Management in Medical Practice
Pain Management Goals and Types
Pain management aims to relieve pain effectively while minimizing side effects, dependency,
and functional impairment. Treatment strategies should be tailored to the specific type of pain,
including acute, chronic, neuropathic, or cancer-related pain. Proper assessment and
individualized therapy are essential to optimize patient outcomes and quality of life.
Non-Opioid Analgesics
Acetaminophen (Tylenol) and NSAIDs (e.g., ibuprofen, naproxen, celecoxib) are frontline
agents for mild to moderate pain and inflammation. Acetaminophen is preferred in pregnancy
and for fever reduction, but exceeding 4 grams per day increases the risk of hepatotoxicity,
especially in patients with liver disease or alcohol use. NSAIDs effectively treat inflammatory
conditions such as arthritis but carry risks like gastrointestinal (GI) bleeding, renal
impairment, and cardiovascular events. Use should be at the lowest effective dose and for the
shortest duration necessary, with careful monitoring.
Opioid Analgesics and Risk Management
Opioids (e.g., morphine, oxycodone, hydrocodone, fentanyl) are reserved for moderate to
severe pain. They act on mu-opioid receptors in the central nervous system to produce
analgesia but can cause sedation, respiratory depression, constipation, and dependence. Risks
of misuse or abuse necessitate thorough evaluation, utilization of prescription monitoring
programs (PMPs), and gradual tapering to prevent withdrawal. Use opioids cautiously,
especially in vulnerable populations.
Opioid overdose can be rapidly reversed with naloxone (Narcan), available as nasal spray, IM,
or IV. Due to its short half-life, repeat doses may be necessary, and emergency protocols should
be in place.
Adjuvant Medications in Pain
Antidepressants (e.g., amitriptyline, duloxetine) and anticonvulsants (e.g., gabapentin,
pregabalin) are effective for neuropathic and chronic pain by modulating CNS pathways
involved in pain perception. They work by increasing serotonin/norepinephrine levels or
reducing nerve excitability, respectively. Side effects include dry mouth, sedation, dizziness, and
weight gain.
, Topical agents like lidocaine patches and capsaicin cream provide localized relief with
minimal systemic effects. Muscle relaxants such as cyclobenzaprine and tizanidine are used
for muscle spasms, but they can cause drowsiness and dry mouth.
Chronic Pain Multimodal Approach
Effective management of chronic pain involves combining pharmacologic treatments with
physical therapy and psychological support (e.g., cognitive-behavioral therapy). This
multimodal approach reduces reliance on opioids, minimizes side effects, and enhances
functional outcomes.
Drugs for Behavioral Health Conditions
Medications for mood, anxiety, psychosis, attention disorders, and substance use disorders aim to
improve functioning, reduce distress, and support adherence. These include:
Antidepressants: SSRIs, SNRIs, atypical agents, TCAs, MAOIs
Anxiolytics: Benzodiazepines, buspirone
Mood Stabilizers: Lithium, anticonvulsants
Antipsychotics: Typical and atypical agents
ADHD Medications: Stimulants and non-stimulants
Substance Use Disorder Medications: Naltrexone, disulfiram, acamprosate, nicotine
replacement, bupropion
Antidepressants' Roles and Side Effects
SSRIs (e.g., fluoxetine, sertraline) and SNRIs (e.g., venlafaxine, duloxetine) are first-line for
depression and anxiety, taking 2–6 weeks for full effect. Common side effects include GI upset,
insomnia, and sexual dysfunction. They carry a Black Box warning for increased suicidal risk
in patients under 25.
TCAs and MAOIs are less frequently used due to their toxicity profiles, dietary restrictions
(MAOIs), and anticholinergic effects.
Mood Stabilizers and Antipsychotics
Lithium remains a cornerstone for bipolar disorder management, requiring regular monitoring of
serum levels, kidney, and thyroid function. Side effects include tremor, weight gain, and GI
upset.
Antipsychotics are classified into first-generation (typical), which target dopamine receptors
and are effective for positive symptoms but carry risks like extrapyramidal symptoms (EPS)
and tardive dyskinesia, and second-generation (atypical) agents, which have broader efficacy
and fewer motor side effects but may cause metabolic syndrome.