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Severe pulmonary complications after cytoreductive surgery and hyperthermic intraperitoneal chemotherapy are common and contribute to decreased overall survival

  • Olivia Sand ,

    Contributed equally to this work with: Olivia Sand, Mikael Andersson, Wilhelm Graf

    Roles Conceptualization, Data curation, Formal analysis, Methodology, Project administration, Validation, Visualization, Writing – original draft, Writing – review & editing

    olivia.sand@surgsci.uu.se

    Affiliation Department of Surgical Sciences, Uppsala University Hospital, Uppsala, Sweden

  • Mikael Andersson ,

    Contributed equally to this work with: Olivia Sand, Mikael Andersson, Wilhelm Graf

    Roles Conceptualization, Data curation, Formal analysis, Methodology, Supervision, Validation, Writing – review & editing

    Affiliation Department of Medical Sciences, Respiratory, Allergy and Sleep Research, Uppsala University, Uppsala, Sweden

  • Erebouni Arakelian ,

    Roles Conceptualization, Supervision, Validation, Writing – review & editing

    ‡ These authors also contributed equally to this work.

    Affiliation Department of Surgical Sciences, Uppsala University Hospital, Uppsala, Sweden

  • Peter Cashin ,

    Roles Conceptualization, Formal analysis, Methodology, Supervision, Validation, Writing – review & editing

    ‡ These authors also contributed equally to this work.

    Affiliation Department of Surgical Sciences, Uppsala University Hospital, Uppsala, Sweden

  • Egidijus Semenas ,

    Roles Conceptualization, Methodology, Resources, Supervision, Validation, Writing – review & editing

    ‡ These authors also contributed equally to this work.

    Affiliation Department of Surgical Sciences, Uppsala University Hospital, Uppsala, Sweden

  • Wilhelm Graf

    Contributed equally to this work with: Olivia Sand, Mikael Andersson, Wilhelm Graf

    Roles Conceptualization, Formal analysis, Funding acquisition, Methodology, Resources, Supervision, Validation, Writing – review & editing

    Affiliation Department of Surgical Sciences, Uppsala University Hospital, Uppsala, Sweden

Abstract

Background and objectives

Extensive abdominal surgery is associated with the risk of postoperative pulmonary complications. This study aims to explore the incidence and risk factors for developing postoperative pulmonary complications after cytoreductive surgery and hyperthermic intraperitoneal chemotherapy and to analyze how these complications affect overall survival.

Methods

Data were collected on 417 patients undergoing surgery between 2007 and2017 at Uppsala University Hospital, Sweden. Postoperative pulmonary complications were graded according to the Clavien-Dindo classification system where Grade ≥ 3 was considered a severe complication. A logistic regression analysis was used to analyze risk factors for postoperative pulmonary complications and a Cox proportional hazards model to assess impact on survival.

Results

Seventy-two patients (17%) developed severe postoperative pulmonary complications. Risk factors were full thickness diaphragmatic injury and/or diaphragmatic resection [OR 5.393, 95% CI 2.924–9.948, p = < 0.001]. Severe postoperative pulmonary complications, in combination with non-pulmonary complications, contributed to decreased overall survival [HR 2.285, 95% CI 1.232–4.241, p = 0.009].

Conclusions

Severe postoperative pulmonary complications were common and contributed to decreased overall survival. Full thickness diaphragmatic injury and/or diaphragmatic resection were the main risk factors. This finding emphasizes the need for further research on the mechanisms behind pulmonary complications and their association with mortality.

Introduction

Peritoneal metastasis (PM) represents the third most frequent metastatic site after hepatic and pulmonary deposits in colorectal cancer [1]. Historically, the diagnosis has been associated with a poor prognosis [2] but the 1990s saw the introduction of a curative treatment for selected patients with PM: cytoreductive surgery (CRS) and hyperthermic intraperitoneal chemotherapy (HIPEC) [3]. The aim of this procedure is to resect all visible tumor tissue and perioperatively flush the abdominal cavity with heated chemotherapy, targeting microscopic residual tumor tissue [3]. CRS and HIPEC has led to an increased survival rate in patients with PM [4] but postoperative morbidity and mortality rates still range between 10% and 30% and 1% and 5% respectively [58].

Postoperative pulmonary complications (PPCs), such as pneumonia and respiratory failure, are common in the period after abdominal surgery [9] and studies on PPCs after CRS and HIPEC quote an incidence between 6.8% and 69% [1013]. Non-pulmonary complications such as hemorrhage and wound infection are also frequent after CRS and HIPEC: reports suggest that the overall severe morbidity rate is around 12% [8]. Some of the proposed risk factors for developing PPCs after abdominal surgery are poor general health status, smoking, lung disease, and the type and duration of surgery [9,14]. Suggested prophylactic measures include pre- and postoperative interventions such as smoking cessation, prophylactic physical therapy, and continuous positive airway pressure (CPAP) in the postoperative period [1517]. A better understanding of the risk factors for developing PPCs after CRS and HIPEC could improve the perioperative treatment of patients with PM and potentially decrease the incidence of PPCs.

There is currently limited information regarding risk factors related to PPCs after CRS and HIPEC, and to what extent PPCs impact survival rates. The aim of this study was to determine the incidence and risk factors for developing severe PPCs after CRS and HIPEC. Another aim was to investigate whether PPCs impact overall survival.

Materials and methods

Patient selection and data collection

This was a cross-sectional study on all patients who underwent CRS and HIPEC at the Uppsala University Hospital between 2007 and 2017. Data were extracted from both medical records and the Swedish Intensive Care Unit Registry (PasIva) [18]. Demographic and clinical data were collected on gender, age, body mass index (BMI), lung disease (defined as chronic obstructive pulmonary disease, asthma, chronic bronchitis and/or sleep apnea), smoking (current or former smoker), the American Society of Anesthesiologists’ physical status classification (ASA), and primary tumor origin. Data were also collected on operative variables such as the peritoneal cancer index (PCI) [19], completeness of cytoreduction score (CC score) [20], duration of surgery, liver resection, splenectomy, diaphragmatic peritonectomy, full thickness diaphragmatic injury and/or diaphragmatic resection, type and grade of pulmonary complications, as well as type and grade of non-pulmonary complications. The study was approved by the Swedish Ethical Review Authority in Uppsala, Sweden (reference no. 2013/203). The data were analyzed anonymously and therefore, written/verbal consent was not required or obtained.

Patient selection for CRS and HIPEC is based on the absence of unresectable metastatic disease, PCI and patient ability to withstand extensive surgery [21]. To identify patients for inclusion, we used a local register from Uppsala University Hospital of patients who had undergone surgery because of PM. All 438 adult patients who underwent CRS and HIPEC between January 1, 2007 and December 31, 2017 were eligible for the study and the primary tumor origin was colon, rectum, appendix, small intestine, stomach, ovarium or peritoneum. The most frequently used chemotherapy regimens were Mitomycin C (for 90 minutes) for appendiceal tumors or Oxaliplatin (for 30 minutes) for tumors of colorectal origin.

Grading of complications

In this study the Clavien-Dindo classification of surgical complications [22] was used to grade both pulmonary and non-pulmonary complications. The classification system consists of seven severity grades including two subgrades for Grades 3 and 4. Grade 1 refers to a deviation from the normal postoperative course without the need for pharmacological (with some exceptions), surgical, radiological or endoscopic treatment. Grade 2 corresponds to complications that need pharmacological treatment, blood transfusion or total parenteral nutrition. Complications that require surgical, endoscopic or radiological interventions are classified as Grade 3 and the two subcategories within Grade 3 divide the interventions into (a) interventions not under general anesthesia or (b) interventions under general anesthesia. Examples of a Grade 3 complication are pleural effusion that requires drainage and reoperation because of anastomotic leaks. A Grade 4 category corresponds to life-threatening complications requiring ICU management where single organ dysfunction is graded 4a and multi-organ dysfunction is graded 4b. In this study respiratory complications that required prolonged mechanical ventilation (defined as longer than what was routine) and/or reintubation or non-invasive ventilation due to respiratory complications were graded 4. Surgical complications that required intensive care were sepsis and various heart conditions. Death is graded 5. In this study, we classified PPCs Grade ≥ 3 as being severe PPCs. For the purpose of this study, patients were divided into two groups based on the occurrence of PPCs: patients with PPCs Grade < 3 (including those with no PPCs) and patients with PPCs Grade ≥ 3 according to the Clavien-Dindo classification of surgical complications. All PPCs occurring during the hospital stay at Uppsala University Hospital were identified and graded. All non-pulmonary complications were grouped together and split into two groups: Grade < 3 or Grade ≥ 3.

Statistical analysis

Demographic, clinical and operative characteristics were presented descriptively in relation to the presence or absence of severe PPCs. Continuous data were presented with means and standard deviations. Categorical data were presented with frequencies and percentages. A univariate analysis of risk factors considered to be associated with severe PPCs was performed. Variables with a p-value ≤ 0.1 in the univariate analysis and variables previously well established as risk factors were included in the multivariate logistic regression model and the odds ratio (OR) for each variable was estimated. A Kaplan-Meier estimation including a log rank test and a Cox proportional hazards model was performed to analyze survival rates between patients with different grades of PPCs and/or non-pulmonary complications. Variable selection was performed by conducting a univariate analysis of variables considered to be associated with overall survival. A Cox proportional hazards model was then built from the variables with a p-value ≤ 0.1 in the univariate analysis and variables known to be correlated with overall survival. Overall survival was defined as the time from surgery to date of death. Patients who were alive at the end of the data collection (April 25, 2019) were censored. All data were processed and analyzed with IBM SPSS Statistics for Windows version 23 (IBM Corp, Armonk, NY, USA). The significance threshold was set at < 0.05.

Results

Baseline characteristics

A total of 438 patients underwent CRS and HIPEC between January 1, 2007 and December 31, 2017. After excluding patients with an unknown CC score (n = 4), CC-2 (n = 6) and CC-3 (n = 11), 417 patients were included in the analyses (Fig 1). Patient characteristics are presented in Table 1.

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Fig 1. Flowchart of inclusions and exclusions of the study.

CRS Cytoreductive surgery HIPEC Hyperthermic intraperitoneal chemotherapy CC score Completeness of cytoreduction score.

https://doi.org/10.1371/journal.pone.0261852.g001

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Table 1. Characteristics of 417 patients undergoing CRS and HIPEC between 2007 and 2017.

https://doi.org/10.1371/journal.pone.0261852.t001

Incidence of complications and risk factors for severe PPCs

The incidence of PPCs Grade ≥ 3 was 17% (72 out of 417 patients) and the types of PPCs were pleural effusion or pneumothorax requiring drainage (n = 60) and postoperative reintubation or prolonged need of mechanical ventilation/non-invasive ventilation because of pulmonary complications such as respiratory failure and pneumothorax (n = 25). The percentage of patients developing one or more non-pulmonary complications Grade ≥ 3 was 9% (38 out of 417 patients) and reoperation was required in 25 (66%) of these patients. The types of non-pulmonary complications Grade ≥ 3 were abdominal abscess (n = 15), hemorrhage (n = 11), cardiac complications (n = 6), gastrointestinal perforations (n = 6), sepsis (n = 5), wound dehiscence (n = 5), anastomotic leaks (n = 4) and ileus (n = 2). In all, 52/72 of PPCs Grade ≥ 3 were isolated pulmonary complications whereas 20 (28%) occurred together with non-pulmonary complications Grade ≥ 3 (Table 1). Full thickness diaphragmatic injury and/or diaphragmatic resection [OR 5.393, 95% CI 2.924–9.948, p = < 0.001] were the most influential variables in the multivariate model, while neither age, smoking, PCI, liver resection nor diaphragmatic peritonectomy contributed statistically significantly to the model (Table 2).

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Table 2. Unadjusted and adjusted results of odds ratios and p-values for the variables included in the final model on risk factors for severe pulmonary complications after CRS and HIPEC.

https://doi.org/10.1371/journal.pone.0261852.t002

PPCs and overall survival

In the Cox proportional hazards model, PPCs Grade ≥3 were not independently associated with decreased overall survival (p = 0.3). However, having both PPCs Grade ≥3 and non-pulmonary complications Grade ≥3 was associated with decreased overall survival (Fig 2), [HR 2.285, 95% CI 1.232–4.241, p = 0.009] when adjusted for gender, age, BMI, ASA score, diagnosis, CC score and PCI (Table 3).

thumbnail
Fig 2. Kaplan-Meier curves on overall survival in relation to PPCs Grade ≥3, non-pulmonary complications Grade ≥3 or combined PPCs Grade ≥3 and non-pulmonary complications Grade ≥3.

PPCs Postoperative pulmonary complications Non-pulmonary complications Including abdominal abscess, hemorrhage, cardiac complications, gastrointestinal perforations, sepsis, wound dehiscence, anastomotic leaks and ileus.

https://doi.org/10.1371/journal.pone.0261852.g002

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Table 3. Unadjusted and adjusted results of hazard ratios and p-values for the variables included in the final model on overall survival after CRS and HIPEC.

https://doi.org/10.1371/journal.pone.0261852.t003

Discussion

In this large cohort of patients, we found severe PPCs to be common after CRS and HIPEC and to contribute to decreased overall survival. The multivariate model of risk factors identified full thickness diaphragmatic injury and/or diaphragmatic resection as significantly associated with severe PPCs.

To date, our study is the largest one conducted on the incidence and risk factors for PPCs after CRS and HIPEC. Previous studies have presented a wide range of incidence numbers, 6.8%-69%, and have also used a variety of grading systems [1013], which complicates comparison. Sinukumar et al. [10], Arakalian et al. [11], and Cascales Campos et al. [12] all used different versions of the Common Terminology Criteria for Adverse Events (CTCAE) [23] whereas Preti et al. [13] used a customized classification system for their study. We found a higher incidence of PPCs than the majority of these studies and we believe that this could be partially explained by the use of a different grading system. Unfortunately, we could find no previous studies on PPCs in patients with peritoneal metastases using the same classification system as we did, the Clavien-Dindo classification system, making it difficult to conduct a valid comparison between the results.

The main risk factors in our study were full thickness diaphragmatic injury and/or diaphragmatic resection, both of which are sometimes unavoidable when trying to reach a complete cytoreduction [2426]. The role of diaphragmatic procedures such as peritonectomy along with full thickness diaphragmatic injury and/or diaphragmatic resection as risk factors for PPCs is controversial [12,13]. In our cohort, diaphragmatic peritonectomy was not a significant risk factor for PPCs, in contrast to previous studies such as the one from Cascales Campos et al. [12] who identified diaphragmatic peritonectomy as the main risk factor. However, they did not find prophylactic chest tubes indicated since the number of patients requiring chest tubes in their study was low. Likewise, Ye et al. [27] did not recommend prophylactic chest tubes after diaphragmatic peritonectomy, but they proposed that they should be considered after full thickness diaphragmatic resection. With the knowledge that severe PPCs, such as pleural effusion requiring chest tubes, might be related to increased mortality, our study suggests a re-evaluation of the use of prophylactic chest tubes. This is supported by Sandadi et al [28] who found that prophylactic chest tubes decreased the incidence of pleural effusion after diaphragmatic procedures as a part of CRS. The management of chest tubes is not without complications since they present the potential for injuries to the stomach and infections [29]. However, tubes inserted intraoperatively under full control are probably safer to use.

Surprisingly, neither smoking nor age, both established risk factors for the development of PPCs [14,3032], were associated with severe PPCs in this cohort. This is interesting and might be a result of patient selection for CRS and HIPEC where heavy smokers with obstructive pulmonary disease might have been ineligible for surgery. Patients with PM are also younger on average than many other cancer patient groups and this might reduce the impact of age in this cohort. These results concur with previous studies of patients with PM [12,13].

This study adds a new perspective regarding the impact of PPCs on overall survival after CRS and HIPEC. Both increased in-hospital mortality [33] and long-term mortality [34] have been associated with PPCs, but this is the first study to examine the effects in patients with peritoneal metastases. In our cohort, neither PPCs Grade ≥ 3 nor non-pulmonary complications ≥ 3 alone affected survival rates but when combined, they were associated with decreased overall survival. It has not been established whether it is the PPC itself or the effect of multiple complications that contributes to the decreased overall survival and further studies are required to fully understand the mechanisms behind the increased mortality rates. It would also be useful to investigate whether PPCs are working as a proxy for some other processes in the body affecting mortality.

Some limitations of this study must be considered when interpreting the results. First, data on cause of death were not available in the medical records. Unfortunately, data on recurrence were only partly registered in the medical records since follow up was handled by the referring hospitals. Furthermore, we must also consider that only data on PPCs occurring during the hospital stay at Uppsala University Hospital were accessible. This means that complications occurring later in the postoperative period that might have had an impact on survival rates could have been missed. The incidence rate of severe PPCs presented in this study might also be affected by the short follow-up period. This study suggests that severe PPCs might play a major role for overall survival. However, this needs more thorough investigation.

One of the strengths of our study is that it uses a standardized grading system that is well established in surgical care and all grades of complications are included. This gives a broad picture on the incidence of severe PPCs after CRS and HIPEC and facilitates future comparisons. Another strength of the study is that we included all tumor types, which resulted in a large cohort and a valid representation of the CRS and HIPEC population.

We are unable to draw conclusions on whether it is the PPC itself or the effect of multiple complications that is responsible for the negative correlation with overall survival in this study but regardless of the underlying mechanisms, we suggest that the prevention of severe PPCs can benefit survival rates. It has previously been established that PPCs after abdominal surgery can, to some extent, be prevented [35] and while some complications such as pleural effusion might be rather difficult to avoid when performing diaphragmatic interventions [12,36], others can be more easily prevented. Preoperative physical therapy including inspiratory muscle training (IMT) is one example that has been shown to decrease the risk of pneumonia after major abdominal surgery [35]. There are no studies on physical therapy focused on pre-habilitation performed on patients undergoing CRS and HIPEC, but this might be a promising preoperative intervention to decrease the risk of PPCs and, by extension, it might also affect overall survival.

This study highlights the impact severe PPCs might have on survival rates, but the underlying mechanisms are still unclear. Evaluating the effect of pre-habilitation interventions on PPCs in patients with peritoneal metastases would be an interesting research subject which might shed light on whether the prevention of PPCs, and thus the potential for avoiding decreased overall survival after CRS and HIPEC, is possible.

Conclusion

Severe PPCs are common after CRS and HIPEC and in our study, full thickness diaphragmatic injury and/or diaphragmatic resection were the most influential risk factors. We also found that having both PPCs Grade ≥ 3 and non-pulmonary complications Grade ≥ 3 was associated with decreased overall survival. These results suggest the need for further research on PPCs and mortality to be able to fully understand the mechanisms.

Supporting information

S1 Appendix. Supplementary file regression analyses.

https://doi.org/10.1371/journal.pone.0261852.s001

(DOCX)

Acknowledgments

The authors thank Patrik Öhagen, Uppsala Clinical Research Center, and Jonas Selling, Academy of Statistics (Statistikakademin), for statistical advice.

References

  1. 1. Segelman J, Granath F, Holm T, Machado M, Mahteme H, Martling A. Incidence, prevalence and risk factors for peritoneal carcinomatosis from colorectal cancer. Br J Surg. 2012;99(5):699–705. pmid:22287157
  2. 2. Hall B, Padussis J, Foster JM. Cytoreduction and Hyperthermic Intraperitoneal Chemotherapy in the Management of Colorectal Peritoneal Metastasis. Surg Clin North Am. 2017;97(3):671–82. pmid:28501254
  3. 3. Sugarbaker PH. Peritonectomy procedures. Ann Surg. 1995;221(1):29–42. pmid:7826158
  4. 4. Chi DS, Eisenhauer EL, Lang J, Huh J, Haddad L, Abu-Rustum NR, et al. What is the optimal goal of primary cytoreductive surgery for bulky stage IIIC epithelial ovarian carcinoma (EOC)? Gynecol Oncol. 2006;103(2):559–64. pmid:16714056
  5. 5. Elias D, Goere D, Blot F, Billard V, Pocard M, Kohneh-Shahri N, et al. Optimization of hyperthermic intraperitoneal chemotherapy with oxaliplatin plus irinotecan at 43 degrees C after compete cytoreductive surgery: mortality and morbidity in 106 consecutive patients. Ann Surg Oncol. 2007;14(6):1818–24. pmid:17356950
  6. 6. Gupta H, Gupta PK, Fang X, Miller WJ, Cemaj S, Forse RA, et al. Development and validation of a risk calculator predicting postoperative respiratory failure. Chest. 2011;140(5):1207–15. pmid:21757571
  7. 7. Ceelen WP, Peeters M, Houtmeyers P, Breusegem C, De Somer F, Pattyn P. Safety and Efficacy of Hyperthermic Intraperitoneal Chemoperfusion with High-Dose Oxaliplatin in Patients with Peritoneal Carcinomatosis. Ann Surg Oncol. 2008;15(2):535–41. pmid:17960463
  8. 8. Desantis M, Bernard J-L, Casanova V, Cegarra-Escolano M, Benizri E, Rahili AM, et al. Morbidity, mortality, and oncological outcomes of 401 consecutive cytoreductive procedures with hyperthermic intraperitoneal chemotherapy (HIPEC). Langenbecks Arch Surg. 2015;400(1):37–48. pmid:25319432
  9. 9. Smetana GW, Lawrence VA, Cornell JE. Preoperative Pulmonary Risk Stratification for Noncardiothoracic Surgery: Systematic Review for the American College of Physicians. Ann Intern Med. 2006;144(8):581. pmid:16618956
  10. 10. Sinukumar S, Mehta S, Damodaran D, Rajan F, Zaveri S, Ray M, et al. Failure-to-Rescue Following Cytoreductive Surgery with or Without HIPEC is Determined by the Type of Complication—a Retrospective Study by INDEPSO. Indian J of Surg Oncol. 2019;10(Suppl 1):71–79.
  11. 11. Arakelian E, Torkzad MR, Bergman A, Rubertsson S, Mahteme H. Pulmonary influences on early post-operative recovery in patients after cytoreductive surgery and hyperthermic intraperitoneal chemotherapy treatment: a retrospective study. World J Surg Oncol. 2012;10:258. pmid:23186148
  12. 12. Cascales Campos P, Martinez Insfran LA, Wallace D, Gil J, Gil E, Gonzalez Gil E, et al. Identifying the incidence of respiratory complications following diaphragmatic cytoreduction and hyperthermic intraoperative intraperitoneal chemotherapy. Clin Transl Oncol. 2019;22(6):852–859. pmid:31392644
  13. 13. Preti V, Chang D, Sugarbaker PH. Pulmonary Complications following Cytoreductive Surgery and Perioperative Chemotherapy in 147 Consecutive Patients. Gastroenterology Research and Practice. 2012;2012: 635314. pmid:22927838
  14. 14. Yang CK, Teng A, Lee DY, Rose K. Pulmonary complications after major abdominal surgery: National Surgical Quality Improvement Program analysis. J Surg Res. 2015;198(2):441–9. pmid:25930169
  15. 15. Quan H, Ouyang L, Zhou H, Ouyang Y, Xiao H. The effect of preoperative smoking cessation and smoking dose on postoperative complications following radical gastrectomy for gastric cancer: a retrospective study of 2469 patients. World J Surg Oncol. 2019;17(1):61. pmid:30940207
  16. 16. Odor PM, Bampoe S, Gilhooly D, Creagh-Brown B, Moonesinghe SR. Perioperative interventions for prevention of postoperative pulmonary complications: systematic review and meta-analysis. The BMJ [Internet]. 2020;368:m540. pmid:32161042
  17. 17. Ireland CJ, Chapman TM, Mathew SF, Herbison GP, Zacharias M. Continuous positive airway pressure (CPAP) during the postoperative period for prevention of postoperative morbidity and mortality following major abdominal surgery. Cochrane Database Syst Rev. 2014;(8):CD008930. pmid:25081420
  18. 18. PASIVA [Internet]. [cited 2021 Apr 10]. https://www.pasiva.se/.
  19. 19. Sugarbaker PH. Peritoneal Carcinomatosis: Principles of Management. Springer Science & Business Media; 1996.
  20. 20. Jacquet P, Sugarbaker PH. Clinical research methodologies in diagnosis and staging of patients with peritoneal carcinomatosis. Cancer Treat Res. 1996;82:359–74. pmid:8849962
  21. 21. Harmon RL, Sugarbaker PH. Prognostic indicators in peritoneal carcinomatosis from gastrointestinal cancer. Int Semin Surg Oncol ISSO. 2005;2(1):3. pmid:15701175
  22. 22. Dindo D, Demartines N, Clavien P-A. Classification of Surgical Complications. Ann Surg. 2004;240(2):205–13. pmid:15273542
  23. 23. US Department of Health and Human Services, National Institutes of Health, National Cancer Institute. Common Terminology Criteria for Adverse Events (CTCAE) Version 5. [Internet]. Published: 2017 November 27. [cited 2021 Dec 3]. Common Terminology Criteria for Adverse Events (CTCAE) (cancer.gov).
  24. 24. Cliby W, Dowdy S, Feitoza SS, Gostout BS, Podratz KC. Diaphragm resection for ovarian cancer: technique and short-term complications. Gynecol Oncol. 2004;94(3):655–60. pmid:15350355
  25. 25. Aletti GD, Dowdy SC, Podratz KC, Cliby WA. Surgical treatment of diaphragm disease correlates with improved survival in optimally debulked advanced stage ovarian cancer. Gynecol Oncol. 2006;100(2):283–7. pmid:16182350
  26. 26. Tsolakidis D, Amant F, Van Gorp T, Leunen K, Neven P, Vergote I. Diaphragmatic surgery during primary debulking in 89 patients with stage IIIB-IV epithelial ovarian cancer. Gynecol Oncol. 2010;116(3):489–96. pmid:19954825
  27. 27. Ye S, He T, Liang S, Chen X, Wu X, Yang H, et al. Diaphragmatic Surgery and Related Complications In Primary Cytoreduction for Advanced Ovarian, Tubal, and Peritoneal Carcinoma. BMC Cancer. 2017;17(1):317. pmid:28476108
  28. 28. Sandadi S, Long K, Andikyan V, Vernon J, Zivanovic O, Eisenhauer EL, et al. Postoperative outcomes among patients undergoing thoracostomy tube placement at time of diaphragm peritonectomy or resection during primary cytoreductive surgery for ovarian cancer. Gynecol Oncol. 2014;132(2):299–302. pmid:24296344
  29. 29. Kwiatt M, Tarbox A, Seamon MJ, Swaroop M, Cipolla J, Allen C, et al. Thoracostomy tubes: A comprehensive review of complications and related topics. Int J Crit Illn Inj Sci. 2014;4(2):143–55. pmid:25024942
  30. 30. Gajdos C, Hawn MT, Campagna EJ, Henderson WG, Singh JA, Houston T. Adverse effects of smoking on postoperative outcomes in cancer patients. Ann Surg Oncol. 2012;19(5):1430–8. pmid:22065194
  31. 31. McAlister FA, Bertsch K, Man J, Bradley J, Jacka M. Incidence of and Risk Factors for Pulmonary Complications after Nonthoracic Surgery. Am J Respir Crit Care Med. 2005;171(5):514–7. pmid:15563632
  32. 32. Sabaté S, Mazo V, Canet J. Predicting postoperative pulmonary complications: implications for outcomes and costs. Curr Opin Anesthesiol. 2014;27(2):201–9.
  33. 33. Canet J, Sabaté S, Mazo V, Gallart L, Gama de Abreu M, Belda J, et al. Development and validation of a score to predict postoperative respiratory failure in a multicentre European cohort: A prospective, observational study. Eur J Anaesthesiol. 2015;32(7):458–70. pmid:26020123
  34. 34. Khuri SF, Henderson WG, DePalma RG, Mosca C, Healey NA, Kumbhani DJ, et al. Determinants of Long-Term Survival After Major Surgery and the Adverse Effect of Postoperative Complications. Ann Surg. 2005;242(3):326–43. pmid:16135919
  35. 35. Katsura M, Kuriyama A, Takeshima T, Fukuhara S, Furukawa TA. Preoperative inspiratory muscle training for postoperative pulmonary complications in adults undergoing cardiac and major abdominal surgery. Cochrane Database Syst Rev. 2015;(10):CD010356. pmid:26436600
  36. 36. Bristow RE, Tomacruz RS, Armstrong DK, Trimble EL, Montz FJ. Survival effect of maximal cytoreductive surgery for advanced ovarian carcinoma during the platinum era: a meta-analysis. J Clin Oncol. 2002;20(5):1248–59. pmid:11870167