Readmission after pancreatectomy for pancreatic cancer in Medicare patients.

OBJECTIVE: The objective of this study was to use a population-based dataset to evaluate the number of readmissions and reasons for readmission in Medicare patients undergoing pancreatectomy for pancreatic cancer.
METHODS: We used Surveillance, Epidemiology, and End Results-Medicare linked data (1992-2003) to evaluate the initial hospitalization, readmission rates within 30 days (early), and between 30 days and 1 year (late) after initial discharge and reasons for readmission in patients 66 years and older undergoing pancreatectomy.
RESULTS: We identified 1,730 subjects who underwent pancreatectomy for pancreatic cancer. The in-hospital mortality was 7.5%. The overall Kaplan-Meier readmission rate was 16% at 30 days and 53% at 1 year, accounting for 15,409 additional hospital days. Early readmissions were clearly related to operative complications in 80% of cases and unrelated diagnoses in 20% of cases. Late readmissions were related to recurrence in 48%, operative complications in 25%, and unrelated diagnoses in 27% of cases. In a multivariate analysis, only distal pancreatic resection (P = 0.02) and initial postoperative length of stay > or =10 days (P = 0.03) predicted early readmission. When compared to patients not readmitted, patients readmitted early had worse median survival (11.8 vs.16.5 months, P = 0.04), but the 5-year survival was identical (18%). Late readmission was associated with worse median and 5-year survival (19.4 vs. 12.1 months, 12% vs. 21%, P < 0.0001).
CONCLUSIONS: Our study demonstrates overall 30-day and 1-year readmission rates of 16% and 53%. The majority of early readmissions were related to postoperative complications but not related to patient and tumor characteristics. Complications causing early readmission are a cause of early mortality and are potentially preventable. Conversely, late readmissions are related to disease progression and are a marker of early mortality and not the cause.

Introduction

Over the last three decades, the operative mortality and lengths of stay have decreased following pancreatic resection,1–6 which can be attributed to increasing regionalization of care,7–10 improved perioperative and critical care,11–13 improved prevention and management of complications, implementation of critical pathways,14,15 and improved post-hospital inpatient and outpatient care. Despite the improvements in mortality and lengths of stay, the morbidity rates, usually defined as the occurrence of any complication in the postoperative period, remain high with reported rates in excess of 30% even at major centers.3,4,6,16–20 Readmission, a good measure of morbidity, is rarely reported. In addition, when reported, the focus is on readmissions within the first year.

There are three previous studies evaluating readmission following pancreatic surgery.16,21,22 Two studies are single-institution studies, both of which included pancreaticoduodenectomy for benign and malignant disease.16,21 Neither study reported readmissions within 30 days of discharge. Emick and colleagues16 reported a 19% readmission rate in the year after surgery in 1,643 patients undergoing pancreaticoduodenectomy. van Geenen and colleagues21 reported an overall 1 year readmission rate of 38% in 283 patients undergoing pancreaticoduodenectomy. Given the single-institution nature of these studies, readmissions to other facilities may not be identified, so the reported rates may not reflect national readmission rates.

A population-based study using the California tumor registry and hospital discharge data reports a 59% readmission rate in the year after pancreaticoduodenectomy in patients with pancreatic cancer.22 They also report decreased long-term survival in the group requiring readmission. The majority of readmissions were related to disease progression. As such, they are a marker of early mortality and not the cause. None of the above studies evaluated readmissions using a time-to-event analysis and therefore potentially underestimated readmission rates.

The goals of our study were to use a population-based data set [Surveillance, Epidemiology, and End Results (SEER)–Medicare-linked data] to evaluate the readmission rates using time-to-event methods. We also evaluate the reasons for readmission within 30 days of pancreatic resection (early readmission) and between 30 days and 1 year (late readmissions). We hypothesize that early readmissions are related to operative complications, contribute to early mortality, and are potentially preventable. Conversely, late readmissions are associated with disease progression and are a marker, rather than a cause, of early mortality. Therefore, it is critical to analyze 30-day readmissions separately. We also determine the patient and tumor factors associated with early readmission and perform a survival analysis to determine the effect of early and late readmission on survival.

Methods

This study was approved by the Institutional Review Board at the University of Texas Medical Branch at Galveston. A Data Use Agreement for the use of SEER–Medicare data has been signed.

Data Source

We used data from the SEER–Medicare Linked Data Project (SMLDP) for the analysis. The SEER tumor registry is a National Cancer Institute (NCI) program, which tracks the incidence of cancer in the USA. The SEER database contains information on patient demographics, tumor characteristics, first course of treatment, and survival data (obtained via linkage to the National Death Index). From 1992–1999, SEER was comprised of 14 registries, 12 of which participated in the SEER–Medicare linkage. After 2000, SEER had 18 registries, 16 of which participated in the SEER–Medicare linkage.23,24

The SMLDP includes the SEER program, the NCI, and the Centers for Medicare and Medicaid Services). Ninety-three percent of all SEER patients older than age 65 are matched with Medicare enrollment files. In addition to the variables available in SEER, claims data for hospital stays, physician services, and hospital outpatient visits are included. The data used in this proposal include SEER subjects through 2002 and their Medicare claims through 2003.

Patient Cohort Selection

Using the SEER–Medicare-linked data, the following subjects were included in the study: (1) patients with International Classification of Diseases (ICD)-O-3 histology codes consistent with adenocarcinoma to eliminate other pancreatic tumor types such as neuroendocrine and acinar cell cancers, (2) patients diagnosed between 1992 and 2002, (3) patients with a pancreatic cancer as their first primary cancer, (4) patients enrolled in both Medicare Parts A and B without HMO for 12 months before their cancer diagnosis and for 1 year after their diagnosis, (5) patients aged ≥66 (to ensure available Medicare claims data for a full year prior to diagnosis), and (6) patients undergoing pancreatic resection (complete resection of the primary tumor). Pancreatic resection was identified by searching MEDPAR inpatient claims files for ICD-9 CM codes for total pancreatectomy, radical pancreaticoduodenectomy, proximal pancreatectomy, distal pancreatectomy, radical subtotal pancreatectomy, or other partial pancreatectomy (codes shown in Table 1). Patients diagnosed at autopsy only or patients diagnosed by death certificate only were excluded.

Table 1

ICD-9 Procedure and Diagnosis Codes

Procedure	ICD-9 procedure codes
Total pancreatectomy	52.7
Radical pancreaticoduodenectomy	52.6
Proximal pancreatectomy	52.51
Distal pancreatectomy	52.52
Radical subtotal pancreatectomy	52.53
Other partial pancreatectomy	52.29
Upper endoscopy with or without intervention	44.13, 44.12, 44.14, 44.19, 44.12, 44.22, 44.43, 45.13, 45.16, 45.22, 45.23, 45.24, 45.25, 45.28, 45.29, 45.30, 54.59
Biliary drainage via percutaneous, endoscopic, or operative approach	51.98, 51.87, 51.10, 51.11, 51.86, 51.85, 57.84, 51.1, 51.31, 51.51, 51.59, 51.3, 51.32, 51.42, 51.37, 51.34, 51.43, 51.49, 87.51
Diagnosis	ICD-9 Diagnosis Codes
Operative complications	998, 998.0, 998.11, 998.12, 998.13, 998.3, 998.30, 998.31, 998.32, 998.4, 998.51, 998.59, 998.6, 998.83, 998.89, 998.9, 997.4, 997.5, 997.9
Metastatic disease	197, 197.0, 197.1, 197.2, 197.3, 197.4, 197.5, 197.6, 197.7, 197.8, 197.9, 198, 198.0, 198.1, 198.2, 198.3, 198.4, 198.5, 198.6, 198.7, 198.8, 198.81, 198.82, 198.89, 196.1, 196.2, 196.3, 196.4, 196.5, 196.6, 196.7, 196.8, 196.9, 199, 199.0, 199.1, 789.5
Dehydration	276, 276.0, 276.2, 276.4, 276.5, 276.50, 276.51, 276.52
Gastric outlet obstruction/delayed gastric emptying	537, 537.0, 537.3, 537.89, 537.9, 536.3, 536.8, 536.9
Venous thromboembolism/ pulmonary embolism	453.8, 444.21, 444.42, 453.1, 453.2, 453.40, 453.4, 453.42, 453.9, 415.19
Pneumonia	480.0, 480.1, 480.2, 480.3, 480.8, 480.9, 481, 481.0, 482.0, 482.1, 482.2, 482.30, 482.31, 482.32, 482.39. 482.40, 482.41, 482.42, 482.49, 482.81, 482.82, 482.83, 482.84, 482.89, 482.9, 483.0, 483.1, 483.8, 484.1, 484.3, 484.5, 484.6, 484.7, 484.8, 487.0, 486, 485
Cholangitis	576.1, 576.2, 576.8, 576.9, 572
Small bowel obstruction	560.2, 560.81, 560.89, 560.9
Gastritis/duodenitis/gastric ulcer/ duodenal ulcer	531.00, 531.01, 531.10, 531.11, 531.20, 531.21, 531.30, 531.31, 531.40, 531.41, 531.50, 531.51, 531.60, 531.61, 531.70, 531.71, 531.90, 531.91, 532.00, 532.01, 532.10, 532.11, 532.20, 532.21, 532.30, 532.31, 532.40, 532.41, 532.50, 532.51, 532.60, 532.61, 523.70, 532.71, 532.90, 532.91, 533.00, 533.01, 533.10, 533.11, 533.20, 533.21, 533.30, 533.31, 533.40, 533.41, 533.50, 533.51, 533.60, 533.61, 533.70, 533.71, 533.90, 533.91, 534.00, 534.01, 534.10, 534.11, 534.20, 534.21, 534.30, 534.31, 534.40, 534.41, 534.60, 534.61, 534.70, 534.71, 534.90, 534.91, 535.00, 535.01, 535, 535.0, 535.10, 535.11, 535.20, 535.21, 535.30, 535.31, 535.40, 535.41, 535.50, 535.51, 535.60, 535.61, 535.70, 535.71
Incisional hernia	553.20, 553.2, 553.21, 553.29, 552.2, 552.20, 552.21, 552.29, 551, 551.10, 551.00)
Pancreatic pseudocyst	577.2
Acute myocardial infarction	410, 410.0, 410.00, 410.01, 410.02, 410.10, 410.11, 410.12, 410.20, 410.21, 410.22, 410.30, 410.40, 410.41, 410.42, 410.50, 410.51, 410.52, 410.60, 410.61, 410.62, 410.70, 410.71, 410.72, 410.80, 410.82, 410.90. 410.91, 410.92
Cerebrovascular accident	435, 435.0, 435.1, 435.2, 435.3, 435.8, 235.9, 436, 437.1
Bile leak	576.4
Hip fracture	820, 820.0, 820.00, 820.01, 820.02, 820.03, 820.09, 820.10, 820.11, 820.12, 820.13, 820.19, 820.20, 820.21, 820.22, 820.30, 820.31, 820.32, 820.8, 820.9, 821.00, 821.10

Assessment of Readmissions and Diagnoses

We defined readmission as the number of patients who were discharged from an acute care hospital and readmitted to the hospital within (1) 30 days (early) or (2) between 30 days and 1 year (late) from the date of discharge from the index admission for pancreatic resection. To account for a decrease in the number of patients at risk in each time period as a result of tumor- and operative-related deaths, a Kaplan–Meier analysis modeling the time to readmission was used to obtain accurate readmission rates. We cannot directly identify patients that were transferred from one acute care hospital to another acute care hospital or rehabilitation facility. Therefore, we excluded patients who were readmitted on the same day they were discharged, assuming these represented hospital to hospital transfers. In many cases, patients were readmitted more than one time over the 1-year time period.

A record was created for each readmission including the first seven discharge diagnosis codes and the first seven procedure codes for each hospitalization. Many patients were readmitted more than one time. On examining the reasons for readmissions, it was clear that reasons for readmission were clustered among multiple readmissions in the same patient. Over 95% of multiple readmissions in a single patient were for the same or related diagnoses. For this reason, we evaluated only the first readmission. For example, if a patient was readmitted for the first time in the early time period and again in the late time period, only the readmission in the early time period was reexamined. We also evaluated late readmission using a conditional repeated events analysis, and the conclusions did not change. We report the former.

Each readmission record was independently reviewed by two authors. After examining the diagnosis and procedure codes, each readmission was assigned a primary reason for the admission. The proportion of readmissions clearly related to postoperative complications was reported. However, these were subject to the reviewers’ interpretation. Therefore, we also report the frequency of specific diagnoses based on the appearance of the ICD-9 diagnosis code anytime during admission. Each readmission record was queried to identify the incidence of several specific diagnoses and procedures present. The incidence of each diagnosis or procedure in each time period was calculated by identifying the frequency of the ICD-9 codes for each respective diagnosis or procedure and dividing this number by the number of first readmissions during the same time period. These diagnoses need only be present in the readmission diagnosis codes but did not need to be the primary reason for readmission. As such, they do not add up to 100%.

The ICD-9 codes used to identify specific procedures and diagnoses are shown in Table 1. Specific procedures evaluated included upper endoscopy with or without intervention and biliary drainage via a percutaneous, endoscopic, or operative approach. Specific diagnoses evaluated included operative complications, metastatic disease, dehydration, gastric outlet obstruction/delayed gastric emptying, venous thromboembolism (VTE) and/or pulmonary embolus (PE), pneumonia, cholangitis, small bowel obstruction, gastritis/duodenitis/gastric ulcer/duodenal ulcer/marginal ulcer, incisional hernia, pancreatic pseuodcyst, acute myocardial infarction, cerebrovascular accident, bile leak, and hip fracture.

Statistical Analysis

SAS version 9.1.3 (Cary, NC) was used for all statistical analyses. Descriptive statistics were reported for the patient demographics, operative details, the in-hospital and 30-day mortality, the number of patients requiring readmission (total, within 30 days, and between 30 days and 1 year), number of total readmissions in each time period, the primary reason for each readmission, and the incidence of specific diagnoses during readmissions. The diagnoses during readmission were compared between the early and late readmission groups using univariate statistics (chi-square, Fisher’s exact test).

Kaplan–Meier survival curves were used to determine readmission rates over the first year. Deaths related to pancreatic cancer were censored at their time of death if death occurred within the first year of discharge and prior to any readmission. Within 30 days of discharge, there were only 13 deaths (11 occurring without a previous readmission), so death was not a significant competing event. Beyond 30 days, the number of deaths increased with time, and death became a significant competing cause. We used a Cox proportional hazards model with deaths treated as censored values to assess patient-level predictors of readmission within 30 days. Between 30 days and 1 year, we excluded patients who died or were readmitted within the first 30 days. We then used two separate Cox models: the first treated deaths within the first year as censored and the second treated deaths as a competing cause. The patient-level factors determining late readmission in each model were analyzed. The assumption of proportionality was tested using Schoenfeld residuals. Significance was accepted at the P < 0.05 level.

Results

Overall Cohort

Between 1992 and 2003, 1,730 subjects met the inclusion criteria for the study. The demographic data, type of procedure, number of in-hospital deaths, postoperative length of stay, 30-day mortality rate (including in-hospital deaths), and stage of disease for the overall cohort are shown in Table 2. The mean age of the study population was 72.6 ± 6.4 years. Forty-eight percent of patients were male and 82% were white. The location of the tumor dictated the type of procedure performed. Pancreaticoduodenal resections were performed in 76% of patients, distal pancreatectomy in 18% of patients, total pancreatectomy in 3% of patients, and 3% underwent pancreatectomy not otherwise specified. The median postoperative length of stay for all patients was 14 days (25th percentile = 10 days, 75th percentile = 21 days).

Table 2

Demographics of Overall Cohort (N = 1,730)

	Number of patients	Percent
Age at surgery	1,730	72.6 ± 6.4 years
Gender
Male	822	48%
Female	908	52%
Race
White	1,427	82%
Black	132	8%
Hispanic	74	4%
Other	97	6%
Marital status
Married	1,044	60%
Single	250	14%
Widowed	380	22%
Unknown	56	3%
Charlson comorbidity score
0	1,108	64%
1	411	24%
2	138	8%
3 or more	73	4%
Type of procedure
Pancreaticoduodenal resection	1,309	76%
Distal pancreatectomy	311	18%
Total pancreatectomy	62	3%
Pancreatectomy, not otherwise specified	48	3%
Stage of disease
Locoregional	1,493	86%
Distant/unknown	237	14%
Postoperative length of stay	1,730	17.5 ± 11.6 days
In-hospital mortality	130	7.5%
30-day mortality	143	8.3%

Among the 1,730 patients, there were 130 in-hospital deaths (7.5%) following surgery, leaving a total of 1,600 patients with the potential for readmission. The 30-day mortality was 8.3% (including in-hospital mortalities); 13 patients died after the first discharge but within 30 days.

Overall Readmissions

Of the 1,600 patients with the potential for readmission, 784 patients were readmitted a total of 1,766 times within the first year of discharge. Three hundred twenty-six patients were readmitted once, 211 patients were readmitted twice, 117 patients were readmitted three times, and 130 patients were readmitted four or more times. Figures 1a and 1b are Kaplan–Meier curves showing the time to readmission over the first year following discharge. Operative deaths are censored in Fig. 1a and treated as competing events in Fig. 1b. In addition to the survival curve, Fig. 1c depicts the number at risk in each time period, the cumulative readmissions at the end of each time period, the cumulative deaths without readmission at the end of each time period, and the Kaplan–Meier estimates for readmission rates at the same time points. The Kaplan–Meier curve shows a 15.5% readmission rate at 30 days and a 52.6% readmission rate at 1 year.

Figure 1

Kaplan–Meier curves showing the time to readmission over the first year following initial discharge after pancreatectomy in Medicare patients. a Kaplan–Meier curve for time to readmission with deaths treated as censored. b Kaplan–Meier curve for time to readmission with deaths treated as a competing event. c The table shows the patients at risk at five different time intervals over the first year following discharge, the cumulative readmissions, and the cumulative deaths for five time periods, and the Kaplan–Meier estimates of readmission rates as well as combined readmission and death rates.

The mean duration for readmission was 8.8 ± 9.7 days (median = 6 days). Readmissions accounted for 15,409 additional hospital days in the 784 patients.

Early Readmissions

Within 30 days after discharge, 248 patients (16%) who survived the initial hospitalization were readmitted a total of 320 times; 190 patients were readmitted once, 46 patients were readmitted twice, and 12 patients were readmitted three or more times. When evaluating the individual reason for each readmission (first readmission only), 80% were related to operative complications and included abscess, sepsis, hemorrhage, probable pancreatic fistula, GI bleed, UTI, pneumonia, respiratory failure, and VTE/PE. When looking for specific ICD-9 codes, the most common diagnosis codes noted during readmission were for operative complications (27.4%), dehydration (27.8%), and gastric outlet obstruction/delayed gastric emptying (8.1%). Of the patients, 19.4% had a diagnosis code for metastatic disease, but this was often not the primary reason for admission. A complete list of diagnoses noted during early readmission is shown in Table 3.

Table 3

Comparison of Reasons: Early vs. Late

	Early (N = 248)	Late (N = 536)	P value
	Number (%)	Number (%)	<0.0001
Operative complications	68 (27.4)	20 (3.7)	<0.0001
Metastases	48 (19.4)	236 (44.0)	<0.0001
Dehydration	69 (27.8)	125 (23.3)	0.17
Gastric outlet obstruction/delayed gastric emptying	20 (8.1)	21 (3.9)	0.02
VTE/PE	12 (4.8)	49 (9.1)	0.04
Pneumonia	<11	32 (6.0)	0.10
Cholangitis	14 (5.6)	32 (6.0)	0.86
Small bowel obstruction	11 (4.4)	35 (6.5)	0.24
Gastritis/duodenitis/gastric ulcer/duodenal ulcer/marginal ulcer	15 (6.0)	34 (6.3)	0.87
Incisional herniaa	0 (0%)	<11 (<2.1%)	0.09
Pancreatic pseudocyst	<11 (<4.4%)	<11 (<2.1%)	0.21
Acute myocardial infarction	<11 (<4.4%)	<11 (<2.1%)	0.91
Cerebrovascular accident	<11 (<4.4%)	<11 (<2.1%)	0.93
Bile leakb	<11 (<4.4%)	0 (0%)	0.04
Hip fracturea	0 (0%)	<11 (<2.1%)	0.03
Esophagogastroduodenoscopy and related procedures	22 (8.9)	71 (13.3)	0.08
Biliary drainage (endoscopic, percutaneous, or operative)	15 (6.1)	49 (9.1)	0.14

aBoth groups <11 patients but significantly higher incidence of incisional hernias and hip fractures in the late readmission group.

bBoth groups <11 patients but significantly higher incidence of bile leaks in early readmission group.

Late Readmissions

There were 688 patients readmitted a total of 1,446 times between 30 days and 1 year following the initial pancreatectomy. Of the 688 patients, 152 were also readmitted within the first 30 days following surgery, leaving 536 patients in the late group at risk for first readmission. Late readmission was related to recurrence in 48%, operative complications in 25%, and unrelated diagnoses in 27% of cases. The diagnoses recorded during readmission in this time period differed significantly from the reasons observed in the first 30 days following discharge (Table 3). The most common diagnoses during late readmissions were metastatic disease (44.0%), dehydration (23.3%), and VTE/PE (9.1%).

Comparison of Reasons for Early and Late Readmissions

We compared the incidence of specific diagnoses during readmission in the early and late readmission groups. These diagnoses may not have been the primary reason for readmission. When compared to patients in the late readmission group, patients readmitted early were more likely to be readmitted with a diagnosis of postoperative complications, gastric outlet obstruction/delayed gastric emptying, and pancreatic pseudocyst. They were less likely to be readmitted with metastatic disease, VTE/PE, and hip fractures (Table 3). The incidence of dehydration was similar between the two groups; however, in the late group, this diagnosis is more related to metastatic disease and failure to thrive, whereas in the early group, it is related postoperative complications.

Cox Proportional Hazards Model: Factors Predicting Early Readmission

The year of surgery, age, race, sex, marital status, income, education, Charlson comorbidity score, type of operation, complications recorded in the billing records for the initial hospitalization, postoperative length of stay (<10 days or ≥10 days), tumor stage, and nodal status were included in all multivariate models. For early readmissions, only the type of operation and the postoperative length of stay (LOS) predicted readmission. Patients undergoing distal pancreatectomy had a hazard ratio (HR) for readmission of 1.66 (95% CI, 1.19–2.33) when compared to those undergoing pancreaticoduodenectomy. Patients undergoing total pancreatectomy and pancreatectomy not otherwise specified had the same likelihood of readmission as patients undergoing pancreaticoduodenal resection. Patients with an initial postoperative LOS of ≥10 days had a HR for readmission of 1.46 (95% CI, 1.04–2.05). A recorded diagnosis code for operative complications during initial hospitalization (see methods) did not predict survival. The final model is shown in Table 4.

Table 4

Cox Proportional Hazards Model: Factors Associated with Early Readmission

Factor (reference group)	HR	95% CI	Type 3, P value
Length of stay ≥10 days (<10 days)	1.46	1.04–2.05	0.03
Operation (pancreaticoduodenectomy)			0.02
Distal pancreatectomy	1.66	1.19–2.33
Total pancreatectomy	1.29	0.67–2.46
Other pancreatectomy	0.76	0.31–1.88
Operative complications initial stay (yes)	0.98	0.71–1.34	0.91
Age (per year of age)	1.00	0.98–1.02	0.78
Year of surgery (per year)	1.04	1.00–1.08	0.07
Gender (male)	0.87	0.66–1.14	0.30
Race (non-Hispanic white)			0.20
Non-Hispanic black	1.03	0.62–1.70
Hispanic	0.29	0.09–0.91
Marital status (married)			0.92
Single	1.05	0.71–1.56
Widowed	1.08	0.77–1.51
Highest income quartile (1 = lowest)			0.18
2	0.86	0.58–1.26
3	0.67	0.47–1.04
4	0.61	0.38–0.99
Highest education quartile (1 = lowest)			0.25
2	1.28	0.85–1.93
3	1.31	0.84–2.03
4	1.67	1.01–2.75
Charlson comorbidity score (0)			0.39
1	1.06	0.77–1.44
2	1.45	0.95–2.23
3 or more	1.01	0.58–1.93
Tumor stage (distant)	0.82	0.56–1.18	0.28
Nodal status (negative)	0.98	0.74–1.30	0.98

For late readmissions, deaths due to pancreatic cancer became a significant competing cause. Figure 1b shows a Kaplan–Meier curve where death and readmission are both treated as events. The rate of readmission or death within the first year was 35% (Fig. 1c).

We ran multivariate Cox proportional hazards models, the first with deaths as censored values at the time of death and the second with deaths as a competing event (Table 5). Considering deaths as censored creates informative censoring, since the same factors that influence cancer deaths likely influence late readmissions. As a result, in the first model, treating deaths as censored, only Hispanic race and a Charlson score of 3 or more (Table 4) predicted readmission. In the model with death as a competing event, the presence of distant disease at the time of surgery, positive nodal status, a Charlson score of 3 or more, and an initial length of stay ≥10 days predicted readmission (Table 5).

Table 5

Cox Proportional Hazards Model: Factors Associated with Early Readmission

Factor (reference group)	Model with deaths censored	Model with deaths as competing cause
	HR (95% CI)
Race (non-Hispanic white)
Non-Hispanic black	1.21 (0.88–1.67)	1.13 (0.85–1.50)
Hispanic	0.42 (0.23–0.75)	0.69 (0.46–1.01)
Charlson comorbidity score (0)
1	1.12 (0.91–1.35)	1.09 (0.91–1.29)
2	1.06 (0.74–1.50)	0.98 (0.73–1.32)
3 or more	1.78 (1.18–2.68)	1.48 (1.04–2.12)
Tumor stage (distant)	0.82 (0.62–1.08)	0.71 (0.57–0.88)
Nodal status (negative)	1.19 (0.98–1.45)	1.30 (1.11–1.53)
Length of stay ≥10 days (<10 days)	1.14 (0.91–1.44)	1.23 (1.02–1.49)
Operation (pancreaticoduodenectomy)
Distal pancreatectomy	1.07 (0.83–1.38)	1.16 (0.95–1.43)
Total pancreatectomy	1.11 (0.68–1.81)	1.12 (0.75–1.66)
Other pancreatectomy	1.34 (0.83–2.17)	1.46 (0.98–2.18)
Operative complications initial stay (yes)	1.09 (0.87–1.37)	1.07 (0.88–1.28)
Age (per year of age)	0.98 (0.97–1.00)	1.00 (0.99–1.01)
Year of surgery (per year)	0.99 (0.97–1.02)	1.01 (0.98–1.03)
Gender (male)	0.84 (0.70–1.01)	0.99 (0.80–1.09)
Marital status (married)
Single	0.98 (0.75–1.28)	0.93 (0.74–1.16)
Widowed	1.08 (0.55–1.36)	1.03 (0.85–1.25)
Highest income quartile (1 = lowest)
2	0.83 (0.64–1.08)	1.01 (0.80–1.26)
3	0.80 (0.60–1.07)	1.01 (0.79–1.29)
4	0.69 (0.50–0.95)	0.91 (0.70–1.20)
Highest education quartile (1 = lowest)
2	1.27 (0.96–1.66)	1.10 (0.87–1.38)
3	1.19 (0.89–1.60)	1.02 (0.80–1.29)
4	1.19 (0.84–1.67)	1.00 (0.76–1.33)

Deaths or readmissions within 30 days were excluded. The first model treats deaths within the first year as censored. The second treats death as a competing event

Survival Analysis

Patients readmitted within 30 days of discharge had worse median survival (median = 11.8 months; 5-year survival, 18%) than patients not requiring readmission (median = 16.5 months; 5-year survival, 18%, p = 0.04, Fig. 2, N = 248). From the curves, you can see that this difference in mortality is early and likely attributable to postoperative complications. Patients surviving the insult of the postoperative complications have similar 5-year survival rates to those who did not suffer complications.

Figure 2

Kaplan–Meier actuarial survival curves showing comparing survival in patients who did not require readmission and those who were readmitted early (within 30 days, N = 248). When compared to patients not readmitted, patients readmitted early had worse median survival (11.8 vs.16.5 months, P = 0.04), but the long-term survival was identical (18%).

Readmission between 30 days and a year was associated with worse median survival (12.1 vs. 19.4 months) and 5-year survival (12% vs. 21%, p < 0.0001, Fig. 3, N = 536) when compared to those not requiring late readmission. As a quarter of late readmissions are related primarily to progression of disease requiring readmission, this is expected.

Figure 3

Kaplan–Meier actuarial survival curves showing comparing survival in patients who did not require readmission and those who were readmitted late (between 30 days and 1 year, N = 536). Late readmission was associated with worse median and long-term survival (19.4 vs. 12.1 months, 21% vs. 12%, P < 0.0001).

Multiple readmissions in the early time period were not correlated with survival. Multiple readmissions in the late time period were correlated with worse survival, presumably from recurrent disease requiring rehospitalization, whereas those who remained disease-free did not require hospital admission.

Discussion

Our study demonstrates an overall readmission rate of 53% and an early (within 30 days) readmission rate of 16% after pancreatectomy for pancreatic cancer in Medicare patients. The overall readmission rate, calculated using at time-to-event analysis, is similar to the 59% readmission rate in a previous population-based study22 and higher than the reported rates in previous single-institution studies.16,21 The higher rates in population-based studies more likely represent true readmission rates in the general population. Moreover, Yermilov and colleagues22 found that 47% of readmissions were not to the hospital performing the primary surgery. It is likely that the single-institution studies did not capture readmissions to outside hospitals and may grossly underestimate readmission rates even in their own patients. In addition, the non-time-dependent methods used in previous studies will inflate the denominator or number at risk in a given period, decreasing the observed readmission rates.

As hypothesized, the length of the time period elapsed since undergoing pancreatectomy determined the reason for readmission. Early readmissions were more commonly associated with postoperative complications, while late readmission after 30 days was more likely to be due to disease progression (metastases or recurrence).

Dehydration occurred in approximately one quarter of patients in both the early and late groups. When evaluating diagnosis codes concurrent with dehydration, dehydration was more commonly related to surgical complications in the early readmission group while dehydration in the late group was more commonly related to chemotherapy or recurrence of pancreatic cancer and general failure to thrive. Likewise, the nature of postoperative complications differed between the early and late groups. Postoperative complications requiring early readmission most commonly included sepsis, abscess, anastomotic leak, and acute hemorrhage, whereas late complications included small bowel obstruction, incisional hernias, biliary strictures, and cholangitis. A diagnosis of delayed gastric emptying or gastric outlet obstruction was seen in 8% of early readmissions and 4% of late readmissions. Similar to dehydration, the reasons for the delayed gastric emptying or gastric outlet obstruction differed between the early and late groups. Early delayed gastric emptying following pancreaticoduodenectomy has been reported in 10–20% of patients immediately following pancreatic resection3,25 and accounts for the majority of delayed gastric emptying or gastric outlet obstruction in the early group. In the late group, however, this diagnosis was associated with gastric outlet obstruction secondary to tumor recurrence.

Only the initial length of stay and the type of resection predicted early readmission. Those who had an initial length of stay of ten or more days were more likely to require early readmission. A diagnosis code for operative complications did not predict readmission. This suggests two things: first, not all operative complications are noted during initial admission and second, not all complications lead to readmission. A prolonged initial length of stay does not cause readmission; rather, it is likely a marker of serious postoperative complications, the most common diagnosis during early readmission. In addition, longer lengths of stay predispose patients to developing additional iatrogenic infections, as well as VTE/PE and atelectasis associated with prolonged immobility, which typically occur in a hospital setting. There was no association of age or patient comorbidities with early readmission.

This is the first study to demonstrate that patients undergoing distal pancreatectomy have an increased risk of readmission. This is unexpected as pancreaticoduodenectomy is a more complex procedure and thought to be fraught with more complications. However, pancreatic fistula rates have been reported to be higher following distal pancreatectomy than pancreatic head resection.26–28 This fact, coupled with the fact that distal pancreatectomy is less likely to be performed at high-volume centers by experienced surgeons,8 likely contribute to this finding.

In the first year after initial discharge, deaths due to pancreatic cancer became a significant competing event. Considering deaths as censored creates informative censoring, since the same factors that influence cancer deaths, likely influence late readmissions. As a result, the multivariate model evaluating the factors associated with late readmission, which treated deaths as censored, does not demonstrate the same predictive factors as the model that treats death as a competing event. By treating deaths a censored, patients with advanced tumor stage (distant disease and positive nodes) are removed from the at risk cohort. However, these factors are related to recurrence, the most common reason for readmission, and would likely have led to readmission in the absence of death.

While the median survival was lower in patients requiring early readmission compared to those who did not, the long-term survival was identical at 18%, suggesting that operative complications increase early deaths. However, survivors of these complications can expect similar survival to their counterparts who had an uncomplicated postoperative course. Late readmission is more commonly due to recurrence and is a marker of early mortality. As expected, it was associated with significantly worse median and long-term survival as shown previously.22

This study has several limitations, mostly related to the use of administrative data. The reported reasons for readmission in Table 3 were based on identification of specific ICD-9 diagnosis codes both in the primary discharge diagnosis and additional diagnoses provided for the same discharge. We also individually reviewed each readmission record and looked at the diagnosis and procedure codes and gave each readmission a primary reason for the admission. The results were similar using the two methods, in that early readmissions were related to surgical complications and late readmissions were related to recurrence; however, these were subject to the reviewers’ interpretation.

It is often difficult to identify specific complications commonly reported after pancreatic surgery using administrative data, including pancreatic fistula and bile leak. For example, there are codes for postoperative complications and anastomotic leak, but they are not specific. In addition, the administrative data is used for billing purposes, so diagnosis codes mandating reimbursement may be more likely to be coded. While we were able to look at nodal status, data were not available on margin status to evaluate its effect on early and late readmission.

In summary, this study demonstrates the rates and the most frequent causes of early and late readmissions and identifies predictors of hospitalization during these time periods after initial discharge following pancreatectomy for pancreatic cancer. These findings reinforce the finding that readmission rates in the general population following pancreatectomy occur in over 50% of patients and are underreported in single-institution studies. Additionally, this study delineates the factors contributing to early and late readmissions. It demonstrates that early readmission related to complications shortens median but does not affect long-term survival if the patient survives the operative complication. Late readmissions are a marker of early mortality. Death due to cancer is a competing event with late readmission. As such, the factors influencing late readmission are similar to those that predict early mortality. The 15% of readmissions related to operative complications are, therefore, potentially preventable. The reasons for early readmissions need to be studied further to identify individual factors and operative techniques that decrease these preventable readmissions.