- Research article
- Open Access
- Open Peer Review
Risk factors for postoperative hypoxemia in patients undergoing Stanford A aortic dissection surgery
© Wang et al.; licensee BioMed Central Ltd. 2013
- Received: 4 November 2012
- Accepted: 29 April 2013
- Published: 30 April 2013
The purpose of this study is to identify the risk factors for postoperative hypoxemia in patients with Stanford A aortic dissection surgery and their relation to clinical outcomes.
Clinical records of 186 patients with postoperative hypoxemia in Stanford A aortic dissection were analyzed retrospectively. The patients were divided into two groups by postoperative oxygen fraction (PaO2/FiO2):hypoxemia group (N=92) and non-hypoxemia group (N=94).
We found that the incidence of postoperative hypoxemia was 49.5%. Statistical analysis by t-test and χ2 indicated that acute onset of the aortic dissection (p=0.000), preoperative oxygen fraction (PaO2/FiO2) ≤200 mmHg(p=0.000), body mass index (p=0.008), circulatory arrest (CA) time (p=0.000) and transfusion more than 3000 ml(p=0.000) were significantly associated with postoperative hypoxemia. Multiple logistic regression analysis showed that preoperative hypoxemia, CA time and transfusion more than 3000 ml were independently associated with postoperative hypoxemia in Stanford A aortic dissection.
Our results suggest that postoperative hypoxemia is a common complication in patients treated by Stanford A aortic dissection surgery. Preoperative oxygen fraction lower than 200 mmHg, longer CA time and transfusion more than 3000 ml are predictors of postoperative hypoxemia in Stanford A aortic dissection.
- Obstructive Sleep Apnea
- Aortic Dissection
- Acute Aortic Dissection
- Prolonged Mechanical Ventilation
- Oxygen Fraction
Aortic dissection can be divided into type A and type B by Stanford classification and is one of the most urgent medical cases for its high mortality and morbidity. Although open heart surgery for treating Stanford A aortic dissection has been a universal option, the patients are still threatened by the lethal perioperative complications such as hemorrhage, hypoxemia, renal dysfunction, cerebral dysfunction and etc. Postoperative hypoxemia is defined as an oxygen fraction (PaO2/FiO2) ≤200 mmHg under mechanical ventilation in the first 24 hour after surgery . As a matter of fact, postoperative hypoxemia resembles ARDS (acute respiratory distress syndrome) when oxygen fraction is below 200 mmHg.
Patients who undergo cardiac surgery generally have a more or less increased risk of postoperative hypoxemia. Postoperative hypoxemia has been reported to occur in 12.2-27.1% of patients after cardiopulmonary bypass, and in as high as 51% after open heart aortic dissection surgery [1–3]. Hypoxemia is a dangerous complication and usually accompanied by a number of untoward consequences such as prolonged ventilator support, longer stay in ICU and hospital. Prolonged mechanical ventilation would lead to more and serious complications. Continuous postoperative hypoxemia may cause dysfunctions of other organs besides lungs. The aim of our study is to evaluate the risk factors of postoperative hypoxemia in Stanford A aortic dissection and its impact on the clinical outcomes.
From Dec 2004 to July 2012,186 consecutive patients with acute Stanford A aortic dissection underwent open heart surgery in RenJi Hospital. This study was approved by RenJi Hospital Clinical Research Ethics Committee(2012027) Acute Stanford A aoritic dissection was diagnosed by enhanced computed tomography scan and aoritc valve regurgitation was confirmed by echocardiography. About 70% of the patients underwent surgical procedure within 48 hours, others within 21 days. 4 patients who died during the first 48 hours after surgery were the result of multiorgan dysfunction syndrome and refractory bleeding. They have been excluded from the 186 patients above. In the present study, namely postoperative hypoxemia was defined as a PaO2/FiO2 ≤200 mmHg in the first 24 hour after surgery, according to the diagnostic criteria for ARDS established by American-European consensus conference. The 186 patients were divided into two groups by postoperative oxygen fraction (PaO2/FiO2): hypoxemia group(N=92) and non-hypoxemia group (N=94). We compared 17 perioperative factors between the two groups. Mortality, morbidity and long-term survival were compared between the two groups. In-hospital outcome variables were obtained from patients’ medical records. Follow-up information including survival, cardiovasucular-related events and causes of death were obtained through out-patient clinic visit or from telephone correspondence with the patients or their relatives.
Operative variables and concomitant procedures
Right subclavical artery
Total arch replacement (TAR)
Hemiarch replacement (HAR)
Intraoperative aortic arch endograft deployment (IAAED)
Intraoperative descending aorta endograft deployment (IDAED)
Ascending aorta replacement (AAR)
Cornary artery bypass grafting
Mitral valve replacement
Atrial septal defect repair
Preoperative patient characteristics
Age (years), M±SD
Height (cm), M±SD
Weight (kg), M±SD
BMI (kg/m2), M±SD
History of smoking (%)
Acute onset (%)
Preoperative hypoxemia (%)
History of previous cardiac operation (%)
Preoperative LVEF, M±SD
Diabetes mellitus (%)
Univariate analysis in postoperative hypoxemia
Age (years), mean (sd)
Gender (male) (%)
Height (cm), mean (sd)
Weight (cm), mean (sd)
BMI (kg/m2), mean (sd)
History of smoking (%)
Acute onset (%)
Preoperative hypoxemia (%)
History of previous cardiac operation (%)
Preoperative LVEF (%), mean (sd)
Diabetes mellitus (%)
CPB time (min), mean (sd)
AO time (min), mean (sd)
CA time (min), mean (sd)
Postoperative LVEF<40% (%)
mechanical ventilation duration (hour), mean (sd)
Postoperative transfusion ≥3000 ml (%)
Multivariate logistic regression analysis model for postoperative hypoxemia
Variables in the equation
95.0% C.I. for EXP(B)
All patients have been followed up through out-patient clinic visit or by telephone contacts. The follow-up period was from one month to ninety months (43.65±23.70 month),with a period of 47.96±24.10 month for hypoxemia group and 39.44±22.64 month for non-hypoxemia group. Four patients died, two died of respiratory failure during the first three month after operation in the hospital, others died of stroke or sudden death during follow-up period. Kaplan-Meier survival curve was shown in Figure 1 which revealed a significant difference in the 90-month survival between the hypoxemia group and non-hypoxemia group(p=0.014).
Stanford A aortic dissection has been known for its high mortality and morbidity. Since deep hypothermia, ultrafiltration and selective cerebral perfusion technique were applied in surgery for Stanford A aortic dissection, the incidence of postoperative cerebral complications has decreased. Hypoxemia, as another lift-threatening postoperative complication for Stanford A aortic dissection, may be attributed to prolonged mechanical ventilation and ICU-stay. Acute aortic dissection is frequently accompanied by hypoxemia. Yet currently, few studies revealed the clinical entity in such patients and the management after surgery for acute Stanford A aortic dissection surgery. The aim of our study is to reveal the incidence, risk factors and management of hypoxemia after the surgery for acute Stanford A aortic dissection.
Previous studies disclosed that persistent hypoxemia was the most common cause of PMV (prolonged mechanical ventilation) and ARDS was the most common cause of hypoxemia [4–6]. The etiology of acute respiratory distress syndrome and its less severe form acute lung injury (ALI) may be systemic, rather than pulmonary confirmed to. One of the diagnostic criteria of ARDS is oxygenation impairment (PaO2/FiO2 ≤200 mmHg). Nevertheless, the respiratory failure in patients with hypoxemia in this study could not be diagnosed technically as ARDS or ALI, because it was not usually accompanied by typical radiological pulmonary infiltrates. Therefore, in the present study, postoperative hypoxemia was defined as PaO2/FiO2 ≤200 mmHg in the first 24 hour after surgery, according to the diagnostic criteria for ARDS established by American-European consensus conference [4–8].
Patients who undergo cardiac surgery have an increased risk of postoperative hypoxemia . Postoperative hypoxemia has been reported to occur in 12.2%-27.1% of patients after cardiopulmonary bypass and usually is 51% in open heart aortic dissection surgery [1–3]. In this study, the incidence of postoperative hypoxemia is 49.5% in open heart Stanford A dissection surgery. Previously reported risk factors for hypoxemia after cardiac surgery include advanced age, obesity, smoking history, previous heart surgery, emergency surgery, low LVEF, preoperative chronic pulmonary disease, preoperative myocardial infarction, preoperative diabetes, cardiogenic and noncardiogenic pulmonary edema, pneumonia, excessive blood transfusion and prolonged CPB time [9–11]. In the present study, we identified BMI, preoperative hypoxemia (PaO2/FiO2) ≤200 mmHg, acute onset of Stanford A aortic dissection, CA time, postoperative transfusion ≥3000 ml as the risk factors for postoperative hypoxemia after Stanford A aortic dissection surgery.
Postoperative hypoxemia is a common complication in cardiac surgery. CPB (cardiopulmonary bypass) and CA(circulatory arrest) have been reported to play important roles in the postoperative hypoxemia [12–16]. Stanford A aortic dissection surgery is associated with a high incidence of postoperative hypoxemia compared with other elective cardiac surgical procedures [5, 14–16]. During cardiac surgery, both experimental and clinical studies have well documented that open heart surgery with CPB could result in systemic inflammatory response, activation of complements, thrombin, cytokines, endothelin, endotoxins, neutrophils, adhesion molecule, macrophages, multiple inflammatory mediators and impaired immune reaction and organ dysfunction [17–23]. As CPB represents a kind of non-physiological circulation affecting the peripheral tissue perfusion, particularly in the case of prolonged pump time, which might lead to impaired capillary membrane permeability, malperfusion, tissue anoxia and pulmonary complications [24–27]. Although deep hypothermia and antegrade selective cerebral perfusion may preserve better cerebral function during circulatory arrest, the malperfusion of other organs may still lead to generally ischemic reperfusion injury. A prospective study by De Santo et al. analysed the effect of pulmonary perfusion during hypothermic circulatory arrest which may preserve better lung function but that was not used in our study .
Deep hypothermia is an important technique commonly used in acute Stanford A aortic dissection surgery. However, deep hypothermia participates in both platelet activation pathways and the enzymatic activity of clotting factors which may lead to bleeding and subsequent transfusion. Excessive transfusion is attributed to active bleeding or coagulation abnormalities. Loss of coagulation factors, destruction of platelets and microthrombosis may all lead to lung injury [29–31]. In our study, prolonged CA time and transfusion more than 3000 ml are associated with the hypoxemia.
According to our experience, large dose of methylperdnisolone in the operation and a rather small dose of methylperdnisolone during the first three day after the operation are regularly used in order to decrease the inflammatory reaction. We also run the operation and control bleeding as fast as possible to reduce the CPB or DHCA (deep hypothermic circulatory arrest) time and excessive transfusion.
In the present study, 78.49% of patients who were sent to emergency department for acute onset of Stanford A aortic dissection were found to be hypoxemia (PaO2/FiO2 ≤200 mmHg) before the operation. In our study, all patients breathed spontaneously with nasal prongs or face mask with inhaled oxygen 5-8 L/min before operation. The arterial blood gas and preoperative PaO2/FiO2 were calculated before machanical ventilation. Both acute onset of dissection and preoperative hypoxemia are associated with postoperative hypoxemia. Acute onset of aortic dissection indicates sudden rupture of intima, propagation of the dissection into the medial layer, acute bleeding and activation of cellular and humoral inflammatory systems. In the process of acute bleeding, ventilation and perfusion are out of balance, which leads to hypoxemia. Quite a number of investigators reported that oxygenation was impaired from the onset of dissection due to the inflammatory cascade reaction, increased endothelial and epithelial permeability, increased pulmonary vascular pressure and impaired alveolar surfactant function, which can lead to decrease in the preoperative PaO2/FiO2 ratio. The preoperative inflammatory status of the patient significantly affects the degree of systemic inflammatory response during the Stanford A aortic dissection surgery in succession [1, 9]. Therefore, postoperative hypoxemia may be related to preoperative disturbance in oxygenation. In our opinion, we try all the best to maintain the perioperative fluid balance and meticulous ventilation manipulation, especially in the very first day after the operation.
Obesity have been reported as predictors for hypoxemia [4, 32]. Consistently, we found that obese patients, with BMI>25 kg/m2 are more likely to develop postoperative hypoxemia. It is well-known that obesity is frequently accompanied by some co-morbidity, including obstructive sleep apnea and hypoventilation syndrome which all related to hypoxia [32, 33]. In the present study, the body mass index showed a significant influence in univariate analysis, but not in the multivariate regression model.
In our study, the long-term survival in non-hypoxemia group was better than that in hypoxemia group, which was in accordance with previous studies . Survivors following cardiac surgery are found to enjoy a good quality of life after discharge.
In conclusion, our study demonstrated that BMI (Body mass index), preoperative hypoxemia (PaO2/FiO2 ≤200 mmHg),acute onset of Stanford A aortic dissection, CA time, postoperative transfusion ≥3000 ml were the key risk factors for Stanford A aortic dissection surgery. And preoperative hypoxemia, CA time and transfusion ≥3000 ml were independent predictors of postoperative hypoxemia after Stanford A aortic dissection surgery. Optimized treatments including preoperative respiratory tract management to control those predictors should be helpful to improve the clinical outcomes.
Like all retrospective studies, this investigation also has several limitations. First, the patient population collected for investigation was relatively small. Second, owing to the emergency nature of the Stanford A aortic dissection surgery, detailed information about preoperative pulmonary disease was not completely available. The presence of COPD (chronic obstructive pulmonary disease) was judged on the basis of the patient’s medical history which might not be well defined. Finally, as this is a retrospective study, the potential misclassification bias could not be completely excluded.
We acknowledge the Dr. Weijun Wang from RenJi Hospital for his help in acquisition of data. Tao Zhang from Ruijin Hosptial for her assistance with statistical analysis.
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