Cancer surgery cancellation: incidence, outcomes and recovery in a universal health care system =============================================================================================== * Antoine Eskander * Claudia Zanchetta * Natalie Coburn * Danny Enepekides * Lilian T. Gien * Reeza Menalo * Gener Austria * Ordeena Linton * Sue Su-Myat * Olga Yermakhanova * Jonathan Irish ## Abstract **Background:** Cancer surgery cancellation can have negative consequences for the patient, the surgeon and the health care system. There is a paucity of literature on cancer surgery cancellation and its association with wait times, perioperative outcomes, survival and costs of care. Therefore, the objective of this study was to determine the incidence of same-day cancer surgery cancellation in a universal health care context and its association with short and long-term outcomes. **Methods:** This was a population-based retrospective cancer cohort study in Ontario, Canada (2010–2016). There were 199 599 patients in the control cohort and 3539 patients in the cohort that experienced a cancellation. We assessed the cohorts for differences in survival, perioperative complications and costs of care. **Results:** The overall cancellation rate was 1.74% and was predicted by cancer type (genitourinary), lower income quintile, and more central region of residence. Wait times in the cancelled cohort were longer than in the control cohort; however, this difference was not associated with worse survival outcomes. Patients in the cancelled cohort had higher complication rates while in hospital (7.3 %) than those in the control cohort (4.9%; *p* < 0.01). After adjusting for important confounders, the cancelled cohort was more costly ($1100). **Conclusion:** Same-day cancer surgery cancellation rates were low. They were associated with longer wait times, higher complication rates and increased costs of care. Survival was not worse in the cancelled cohort, suggesting that appropriate cancer urgency prioritization occurs. Preventable causes of cancellation should be targeted to improve outcomes in patients with cancer. Cancer surgery cancellation can have negative consequences for the patient, the surgeon and the health care system. Delays in cancer surgery, even by a few weeks, can have a negative impact on curability and overall survival, particularly for aggressive malignancies.1,2 During the first wave of the COVID-19 pandemic in Canada, many surgeries were cancelled, of which cancer surgeries were relatively protected, likely owing to prioritization over nononcologic procedures.3 Although many studies have looked at surgery cancellation with a broad overview of incidence and causes (40% unavoidable; medical/patient causes and health system capacity reasons), to our knowledge none have focused on cancer surgery specifically.4–6 Furthermore, there are no studies comparing outcomes between those who experienced a cancellation followed by eventual completion of the intended procedure and those who did not experience a cancellation. There is therefore a paucity of literature on cancer surgery cancellation and its association with wait times, perioperative outcomes, survival and costs of care. The objective of our study was to determine the incidence of same-day cancer surgery cancellation in a universal health care context. The secondary objective was to determine the association of cancellations with outcomes, including wait times, survival, perioperative complications, 30-day readmission and emergency department (ED) use, and costs of care. ## Methods ### Study design and setting This was a population-based retrospective cohort study in Ontario, Canada, using linked health administrative databases available at Ontario Health — Cancer Care Ontario (OH-CCO). Cohort development was based on prespecified inclusion and exclusion criteria to develop a comprehensive cohort of patients who had cancer surgery in Ontario during the study period. ### Cohort development (inclusion/exclusion criteria) The study used an initial list of patients who had a diagnosis of cancer in the Ontario Cancer Registry (OCR) from January 1, 2010, to December 31, 2016. This period was selected to allow for mature survival data given it was one of our secondary outcomes. Furthermore, at the time of study inception, cancer data around the pandemic period in our jurisdiction were not mature. The OCR is a well-validated cancer registry with a cancer capture rate greater than 98% for all noncutaneous malignancies.7,8 The OCR has a much higher cancer capture rate than the 2 most commonly used US databases (Surveillance, Epidemiology, and End Results [26%] and the National Cancer Database [70%]), providing a less biased initial cohort. We identified 2 cohorts: a control cohort who had a cancer surgery without prior history of cancellation, and a cancelled cohort who ultimately received a cancer surgery, but had a prior history of cancellation. To identify patients who underwent cancer surgery, we used the Canadian Institute for Health Information (CIHI) databases. Cancer surgery could have occurred up to 3 months before cancer diagnosis date, as procedures can be both diagnostic and therapeutic in the prediagnosis period. All hospitals in Ontario, Canada, are required to submit demographic and clinical information about all hospital admissions and discharges, including cancelled surgery, transfers and deaths, to CIHI. The CIHI data have a specific *International Classification of Diseases* (ICD) code for cancelled surgeries: Z53. Similarly, the Wait Time Information System (WTIS) was also used to identify patients whose oncology procedures occurred during the same time period. The WTIS is an Ontario database that collects prospective wait time data for a variety of scheduled clinical services in the province. It captures wait times for all publicly funded surgical procedures performed in an operating room; the exception is cataract procedures, which are captured regardless of location. In addition to demographic data allowing linkage with other databases, the WTIS also includes information on priority categorization, referral source, system delay reasons, Wait 2 (time from the decision to treat to the procedure date), Dates Affecting Readiness to Treat (DART), and reasons for delay.9 The WTIS also codes cancelled surgeries and when they are rebooked. This allows a restrictive approach to identify patients with cancer surgery cancellations; to be included in the cancelled cohort, a patient had to have a Z53 ICD code in CIHI databases and a cancelled surgery intervention code in the WTIS. The coding regarding reason for cancellation is not reliable and was not used. As such, whether the cancellation was related to administrative limitations (e.g., lack of operating room time, nursing, beds) or to medical concerns could not be assessed. To be included in the cancelled cohort, the same cancer surgery that was initially booked must have eventually been completed; those who ultimately never had cancer surgery were not included. Finally, a linkage with the OCR was then used to validate that the cancer diagnosis site and date matched that of the cancer surgical procedure received. We excluded patients if they were not adults (age < 18) at the index date, had a Priority 1 or emergency nonelective cancer surgery, had an out-of-province postal code at the time of surgery, had a missing or invalid health care number, or were not eligible for the Ontario Health Insurance Plan (OHIP) at the time of their index surgery. The study protocol was approved by the Privacy Office at OH-CCO and is otherwise exempt from the requirement for research ethics board approval. ### Covariates Age was defined at the time of cancer diagnosis. Charlson Comorbidity score (categorical; 0, 1, 2 or more) was defined by the sum of comorbidities from administrative data. Data from the 2016 Census Profile available at the dissemination area geographic level were used to calculate neighbourhood income quintiles and deciles. This analysis relied on singleperson equivalent (SPE) to take into consideration household size; SPE is the person-weights implicit in the Statistics Canada low-income cut-offs needed to specify an appropriate multiplier for different house-hold sizes. This adjustment is necessary because it generally costs less per person for 2 or more persons living together than for 1 person living alone.10 Regions were defined according to the new Ontario Health categorization: Toronto, North, West, East, and Central. Cancer sites were categorized into breast, lung, genitourinary (not including prostate), prostate, gastrointestinal, gynecologic and other. It should be noted that lymphomas and cutaneous malignancies (including melanoma, squamous cell carcinoma and basal cell carcinoma) were not included. Race and ethnicity data are not readily available in the OH-CCO data set holdings that were used for this study and as such could not be included as covariates. ### Wait times and survival Patients in the different cohorts were compared for median and 90th percentile wait time using the Student *t* test. Cohorts were then compared based on the aforementioned covariates using the χ2 test for categorical variables and a *t* test for continuous variables. Vital status was captured from the Registered Persons Database (RPDB), which contains information on all persons who are registered for the purposes of OHIP and the Ontario Drug Benefits. For the survival output, we generated a Kaplan–Meier curve using the unadjusted association between cohort status and overall survival. A multivariable Cox regression analysis was to be performed if the cancelled cohort had worse survival than the control cohort on univariable analysis necessitating adjustment for confounders. However, if no difference was noted or if the opposite effect was identified, the a priori statistical plan would not involve a multivariable model. ### Complications, 30-day ED visit and unplanned hospitalization Patients who died while still in hospital (any time from admission to discharge) or who died during surgery were excluded for this portion of the analysis. Similarly, patients who had a return visit or admission on the same day of discharge or surgery were excluded in the numerator, as these are often considered coding errors with patient transfers from one admission type to another or between institutions. Readmission or visit to the ED within 30 days for our surgical cohorts was captured using the CIHI Discharge Abstract Database (DAD) and the National Ambulatory Care Reporting System (NACRS). ### Costs of care Similarly, costs from Sept. 1, 2015, to Mar. 31, 2016, were calculated using a well-described algorithm that uses both hospital and physician claims data. Cost is defined as the amount of hospital expenditures for resources used to deliver care, including physician fees. Operating room costs depend on start time, turnover times, cancellation rates, supplies, equipment and staffing.11,12 The costing window start date was 180 days before the surgical date and ended 180 days after the surgery date. To ensure full cost capture, and given the limitations of the costing database, which starts on Apr. 1, 2012, and ends on Mar. 31, 2019, cases with a start date before these 2 dates were removed. Costs were adjusted for inflation; base year was set at 2017. Costs are based on a methodology similar to that outlined and used by ICES. The most notable difference is that the CIHI data sets use the Health Based Allocation Model Inpatient Group/Ontario Specific Comprehensive Ambulatory Classification System (CAC) weights rather than Case Mix Groups/National CAC weights and use facility-specific costs, whereas Community Care Access Centre methodology uses costs from the Healthcare Indicator Tool. Physician costs included are those billed through OHIP. Any non-fee-for-service physician compensation is not included, and any shadow billing has no associated cost. ### Modelling statistical analysis For the outcome of ED visits and unplanned readmission within 30 days, we used a logistic regression model. To compare costs, we used a generalized linear model. Covariates with a *p* value < 0.25 on univariable analysis were considered for inclusion in the final multivariable models. Other variables were included based on a priori hypotheses and for face validity. All potential covariates were assessed for collinearity, defined as a variance inflation factor > 2.5. None of the variables in our analysis were found to be collinear. Statistical significance was defined by a 2-sided *p* value of 0.05 or a standardized difference > 0.10. All analyses were performed using SAS version 9.4 (SAS Institute). ## Results ### Cohort description – cancellation rate The overall cancellation rate in our cohort was 1.74%, with the cancelled cohort comprising 3539 patients compared with 199 599 patients in the control cohort. Patients in the cancelled cohort were more likely to be younger and male; however, this difference was not clinically meaningful in the standard difference analysis (Table 1). The cancelled cohort had a clinically and significantly higher comorbidity index than the control cohort. The cohorts did not differ by income quintile. Genitourinary cancers were more likely to be cancelled, while gastrointestinal and “other” cancers were less likely to be cancelled. There was a higher proportion of patients cancelled in the Central region than in other regions. View this table: [Table 1](http://canjsurg.ca/content/65/6/E782/T1) Table 1 Sociodemographic and clinic differences between the control cohort and the cancelled cohort #### Wait times comparison Figure 1 and Figure 2 represent the median and 90th percentile wait times, respectively, for the cancelled and control cohorts by year of surgery. The median overall wait time was very stable throughout the study years (Figure 1): 19–20 days for the control cohort and 41–49 days for the cancelled cohort. The median wait time of patients without prior cancellations was 57% shorter than that of patients whose surgery was cancelled. Patients with cancelled cancer procedures who ultimately went on to receive surgery did so within a median of 21–29 days. Similarly, the 90th percentile wait time was very stable throughout the study years (Figure 2): 49–55 days for the control cohort and 98–143 days for the cancelled cohort. The wait times in the cancelled cohort (mean 66.9 d ± standard deviation [SD] 67 d) were significantly longer (*p* < 0.01) than in the control cohort (mean 25.4 d ± SD 25 d). The much longer 90th percentile wait times for the cancelled cohort suggest a distribution with longer tail in a minority of patients. ![Fig. 1](http://canjsurg.ca/https://www.canjsurg.ca/content/cjs/65/6/E782/F1.medium.gif) [Fig. 1](http://canjsurg.ca/content/65/6/E782/F1) Fig. 1 Comparison of the overall median wait times for cancer surgery between patients who experienced a same-day cancellation but ultimately went on to receive cancer surgery (cancelled cohort) and those whose cancer surgeries were not cancelled (control cohort). ![Fig. 2](http://canjsurg.ca/https://www.canjsurg.ca/content/cjs/65/6/E782/F2.medium.gif) [Fig. 2](http://canjsurg.ca/content/65/6/E782/F2) Fig. 2 Comparison of the 90th percentile median wait times for cancer surgery between patients who experienced a same-day cancellation but ultimately went on to receive cancer surgery (cancelled cohort) and those whose cancer surgeries were not cancelled (control cohort). #### Survival analysis Notable survival differences were found when comparing the cancelled and control cohorts (Figure 3). Patients who had a prior cancer surgery cancellation had a higher overall survival (hazard ratio 0.921, 95% confidence interval [CI] 0.882–0.960, *p* < 0.01). The control cohort had a 3-year survival of 83.5% (95% CI 82.2%–84.6%) and the cancelled cohort, 84.8% (95% CI 84.7%–85%). ![Fig. 3](http://canjsurg.ca/https://www.canjsurg.ca/content/cjs/65/6/E782/F3.medium.gif) [Fig. 3](http://canjsurg.ca/content/65/6/E782/F3) Fig. 3 Comparison of overall survival between patients who experienced a same-day cancellation but ultimately went on to receive cancer surgery (cancelled cohort) and those whose cancer surgeries were not cancelled (control cohort). Patients who had a prior cancer surgery cancellation had a higher overall survival (hazard ratio 0.921, 95% confidence interval [CI] 0.882–0.960, *p* < 0.01). #### Complications Patients in the cancelled cohort had higher complication rates while in hospital than the control cohort (7.3% v. 4.9%, *p* < 0.01). When each complication was assessed individually, there was a higher rate of only myocardial infarctions in the cancelled cohort than the control cohort (1.5% v. 0.7%, *p* = 0.01). Rates of inpatient infection, reoperation/ readmission to the intensive care unit (ICU), pneumonia, stroke and pulmonary embolism did not differ between the cohorts. #### Readmission or ED return within 30 days Hospital readmission and/or ED visits within 30 days for any reason were higher in the cancelled cohort than the control cohort (35.8% v. 31.7%, *p* < 0.01). When the cause for readmission and/or ED visit was narrowed to surgical complications, the rates were much lower and were no longer significantly different between the cohorts (4.2% event rate in the cancelled cohort v. 3.6% in the control cohort, *p* = 0.08). Univariable and multivariable predictors for all cause hospital readmission and/or ED visit within 30 days are shown in Table 2. On univariable analysis, rates of readmission or ED visits were higher in the cancelled cohort (odds ratio [OR] 1.12, *p* < 0.01); however, after controlling for confounders, this was no longer significant (OR 1.01, *p* = 0.76). View this table: [Table 2](http://canjsurg.ca/content/65/6/E782/T2) Table 2 Predictors of all-cause readmission or ED return visits within 30 days ### Costs of care Costs of care in the 2 years following surgery were also assessed (Table 3). On univariable analysis, the cancelled cohort cost significantly more than the control group ($35 568 v. $30 573). After adjusting for important clinical and sociodemographic confounders that may be associated with costs using a generalized linear model, these differences were sustained and the cancelled cohort cost $1100 more (95% CI $3–$2196, *p* = 0.049). View this table: [Table 3](http://canjsurg.ca/content/65/6/E782/T3) Table 3 Univariable and multivariable costs of care ## Discussion In Ontario, between 2010 and 2016, 1.74% of cancer surgeries experienced a same-day cancellation and were eventually completed. Cancellations were more common in patients with comorbidities and in those with genitourinary cancers, but less common in patients with other cancers (gastrointestinal and “other,” which includes head and neck). Not surprisingly, the wait times in the cancelled cohort were longer than in the control cohort (mean 66.9 d ± SD 67d v. mean 25.4 d ± SD 25 d), showing the significant association this has on overall wait time. Paradoxically, patients who experienced a cancellation had improved overall survival on univariable analysis. Further work is required to corroborate this finding; however, it may be related to appropriate cancer prioritization, with the most urgent cancer procedures being performed sooner than those that were less acute. Overall surgical complication rates were higher in the cancelled cohort than the control cohort. Emergency department and readmission rates within 30 days did not differ between the cohorts; however, the cancelled cohort was more costly to treat ($1100/patient) after multivariable model adjustment. The rates of cancellation in this study are much lower than those reported in the literature in many other countries and health systems, largely because those studies examined elective procedures and did not focus on cancer surgery specifically. In the United Kingdom, a study of 245 hospitals in a 7-day period reported a 13.9% same-day cancellation rate owing to lack of bed capacity, with cancer surgery being cancelled less often (OR 0.32).13 In Australia, a cross-sectional single-institution assessment in 2002 reported an 11.9% cancellation rate, which was highest for ear, nose and throat surgery (19.6%) and cardiothoracic surgery (15.8%).5 In Korea, a 10-year retrospective study in a single general hospital reported an 8.0% cancellation rate that was predominantly related to patient (93.2%) rather than hospital (6.8%) factors.6 Another study identified that larger academic hospitals had higher cancellation rates (12.4%) than mid- to small-size community hospitals (5.0%).14 Although this was not specifically examined in our study, we suspect this to also be true in our health care environment as many academic hospitals are responsible for trauma and transplant surgery, which are resource intensive and unscheduled. Overall, these rates are much higher than reported in our study because they include all surgical procedures rather than cancer surgery specifically. Despite a lack of oncology-specific data, there are some reports on other high-risk time-sensitive elective procedures, such as vascular and cardiac surgery, which show far lower cancellation rates (2%).15,16 In the vascular and cardiac cohorts, there was a 7% and 5% 30-day mortality, respectively, in those who experienced cancellations, with an additional wait time of 46 and 12 days, respectively.15,16 In the present study, we did not identify a lower overall survival in the cancelled cohort; however, the additional wait time (25 d) is in keeping with those reported for these vascular and cardiac cohorts. We hypothesize that appropriate prioritization of more urgent cancers on days where cancellations were required may explain the paradoxically higher survival in the cancelled cohort (which may have included patients with cancers for which a longer wait time may have had less of an association with survival). Our broad capture of all cancers would not allow us to determine whether delays led to more extensive adjuvant therapies. From an equity lens, we did not identify any sociodemographic factors that predicted a higher rate of sameday cancellation. There is a paucity of literature comparing sociodemographic factors between patients who have had a cancelled cancer procedure and those who did not experience a cancellation. There was little geographic variation, and the most rural health region (North) had a lower rate of cancellation than the other regions. Age, gender, and socioeconomic status did not predict cancellation, which speaks to the fact that cancellations are multifactorial and occur equally for all patients in a publicly funded cancer care system. Patients with greater comorbidities had higher rates of cancellations potentially related to medical reasons for cancellation, which has been previously reported in a noncancer cohort.4 It is therefore not surprising that we observed an overall higher complication rate in our cancelled cohort (largely related to myocardial infarction postoperatively) that did not translate into differences in surgical complications between the cohorts. The variations we observed between cancer sites is worth noting: higher rate of cancellation for genitourinary cancer procedures and lower rates of cancellation for gastrointestinal and “other” cancers, which include sarcoma, and head and neck cancers. We hypothesize that this is related to within-hospital prioritization of urgent cancers. Further work will be required to confirm this using more granular data, which are not available in the current data set. Despite similar surgical complications and comparable readmission/ED visit rates, surgery in the cancelled cohort was more costly ($1100/patient), highlighting the detrimental cost implications of cancellations on the health care system. ### Limitations These data must be interpreted in the context of the study design. Our cohort included only patients who ultimately went on to receive their planned procedure. While some patients whose surgeries are cancelled never go on to receive cancer surgery, this is quite rare and is unlikely to influence our overall findings or conclusions. Also, our study was able to ascertain only those who had cancellation on the same day as their planned surgery, and therefore underestimates the true cancer surgery cancellation rate. Nonetheless, same-day cancer surgery cancellation is a negative outcome for the patient, their family, the surgeon and the health care system overall. Although our data show the incidence and clinical predictors of cancellations from an advanced wait times information capture system, our study did not include more granular data on the reason for the same-day cancellation. Such data would likely require a single-institution type of study. Fortunately, this has been well studied in the past with fairly consistent findings showing that cancellations are partly patient driven (17%–90%) and partly system driven (e.g., lack of ward/ICU beds, staff; 7%–50%).5,13,15–17 Nonetheless, to our knowledge, our study is the largest examining cancer surgery cancellation and the first to assess predictors of these events and their downstream health care implications (wait time, survival, complications, ED use, and costs). Cancellations are unavoidable in 40% of surgical cases (not exclusively oncology).5 However, given the negative impact of cancellations on patients and the health care system, a focus on avoidable cancellations is required. Although operating room time is often listed as a limiting factor, adding additional operating room capacity has been previously well studied and does not decrease cancellation rates, as often ward and ICU bed flow issues become the next limiting factor.18,19 In our publicly funded and administered health care environment it is unlikely that adding private operating room facilities will improve cancellation rates for cancer surgery, as cancellation rates are already quite low. In the United Kingdom, it was noted that private facilities have the lowest cancellation rates, with large variation compared with publicly funded institutions, which raises concerns around case mix and equity.4 Finally, although we hypothesized that appropriate prioritization is taking place, more formal guidelines are required that should consider the differential impact of additional wait time on different cases to assist those making such decisions at the institutional level.1 ## Conclusion We identified a low rate (1.74%) of cancellation of cancer surgery in a publicly funded health care context. This leads to increased wait times and costs of care, but does not have an apparent association with survival, increased complication rates or ED use postoperatively. ## Acknowledgements This study was not supported by any internal or external grants. This work was completed through a team from Ontario Health — Cancer Care Ontario. The authors would also like to thank Shannon Milroy from Ontario Health — Cancer Care Ontario for her contributions to the methodology and data acquisition. ## Footnotes * **Competing interests:** None declared. * Accepted March 28, 2022. This is an Open Access article distributed in accordance with the terms of the Creative Commons Attribution (CC BY-NC-ND 4.0) licence, which permits use, distribution and reproduction in any medium, provided that the original publication is properly cited, the use is noncommercial (i.e., research or educational use), and no modifications or adaptations are made. See: [https://creativecommons.org/licenses/by-nc-nd/4.0/](https://creativecommons.org/licenses/by-nc-nd/4.0/) ## References 1. Hanna TP, King WD, Thibodeau S, et al. Mortality due to cancer treatment delay: systematic review and meta-analysis. BMJ 2020;371:m4087. 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