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Volume 2015 |Article ID 265165 | https://doi.org/10.1155/2015/265165

Yue Jin, Guohao Xie, Haihong Wang, Lielie Jin, Jun Li, Baoli Cheng, Kai Zhang, Andreas Hoeft, Xiangming Fang, "Incidence and Risk Factors of Postoperative Pulmonary Complications in Noncardiac Chinese Patients: A Multicenter Observational Study in University Hospitals", BioMed Research International, vol. 2015, Article ID 265165, 10 pages, 2015. https://doi.org/10.1155/2015/265165

Incidence and Risk Factors of Postoperative Pulmonary Complications in Noncardiac Chinese Patients: A Multicenter Observational Study in University Hospitals

Academic Editor: Stephen M. Pastores
Received09 Jan 2014
Revised01 Jul 2014
Accepted06 Aug 2014
Published02 Mar 2015

Abstract

Purpose. To assess the incidence of postoperative pulmonary complications (PPCs) in Chinese inpatients, and to develop a brief predictive risk index. Methods. Between August 6, 2012, and August 12, 2012, patients undergoing noncardiac operations in four university hospitals were enrolled. The cohort was divided into two subsamples, cohort 1 to develop a predictive risk index of PPCs and cohort 2 to validate it. Results. 1673 patients were enrolled. PPCs were recorded for 163 patients (9.7%), of whom the hospital length of stay (LOS) was longer (). The mortality was 1.84% in patients with PPCs and 0.07% in those without. Logistic Regression modeling in cohort 1 identified nine independent risk factors, including smoking, respiratory infection in the last month, preoperative antibiotic use, preoperative saturation of peripheral oxygen, surgery site, blood lost, postoperative blood glucose, albumin, and ventilation. The model was validated within cohort 2 with an area under the receiver operating characteristic curve of 0.90 (95% CI 0.86 to 0.94). Conclusions. PPCs are common in noncardiac surgical patients and are associated with prolonged LOS in China. The current study developed a risk index, which can be used to assess individual risk of PPCs and guide individualized perioperative respiratory care.

1. Introduction

More than 230 million major surgical procedures are undertaken each year worldwide [1] and postoperative complications imposed a significant clinical and economic burden to surgical patients as well as the public health systems [2, 3]. Postoperative pulmonary complications (PPCs) are common postoperative complications that occur in 2% to 40% of patients and are associated with increased morbidity, mortality, and length of stay (LOS) [39]. In noncardiac patients, PPCs occur more frequently than cardiac complications [10]. Though it came to wide attention in recent years, the literature investigating the incidence and outcome of PPCs in Chinese inpatients remains scarce.

It is known that PPCs have a multifactorial etiology and had been defined broadly, including respiratory tract infection, pneumonia, respiratory failure, atelectasis, pleural effusion, pneumothorax, bronchospasm, and aspiration pneumonitis [11]. Previous studies demonstrated that PPCs were associated with a series of perioperative risk factors, such as age, smoking, chronic obstructive pulmonary disease (COPD), type of surgery, and serum albumin [4, 6, 7, 1114]. A majority of these risk factors can be intervened and improved [1517]. Therefore, identifying perioperative risk factors of PPCs is an important step toward improving quality of care in surgical patients, which has been already explored in several studies [11, 12, 18].

In the United States, Arozullah et al. developed a multifactorial risk index to predict the postoperative pneumonia after major noncardiac surgery [12]. In Canada, McAlister et al. paid attention to the nonthoracic surgery [7]. They found the incidence of PPCs is 8% and identified the preoperative risk factors. Dupont et al. also investigated five independent predictive factors of postoperative pneumonia in France [19]. A recently published risk-prediction equation for PPCs was a significant advance in this field, which identified seven independent risk factors for PPCs by Canet et al. [11]. The researchers further tested this predictive risk score in a large European cohort and found this risk score performed differently between geographic areas [20]. In China, the most populous developing country in the world, however, very limited information about PPCs has been reported so far. Since China is different from the USA and European countries in geographic areas, race, disease spectrum, and social psychological background, investigations assessing the incidence and characteristics of PPCs in Chinese surgical cohorts are indispensable. Hence we conducted the present study to assess the incidence and risk factors of PPCs after noncardiac surgery in China and to develop a risk index of PPCs which is applicable for Chinese inpatients. The results of the present study would help health care providers to understand the existing situation of PPCs in China, to identify high-risk patients from the generic surgical population, and to guide individualized perioperative respiratory care.

2. Materials and Methods

2.1. Study Settings and Patients

We conducted a prospective, multicenter, and observational study of inpatients undergoing noncardiac surgical procedures. This study was performed at 4 university hospitals located in Zhejiang province, China (the First Affiliated Hospital, Zhejiang University School of Medicine, the Sir Run Run Shaw Hospital, Zhejiang University School of Medicine, the First Affiliated Hospital, Wenzhou Medical College, and the Second Affiliated Hospital, Wenzhou Medical College). The inpatients undergoing surgical procedures between August 6, 2012, and August 12, 2012 were enrolled into the study. All patients would receive routine care, and no research-related intervention would be introduced.

2.2. Inclusion and Exclusion Criteria

All noncardiac operations performed under general, spinal, epidural, or regional anesthesia were eligible for inclusion. The exclusion criteria were as follows: (1) younger than 18 years; (2) pregnancy; (3) organ transplantation; (4) procedures performed under local nerve anesthesia; (5) procedures outside the operating room; (6) outpatient procedures (who had an LOS in hospital less than 24 hours); (7) reoperation related to a previous surgical complication; (8) patients with preoperatively intubated trachea.

2.3. Data Collection

Two trained anesthesiologists were assigned at each center to collect the following data: (1) generic information: date of surgery and hospital admission/discharge, age, gender, American society of anesthesiologists (ASA) physical status, height and weight, smoking status, alcohol use, and chronic comorbid disease; (2) preoperative variables: respiratory infection in the last month, antibiotic use, nasogastric tube, saturation of peripheral oxygen (SpO2), and laboratory results (leucocytes count, neutrophil, hemoglobin, serum creatinine, serum albumin, and fasting blood glucose); (3) intraoperative variables: anaesthetic technique, surgery (type, site, and duration), nasogastric tube, bladder catheter, central venous catheter, blood loss, blood transfusion, pulmonary, and cardiovascular complications; (4) postoperative variables: clinic (SpO2, mechanical ventilation, vasoactive drugs) and laboratory results within 2 hours after surgery. After operation, surgeon and nurses visited the patients every day and recorded incidence of PPCs. The PPCs were defined in Table 1 [11]. Postoperative mortality was defined as death within 60 days of surgery.


Respiratory infection
Treatment with antibiotics for a respiratory infection, plus at least one of the following criteria: new or changed sputum, new or changed lung opacities, fever, and leukocyte count >12,000/mm3

Respiratory failure
Postoperative PaO2 <60 mmHg on room air, a ratio of PaO2 to inspired oxygen fraction <300, or SaO2 <90% and requiring oxygen therapy

Pleural effusion
Chest radiograph demonstrating blunting of the costophrenic angle, evidence of displacement of adjacent anatomical structures, or (in supine position) a hazy opacity in one hemithorax with preserved vascular shadows

Atelectasis
Collapse of the alveoli, lung opacification with shift of the mediastinum, hilum, or hemidiaphragm toward the affected area, and compensatory overinflation in the adjacent nonatelectatic lung

Pneumothorax
A collection of air in the pleural space (the area with no vascular bed surrounding the visceral pleura)

Bronchospasm
Newly detected expiratory wheezing treated with bronchodilators

Aspiration pneumonitis
Acute lung injury after the inhalation of regurgitated gastric contents

PaO2: partial pressure of oxygen in arterial blood; SaO2: arterial oxyhemoglobin saturation.
2.4. Outcomes

The primary outcome was the occurrence of PPCs, the postoperative LOS, and the postoperative mortality rate. The secondary outcome is the predictive risk index of PPCs.

2.5. Statistical Analysis

Quantitative data were presented as means and standard deviations (SD) or median and interquartile range (IQR; from 25th to 75th percentiles) as appropriate. Qualitative data were reported as (%). Student’s -test or Mann-Whitney test were used for comparison of continuous variables and the chi-squared test or Fisher’s exact test for categorical variables to test the relationship between each potential risk factors and PPCs.

In order to develop a risk index of PPCs, enrolled patients were further divided into two cohorts. Cohort 1 composed of patients from two hospitals and was used to develop the predictive index, while cohort 2 was used to validate the index. In cohort 1, risk factors were firstly analyzed using univariate analysis (). Then a multivariate logistic regression was conducted in cohort 1 with the occurrence of PPCs as the dependent factor, incorporating all risk factors on the basis of correlation coefficients between variables lower than 0.4. The forward LR mode was adopted in the process of regression. The adjusted odds ratios (OR) and the confidence intervals (CI) were also calculated. A brief predictive index was then calculated by multiplying the regression (β) by 10 and rounding off to the nearest integer [12]. The brief predictive index then validated in cohort 2 to evaluate the model’s discriminatory capability, and the area under the receiver operating characteristic (ROC) curve was displayed (-statistic).

Data were analyzed using SPSS 16.0 (SPSS inc., Chicago, USA). All these tests were two-tailed and statistical significance was considered when a value was less than 0.05.

3. Results

3.1. Demographic and Clinical Characteristics

Between August 6, 2012, and August 12, 2012, 2001 patients were undergoing noncardiac surgery, of which 328 were excluded according to the inclusion criteria or lost. Consequently, the final sample included in the statistical analysis consisted of 1673 patients, 902 in cohort 1 and 771 in cohort 2 (Figure 1). The basic characteristics of the study subjects are detailed in Table 2.


OverallCohort 1 Cohort 2
(n = 1673)(n = 902)(n = 771)

Male, n (%)770 (46.0)436 (48.3)334 (43.3)0.04
Age, yr49 (37–60)48 (36–60)49 (39–60)0.69
Education, yr9 (6–9)9 (6–9)9 (9–14.5)0.31
Smoking status, n (%)0.85
 Never smoker1397 (83.5)753 (83.5)644 (83.5)
 Former smoker222 (13.3)118 (13.1)104 (13.5)
 Current smoker54 (3.2)31 (3.4)23 (3.0)
Drinker, n (%)0.47
 Never drinker1487 (88.9)804 (89.1)683 (88.6)
 Former drinker152 (9.1)83 (9.2)69 (8.9)
 Current drinker34 (2.0)15 (1.7)19 (2.5)
Body mass index, kg/m222.3 (20.3–24.3)22.1 (20.3–24. 2)22.4 (20.3–24.3)0.85
Preoperative SpO2, %98 (98-99)98 (98-99)98 (98-98)0.45
Respiratory infection in the last month, n (%)28 (1.7)16 (1.8)12 (1.6)0.85
ASA physical status, n (%)0.43
 1830 (49.6)464 (51.4)366 (47.5)
 2722 (43.2)380 (42.1)342 (44.4)
 3114 (6.8)54 (6.0)60 (7.8)
 45 (0.3)3 (0.3)2 (0.3)
 52 (0.1)1 (0.1)1 (0.1)
Emergency surgery, n (%)102 (6.1)55 (6.1)47 (6.1)0.99
Anesthesia, n (%)0.24
 General and combined#1251 (74.8)664 (73.6)587 (76.1)
 Neuraxial/regional422 (25.2)238 (26.4)184 (23.9)
Surgical site, n (%)<0.001
 Peripheral1015 (60.7)620 (68.7)395 (51.2)
 Abdominal600 (35.9)243 (26.9)357 (46.3)
 Intrathoracic58 (3.5)39 (4.3)19 (2.5)
Duration of surgery, h0.63
 ≤2 h1238 (74.0)659 (73.1)579 (75.1)
 2-3 h235 (14.0)132 (14.6)103 (13.4)
 >3 h200 (12.0)111 (12.3)89 (11.5)
LOS, d8 (5–14)9 (6–14)8 (5–13)0.01

Data are median (quartile) unless otherwise specified.
SpO2: saturation of peripheral oxygen; ASA: American society of anesthesiologists; LOS: length of stay.
*Cohort 1 versus cohort 2; #this category included general anesthesia alone and general anesthesia combined with regional blockade.
3.2. PPCs, LOS, and Mortality

A total of 163 (9.7% of the 1673 patients) patients were recorded with 237 episodes of PPCs. Postoperative respiratory failure developed in 30 patients (1.8%), bronchospasm in 48 (2.9%), pleural effusion in 7 (0.4%), respiratory infection in 131 (7.8%), atelectasis in 19 (1.1%), cardiopulmonary edema 1 (0.06%), and pneumothorax in 1 (0.06%). Most PPCs occurred after upper gastrointestinal surgery (40.4%), followed by thoracic (38.8%), neurosurgery (22.2%), kidney (14.3%), hepatobiliary (13.5%), and lower gastrointestinal surgeries (11.8%). The median postoperative LOS was longer in patients with PPCs (16 days, IQR 10–23 days) than in those without PPCs (8 days, IQR 5–13 days) (), especially in orthopaedics (), breast (), gynaecology (), lower gastrointestinal (), and hepatobiliary () surgery. The detailed information on the characteristics of PPCs and LOS was shown in Table 3.


All patientsPPCs, n (%)LOS (day)P
With PPCs (n = 163)Without PPCs (n = 1510)

Total 1673163 (9.7)16 (10–23)8 (5–13)<0.001
Surgical specialty
 Orthopaedics30310 (3.3)22 (14–31)11 (6–17)0.03
 Breast722 (2.8)20 (19–21)4 (3–8)<0.001
 Gynaecology20816 (7.7)10 (7–19)6 (4–8)<0.001
 Vascular331 (3.0)16 (16–16)9 (7–13)0.45
 Upper gastrointestinal4719 (40.4)18 (16–21)17 (13–20)0.68
 Lower gastrointestinal13616 (11.8)17 (15–28)11 (6–15)<0.001
 Hepatobiliary22931 (13.5)24 (16–33)8 (5–14)<0.001
 Urology1687 (4.2)16 (13–38)8 (6–11)0.16
 Kidney568 (14.3)13 (10–17)10 (7–14)0.65
 Head and neck1479 (6.1)4 (3–7)7 (5–9)0.21
 Thoracic4919 (38.8)12 (10–15)14 (9–16)0.36
 Neurosurgery368 (22.2)22 (12–27)18 (12–25)0.40
 Endocrinology14714 (9.5)8 (7–14)7 (6–8)0.11
 Others414 (2.4)10 (7–26)7 (5–9)0.16

Data are median (quartile) unless otherwise specified.
PPCs: postoperative pulmonary complications; LOS: length of stay.

Four (0.24%) patients died in the hospital, 3 (1.84%) of the 163 patients with PPCs and 1 (0.07%) of the 1510 patients without PPCs; the mortality was significantly higher in patients with PPCs than those without ().

3.3. Risk Factors and PPCs

The variables having a statistically significant impact on the incidence of PPCs detected from the cohort 1 are shown in Table 4. Then the independent variables were entered into the logistic regression model, except for these have high collinearity with others (intraoperative blood loss and duration of surgery; intraoperative blood loss and central venous catheter; intraoperative blood loss and blood transfusion; postoperative ventilation and vasoactive drug; pre- and intraoperative nasogastric tube; pre- and postoperative hemoglobin). Multivariable logistic regression indicated that 9 of those potential predictors were present in the final model. The raw and adjusted odds ratios for the nine variables are shown in Table 5, which also shows the brief predictive index derived from the β coefficient for each variable. This nine-variable regression model had good discrimination and calibration values in cohort 1 (-statistic 0.91, 95% CI, and from 0.89 to 0.94). The ROC curves and the -statistics for the validation subsamples (cohort 2) are shown in Figure 2. The brief predictive index developed in the present study has potential advantage in predicting PPCs in Chinese inpatients (better -statistic than the risk index in the study of Canet et al.) [11]. The most relevant cut point was the score of 13 (sensitivity 90.2%, specificity 79.4%). Table 6 shows the incidence of PPCs by risk index score, the number of patients in each risk class, and the actual incidence of PPCs in cohort 1 and cohort 2.


Number of patientsNumber (%) of patients with PPCsP

Age, yr<0.001
 <5967065 (9.7)
 ≥6023247 (20.3)
ASA physical status<0.001
 146420 (4.3)
 238077 (20.3)
 35413 (24.1)
 431 (33.3)
 511 (100.0)
Smokers0.001
 No75379 (10.5)
 Yes 14933 (22.1)
Respiratory infection in the last month<0.001
 No 886101 (11.4)
 Yes 1611 (68.8)
Diabetes0.001
 No 84697 (11.5)
 Yes 5615 (26.8)
COPD<0.001
 No 890106 (11.9)
 Yes 126 (50.0)
Cirrhosis0.014
 No 895109 (12.2)
 Yes 73 (42.9)
Stroke/transient ischaemic attack0.001
 No 887106 (12.0)
 Yes 156 (40.0)
Preoperative antibiotic use<0.001
 No 29819 (6.4)
 Yes 60493 (15.4)
Preoperative SpO2, %<0.001
 ≥9684592 (10.9)
 <965720 (35.1)
Preoperative anemia0.007
 No 83797 (11.6)
 Yes 6515 (23.1)
Preoperative LOS, d0.002
 <21265 (4.0)
 ≥2776107 (13.8)
Surgery site<0.001
 Peripheral62036 (5.8)
 Abdominal24356 (23.0)
 Intrathoracic3920 (51.3)
Anesthesia<0.001
 Regional23810 (4.2)
 General664102 (15.4)
Intraoperative nasogastric tube<0.001
 No 84785 (10.0)
 Yes 5527 (49.1)
Intraoperative bladder catheter<0.001
 No 46628 (6.0)
 Yes 43684 (19.3)
Intraoperative central venous catheter<0.001
 No 82185 (10.4)
 Yes 8127 (33.3)
Intraoperative blood loss, mL<0.001
 <10063632 (5.0)
 ≥10026680 (30.1)
Intraoperative blood transfusion<0.001
 No 875102 (11.7)
 Yes 2710 (37.0)
Duration of surgery, h<0.001
2 h65947 (7.1)
2 to 3 h13227 (20.5)
3 h11138 (34.2)
Postoperative SpO2, %<0.001
 ≥96891101 (11.3)
 <961111 (100.0)
Postoperative leucocyte, 109/L<0.001
462 (33.3)
 4–1066547 (7.1)
1023163 (27.3)
Postoperative anemia0.009
 No 79390 (11.3)
 Yes 10922 (20.2)
Postoperative fasting blood glucose, mmol/L<0.001
 ≤6.177850 (6.4)
 >6.112462 (50.0)
Postoperative creatinine, μmol/L<0.001
11587299 (11.4)
1153013 (43.3)
Postoperative albumin, g/L<0.001
 <3524485 (34.8)
 ≥3565827 (4.1)
Postoperative ventilation<0.001
 No87897 (11.0)
 Yes2415 (62.5)
Postoperative vasoactive drug<0.001
 No 893105 (11.8)
 Yes 97 (77.8)

Smoking: defined as patients who smoked up to 1 year before surgery; Anemia: defined as hemoglobin <100 g/L.
PPCs: postoperative pulmonary complications; ASA: American society of anesthesiologists; COPD: chronic obstructive pulmonary disease; SpO2: saturation of peripheral oxygen; LOS: length of stay.

OR (95% CI) 
n = 902
coefficientRisk score

Respiratory infection in the last month7.03 (1.66–29.80)1.95020
Smokers2.37 (1.27–4.42)0.8619
Preoperative antibiotic use0.238 (0.11–0.54)−1.436−14
Preoperative SpO2 <96%5.56 (2.38–12.98)1.71517
Surgery site
 Peripheral1
 Abdominal 2.88 (1.49–5.59)1.05811
 Intrathoracic12.20 (4.61–32.28)2.50125
Intraoperative blood loss ≥100 mL3.00 (1.64–5.50)1.10011
Postoperative fasting blood glucose >6.1 mmol/L2.60 (1.91–3.54)0.95610
Postoperative albumin <35 g/L4.21 (2.24–7.92)1.43814
Postoperative ventilation7.20 (1.96–26.45)1.97520

PPCs: postoperative pulmonary complications; SpO2: saturation of peripheral oxygen.

Risk class
Low risk
(<13 points)
Intermediate risk
(13–30 points)
High risk
(31–42 points)
Extremely high risk
(>42 points)

Cohort 1, n (%)672 (74.5)127 (14.1)67 (7.4)36 (4.0)
Cohort 2, n (%)577 (74.8)110 (14.3)54 (7.0)30 (3.9)
Rate of PPCs in cohort 1, n (%)21 (3.1)22 (17.3)38 (56.7)31 (86.1)
Rate of PPCs in cohort 2, n (%)5 (0.9)17 (15.5)12 (22.2)17 (56.7)

PPCs: postoperative pulmonary complications.
3.4. Strategies to Reduce PPCs

Opportunities to reduce risk for PPCs occur throughout the perioperative period. Table 7 summarizes perioperative interventions that have been recommended to decrease the risk of PPCs [15, 16, 21, 22].


Preoperative interventions
 A careful history taking and physical examination
 Encourage cessation of smoking for at least 2 months
 Appropriate use of antibiotics and delay surgery if respiratory infection is present
 Recommend a regular exercise program (e.g., walking, upper limb exercises, swimming, pool exercises, etc.)
 Treat patients with established asthma with inhaled corticosteroids
 Treat patients with established COPD with regular bronchodilators

Intraoperative interventions
 Substitute less ambitious procedure for upper abdominal or thoracic surgery when possible
 Minimize blood loss
 Limit duration of surgery to less than 3 hr
 Whenever possible, use spinal or epidural anesthesia

Postoperative interventions
 Recommend regular lung expansion modalities such as deep breathing exercises
 Perform selective decompression of abdominal contents using nasogastric tube if patient is experiencing symptomatic gastric
 distension
 As soon as possible after surgery, have the patient sit up in a chair

PPCs: postoperative pulmonary complications; COPD: chronic obstructive pulmonary disease.

4. Discussion

This prospective study assessed the 9.7% incidence of PPCs after noncardiac surgery in Chinese university hospitals and found increased hospital LOS by 8 days in patients with PPCs than those without. Furthermore, we identified the perioperative risk factors of PPCs and developed a brief risk index for predicting PPCs in Chinese inpatients.

In the current study, the incidence of PPCs after noncardiac surgery and the hospital LOS in patients with PPCs were comparable to the incidence observed in some previous studies [11, 2325]. The high incidence of PPCs and the increased hospital LOS indicating PPCs is also an important public health issue demanding nationwide attention in China. Unexpectedly, we found the postoperative mortality in patients with PPCs was lower than several previous results [3, 11]. This may be in association with the higher percentage of ASA class 1 to 2 patients and younger median age. Firstly, the medical resources in China were mainly concentrated in larger hospitals, especially the university hospitals and tertiary hospitals. So the patients always chose to go to large hospitals directly, even if they only have a cold or want to remove a small lipoma on body surface. Secondly, the percentage of emergency surgery in the present study was low, since none of the four studied hospitals had a major trauma center.

Nine independent risk factors were finally selected to participate in the brief predictive index for PPCs, including smoking, respiratory infection in the last month, antibiotic use, SpO2, surgery site and blood lost, blood glucose, albumin, and ventilation.

Among the preoperative risk factors, smoking, a history of respiratory infection in the last month, SpO2, and antibiotic use are strong PPC risk factors. Smoking and respiratory infection may lead to local changes in airway reactivity, pulmonary function, and residual impairment of immunity, which could increase the risk of PPCs for several folds [6, 7]. SpO2 is an easily recorded objective measure, which reflects the respiratory function as well as cardiovascular functional status [11]. Antibiotic use is a protective factor in the current cohort. It seems to be helpful to use prophylactic antibiotic, especially in these high-risk patients.

The intraoperative risk factors were identified in the present study including surgery site and blood loss, which were similar to many previous studies [4, 7, 14, 26]. Thoracic and abdominal surgeries are always performed via a large painful incision associated with obviously changes in lung compliance and functional residual capacity. As a result, the incidence of PPCs in these surgeries is much higher than others. Significant intraoperative blood loss gives rise to haemodynamic instability and relative ischaemia and so causes ischaemia-reperfusion injury, which can lead to organ dysfunction.

Factors in early stage of postoperative may have a better performance in predicting PPCs. We found postoperative mechanical ventilation, albumin, and blood glucose could increase the risk of PPCs. Among them, ventilation is the most important risk factor for PPCs. Researchers found an increased risk of respiratory events in patients with ventilation [26, 27]. It is important to follow the guidelines for the management of ventilation and the prevention of nosocomial infection.

A brief risk score based on these factors was calculated to predict the incidence of PPCs. In Spain, Canet and coworkers also developed a similar risk index of PPCs [11]. Three of these risk factors (preoperative SpO2, respiratory infection in the last month, and surgery site) were also identified in the current study. What is more, the brief predictive index developed in the present study has potential advantage in predicting PPCs in Chinese inpatients (better -statistic than the risk index of Canet). This disparity may be due to the different geographic areas, ethnic, cultural, socioeconomic, and political differences between China and Spain. In fact, the risk index developed by Canet also performed differently between the Western Europe sample and the Eastern Europe sample [20]. In general, the current brief predictive index predicted the risk of PPCs well in both the development and validation cohorts. These findings suggest patients with high risk of PPCs should be closely monitored and early intervened if the risks factors could be modified.

Several limitations in our study should be acknowledged. First of all, only four university hospitals participated. This may result in some bias. Further studies targeting general Chinese hospitals with a larger population are still needed. Another limitation is that the 7-day study period was arbitrarily decided. All patients were enrolled in August. Englesbe et al. demonstrated a significant seasonal variation in surgical morbidity and mortality [28]. They found a dramatic worsening of surgical mortality in July, which was attributed to the influx of inexperienced trainees. However, Ehlert and colleagues refuted the “July Phenomenon” in a larger population [29]. In most hospitals in China, July is marked by an influx of intern. Instead of managing patients directly, they only do the paperwork. Therefore, they may have little effect on the present results. Further study is needed to confirm the impact of seasonal variation in surgical morbidity and mortality.

5. Conclusion

The present prospective, multicenter study found there was high incidence of PPCs which increased hospital LOS in noncardiac surgical inpatients in China. We identified nine objective and easily assessed factors associated with the occurrence of PPCs. A simple risk index based on these factors predicted the development of PPCs. This brief predictive index may be useful for clinicians in estimating patients’ risk for PPCs and guide individualized perioperative respiratory care.

Conflict of Interests

The authors declare that there is no conflict of interests regarding the publication of this paper.

Acknowledgments

This research was supported by National Natural Science Foundation of China (no. 81301652) and Zhejiang Provincial Program for the Cultivation of High-level Innovative Health Talents.

References

  1. T. G. Weiser, S. E. Regenbogen, K. D. Thompson et al., “An estimation of the global volume of surgery: a modelling strategy based on available data,” The Lancet, vol. 372, no. 9633, pp. 139–144, 2008. View at: Publisher Site | Google Scholar
  2. A. A. Ghaferi, J. D. Birkmeyer, and J. B. Dimick, “Variation in hospital mortality associated with inpatient surgery,” The New England Journal of Medicine, vol. 361, no. 14, pp. 1368–1375, 2009. View at: Publisher Site | Google Scholar
  3. A. Shander, L. A. Fleisher, P. S. Barie, L. M. Bigatello, R. N. Sladen, and C. B. Watson, “Clinical and economic burden of postoperative pulmonary complications: patient safety summit on definition, risk-reducing interventions, and preventive strategies,” Critical Care Medicine, vol. 39, no. 9, pp. 2163–2172, 2011. View at: Publisher Site | Google Scholar
  4. L. G. G. Serejo, F. P. da Silva-Júnior, J. P. C. Bastos, G. S. de Bruin, R. M. S. Mota, and P. F. C. de Bruin, “Risk factors for pulmonary complications after emergency abdominal surgery,” Respiratory Medicine, vol. 101, no. 4, pp. 808–813, 2007. View at: Publisher Site | Google Scholar
  5. K. J. Haines, E. H. Skinner, and S. Berney, “Association of postoperative pulmonary complications with delayed mobilisation following major abdominal surgery: an observational cohort study,” Physiotherapy, vol. 99, no. 2, pp. 119–125, 2013. View at: Publisher Site | Google Scholar
  6. R. L. Scholes, L. Browning, E. M. Sztendur, and L. Denehy, “Duration of anaesthesia, type of surgery, respiratory co-morbidity, predicted VO2max and smoking predict postoperative pulmonary complications after upper abdominal surgery: an observational study,” Australian Journal of Physiotherapy, vol. 55, no. 3, pp. 191–198, 2009. View at: Publisher Site | Google Scholar
  7. F. A. McAlister, K. Bertsch, J. Man, J. Bradley, and M. Jacka, “Incidence of and risk factors for pulmonary complications after nonthoracic surgery,” The American Journal of Respiratory and Critical Care Medicine, vol. 171, no. 5, pp. 514–517, 2005. View at: Publisher Site | Google Scholar
  8. S. F. Khuri, W. G. Henderson, R. G. DePalma et al., “Determinants of long-term survival after major surgery and the adverse effect of postoperative complications,” Annals of Surgery, vol. 242, no. 3, pp. 326–343, 2005. View at: Publisher Site | Google Scholar
  9. D. L. Davenport, W. G. Henderson, S. F. Khuri et al., “Preoperative risk factors and surgical complexity are more predictive of costs than postoperative complications: a case study using the National Surgical Quality Improvement Program (NSQIP) database,” Annals of Surgery, vol. 242, no. 4, pp. 463–471, 2005. View at: Publisher Site | Google Scholar
  10. V. A. Lawrence, S. G. Hilsenbeck, C. D. Mulrow, R. Dhanda, J. Sapp, and C. P. Page, “Incidence and hospital stay for cardiac and pulmonary complications after abdominal surgery,” Journal of General Internal Medicine, vol. 10, no. 12, pp. 671–678, 1995. View at: Publisher Site | Google Scholar
  11. J. Canet, L. Gallart, C. Gomar et al., “Prediction of postoperative pulmonary complications in a population-based surgical cohort,” Anesthesiology, vol. 113, no. 6, pp. 1338–1350, 2010. View at: Publisher Site | Google Scholar
  12. A. M. Arozullah, S. F. Khuri, W. G. Henderson, and J. Daley, “Development and validation of a multifactorial risk index for predicting postoperative pneumonia after major noncardiac surgery,” Annals of Internal Medicine, vol. 135, no. 10, pp. 847–857, 2001. View at: Publisher Site | Google Scholar
  13. G. W. Smetana, V. A. Lawrence, and J. E. Cornell, “Preoperative pulmonary risk stratification for noncardiothoracic surgery: Systematic review for the American College of Physicians,” Annals of Internal Medicine, vol. 144, no. 8, pp. 581–595, 2006. View at: Publisher Site | Google Scholar
  14. A. M. Arozullah, J. Daley, W. G. Henderson, and S. F. Khuri, “Multifactorial risk index for predicting postoperative respiratory failure in men after major noncardiac surgery. The National Veterans Administration Surgical Quality Improvement Program,” Annals of Surgery, vol. 232, no. 2, pp. 242–253, 2000. View at: Publisher Site | Google Scholar
  15. A. Qaseem, V. Snow, N. Fitterman et al., “Risk assessment for and strategies to reduce perioperative pulmonary complications for patients undergoing noncardiothoracic surgery: a guideline from the American College of Physicians,” Annals of Internal Medicine, vol. 144, no. 8, pp. 575–580, 2006. View at: Publisher Site | Google Scholar
  16. V. A. Lawrence, J. E. Cornell, and G. W. Smetana, “Strategies to reduce postoperative pulmonary complications after noncardiothoracic surgery: systematic review for the American College of Physicians,” Annals of Internal Medicine, vol. 144, no. 8, pp. 596–608, 2006. View at: Publisher Site | Google Scholar
  17. D. O. Warner, “Preventing postoperative pulmonary complications: The role of the anesthesiologist,” Anesthesiology, vol. 92, no. 5, pp. 1467–1472, 2000. View at: Publisher Site | Google Scholar
  18. J. Canet and L. Gallart, “Predicting postoperative pulmonary complications in the general population,” Current Opinion in Anaesthesiology, vol. 26, no. 2, pp. 107–115, 2013. View at: Publisher Site | Google Scholar
  19. H. Dupont, P. Montravers, R. Gauzit, B. Veber, J. Pouriat, and C. Martin, “Outcome of postoperative pneumonia in the Eole study,” Intensive Care Medicine, vol. 29, no. 2, pp. 179–188, 2003. View at: Google Scholar
  20. V. Mazo, S. Sabate, J. Canet et al., “Prospective external validation of a predictive score for postoperative pulmonary complications,” Anesthesiology, vol. 121, no. 2, pp. 219–231, 2014. View at: Google Scholar
  21. J. M. Torpy, C. Lynm, and R. M. Glass, “JAMA patient page. Lung complications after surgery.,” The Journal of the American Medical Association, vol. 302, no. 14, p. 1610, 2009. View at: Publisher Site | Google Scholar
  22. G. W. Smetana, “Preoperative pulmonary evaluation,” New England Journal of Medicine, vol. 340, no. 12, pp. 937–944, 1999. View at: Publisher Site | Google Scholar
  23. P. G. Noordzij, D. Poldermans, O. Schouten, J. J. Bax, F. A. G. Schreiner, and E. Boersma, “Postoperative mortality in the Netherlands: A population-based analysis of surgery-specific risk in sdults,” Anesthesiology, vol. 112, no. 5, pp. 1105–1115, 2010. View at: Publisher Site | Google Scholar
  24. N. A. Khan, H. Quan, J. M. Bugar, J. B. Lemaire, R. Brant, and W. A. Ghali, “Association of postoperative complications with hospital costs and length of stay in a tertiary care center,” Journal of General Internal Medicine, vol. 21, no. 2, pp. 177–180, 2006. View at: Publisher Site | Google Scholar
  25. D. A. Thompson, M. A. Makary, T. Dorman, and P. J. Pronovost, “Clinical and economic outcomes of hospital acquired pneumonia in intra-abdominal surgery patients,” Annals of Surgery, vol. 243, no. 4, pp. 547–552, 2006. View at: Publisher Site | Google Scholar
  26. J. Chastre and J. Fagon, “Ventilator-associated pneumonia,” The American Journal of Respiratory and Critical Care Medicine, vol. 165, no. 7, pp. 867–903, 2002. View at: Publisher Site | Google Scholar
  27. A. R. Tait, S. Malviya, T. Voepel-Lewis, H. M. Munro, M. Siewert, and U. A. Pandit, “Risk factors for perioperative adverse respiratory events in children with upper respiratory tract infections,” Anesthesiology, vol. 95, no. 2, pp. 299–306, 2001. View at: Publisher Site | Google Scholar
  28. M. J. Englesbe, S. J. Pelletier, J. C. Magee et al., “Seasonal variation in surgical outcomes as measured by the American College of Surgeons-National Surgical Quality Improvement Program (ACS-NSQIP),” Annals of Surgery, vol. 246, no. 3, pp. 456–462, 2007. View at: Publisher Site | Google Scholar
  29. B. A. Ehlert, J. T. Nelson, C. E. Goettler et al., “Examining the myth of the “july Phenomenon” in surgical patients,” Surgery, vol. 150, no. 2, pp. 332–338, 2011. View at: Publisher Site | Google Scholar

Copyright © 2015 Yue Jin et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.


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