Investigators will identify patients with AP based on the 2012 revised Atlanta
criteria for diagnosis, i.e., AP is diagnosed if 2 out of the following 3 criteria
are met:
Acute onset of persistent, severe, epigastric pain often radiating to the back,
Elevation in serum lipase or amylase to three times or greater than the upper limit
of normal,
Characteristic findings of acute pancreatitis on imaging (contrast-enhanced computed
tomography [CT], magnetic resonance imaging [MRI], or transabdominal
ultrasonography).
Patients will be recruited for participation in this study while they are
hospitalized with AP at Beth Israel Deaconess Medical Center. Once the patient has
been transferred from the emergency department to the hospital floor, we will
identify and recruit them for participation in our study.
After obtaining informed consent from the patient, the patient will be enrolled by
simple randomization to either the PCA or the PDA arm of the study. The research
staff will assign patients to either the PCA arm or the PDA arm based on a standard
randomization. Once, a patient has consented, the research staff will assign them to
the next sequential study identidication number and corresponding study arm and let
the attending hospitalist know of the result. The patient will then be enrolled in
their assigned arm.
The initial protocol for analgesic administration in each arm is as follows:
Recommended algorithm for physician directed analgesia (PDA) arm:
IV Hydromorphone 0.4 mg every 4 hours PRN for pain 4-6
IV hydromorphone 0.6 mg every 2 hours PRN for pain 7-10
Rescue IV hydromorphone 0.4 mg every 2 hours PRN for pain 4-10 = only to
be given as a 'rescue dose' if patient has persistent pain despite using
every 4 hours PRN IV hydromorphone (breakthrough pain)
Maximum opioid dosing: 1 mg per hour and 3 mg of IV hydromorphone per 4
hours
If patient has received more than 2 rescue doses for breakthrough pain in
12 hours or is in uncontrolled pain: Hospitalist's recommended step-up
orders: IV hydromorphone 0.8 mg every 4 hours PRN 4-6
Recommended algorithm for patient controlled analgesia (PCA) arm:
IV Hydromorphone 0.1 mg every 10 minutes
Rescue IV hydromorphone 0.4 mg every 2 houra PRN for pain 4-6,
hydromorphone 0.6 mg every 2 hours PRN for pain 7-10 = only to be given as
a 'rescue' dose for if patient has persistent pain despite using PCA
(breakthrough pain)
Maximum opioid dosing: 1 mg per hour and 3 mg of IV hydromorphone per 4
hours
If patient has received more than 2 rescue doses for breakthrough pain in
12 hours or is in uncontrolled pain: Hospitalist's recommended step-up
orders: IV hydromorphone 0.2 mg every 10 minutes
Recommended for all patients:
PO Acetaminophen 1000 mg every 8 hours scheduled
IV Naloxone 40-80 mcg PRN for respiratory depression (RR<10) or
significant somnolence
PO Benadryl 25mg every 4 hours PRN moderate to severe pruritis
Recommended algorithm for transition to oral:
PO Oxycodone 5mg every 4 hours PRN for pain 4-6
PO Oxycodone 10mg every 4 hours PRN for pain 7-10
Rescue PO Oxycodone 5mg every 2 hours PRN for pain 4-10 = only to be given
as a 'rescue dose' if patient has persistent pain despite using every 4
hours PO oxycodone (breakthrough pain)
Dosing and frequencies of medications in the above algorithms are recommendations.
The recommended doses are not required for maintenance in the study and we
anticipate that they may change given patient characteristics and variable response
to medication, the rapidly evolving nature of acute pancreatitis, and hospitalist
preferences. However, the mode of IV opioid administration (PDA vs PCA) should
remain as assigned until transition to PO opioid.
Each patient will be closely monitored for adverse events related to opioid
administration to include cardiorespiratory decompensation, hemodynamic instability,
nausea, vomiting, confusion, altered mental status, headache, drowsiness, etc. This
monitoring will include continuous pulse oximetry in addition to vital sign
measurement every 4 hours.
The efficacy of each treatment arm to adequately control the patient's pain will be
assessed with scheduled use of the Numeric Rating Scale (NRS) every 4 hours by the
nursing staff. Pain rating on the NRS will be documented by the nursing staff after
each assessment. In an NRS, patients are asked to circle the number between 0 and 10
that fits best to their pain intensity. Zero usually represents 'no pain at all'
whereas 10 represents 'the worst pain ever possible'.
Likert scale of 1 to 10 (1 = Very poor, 10= excellent) will be used to grade overall
patient satisfaction with pain control.
Once each patient's pain is well controlled on IV opioid administration (as
determined by the attending physician) and they can tolerate intake by mouth,
transition from IV to PO opioid medication can be made in each arm by the attending
physician. If the patient is unable to tolerate either the PDA or the PCA arm for
any reason and requires switching over to the other arm as part of his/her clinical
care, they will be withdrawn from the study and their data will be excluded while
analyzing the results. AP has a variable course and may require IV opioids after
transition to PO opioids. The modality of IV opioid administration will revert to
the assigned treatment arm.
Other aspects of each patient's routine clinical care will continue as per the
attending physician under whom the patient is admitted regardless of treatment arm
status (PDA vs PCA).
At the end of their hospital stay, investigators will document study outcomes.
Investigators expect to enroll patients over a 36-month period from the start date
of the study. Based on this, investigators expect patient enrollment to end by
4/30/2024. Investigators will plan to perform data analysis at two points: 1.
Interim data analysis at a predetermined point in the study (mid-point of study),
and 2. At the end of the study once patient enrollment has been completed.