Literature DB >> 35117459

Impact of interstitial lung disease on postoperative morbidity and 90-day mortality after pulmonary resection.

Weipeng Shao1, Jingjing Huang2, Hongxiang Feng2, Hongliang Sun3, Yanhong Ren4, Xiaowei Wang5, Zhenrong Zhang2, Deruo Liu1.   

Abstract

BACKGROUND: To evaluate the effect of interstitial lung disease (ILD) on postoperative morbidity and mortality in pulmonary resection and identify the factors of AE-ILD.
METHODS: We retrospectively analyzed 1,309 patients underwent pulmonary operation between January 2010 and January 2018 in our hospital. Clinical data including age, sex, history of chronic obstructive pulmonary disease (COPD), smoking history, smoking index, American Society of Anesthesiologists (ASA) classification, Charlson comorbidity index (CCI), forced expiratory volume in 1 s (FEV1) % predict, surgical procedure, video-assisted thoracoscopic surgery (VATS) or not, intraoperative blood transfusion, anesthesia time, operation time/one-lung ventilation time, blood loss, histology, postoperative morbidity, 90-day mortality, onset of acute exacerbation of ILD (AE-ILD), and postoperative stay were collected and analyzed.
RESULTS: There were 97 (7.4%) and 1,212 (92.6%) patients in the ILD and non-ILD groups, respectively. AE-ILD occurred in 6 patients (0.5%), with a mortality of 83.3%, and was the leading cause of 90-day mortality (55.6%). Age (P<0.001) was an independent risk factor for ILD. There were 6 and 91 patients in the AE-ILD and non-AE-ILD groups, respectively. ASA classification (P=0.038) were independent risk factors for AE-ILD. Multivariate regression analysis identified that the sex (P=0.003), ILD (P<0.001), COPD (P=0.007), surgical procedure (P<0.001), blood loss (P<0.001), CCI (P=0.049) were independent risk factors for postoperative morbidity. ILD (P=0.001) and postoperative morbidity (P=0.003) were independent risk factors for 90-day mortality in multivariate analysis.
CONCLUSIONS: Patients with ILD had a higher incidence of postoperative morbidity and 90-day mortality. ASA classification was an important influencing factor for AE-ILD. Based on the obvious postoperative morbidity and mortality, special attention and management should be given to ILD patients. 2020 Translational Cancer Research. All rights reserved.

Entities:  

Keywords:  90-day mortality; Interstitial lung disease (ILD); acute exacerbation of interstitial lung disease; morbidity; pulmonary resection

Year:  2020        PMID: 35117459      PMCID: PMC8797989          DOI: 10.21037/tcr.2019.12.88

Source DB:  PubMed          Journal:  Transl Cancer Res        ISSN: 2218-676X            Impact factor:   1.241


Introduction

Interstitial lung disease (ILD) is a group of diseases with diffuse alveolar chronic inflammation and interstitial fibrosis as the main pathological characteristics, it mainly occurs in the elderly individuals and had no specific predisposing factors (1). Generally, ILD includes idiopathic pulmonary fibrosis, connective tissue disease-related interstitial pulmonary disease, and sarcoidosis (2). The symptoms and signs of many ILD patients lack specificity. The etiology of ILD remains unclear, the history of long-term smoking or some occupational factors might contribute to the occurrence of ILD (3,4). Surgical operation is the primary therapeutic method for ILD patients complicated with lung cancer or suspected lung cancer. However, acute exacerbation of ILD (AE-ILD), as a disastrous postoperative complication, could dramatically increase postoperative mortality in these patients (5,6). Approaches to decrease postoperative mortality and preclude the occurrence of AE-ILD has drawn much attention (5,7-9). This study attempted to clarify the impact of ILD on postoperative morbidity and 90-day mortality of patients undergoing pulmonary resection.

Methods

The patients underwent surgery after providing informed consent, and the requirement for the individual consent of patients whose records were evaluated was waived because they were de-identified in the study. The study was approved by institutional ethics board of China-Japan Friendship Hospital (No. 2018-13-K08). Information about preoperative patient characteristics, disease status, surgical procedures, postoperative morbidity, pathological findings and treatment was collected. We retrospectively analyzed 1,309 patients who underwent pulmonary surgery in our hospital between January 2010 and January 2018. Preoperative, intraoperative, and postoperative data were collected for all patients, including age (≥/<65), sex (male/female), history of chronic obstructive pulmonary disease (COPD), smoking history, smoking index, American Society of Anesthesiologists (ASA) classification, Charlson comorbidity index (CCI), forced expiratory volume in 1 s (FEV1) % predict, surgical procedure, video-assisted thoracoscopic surgery (VATS), intraoperative blood transfusion, anesthesia time, operation time/one-lung ventilation time, blood loss, histology, postoperative morbidity [pulmonary leakage (>1 week), pleural effusion (second-time thoracic puncture), pulmonary infection (fever and culture positive), chylothorax (whether somatostatin therapy is effective)], 90-day mortality, onset of AE-ILD, and postoperative stay. According to the guidelines drafted by the American Thoracic Society (ATS), the European Respiratory Society (ERS), the Japanese Respiratory Society (JRS) and the Latin American Thoracic Society (ALAT), ILD could be divided into two groups according to the CT findings: (I) usual interstitial pneumonia (UIP): this group was characterized by the presence of basal-dominant reticular opacities and a predominantly basal and subpleural distribution of honeycomb lesions with multiple equal-sized cystic lesions of 2 to 10 mm in diameter with a thick wall. (II) non-UIP: This group was characterized by the presence of basal-predominant ground-glass opacities and infiltrative shadows inconsistent with UIP patterns (6). AE-ILD caused by pulmonary resection was defined based on the following criteria: (I) dyspnea of unknown origin within 30 days; (II) decrease in PaO2 by at least 10 mmHg under same respiratory condition; (III) newly found ground glass shadow or diffuse alveolar injury in the background of UIP according to chest CT scan; (IV) no evidence of pulmonary infection; (V) exclusion of alternative causes, such as cardiac failure, pulmonary embolism, or other identifiable causes of lung injury. Exacerbations that occurred from 31 days onward were defined as chronic exacerbations (10). The primary outcome of the study was 90-day mortality (death from any cause within 90 days postoperation).

Statistical analysis

Statistical analysis was performed with SPSS 24.0 software (SPSS, Inc., Chicago, IL, USA). All data were presented as median ± quartile deviation. Continuous variables were compared with the independent sample t-test. Categorical and dichotomic variables were compared by χ2 test and Fisher’s exact test, respectively. All P values were 2-sided, and the statistical significance level was set at less than 0.05.

Results

A total of 1,309 patients who underwent pulmonary resection were reviewed. The median age of the patients was 58.9 years, 755 (57.7%) of 1,309 patients were male, and 508 (38.8%) of 1,309 patients had a smoking history. Among these patients, 97 (7.4%) patients were diagnosed with UIP according to high resolution computed tomography/computed tomography (HRCT/CT). Based on CT characteristics, the enrolled patients were classified into the ILD group and non-ILD group. The clinical data of all patients are shown in . In the ILD group, 54 (55.7%) patients were no younger than 65 years old, 65 (67.0%) patients were male, 10 (10.3%) patients had combined COPD, 47 (48.5%) patients had a smoking history and 33 (34.0%) patients had a smoking index greater than 400, 13 (13.4%) patients received intraoperative blood transfusion. Seventy-six (78.4%) patients were classified as I and II by ASA, 80 (82.5%) patients were diagnosed with malignant tumors, 35 (36.1%) patients had postoperative complications, and 5 (5.2%) patients died within 90 days. The average days of hospitalization were 9 (IQR, 8–13.5) days and 8 (IQR, 7–12) days (P=0.038) in the ILD group and non-ILD group, respectively. The CCI was 3 (IQR, 2–4) in 2 groups (P<0.001). Age (P<0.001) was an independent risk factor for ILD in multivariate analysis ().
Table 1

Patient characteristics

VariablesILD (n=97)Non-ILD (n=1,212)P
Age<0.001
   ≥6554370
   <6543842
Sex0.053
   Male65690
   Female32522
COPD0.859
   Yes10132
   No871,080
Smoking history0.043
   Yes47461
   No50751
Smoking index (>400)0.031
   Yes33293
   No64919
Lobectomy0.532
   No31351
   Yes66861
Approach0.135
   VATS60846
   VAMT23258
   OPEN14108
Blood transfusion0.032
   Yes1389
   No841,123
ASA classification0.005
   I/II761,069
   III/IV21143
Histology0.052
   Malignant80891
   Benign17321
Postoperative morbidity<0.001
   Yes35226
   No62986
Death within 90 days<0.001
   Yes54
   No921,208
FEV1 of predicted (%)77.7 [73.12–79.95]78.1 [74.51–80.66]0.452
Anaesthesia time (min)260 [175–320]250 [190–310]0.955
Operating time (min)200 [120–267.5]195 [130–255]0.703
Blood loss (mL)150 [50–300]100 [50–250]0.427
Postoperative stay (days)9 [8–13.5]8 [7–12]0.038
CCI3 [2–4]3 [2–4]<0.001

ILD, interstitial lung disease; COPD, chronic obstructive pulmonary disease; VATS, video assisted thoracoscopic surgery; VAMT, video-assisted minithoracotomy; ASA, American Society of Anesthesiologists; FEV1, forced expiratory volume in 1 s; CCI, Charlson comorbidity index.

Table 2

Multivariate analysis to identify predictors of interstitial lung disease

VariableOR95% CIP
Age2.8491.868–4.347<0.001

ILD, interstitial lung disease; OR, odds ratio; CI, confidence interval.

ILD, interstitial lung disease; COPD, chronic obstructive pulmonary disease; VATS, video assisted thoracoscopic surgery; VAMT, video-assisted minithoracotomy; ASA, American Society of Anesthesiologists; FEV1, forced expiratory volume in 1 s; CCI, Charlson comorbidity index. ILD, interstitial lung disease; OR, odds ratio; CI, confidence interval. According to AE-ILD status, 97 patients with ILD were divided into AE-ILD group and non-AE-ILD group. Multivariate regression analysis further identified that ASA classification (P=0.038) were independent risk factor of AE-ILD ().
Table 3

ILD patient characteristics

VariablesAE-ILD (n=6)Non-AE-ILD (n=91)P
Age (years)0.325
   ≥65549
   <65142
Sex0.173
   Male659
   Female032
COPD0.222
   Yes28
   No483
Smoking history0.617
   Yes443
   No248
Smoking index (>400)1.000
   Yes229
   No462
Lobectomy1.000
   No229
   Yes462
Approach0.210
   VATS456
   VAMT023
   OPEN212
Blood transfusion1.000
   Yes112
   No579
ASA classification0.024
   I/II274
   III/IV417
Histology1.000
   Malignant575
   Benign116
Postoperative morbidity0.002
   Yes629
   No062
Death within 90 days<0.001
   Yes50
   No191
FEV1 of predicted (%)76.75 [57.75–95.75]77.57 [67.60–87.54]0.920
Anaesthesia time (min)235 [154–315]255 [161–349]0.605
Operating time (min)187 [111–263]215 [61–269]0.664
Blood loss (mL)226 [40–412]218 [68–368]0.933
Postoperative stay (days)28 [6–50]11 [4–18]0.128
CCI4 [3–5]4 [3–5]0.507

ILD, interstitial lung disease; COPD, chronic obstructive pulmonary disease; VATS, video assisted thoracoscopic surgery; VAMT, video-assisted minithoracotomy; ASA, American Society of Anesthesiologists; FEV1, forced expiratory volume in 1 s; CCI, Charlson comorbidity index.

Table 4

Multivariate analysis to identify predictors of AE-ILD

VariableOR95% CIP
ASA0.1300.190–0.8900.038
ILD, interstitial lung disease; COPD, chronic obstructive pulmonary disease; VATS, video assisted thoracoscopic surgery; VAMT, video-assisted minithoracotomy; ASA, American Society of Anesthesiologists; FEV1, forced expiratory volume in 1 s; CCI, Charlson comorbidity index. All included patients were grouped according to the postoperative morbidity and 90-day mortality. A total of 261 (19.3%) patients had postoperative complications, and 9 (0.7%) patients died within 90 days. Univariate analysis identified that sex (P<0.001), ILD (P<0.001), COPD (P<0.001), smoking history (P=0.026), smoking index (P=0.004), surgical procedure (P<0.001), VATS (P<0.001), intraoperative blood transfusion (P<0.001), histology (P=0.001), FEV1% predict (P<0.001), anesthesia time (P<0.001), operation time/one-lung ventilation time (P<0.001), blood loss (P<0.001), CCI (P=0.001) were candidate risk factors for postoperative morbidity (). Multivariate regression analysis further identified male sex (P=0.003), ILD (P<0.001), COPD (P=0.007), lobectomy (P<0.001), blood loss (P<0.001), CCI (P=0.049) as independent risk factors of postoperative morbidity (). There were differences in the following clinical factors between these two groups: age (P=0.010), ILD (P<0.001), ASA classification (P=0.017), and postoperative morbidity (P<0.001). Multivariate analysis revealed that ILD (P=0.006) and postoperative complications (P=0.012) were independent risk factors of 90-day mortality ().
Table 5

Univariate analysis to identify predictors of postoperative morbidity and 90-day mortality among patients with ILD

VariablesMorbidity/not (n=261/1,048)90 death/not (n=9/1,300)P
Age (years)0.066/0.010
   ≥6597/3277/417
   <65164/7212/883
Sex<0.001/0.376
   Male182/5737/748
   Female79/4752/552
ILD<0.001/<0.001
   Yes35/625/92
   No226/9864/1,208
COPD<0.001/0.101
   Yes45/973/139
   No216/9516/1,161
Smoke0.026/0.489
   Yes117/3915/503
   No144/6574/797
Smoking index (>400)0.004/0.081
   Yes83/2425/321
   No178/8064/980
Lobectomy<0.001/1
   No40/3423/379
   Yes221/7066/921
Approach<0.001/0.221
   VATS154/7524/902
   VAMT73/2083/278
   OPEN34/882/120
Blood transfusion<0.001/0.319
   Yes34/682/100
   No227/9807/1,200
ASA classification0.127/0.017
   I/II221/9245/1,140
   III/IV40/1244/160
Histology0.001/0.529
   Malignant214/7578/963
   Benign47/2911/337
Death within 90 days/morbidity<0.001/<0.001
   Yes8/18/253
   No253/1,0471/1,047
FEV1 of predicted (%)76.7 [70.85–80.16]/78.29 [74.91–80.77]74.1 [67.5–85.35]/78.1 [74.27–80.6]<0.001/0.636
Anaesthesia time (min)290 [230–330]/240 [180–303]250 [205–312.5]/250 [190–310]<0.001/0.934
Operating time (min)235 [180–270]/180 [120–250]190 [157.5–252.5]/195 [125–255]<0.001/0.983
Intraoperative bleeding volume (mL)200 [100–350]/100 [50–200]200 [100–400]/100 [50–250]<0.001/0.186
Postoperative stay (days)14 [9–21]/8 [6–10]11 [8–29.5]/8 [7–12]<0.001/0.01
CCI3 [2–4]/3 [2–4]3 [3–5]/3 [2–4]0.001/0.05

ILD, interstitial lung disease; COPD, chronic obstructive pulmonary disease; VATS, video assisted thoracoscopic surgery; VAMT, video-assisted minithoracotomy; ASA, American Society of Anesthesiologists; FEV1, forced expiratory volume in 1 s; CCI, Charlson comorbidity index.

Table 6

Multivariate analysis to identify predictors of postoperative morbidity and 90-day mortality in patients with ILD

AccidentOR95% CIP
Morbidity
   Sex1.5751.163–2.1340.003
   ILD2.3541.479–3.745<0.001
   COPD2.7931.816–1.1810.007
   Lobectomy0.4200.287–0.615<0.001
   Blood loss0.9990.999–1.000<0.001
   CCI0.8940.800–1.0000.049
Death within 90 days
   ILD8.2681.829–37.3820.006
   complication15.1641.798–127.8760.012

ILD, interstitial lung disease; OR, odds ratio; CI, confidence interval.

ILD, interstitial lung disease; COPD, chronic obstructive pulmonary disease; VATS, video assisted thoracoscopic surgery; VAMT, video-assisted minithoracotomy; ASA, American Society of Anesthesiologists; FEV1, forced expiratory volume in 1 s; CCI, Charlson comorbidity index. ILD, interstitial lung disease; OR, odds ratio; CI, confidence interval. Of the 1,309 patients, 9 died within 90 days postoperation, of which 5 died of AE-ILD, 2 died of pulmonary embolism, 1 died of myocardial infarction and 1 died of heart failure. There were 6 patients of AE-ILD, all of whom had a history of ILD and were male. The age of these 6 patients ranged from 62 to 78 years old, with a median age of 69.3 years old. The mean time of AE-ILD onset and time of death were 7.8 and 31 days postoperation, respectively. None of the patients received prophylactic steroid therapy, but steroid therapy was given after the diagnosis of AE-ILD. Only one patient them recovered from AE-ILD, and the other patients died within 90 days ().
Table 7

Clinical characteristics of patients who experienced AE-ILD

Age/genderILDSmoking historySmoking indexSurgery time (min)Surgery methodsThoracoscopyBlood loss (mL)HistologyOnsetOutcome
67/maleUIPno0270lobectomyVATS150Malignant5PODDied in 21POD
70/maleUIPno050wedgeVATS10Benign20PODDied in 85POD
67/maleUIPyes900210lobectomyOpen500Malignant5PODDied in 14POD
62/maleUIPyes800190lobectomyOpen200Malignant3PODDied in 8POD
78/maleUIPyes200165wedgeVATS400Malignant6PODDied in 40POD
72/maleUIPyes1200240lobectomyVATS100Malignant8PODDischarge in 18POD

ILD, interstitial lung disease; UIP, usual interstitial pneumonia; VATS, video assisted thoracoscopic surgery; POD, post of operation.

ILD, interstitial lung disease; UIP, usual interstitial pneumonia; VATS, video assisted thoracoscopic surgery; POD, post of operation.

Discussion

In this study, we found that patients with ILD presented a significantly higher incidence of postoperative morbidity and 90-day mortality than those without ILD. As 55.6% of 90-day deaths were caused by AE-ILD, AE-ILD could be recognized as a factor that leads to disastrous morbidity and should be treated immediately. ILD is a progressive diffuse lung disease with poor prognosis (1), The incidence of ILD in the United States ranged from 6.8 to 16.3 per 100,000 people (11). It is less common in patients younger than 50 years old, and patients with ILD usually have a median survival of approximately 2–3 years (7,12). Increasing exposure of possible pathogenic factors such as smoking and second-hand smoking, environmental exposures and microbial factors could partially explain the higher incidence of ILD in elder patients (6). Similar to this finding, our results showed that age was an independent risk factor for ILD in surgical patients. We deduced that the incidence of ILD was increased with advancing age. As reported in the literature, the postoperative morbidity and 90-day mortality rates in ILD patients were significantly higher than those in the non-ILD patients. AE-ILD, which is a rapidly progressive disorder in patients with ILD, has been reported to be the main factor of 90-day mortality (5,7,13,14). Chiyo et al. believed that the incidence of pulmonary morbidity was significantly higher in ILD patients than in non-ILD patients (9). Takeda and his colleagues found that the incidence of morbidity was greater in the ILD group than in the non-ILD group (P=0.0004) (15). However, Voltolini et al.’s study showed different outcomes. In their study, ILD led to more acute respiratory distress syndrome/acute lung injury (ARDS/ALI) postoperatively but not to other pulmonary complications, such as postoperative air leakage, pulmonary infection, pleural effusion and chylothorax (13). In our study, ILD was an independent risk factor for postoperative morbidity. ILD led to pulmonary fibrosis, weaken the healing ability of lung tissue and thus resulting in postoperative air leakage, and pleural effusion could be a possible explanation. Furthermore, change in the pulmonary interstitium might cause pulmonary hypertension, emphysema and obstructive sleep apnea, which in turn increased the risk of postoperative complications (6). Chiyo et al. retrospectively analyzed 931 patients with lung cancer. Among them, 36 patients were diagnosed with ILD confirmed by HRCT/CT. The incidences of pneumonia and AE-ILD in these 36 patients was significantly higher than those in patients without ILD (P<0.05), but there was no significant difference in 30-day mortality between these two groups (P=0.30) (9). A large-scale multicenter cohort study from 61 hospitals in Japan reported that 164 (9.3% of the 1,763 cases) ILD patients with lung cancer had AE-ILD after pulmonary surgery, with a mortality rate of 43.9%. Approximately 71.7% of the deaths occurred within 30 days postoperation (7). In our study, postoperative morbidity and mortality were similar to those in previous studies; 9 (0.7%) patients died within 90 days postoperation, and a total of 6 patients were diagnosed AE-ILD in the ILD group, of which 5 died of AE-ILD. Most published studies used the 30-day mortality rate as their primary outcome (5,7,9). However, we found that two patients with AE-ILD died at 40 and 85 days after the operation. Three (3.1%) patients died within 30 days of AE-ILD, and 5 (5.2%) patients died within 90 days. Using a 30-day mortality rate would underestimate the short-term mortality rate; thus, the 90-day mortality rate could be a better alternative. A similar outcome has also been reported in Fukui et al.’s study (14). Sato et al. found that the incidence of AE-ILD was 3.83 and 5.70 times higher in patients receiving lobectomy/segmentectomy and combined lobectomy/pneumonectomy, respectively, compared with patients receiving wedge resection (5). Fujimoto et al. proposed that local resection should be performed if possible although it might increase the rate of tumor recurrence (16). In our study, surgical procedures did not differ between the ILD and non-ILD groups, and different surgical procedures showed an influence on postoperative morbidity (P<0.001) but not on 90-day mortality. While limited resection might decrease the postoperative morbidity, it might increase the recurrence rate and decrease the survival rate. Lobectomy should still be performed as the primary choice. Long operation time, anesthesia time and one-lung ventilation time have been considered to induce oxygen-free radicals production, thus result in ARDS/AE-ILD postoperation (17). However, Fukui et al. studied the effect of operation time on lung cancer patients with ILD and found that the average operation time in the ILD and non-ILD groups was 184.8±84.3 min and 189.1±86.5 min (P=0.51), respectively. There was no significant difference of operation time between the AE group and the non-AE group (P=0.052) (14). Similar findings from the study of Omori et al. showed that the mean operation time in ILD and non-ILD patients were 291.7±78.2 and 319.2±109.9 min respectively (P=0.143) (18). In our study, the average operation time in the ILD group and the non-ILD group was 200 (IQR, 120–267.5) min and 195 (IQR, 130–255) min (P=0.700), and the anesthesia time was 260 (IQR, 175–320) min and 250 (IQR, 190–310) min (P=0.955), respectively. ILD patients seemed to have longer operation times, whether a combination of ILD increases operation difficulty still needs further study. As a feasible and safe surgical method, VATS has been widely used in the resection of early-stage lung cancer with an acceptable long-term survival rate (19). We found that there was no significant difference between the postoperative morbidity group and 90-day mortality group. According to the statistical results, we might conclude that surgical approach and non-lung injury (such as incision size) had no effect on postoperative morbidity and 90-day mortality. The average blood loss in the ILD group and non-ILD group was 200 (IQR, 100–400) mL and 100 (IQR, 50–250) mL (P=0.186), in the postoperative morbidity group and non-postoperative morbidity group was 200 (IQR, 100–350) mL and 100 (IQR, 50–200) mL (P<0.001), and in the 90-day death group and 90-day nondeath group was 200 (IQR, 100–400) mL and 100 (IQR, 50–250) mL (P=0.186), respectively. we could see that there was a significant difference between the postoperative morbidity group and non-postoperative morbidity group. Maniwa T et al did not found a significant correlation between blood loss and ILD (20). However, Taniguchi et al. indicated that the blood loss in ILD patients suffering from acute exacerbation postoperation was greater than that in ILD patients without AE (628±338.7 vs. 272.2±451.7 mL, P=0.024) (21). We believed that combined with ILD would increase the difficulty of surgery, increase the operation time and blood loss, and might cause postoperative morbidity. ASA classification was used in the anesthesiology department to evaluate the physical condition and surgical risk of patients (22). Marret et al. found that the ASA classification of III and IV correlated with poor outcome in patients receiving lobectomy (P<0.0001) (23). Similar findings from Limmer et al. showed that patients with an ASA classification of IV undergoing chest operation had a significantly higher mortality rate and longer hospitalization time (P=0.001) (24). Our results showed that there was a significant difference in ASA classification between the ILD group and the non-ILD group (P=0.005), and there was a significant difference in univariate analysis of 90-day mortality (P=0.017), but there was no significant difference in multivariate analysis (P>0.05). Meanwhile, our results showed that there was a significant difference in ASA classification between AE-ILD group and non-AE-ILD group (P=0.038). ILD can cause ASA classification upgrade and influence 90-day mortality. We needed to pay attention to the ASA classification in the perioperative period. CCI is commonly used to predict the mortality rate of patients with chronic diseases according to the assessment of physical function. ILD impairs cardiopulmonary function and thus increased the risk of perioperative mortality (25). In our study, the CCI in the ILD and non-ILD groups were 3 (IQR, 2–4) and 3 (IQR, 2–4) (P<0.001), respectively, which might be due to the increase in CCI indirectly caused by ILD. The average CCI in the postoperative morbidity group and non-postoperative morbidity group was 3 (IQR, 2–4) and 3 (IQR, 2–4) (P=0.049), respectively. This finding suggested that CCI adversely affects postoperative morbidity, and we should pay attention to CCI in clinical practice. Most studies of the lung function test focused on FEV1% and DLCO%. Luca Voltolini et al. reported that the FEV1% and DLCO% in ILD and non-ILD patients were 88.8%±12.3% vs. 84.1%±0.4% (P>0.05) and 59.13%±14.34% vs. 65.53%±19.20% (P>0.05), respectively. However, approximately 50% of ILD patients with FEV1% less than 80% developed ARDS/ALI after surgery, while no ILD patients with FEV1% greater than 90% suffered from ARDS/ALI (13). Fukui et al. reported that FEV1%, VC% and DLCO% in the ILD and non-ILD group were 74.8%±0.7% vs. 74.9%±0.3% (P=0.88), 94.4%±17.7% vs. 97.3%±15.9% (P=0.028) and 48.2±1.2 vs. 64.5±0.5 (P<0.001), respectively. The value of VC% and DLCO% was significantly different between the ILD group and the non-ILD group (14). In our study, the analysis of DLCO and VC was not performed because of a shortage of medical resources and medical insurance. According to whether FEV1/FVC was less than 0.7 as a cutoff point, we found that there was no significant difference between the ILD group and the non-ILD group (P=0.859). The average values of FEV1% predict in the ILD and non-LID groups were 77.7% (IQR, 73.12–79.95%) and 78.1% (IQR, 74.51–80.66%) respectively (P=0.452). We concluded that FEV1% predict had little influence on ILD. Several limitations should be noted in this study. First, as a retrospective study, it is vulnerable to various sources of deviation that might not be identified and controlled. Second, this was a single institutional study with a limited sample size and thus calls for more evidence from further prospective studies (including a larger series of patients). Finally, all patients in this study were Chinese. Some studies have shown that there were racial differences in the frequency of ILD and AE-ILD (26). In conclusion, patients with ILD had a higher incidence of postoperative morbidity and 90-day mortality. ASA classification is an important influencing factor of AE-ILD. AE-ILD could lead to a significantly higher mortality rate. Special attention and management should be given to ILD patients when undergoing pulmonary operation. Based on our clinical experience, steroid therapy was an alternative method for AE-ILD. Hence, when an ILD patient is undergoing surgery, the patient needs to be evaluated jointly by a thoracic surgeon, a respiratory surgeon, and an anesthesiologist.
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Authors:  J M Harris; I D A Johnston; R Rudd; A J Newman Taylor; P Cullinan
Journal:  Thorax       Date:  2009-12-08       Impact factor: 9.139

6.  Long-term results and predictors of survival after surgical resection of patients with lung cancer and interstitial lung diseases.

Authors:  Toshihiko Sato; Atsushi Watanabe; Haruhiko Kondo; Masato Kanzaki; Kenichi Okubo; Kohei Yokoi; Kazuya Matsumoto; Takashi Marutsuka; Hirohiko Shinohara; Satoshi Teramukai; Kazuma Kishi; Masahito Ebina; Yukihiko Sugiyama; Okumora Meinoshin; Hiroshi Date
Journal:  J Thorac Cardiovasc Surg       Date:  2014-09-18       Impact factor: 5.209

7.  Pulmonary Resection for Lung Cancer in Patients With Idiopathic Interstitial Pneumonia.

Authors:  Takahiro Omori; Michihiko Tajiri; Tomohisa Baba; Takashi Ogura; Tae Iwasawa; Koji Okudela; Tamiko Takemura; Mari S Oba; Takamitsu Maehara; Haruhiko Nakayama; Masahiro Tsuboi; Munetaka Masuda
Journal:  Ann Thorac Surg       Date:  2015-06-23       Impact factor: 4.330

8.  Operation for lung cancer in patients with idiopathic pulmonary fibrosis: surgical contraindication?

Authors:  Toshio Fujimoto; Tsuyoshi Okazaki; Tadashi Matsukura; Takeshi Hanawa; Naoki Yamashita; Koichi Nishimura; Masayoshi Kuwabara; Yoshito Matsubara
Journal:  Ann Thorac Surg       Date:  2003-11       Impact factor: 4.330

9.  Impact and predictors of acute exacerbation of interstitial lung diseases after pulmonary resection for lung cancer.

Authors:  Toshihiko Sato; Satoshi Teramukai; Haruhiko Kondo; Atsushi Watanabe; Masahito Ebina; Kazuma Kishi; Yoshitaka Fujii; Tetsuya Mitsudomi; Masahiro Yoshimura; Tomohiro Maniwa; Kenji Suzuki; Kazuhiko Kataoka; Yukihiko Sugiyama; Takashi Kondo; Hiroshi Date
Journal:  J Thorac Cardiovasc Surg       Date:  2013-11-20       Impact factor: 5.209

10.  The rising incidence of idiopathic pulmonary fibrosis in the U.K.

Authors:  V Navaratnam; K M Fleming; J West; C J P Smith; R G Jenkins; A Fogarty; R B Hubbard
Journal:  Thorax       Date:  2011-04-27       Impact factor: 9.139

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