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* From the Physician Research Network, Methodist Healthcare University Hospital, Memphis, TN.
Correspondence to: Sachin Yende, MD, 501 Crews Wing, 1265 Union Ave, Memphis, TN 38104; e-mail: yende{at}juno.com
| Abstract |
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Design: Prospective observational study.
Setting: Cardiovascular surgical ICU.
Patients: Three hundred forty-eight patients underwent CABG. Following surgery, patients were extubated by a standardized respiratory weaning protocol.
Measurements and results: Forty-nine percent of patients had SSS > 0 and had significantly longer duration of mechanical ventilation. The sensitivity, specificity, positive predictive value (PPV), and negative predictive value (NPV) of the SSS for failure to extubate at 48 h are 80, 49, 9%, and 98%, respectively. Two hundred thirty-two patients (67.5%), 101 patients (29%), and 12 patients (3.5%) had a CRS of 0 to 4, 5 to 8, and > 8, respectively. Patients with lower scores had shorter duration of mechanical ventilation. The sensitivity, specificity, PPV, and NPV of the CRS for failure to extubate at 10 h are 42, 73, 47% and 69%, respectively.
Conclusion: The SSS may be used as a preoperative screening tool. A simple questionnaire that includes history of unstable angina, diabetes, congestive heart failure, and smoking prior to hospital admission can be used to calculate the SSS. Patients with SSS
0 are at low risk for PMV and can proceed to surgery without further evaluation.
Key Words: coronary artery bypass grafting failure to wean prolonged mechanical ventilation scoring system
| Introduction |
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Two scoring systems based on clinical criteria alone have been specifically proposed to predict PMV after CABG. Spivack et al5 proposed a scoring system based on preoperative risk factors (the Spivack scoring system [SSS]). Since the SSS is based on preoperative clinical criteria alone, it can be used to predict risk of PMV prior to CABG. Wong et al6 proposed a cardiac risk score (CRS) based on preoperative as well as postoperative risk factors.
We attempted to validate both of these scoring systems in a prospective observational study. Since the complex formula complicates the routine use of the SSS, we also propose a simplified approach to identify low-risk patients using the SSS.
| Materials and Methods |
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Patient Population
Patients were identified prior to surgery. All patients undergoing conventional CABG or off-pump CABG (OPCAB) were included. Patients undergoing combined valve surgery and CABG were excluded.
Data Collection
Preoperative patient characteristics, significant intraoperative risk factors, and both perioperative and postoperative complications were recorded on all patients. The definitions from the Society of Thoracic Surgeons cardiac surgery database were used.2
Patients were followed until discharge to home or a rehabilitation facility. Patients were contacted via telephone 30 days after discharge to determine complications following discharge.
Protocol
A standardized respiratory weaning protocol was followed after surgery to discontinue patients from mechanical ventilation. After arrival in the ICU, fraction of inspired oxygen was decreased from 1.0 to 0.4 while maintaining oxygen saturation > 93%. Once the fraction of inspired oxygen goal was reached, level of consciousness, FVC, and negative inspiratory force were then assessed in all patients. Patients who were alert and had an FVC > 1 L and negative inspiratory force > 20 cm H2O were switched from assist/control mode to the continuous positive airway pressure mode without pressure support. Patients were extubated if a blood gas analysis after 30 min showed pH > 7.3, PCO2 < 50 mm Hg, and PO2 > 70 mm Hg. If patients did not respond to the protocol, the surgeon or critical care physician were contacted and subsequent weaning attempts were continued based on specific physician orders. The total duration of mechanical ventilation in hours (in increments of 15 min) was calculated.
Inotropes were used at the discretion of ICU nurses and physicians, generally to maintain a mean arterial BP of approximately 100 mm Hg, and a cardiac index > 2 L/min/m2. The doses of inotropes were adjusted frequently, and multiple inotropes were often used concomitantly. Therefore, for purposes of analysis, all inotropes were combined, including dopamine, dobutamine, amrinone, milrinone, levophed, and epinephrine. The total duration of all inotropes initiated during surgery and within first 48 h was calculated.
Scoring Systems
SSS:
Comorbid risk factors included history of smoking, diabetes, unstable angina, and congestive heart failure (CHF) prior to hospital admission. Each risk factor was assigned 0.25 points, and the total comorbid risk factor score (COMFAC) was calculated as follows: SSS = 5.409 (COMFAC) - 0.437 (ejection fraction [EF]) - 1.821. Patients with SSS > 0 were considered to be high risk, whereas those with SSS
0 were at low risk for PMV.
CRS: Points were assigned as follows: preoperative, age > 75 years (3 points), age 61 to 75 years (2 points), and female gender (2 points); postoperative, excessive bleeding (6 points), intra-aortic balloon pump (6 points), inotrope use (2 points), and atrial arrhythmia (2 points). Excessive postoperative bleeding was defined as bleeding > 100 mL/h from the chest tube or need for re-exploration secondary to bleeding. Inotrope use was defined as use of any inotrope (defined previously) during the first 48 h following surgery. The CRS was calculated in all patients. Patients were further classified into three groups based on the CRS (0 to 4, 5 to 8, and > 8, respectively).
End Points
Different cutoffs of duration of mechanical ventilation were used to define PMV in the two studies.5
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Spivack et al5
defined PMV as need for mechanical ventilation > 48 h for the SSS. The CRS by Wong et al6
defined PMV as need for mechanical ventilation > 10 h.
Statistical Analysis
All statistical tests were performed as two-tailed tests. Fisher exact test or
2 were used to compare difference in proportions. Continuous variables were expressed as mean (± SD or SEM) and compared with parametric (Student t test) or nonparametric (Wilcoxon) test based on distribution of variables. Kaplan-Meier curves were constructed, and a log-rank test was used to determine association of scoring system and duration of mechanical ventilation, length of ICU, and hospital stay. A p value < 0.05 was considered statistically significant.
A simple linear regression model was used to determine the relation between duration of mechanical ventilation and individual scoring system. For this analysis, the duration of mechanical ventilation (in hours) was considered as the dependent variable. The duration of mechanical ventilation was logarithmically transformed since its distribution was not normal. The point estimate (ß) and Pearson product correlation coefficient (
or r) were calculated for each scoring system. Statistical analysis was performed using software (JMP version 3.2.2; SAS Institute; Cary, NC).
| Results |
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One hundred sixty-eight of 345 patients (49%) had SSS > 0. Preoperative and intraoperative characteristics of patients with SSS
0 and SSS > 0 are summarized in Table 1
. EF, history of smoking, diabetes, CHF, and unstable angina, which are part of the SSS, were significantly different in these two subgroups. In addition, the patients with SSS > 0 had higher incidence chronic lung disease. Patients with SSS > 0 were associated with longer duration of mechanical ventilation (Fig 1 , Table 2
). The patients with a lower score were more likely to be successfully extubated at 48 h (Table 2)
. On multivariable analysis, this association was independent of age, gender, chronic lung disease, type of surgery (conventional vs OPCAB), and duration on bypass machine. The sensitivity, specificity, positive predictive value (PPV), and negative predictive value (NPV) of SSS at 48 h are summarized in Table 3
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0 were associated with shorter duration of mechanical ventilation in the elective subgroup (8.6 h vs 30.6 h, p = 0.003) and urgent subgroup (10.6 h vs 32 h, p = 0.047). However, SSS was not associated with duration of mechanical ventilation in the emergent subgroup (33.6 h vs 28.6 h, p = not significant [NS]).
CRS of 0 to 4, 5 to 8, and > 8 occurred in 232 patients (67%), 101 patients (29%), and 12 patients (3.5%), respectively. Preoperative and intraoperative characteristics of the three groups are summarized in Table 4
. The only factors not specifically included in the CRS (age, gender) were lower incidence of CHF and unstable angina in patients with score
4. A Kaplan-Meier curve was plotted for duration of mechanical ventilation for these three groups (Fig 2
). Patients with lower scores were associated with shorter duration of mechanical ventilation, and were more likely to be successfully extubated at 10 h (Table 5
).
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| Discussion |
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0 (NPV of 98%). However, only 8.5% of patients with SSS > 0 had PMV > 48 h. Therefore, the SSS can be used as a screening tool to identify low-risk patients who may proceed to surgery without further evaluation. However, the poor PPVs among patients with SSS > 0 suggests that further risk stratification is necessary for this group. At first glance, the SSS may appear complicated for routine use. However, careful attention to the formula to calculate the SSS may simplify its clinical application. Patients with none or a single COMFAC risk factor will always have a SSS > 0, whereas those with more than one risk factor always had SSS > 0. This will occur irrespective of EF. Therefore, determining the presence or absence of history of diabetes, unstable angina, smoking, and CHF prior to hospital admission would be adequate to risk stratify these patients. Figure 4 shows a simplified approach to the SSS.
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The ROC compares sensitivity and the false-positive rate for various thresholds of the SSS. The thresholds of 0.6 and 0 are associated with the best combination of sensitivity and false-positive rate. Using a lower threshold would increase the false-positive rate dramatically with minimal improvement in sensitivity. However, using a higher threshold would reduce the sensitivity with minimal reduction in the false-positive rate. The threshold of 0.6 has similar sensitivity but slightly lower false-positive rate (48% vs 51%, respectively) compared to the threshold of zero. However, it is not necessary to calculate the actual score to use the zero threshold. Therefore, the SSS > 0 offers the best combination of sensitivity, false-positive rate, and ease of use at the bedside.
A simple linear regression model to determine association between individual scoring systems and duration of mechanical ventilation demonstrated poor correlation coefficients for both scores. This finding suggests that both scoring systems describe only a small portion of the total variability in duration of mechanical ventilation.
Additional information, such as pulmonary function test (PFT) results, may improve the SSS. However, the role of PFTs in predicting PMV after CABG remains controversial.2 3 7 8 9 Spivack et al5 originally suggested different formulas for patients undergoing elective and urgent CABG. PFT results (FEV1/FVC < 50%) and preoperative PCO2 appeared to have a small effect on the ability to predict PMV only in the subgroups of patients undergoing urgent CABG. PFTs and arterial blood gas analysis are not routinely performed in all patients at our institution, and therefore were not available in our study. We therefore used the same scoring system in all patients. However, our PPV and NPV were similar to the original study (10% and 97% for elective group and 22% and 96% for urgent group, respectively). Patients undergoing emergent or salvage CABG were excluded in the study by Spivack et al.5 The lack of efficacy in patients undergoing emergent and salvage CABG in our study may be a type II statistical error due to fewer patients in this subgroup. In addition, preoperative spirometry is seldom performed in this subgroup, as the benefit of surgery outweighs the risk of postoperative complications.
To conclude, the SSS can be used as a preoperative screening tool to risk-stratify patients undergoing elective and urgent CABG. The SSS is simple and can be calculated based on a four point questionnaire: does the patient have history of unstable angina, diabetes, smoking, and CHF prior to hospital admission? Patients with SSS
0 are at low risk for PMV and can proceed to surgery without further evaluation. Patients with SSS > 0 are at higher risk for PMV and may require further risk stratification.
| Footnotes |
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This study was funded by Methodist Lebonheur Healthcare Foundation.
Received for publication March 5, 2001. Accepted for publication January 16, 2002.
| References |
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