; this deterioration will unfortunately be doubled in case she was pregnant. Playing the same tune, a patient who is non-compliant to OAC is expected to deteriorate 50% faster than a compliant patient, with all other parameters being equal. As such, the ID may be useful to schedule patients for surgery and, in fact, the median ID of our emergency cases was 0.6, which was 3.5 times that of urgent cases and nearly 7 times that calculated in patients who were operated upon electively.
On the other hand, the ID correlated positively with major adverse operative and postoperative outcomes, such as the durations of cardiopulmonary bypass, mechanical ventilation, and need for inotropes. A high ID was an indicator of a limited improvement of LVEF% after surgery, development of non-fatal complications, and mortality. The median ID of patients who developed non-fatal hospital complications was 2.5 times that calculated for uneventful cases (P = 0.011) and the median ID of the 18 hospital mortalities was more than double that of the 68 survivors (P = 0.002). In practice, a patient, whose ID is 0.35 NYHA class/day or higher, is expected to develop non-fatal complications and mortality, with a sensitivity of 78.7% and specificity of 64.1%. An ID > 0.46 or higher is expected to unfortunately join mortality, with a sensitivity of 81% and specificity of 62%. We have previously tested the ID in a group of 75 patients presenting with different types of prosthetic malfunctions including PVT, prosthetic valve endocarditis, severe prosthetic dehiscence, and primary bioprosthetic failure. Due to the inclusion of a large number of patients with slowly progressive valve dehiscence, it was more suitable to calculate LPM in months rather than in days, giving larger crude ID values than the ones calculated in the actual study . The ID calculated for different valve malfunctions also correlated positively and significantly with the early presentation of the malfunction, need for emergency, and longer durations of bypass and positive inotropes as well as hospital mortality .
Although the hospital mortality in our study was as heavy as 21%, yet it was within the widely variable range reported to be as low as 5% in a small selected series of 20 patients  to 20.6% in a large series of 63 patients who developed mainly PVT due to pannus formation  to as much as 41% in a Canadian series of 39 patients . Many risk factors have been identified to influence outcomes of surgery including early presentation [8, 11] myocardial depression, as indicated by low EF , and increased left ventricular diameter [14, 19], advanced NYHA class , prolonged cardiopulmonary bypass time , non-compliance to oral anticoagulation (OAC) regimen [11, 13], and need for any additional procedure  Our study has shown that low LVEF% on admission was the only independent predictor of hospital mortality and not the ID or the EuroScore II.
Although the STS risk score has been found to be highly effective for determining numerous outcomes such as short and long-term mortality, stroke, length of hospital stay and renal failure, prolonged ventilation, infection, and reoperation, yet it was modeled to fit specific surgical cases: isolated coronary artery bypass grafting (CABG), isolated aortic valve replacement (AVR), isolated mitral valve replacement (MVR), mitral valve repair (MV repair), CABG + AVR, CABG + MVR, and CABG + MV repair . Because of this limitation, the STS risk scoring system cannot be used to study other types of cardiac surgery that are not yet included. On the other hand, the other most commonly used scoring system (the EuroScore II) that was designed to expect mortality in various surgical cases showed poor clinical relevance in the segment of patients where it is needed the most, i.e., the high risk and emergency cases [23,24,25]. Many studies have shown a significant discrepancy between observed and expected mortality in those patients when calculated by EuroScore II which sometimes overestimates  and in other times underestimates mortality  in high-risk patients [23, 24] as well as in emergency surgery . In our study, the observed mortality was triple that expected by EuroScore II. Although it discriminated mortality and complications better than the ID, yet the wide gap between observed and expected values may be due to EuroScore II totally disregarding the important effect of time factor on outcome, whether the time delay between the implantation and the development of PVT [8, 10, 11]: the LPM or the speed by which the patient deteriorates: the MPM; which is the basis upon which the ID was founded . Another important forgotten factor is the patient’s compliance to OAC [11,12,13,14,15, 17]which is an independent predictor of deterioration, as expressed in terms of ID.
The simple two-factors based ID (NYHA deterioration and time) was never thought as a replacement for the well-known multifactorial scoring systems, but as a useful numeric index to monitor deterioration and predicting hospital progression and outcomes in patients presenting with PVT. It raised questions about the need to include the time factor and non-compliance to OAC in predicting outcomes in those patients. However, larger studies are needed to show if the index of deterioration can be helpful to take decisions during the course of management of those patients.
Availability of data and materials
Available for public share in the main manuscript and the tables and figures.
Area under the curve
Aortic valve replacement
Coronary artery bypass grafts
Index of deterioration
Latent period of malfunction
- LVEF %:
Left ventricular ejection fraction %
Manifest period of malfunction
Mitral valve replacement
New York Heart Association Classification
Prosthetic valve thrombosis
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This study was approved by the ethical committee of the Faculty of Medicine, Ain-Shams University (Ref FMASU MD 185/2017).
Written informed consent was obtained from all participants in this study.
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Hassouna, A., El-Ghanam, M., Moftah, H. et al. Index of deterioration of patients with mechanical prosthetic heart valve thrombosis. Cardiothorac Surg 28, 23 (2020). https://doi.org/10.1186/s43057-020-00033-0
- Prosthetic valve malfunction
- Prosthetic valve thrombosis
- Mechanical valve thrombosis
- Scoring systems
- EuroScore II