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Accelerated Recovery Pathway for Discharge After Surgery in Patients With Pancreatic Cancer

Not Applicable
Completed
Conditions
Pancreatic Carcinoma
Interventions
Procedure: Pancreaticoduodenectomy
Registration Number
NCT02517268
Lead Sponsor
Sidney Kimmel Cancer Center at Thomas Jefferson University
Brief Summary

This randomized clinical trial studies accelerated recovery pathway for discharge after surgery in patients with pancreatic cancer. A standardized accelerated recovery pathway may improve outcomes after surgery following complex abdominal operations resulting in a shorter length of stay in patients with pancreatic cancer. It may also help patients to mobilize more quickly and return to the home setting, decrease hospital-acquired infectious complications, and increase potential cost savings. It is not yet known whether an accelerated recovery pathway is better than a standard recovery pathway for discharge following surgery in patients with pancreatic cancer.

Detailed Description

PRIMARY OBJECTIVES:

I. The use of an accelerated pathway will result in a shorter postoperative hospital length of stay for patients undergoing pancreaticoduodenectomy (PD) without an increase in perioperative complications or readmission rates.

SECONDARY OBJECTIVES:

I. The investigators anticipate lower cost, lower readmission rate, similar rate of post-operative complications (delayed gastric emptying \[DGE\], anastomotic leaks, intra-abdominal abscesses, wound infection, urinary tract infection \[UTI\], respiratory compromise, renal failure, etc.) in our study group.

OUTLINE: Patients are randomized to 1 of 2 treatment arms.

ARM I: Patients follow the standard 7-day pathway at the end of surgery.

ARM II: Patients follow the Whipple accelerated 5-day pathway at the end of surgery. The accelerated pathway includes more rapidly leaving the ICU setting, early mobilization and enhanced physical therapy, multimodal pain control, dietary modifications, and increased and standardized phone contact by a nurse practitioner during the first week following hospital discharge.

After completion of study treatment, patients are followed up periodically.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
98
Inclusion Criteria
  1. Pancreaticoduodenectomy
  2. Firm gland texture
  3. Subjects able to provide informed consent
Exclusion Criteria
  1. Preoperative factors:

    • Congestive heart failure (CHF)
    • End stage renal disease (ESRD)
    • Chronic obstructive pulmonary disease (COPD)
    • Pregnancy
    • Albumin < 3 gm/dL
    • Poor preoperative performance status as defined by: timed get up and go (< 15 seconds)
    • Patients cannot be homeless or have substance dependence
  2. Intraoperative factors:

    • Estimated blood loss (EBL) > 1 liter
    • Failure to extubate at the conclusion of the case
    • Operative time > 8 hours
    • Need for vascular resection/reconstruction

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Accelerated 5-Day PathwayPancreaticoduodenectomyPatients follow the Whipple accelerated 5-day pathway following pancreaticoduodenectomy. The accelerated pathway includes more rapidly leaving the ICU setting, early mobilization and enhanced physical therapy, multimodal pain control, dietary modifications, and increased and standardized phone contact by a nurse practitioner during the first week following hospital discharge.
Standard 7-Day PathwayPancreaticoduodenectomyPatients follow the standard 7-day pathway following pancreaticoduodenectomy
Primary Outcome Measures
NameTimeMethod
Percentage of Patients Discharged by Post-operative Day 5Up to post-operative day 5

Two-sided alpha 0.05 will be used to detect a increase in the percentage of patients discharged on post-operative day 5

Secondary Outcome Measures
NameTimeMethod
Post-operative Median Length of Stay30 days after operation
Readmission Rate30 days after operation
Cost30 days after operation

Cost will be assessed by reviewing inpatient hospital charges

Incidence of Post-operative Complications (DGE, Anastomotic Leaks, Intra-abdominal Abscesses, Wound Infection, UTI, Respiratory Compromise, Renal Failure, Etc.)30 days after operation

Trial Locations

Locations (1)

Thomas Jefferson University

🇺🇸

Philadelphia, Pennsylvania, United States

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