Opiate potency chart. Understanding Opioid Equivalency: A Comprehensive Guide to Pain Management

17.03.202126.07.2023 by alexxlab

How do opioids work for pain management. What are the different types of opioids available. Which opioids are preferred in specific clinical settings. How is opioid equivalency calculated and why is it important. What are the key factors to consider when switching between opioids. How can healthcare professionals ensure safe and effective opioid use.

Содержание

The Basics of Opioid Therapy and Pain Management

Opioids play a crucial role in managing moderate to severe pain, particularly in cases where non-opioid therapies prove inadequate. These potent analgesics are commonly prescribed for cancer-related pain and chronic pain conditions. However, their use requires careful consideration and monitoring due to their potential for side effects and addiction.

Understanding opioid equivalency is essential for healthcare professionals to provide effective pain management while minimizing risks. This concept allows for the safe conversion between different opioid medications, ensuring patients receive appropriate dosages when switching from one opioid to another.

What are opioids and how do they work?

Opioids are a class of drugs that interact with opioid receptors in the brain and nervous system to produce pain-relieving effects. The majority of clinically useful opioid analgesics primarily bind to mu-opioid receptor sites, where they exert agonist effects. This shared mechanism of action is what allows for the interchangeability of different opioids, provided the doses are adjusted for relative potency.

Common opioids used in clinical practice

Morphine
Hydromorphone
Fentanyl
Oxycodone
Hydrocodone
Methadone

Opioid Selection in Various Clinical Settings

The choice of opioid medication often depends on the specific clinical situation and patient characteristics. The FDA has provided recommendations for opioid selection in various settings:

Mechanical ventilation

For patients on mechanical ventilation, fast-acting and titratable opioids are preferred. Fentanyl, morphine, and hydromorphone are commonly used in this setting. In cases where early extubation is expected, remifentanil may be considered due to its ultrashort duration of action.

Post-extubation pain management

After extubation, patients with moderate to severe non-neuropathic pain can benefit from IV fentanyl, morphine, or hydromorphone. These agents can be easily titrated to provide appropriate analgesia without excessive central nervous system depression.

Renal and hepatic insufficiency

For patients with impaired renal or hepatic function, IV fentanyl or hydromorphone are often better choices, with dose adjustments as needed. In cases of severe multiorgan failure, remifentanil may be considered as its metabolism is independent of hepatic or renal function.

Hemodynamic instability

Fentanyl or remifentanil are preferred in patients with hemodynamic instability. Morphine is typically avoided in these cases due to its potential to cause histamine release, which could exacerbate hypotension.

Bronchospasm

In patients prone to bronchospasm, fentanyl or hydromorphone are preferred over morphine. These agents cause less histamine release, reducing the risk of bronchial constriction.

Routes of Opioid Administration

Opioids can be administered through various routes, each with its own advantages and considerations:

Intravenous (IV) administration

IV administration is commonly used for acute pain relief, particularly in hospital settings. It allows for rapid onset of action and easy dose titration.

Oral (PO) administration

Oral opioids are available in both short-acting and long-acting formulations. Short-acting opioids are typically dosed every 3 to 4 hours, while long-acting formulations can be given every 8 to 12 hours.

Transdermal (TD) administration

Transdermal patches, such as those containing fentanyl, can provide continuous pain relief for patients requiring chronic analgesia. This route is particularly useful for patients who have difficulty swallowing or maintaining oral medication regimens.

Other routes

Intramuscular (IM) and subcutaneous (SQ) routes are less commonly used. IM administration is generally not recommended for pain management, while SQ administration is limited to specific circumstances, such as when IV access is unavailable.

Understanding Opioid Equivalency

Opioid equivalency is a critical concept in pain management that allows healthcare providers to switch between different opioid medications safely and effectively. It involves comparing the analgesic potency of various opioids to a standard reference, usually morphine.

Why is opioid equivalency important?

Opioid equivalency serves several crucial purposes:

Facilitates safe transitions between different opioid medications
Helps prevent under- or over-dosing when changing opioids
Allows for more precise pain management in opioid-tolerant patients
Aids in the development of individualized treatment plans

How is opioid equivalency calculated?

Opioid equivalency is typically expressed as a ratio comparing the potency of a given opioid to morphine. For example, if Drug A has an equivalency ratio of 2:1 to morphine, it means that 1 mg of Drug A is equivalent in analgesic effect to 2 mg of morphine.

To calculate equivalent doses when switching between opioids:

Determine the total daily dose of the current opioid
Convert this dose to its morphine equivalent using established conversion factors
Calculate the equivalent dose of the new opioid using its conversion factor
Adjust the calculated dose based on individual patient factors and clinical judgment

Factors Influencing Opioid Equivalency

While opioid equivalency charts provide a useful starting point, several factors can influence the actual equivalency in clinical practice:

Individual patient variability

Patients may respond differently to various opioids due to genetic factors, metabolism, and other individual characteristics. This variability necessitates careful monitoring and dose adjustments when switching between opioids.

Incomplete cross-tolerance

When switching between opioids, incomplete cross-tolerance can occur, meaning that the new opioid may have a stronger effect than expected based on equivalency calculations alone. To account for this, it’s often recommended to reduce the calculated equivalent dose by 25-50% when switching to a new opioid.

Route of administration

The route of administration can affect opioid bioavailability and, consequently, its potency. For example, oral morphine has lower bioavailability compared to intravenous morphine, necessitating higher oral doses to achieve the same analgesic effect.

Duration of action

When converting between immediate-release and extended-release formulations, consideration must be given to the differences in duration of action and dosing frequency.

Safe Practices in Opioid Rotation

Opioid rotation, or switching from one opioid to another, requires careful consideration and adherence to best practices to ensure patient safety and effective pain management.

Steps for safe opioid rotation

Assess the current pain management regimen and reasons for switching
Calculate the equivalent dose of the new opioid using established conversion factors
Reduce the calculated dose by 25-50% to account for incomplete cross-tolerance
Initiate the new opioid at the adjusted dose
Closely monitor the patient for efficacy and side effects
Titrate the dose as needed based on patient response

Monitoring after opioid rotation

After initiating a new opioid, it’s crucial to monitor patients closely for:

Pain control: Assess whether the new regimen adequately manages the patient’s pain
Side effects: Watch for common opioid side effects such as constipation, nausea, and sedation
Signs of opioid toxicity: Monitor for respiratory depression, excessive sedation, or confusion
Withdrawal symptoms: In cases of significant dose reduction, be alert for signs of opioid withdrawal

The Role of the Interprofessional Team in Opioid Management

Effective opioid management requires a coordinated effort from an interprofessional healthcare team. Each member plays a crucial role in ensuring safe and effective pain management while minimizing the risks associated with opioid use.

Key team members and their roles

Physicians: Prescribe opioids, develop treatment plans, and oversee overall patient care
Nurses: Administer medications, monitor patients for efficacy and side effects, and provide patient education
Pharmacists: Review medication regimens, provide dosing recommendations, and educate on potential drug interactions
Pain specialists: Offer expertise in complex pain management cases and advanced interventions
Mental health professionals: Address psychological aspects of pain and monitor for signs of substance abuse
Physical therapists: Provide non-pharmacological pain management strategies and functional assessments

Importance of team communication

Effective communication among team members is essential for successful opioid management. Regular case discussions, shared electronic health records, and clear documentation of treatment plans and patient responses all contribute to improved patient outcomes and safety.

Challenges and Considerations in Opioid Equivalency

While opioid equivalency is a valuable tool in pain management, it comes with several challenges and considerations that healthcare providers must navigate:

Limitations of equivalency charts

Opioid equivalency charts provide general guidance but may not account for individual patient variability or specific clinical scenarios. They should be used as a starting point rather than a definitive guide.

Risk of opioid misuse and addiction

When rotating opioids or adjusting doses, there’s a potential risk of inadvertently contributing to opioid misuse or addiction. Healthcare providers must balance effective pain management with the need to minimize these risks.

Lack of standardization

Different sources may provide slightly different conversion factors, leading to potential confusion or inconsistencies in practice. It’s important to use reliable, up-to-date resources and maintain consistency within healthcare systems.

Complex pharmacokinetics

Some opioids, such as methadone, have complex pharmacokinetics that make simple linear conversions unreliable. These medications require specialized knowledge and careful monitoring during rotation.

Understanding opioid equivalency is crucial for healthcare professionals involved in pain management. By applying this knowledge carefully and considering individual patient factors, clinicians can improve pain control, minimize adverse effects, and enhance the quality of life for patients living with chronic pain. However, it’s essential to remember that opioid equivalency is just one tool in the comprehensive approach to pain management, which should also include non-pharmacological strategies and regular reassessment of treatment goals and outcomes.

Opioid Equivalency – StatPearls – NCBI Bookshelf

Continuing Education Activity

Opioids are often prescribed for cancer-related pain and moderate-to-severe chronic pain, especially pain that is inadequately controlled with non-opioid therapies. Clinicians can improve the lives of patients living with pain by applying knowledge regarding opioid equivalent dosing for opioid-tolerant patients eligible for opioid rotation. This activity reviews the importance of establishing and calculating opioid equivalence between various agents when making a therapeutic switch and the role of the interprofessional team in ensuring therapeutic and analgesic efficacy while simultaneously minimizing adverse events.

Objectives:

Describe the concept of opioid equivalence.
Outline the steps to take to establish opioid equivalence when changing agents.
Review the monitoring necessary after establishing therapy using opioid equivalence.
Summarize the importance of having all interprofessional team members coordinating their activities regarding opioid equivalence, pain control therapy, and preventing opioid misuse.

Access free multiple choice questions on this topic.

Indications

Opioids are often prescribed for cancer-related pain and moderate-to-severe chronic pain, especially when inadequately controlled with non-opioid strategies. Although morphine is the prototype opioid agent widely used in critically ill patients, it may not always be the first choice, as with other opioids.[1] Here are some of the clinical settings where certain opioid drugs are preferred over others, as per the FDA recommendations:

Patients receiving mechanical ventilation: Fentanyl, morphine, or hydromorphone are preferred because these opioids are fast-acting and titratable. Remifentanil may occasionally be selected if early extubation is expected as it has an ultrashort duration of action.

Patients who are extubated: In case of moderate-to-severe non-neuropathic pain in critically ill patients who have been extubated, IV fentanyl, morphine, or hydromorphone is preferred as these agents can easily be titrated, and patients can be given the appropriate analgesia without central nervous system depression.

Patients with renal and/or hepatic insufficiency: IV fentanyl or hydromorphone is a better choice, with dose adjustments as needed. Remifentanil may occasionally be considered in patients with severe multiorgan failure because its metabolism is independent of hepatic or renal function.

Patients with hemodynamic instability: Morphine is typically not advised in this case as it causes more histamine release, which could exacerbate hypotension, compared with fentanyl or remifentanil, which are preferred in these patients.

Patients with bronchospasm: Fentanyl or hydromorphone is preferred over morphine as they cause the lesser release of histamine compared to morphine.

Patients requiring frequent neurologic assessments: Remifentanil is preferred because of its ultrashort duration of action.

Patients requiring intermittent bolus opioid doses: Morphine or hydromorphone are preferred, especially when they have to endure a painful procedure because of their longer duration of action than fentanyl.

Patients who may benefit from oral, enteral, or transdermal opioid administration: Longer-acting oral opioids (e.g., methadone, extended-release oxycodone, extended-release morphine sulfate) can be used when nonintravenous forms are required, especially on discharge.

A transdermal route is possible for fentanyl, where chronic analgesia may be required.

Mechanism of Action

Mu Receptor Agonists: Dosing Challenges

The majority of clinically useful opioid analgesics bind primarily to mu-opioid receptor sites where they have agonist effects. Examples of these mu receptor agonists include morphine, hydromorphone, fentanyl, oxycodone, hydrocodone, and methadone. Because they act on the same receptor, these drugs are theoretically interchangeable, provided the doses are adjusted for relative potency.[2]

Administration

Routes for common opioids include intravenous (IV), intramuscular (IM), subcutaneous (SQ), Oral (PO), and transdermal (TD). Intramuscular administration is not recommended for pain management while using the SQ route is limited to circumstances such as lack of IV availability. The most common routes of administration of opioids are PO, IV, and TD. Oral short-acting opioids are dosed 3 to 4 hours apart due to their short half-life. Stable patients on chronic opioid therapy benefit from preventive analgesia and often have regimens that combine a long-acting opioid, dosed 8 to 12 hours apart, and a short-acting opioid, the latter being used as a breakthrough opioid when pain transiently increases in intensity above the pain addressed by the ongoing analgesics. Intravenous opioids are generally dosed for acute pain relief in situations where an oral opioid is ineffective, or the oral route is unavailable. Intravenous opioids are dosed 2 to 3 hours apart or can be dosed as a continuous infusion or as patient-controlled analgesia (PCA).

Adverse Effects

Adverse effects are common during opioid therapy. In particular, patients on opioids should be monitored for constipation, nausea, vomiting, sedation, impaired psychomotor function, and urinary retention. Among gastrointestinal side effects, opioid-induced constipation (OIC) affects between 45% and 90% of patients and is a source of significant morbidity.[3] It is the most prevalent reason patients avoid or discontinue opioids and can often result in an increased length of hospital stay and overall healthcare costs.[4][3][5][6][7][8] Nausea is seen most commonly at the start of therapy. Patients commonly develop tolerance to the emetic effects so that within 3 to 7 days, at a constant opioid dose, the emetic effects abate. While there is no research on this effect, morphine and codeine are often mentioned as the worst offenders.

Opioids also have neuroexcitatory effects that might not be easily recognized. Myoclonus is typically a herald symptom. Myoclonus, which is the uncontrollable jerking and twitching of muscles/muscle groups, most frequently occurs in the extremities, initially presenting with only an occasional random jerking movement. Myoclonus can present in patients on chronic therapy with most opioids, including hydromorphone, morphine, and fentanyl. Higher doses more frequently result in myoclonus, but the dose relationship is variable.[9] Myoclonus can occur with all routes of administration. As myoclonus worsens, patients may develop other neuroexcitatory signs: hyperalgesia (increased sensitivity to noxious stimuli), delirium with hallucinations, and eventually grand mal seizures. Treatment usually involves decreasing the opioid dose, opioid rotation, or the addition of a benzodiazepine.

Sedation occurs in 20% to 60% of patients, most commonly when initiating opioid therapy or when doses increase. [10] Mild-to-moderate sedation is usually self-limiting, resolving in a few days. If persistent, it may improve with drug therapy.[11] Moderate-to-severe sedation responds to dose reduction but may also necessitate opioid rotation.

Both pruritus and urinary retention are rare side effects. A combination of topical agents and/or systemic low-dose opioid antagonists is commonly used to treat pruritus. Acute urinary retention needs urgent medical attention; if it is related to the opioid, either the opioid dose can be reduced, or the agent discontinued.

Contraindications

The mu receptor agonists differ in their metabolism, and organ dysfunction can influence their side effect profile.[12] For example, in patients with renal impairment, fentanyl, oxycodone, or methadone are preferred, whereas morphine and hydromorphone are the favored agents for patients with severe liver disease.[13][14]

Monitoring

All patients on chronic opioid therapy regimens require monitoring for continued efficacy as well as an indication for treatment. Monitoring includes a thorough pain assessment that accounts for pain levels, changes in the quality of pain, pain recurrence, and side effects from analgesics. When a decision is made to rotate to a different opioid, there are essential pharmacokinetic principles to consider: equianalgesia and incomplete cross-tolerance.[1]

Equianalgesia and Incomplete Cross-tolerance

The term equianalgesia, meaning “approximately equal analgesia,” refers to the doses of various opioid analgesics that are estimated to provide the same pain relief. Equianalgesic dose calculations are a means for selecting the appropriate initial dosing when changing from one opioid agent or route of administration to another. An equianalgesic chart provides a list of analgesic doses, both oral and parenteral, which approximate each other in their ability to provide pain relief (i.e., the equianalgesic units). The equianalgesic chart (Table 1) lists rough estimates; individual patients may vary. Morphine is considered the gold standard; hence all calculations occur in Oral Morphine Equivalents (OME).

Most patients on chronic opioids develop tolerance to analgesic and non-analgesic effects of opioids such that a previously effective dose gradually loses efficacy. This is usually manifested as a shortened duration of action and often requires dose escalation to maintain adequate analgesia. Cross-tolerance is the development of tolerance to the effects of pharmacologically related drugs, particularly those that act on the same receptor site. However, when switching to another opioid, clinicians need to assume that cross-tolerance is incomplete, which means that the starting dose of the new opioid must be reduced by at least 50% of the calculated equianalgesic dose to prevent overdosing.[12]

Toxicity

Naloxone, a semisynthetic opioid antagonist, is indicated for the complete or partial reversal of life-threatening CNS/respiratory depression induced by opioids. Depending on the dose, naloxone administration to a physically dependent patient on opioids will cause an abrupt return of pain and can precipitate abstinence (withdrawal) syndrome, with symptoms ranging from mild anxiety, irritability, and muscle aches to life-threatening tachycardia and hypertension. [15] Newer peripherally acting opioid antagonists, methylnaltrexone, and naloxegol antagonize peripheral mu-opioid receptors and are used to treat refractory opioid-induced constipation.[16]

Enhancing Healthcare Team Outcomes

Opioid Calculation and Conversion Steps

Determine the total daily dose of the present opioid
Calculate the 24-hour OME: Add all scheduled and breakthrough opioid doses over 24 hours. Using the equianalgesic dose chart, determine the morphine equivalents of the current opioid. This will be the 24-hour equivalent of morphine. (24-hour OME = 24-hour dose of current opioid X 30 /Number of equianalgesic units in current opioid
Determine new opioid and route of administration: Using the equianalgesic dose chart, determine the 24-hour dosage of the new opioid. (24-hour dose of new opioid = Total OME X Equianalgesic units of new opioid / 30)
Decrease dose of new opioid due to incomplete cross-tolerance: Decrease dose of the new opioid by 50% to reach the final amount of the drug to be given
Develop a pain prescription

The following are some examples.

Case Example 1: Changing Route, Same Opioid

Ms. T is a patient with lung cancer and painful bony metastases who takes extended-release morphine 90 mg every twelve hours and has tolerated it well. She is admitted to the hospital for a planned stabilization procedure of lytic bony metastasis. She is likely to suffer from uncontrolled pain if she doesn’t take her scheduled Morphine doses.

Determine the total daily dose of current opioid: morphine 90 mg every twelve hours 90 +90 = 180 mg
Calculate the 24-hour OME: 180 mg OME per 24 hours
Determine new opioid and route of administration: The patient is NPO for surgery, and her oral morphine requirement is replaceable by a continuous infusion of morphine (24-hour dose of the new opioid = 180 X 10 / 30 = 60 mg)
Decrease dose of new opioid due to incomplete cross-tolerance: Since the new drug is unchanged, tolerance to the new formulation of the same drug will be the same. One does not need to decrease the dose.
Develop pain prescription: A continuous infusion of morphine IV would be 60 / 24 = 2.5 mg per hour. In clinical practice, an IV infusion of an opioid frequently allows patients to deliver an additional dose during episodes of pain escalation. The prescription would more likely be for a continuous infusion of 2 mg per hour with a patient capability of 0.5 mg or 1 mg every few minutes (typically 10-15 minutes). This is called patient-controlled analgesia (PCA).

Case Example 2: Rotating opioid, Keeping the Same Route

During her hospital stay, Ms. T develops acute renal failure from IV contrast during a procedure. To avoid toxicity from morphine in the setting of renal failure, you decide to switch her to an opioid that can be administered safely in cases of renal insufficiency, such as fentanyl or hydromorphone. On bedside assessment, her pain is well controlled, and she is receiving morphine IV continuous infusion at 2. 5 mg per hour.

Determine total daily dose of current opioid: (2.5 mg IV morphine per hour = 60 mg per 24 hours)
Calculate the 24-hour OME: 24-hour OME = 24-hour dose of current opioid X 30 /Number of equianalgesic units in current opioid. (24-hour OME for this patient is: 60 x 30 / 10 = 180 mg)
Determine new opioid and route of administration: Unlike morphine, IV hydromorphone has a short half-life and lacks clinically relevant metabolites, and is considered safer for patients with renal insufficiency. Total OME X Equianalgesic units of the new opioid / 30 = 24-hour dose of new opioid. (180 X 1.5 / 30 = 9 mg per 24 hours or 0.375 mg per hour)
Decrease dose of the new opioid due to incomplete cross-tolerance: While the patient is tolerant to morphine, her tolerance to hydromorphone is likely to be incomplete. Her hydromorphone dose will need to be decreased by 50%, which would be 0.1875 mg per hour.
Develop pain prescription: A close approximation to a measurable dose of IV hydromorphone to the amount calculated above is 0. 2 mg per hour. Similar to the solution above, the IV infusion of hydromorphone will allow an additional dose during episodes of pain escalation. The prescription would more likely be for a continuous infusion of 0.2 mg per hour with a patient capability of 0.2mg every 10 to 15 minutes.

Case Example 3: Change Opioid and Route

Towards the end of her hospital stay, Ms. T reports that her pain has been controlled with the IV hydromorphone; however, her renal function has not completely recovered, and she needs to be switched to oral opioids that are safe to use in renal dysfunction.

Determine the total daily dose of current opioid: 0.2 mg IV hydromorphone per hour = 4.8 mg per 24 hours
Calculate the 24-hour OME: 24-hour OME = 24-hour dose of current opioid X 30 /Number of equianalgesic units in current opioid (24-hour OME for this patient is: 4.8 x 30 / 1.5 = 96 mg)
Determine new opioid and route of administration: Hydromorphone is available in a short-acting oral formulation, and a 24-hour dose of oral hydromorphone calculated from the previous steps could be dosed in equal divided doses 4 hours apart. Total OME X Equianalgesic units of the new opioid / 30 = 24-hour dose of the new opioid (96 X 7.5 / 30 = 24 mg). However, there is a strong likelihood that multiple daily doses of the drug will decrease compliance and lead to poorly controlled pain. A different opioid that is long-acting and safely dosed in patients with renal insufficiency is fentanyl. Fentanyl is delivered transdermally as a patch in its long-acting formulation. A fentanyl patch takes 12 to 24 hours to achieve the full effect. Studies clarifying the equianalgesic dosing of fentanyl are lacking. To calculate a comparable dose of fentanyl, a conversion formula is used. While there are several conversion formulas available, we recommend the use of the following: Fentanyl Transdermal Patch Dose calculation: The 24-hour OME divided by 2 is equal to fentanyl dose in mcg per hour (96 / 2= 48 mcg per hour)
Decrease dose of the new opioid due to incomplete cross-tolerance: Decreasing the dose of fentanyl by 50% would yield a dose of 24 mcg per hour. The closest approximation of commercially available formulations of fentanyl patch to that calculation is 25 mcg per hour.
Develop pain prescription: Fentanyl patch is placed on the skin for 72 hours, after which the old patch is removed and replaced with a new one. For patients who are prescribed a long-acting opioid, it is preferable to add a short-acting opioid. The short-acting opioid helps to address breakthrough pain, which is not addressed by the long-acting opioid alone. The dose of the short-acting opioid is determined as follows: Calculate 24-hour OME from the long-acting opioid dose. In the example above it is: (24-hour OME = fentanyl patch dose X 2 = 50 mg) Dose of short-acting opioid is 10% of OME: Morphine 5 mg PO. A short-acting medication is usually dosed every 3 to 4 hours, which the patient takes on an as-needed basis. Equivalent doses of different short-acting formulations of hydromorphone and oxycodone are calculated using the same principles of equianalgesia as outlined above.

Optimal patient analgesia is best accomplished through the efforts of an interprofessional healthcare team that includes clinicians, specialists, nursing staff, and pharmacists. When these team members are involved with patients in scenarios such as the above cases, they must be well familiarized with opioid equivalency and monitoring patient pain control. This responsibility falls to the prescribing or ordering clinician, should be double-checked by the pharmacist. If a nurse is administering or counseling the patient on how to take the medication, they should also be trained on opioid equivalence and equianalgesia. This interprofessional approach will minimize opioid misuse and dependence, prevent adverse events, and provide the patient with the needed analgesia for their situation. [Level 5]

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Figure

Opioid Equivalency Tables. Contributed by Mamta Bhatnagar MD, MS

References

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: Disclosure: Mamta Bhatnagar declares no relevant financial relationships with ineligible companies.
: Disclosure: Jennifer Pruskowski declares no relevant financial relationships with ineligible companies.