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100+ Free ABR Pain Medicine Practice Questions

Pass your ABR Pain Medicine Subspecialty Certificate of Added Qualification (CAQ) exam on the first try — instant access, no signup required.

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According to the IASP 2020 revised definition, pain is best described as which of the following?

A
B
C
D
to track
2026 Statistics

Key Facts: ABR Pain Medicine Exam

~200

Total MCQ Items

Multidisciplinary Pain Medicine subspecialty exam

1 day

Total Exam Time

1-day computer-based test at Pearson VUE

~15%

Interventional Procedures Weight

Largest domain on 2026 Pain Medicine CAQ blueprint

$2,200

2026 CAQ Fee

ABR/ABA subspecialty certification

5+ yr

Required Training

DR/IR-DR primary + 1-year Pain Medicine fellowship

4 boards

Joint Exam Sponsors

ABA, ABR, ABPN, and ABPMR share one Pain Medicine exam

The ABR Pain Medicine CAQ is a 1-day Pearson VUE computer-based exam containing ~200 single-best-answer MCQs. The 2026 multidisciplinary blueprint emphasizes interventional procedures (~15%), opioid pharmacology and prescribing safety (~12%), chronic non-cancer pain (~12%), pain pathophysiology/assessment (~10%), acute pain (~10%), neuropathic pain (~10%), cancer pain (~8%), non-opioid analgesics (~8%), headache (~7%), psychological/rehabilitation (~6%), addiction medicine (~5%), neuromodulation (~5%), and special populations (~5%). CAQ fee ~$2,200; requires ABR DR or IR/DR primary certification plus a 1-year ACGME Pain Medicine fellowship.

Sample ABR Pain Medicine Practice Questions

Try these sample questions to test your ABR Pain Medicine exam readiness. Each question includes a detailed explanation. Start the interactive quiz above for the full 100+ question experience with AI tutoring.

1According to the IASP 2020 revised definition, pain is best described as which of the following?
A.An unpleasant sensory and emotional experience associated with, or resembling that associated with, actual or potential tissue damage
B.A protective sensation that always indicates ongoing tissue injury
C.An entirely subjective psychological phenomenon with no biological basis
D.Activation of nociceptors that produces a reflex withdrawal response
Explanation: The IASP 2020 revised definition explicitly recognizes pain as both sensory and emotional, decoupled from the requirement of demonstrable tissue damage (the 'or resembling that associated with' clause). This wording validates pain in conditions like fibromyalgia and central sensitization syndromes where peripheral pathology is absent.
2Which pain assessment scale is most appropriate for a nonverbal 4-year-old child after surgery?
A.FLACC (Face, Legs, Activity, Cry, Consolability)
B.Numeric Rating Scale 0-10
C.McGill Pain Questionnaire
D.PAINAD scale
Explanation: FLACC is a behavioral observation scale validated for preverbal and nonverbal children. NRS requires self-report (typically ≥7 yr), McGill requires reading/comprehension, and PAINAD is designed for adults with advanced dementia. Faces Pain Scale-Revised is appropriate for verbal children 3-7 yr.
3Wind-up and central sensitization in chronic pain are primarily mediated by which receptor in the dorsal horn?
A.NMDA glutamate receptor
B.GABA-A receptor
C.Mu opioid receptor
D.Alpha-2 adrenergic receptor
Explanation: Repetitive C-fiber input causes Mg2+ block removal from NMDA receptors, allowing Ca2+ influx and progressive amplification (wind-up). This is why NMDA antagonists like ketamine and methadone reduce central sensitization. GABA-A is inhibitory, mu opioid is part of descending modulation, and alpha-2 mediates clonidine analgesia.
4A 62-year-old with diabetes describes burning, electric-shock-like foot pain. Which screening tool is best validated to identify a neuropathic component?
A.DN4 questionnaire
B.Visual Analog Scale
C.PAINAD
D.Brief Pain Inventory severity subscale
Explanation: DN4 (Douleur Neuropathique 4) is a 10-item interview/exam tool with a cutoff of ≥4/10 to identify neuropathic pain. LANSS and painDETECT are alternatives. VAS measures intensity only; PAINAD is for dementia; BPI severity does not differentiate pain mechanisms.
5Discriminative aspects of pain (location, intensity) are primarily transmitted via which pathway to which thalamic region?
A.Lateral spinothalamic tract to ventral posterolateral (VPL) nucleus
B.Anterior spinothalamic tract to medial dorsal nucleus
C.Dorsal column-medial lemniscus to VPL
D.Spinoreticular tract to reticular formation
Explanation: The lateral (neospinothalamic) tract carries fast, well-localized discriminative pain to VPL and then somatosensory cortex (S1, S2). The anterior (paleospinothalamic) tract projects to medial thalamus and limbic structures (ACC, insula) carrying affective/emotional aspects. Dorsal columns transmit proprioception and discriminative touch, not pain.
6The descending pain inhibitory pathway involving the periaqueductal gray (PAG) and rostral ventromedial medulla (RVM) primarily uses which neurotransmitters at the dorsal horn — providing the rationale for which class of analgesics?
A.Serotonin and norepinephrine — TCAs and SNRIs
B.Acetylcholine and glycine — anticholinergics
C.Glutamate and substance P — NMDA antagonists
D.Dopamine and histamine — antipsychotics
Explanation: PAG → RVM → spinal dorsal horn descending modulation uses serotonergic (raphe) and noradrenergic (locus coeruleus) projections that inhibit nociceptive transmission. Augmenting these monoamines (TCAs like amitriptyline; SNRIs like duloxetine and venlafaxine) is the mechanistic basis for their efficacy in chronic and neuropathic pain.
7Fibromyalgia is best classified as which type of pain in the IASP framework?
A.Nociplastic pain
B.Nociceptive somatic pain
C.Peripheral neuropathic pain
D.Visceral pain
Explanation: Nociplastic pain (added by IASP) reflects altered nociception without clear evidence of tissue damage or somatosensory lesion. It encompasses fibromyalgia, IBS, and many chronic widespread pain syndromes. This classification is high-yield because it shapes treatment toward central-acting agents (SNRIs, TCAs, gabapentinoids) and behavioral approaches.
8The fundamental principle of multimodal postoperative analgesia is to:
A.Combine agents with different mechanisms to improve analgesia and reduce opioid requirements
B.Use the highest tolerated dose of a single opioid
C.Avoid all non-opioid agents to minimize drug interactions
D.Provide PRN dosing only after pain reaches severe levels
Explanation: Multimodal analgesia combines acetaminophen, NSAIDs, gabapentinoids, ketamine, regional techniques, and opioids to leverage additive/synergistic effects with reduced individual doses and side effects. This is the core ERAS opioid-sparing strategy and is endorsed by ASA and PROSPECT guidelines.
9Which patient-controlled analgesia (PCA) practice carries the highest risk of respiratory depression in an opioid-naive postoperative patient?
A.Adding a continuous basal infusion to PCA bolus dosing
B.A 6-minute lockout interval
C.An hourly maximum dose limit
D.Use of hydromorphone instead of morphine
Explanation: Basal infusions remove the safety mechanism of patient self-titration — sedated patients continue receiving opioid even when not pressing the button. Multiple ISMP and APSF advisories warn against basal infusions in opioid-naive adults. They may be considered cautiously in opioid-tolerant patients.
10A transversus abdominis plane (TAP) block primarily covers which dermatomes for analgesia after lower abdominal surgery?
A.T10 to L1
B.T4 to T8
C.L2 to L4
D.S1 to S4
Explanation: The TAP block deposits local anesthetic in the fascial plane between internal oblique and transversus abdominis, anesthetizing the anterior rami of T10-L1 spinal nerves. It provides somatic (not visceral) analgesia for cesarean section, hernia repair, and other lower abdominal incisions.

About the ABR Pain Medicine Exam

The ABR Pain Medicine CAQ is the multidisciplinary subspecialty certification examination for radiologists who completed a 1-year ACGME-accredited Pain Medicine fellowship. The exam is jointly developed and shared across the American Board of Anesthesiology (ABA), American Board of Radiology (ABR), American Board of Psychiatry and Neurology (ABPN), and American Board of Physical Medicine and Rehabilitation (ABPMR). The 1-day computer-based exam contains approximately 200 single-best-answer MCQs covering pain pathophysiology and assessment (IASP definitions, sensitization, pain scales, DN4), acute postoperative multimodal analgesia, chronic non-cancer pain (low back pain, CRPS Budapest criteria, fibromyalgia), cancer pain (WHO ladder, methadone rotation, intrathecal pumps, neurolytic blocks), neuropathic pain (PHN, DPN, CIPN, trigeminal neuralgia), headache (ICHD-3, CGRP, PREEMPT botulinum), opioid pharmacology and CDC 2022 prescribing safety, non-opioid analgesics, image-guided interventional procedures (epidurals, facet/MBB, RFA, sympathetic blocks, vertebral augmentation), neuromodulation (SCS, DRG-S, intrathecal pumps), psychological/behavioral approaches (CBT, ACT, MBSR), addiction medicine (DSM-5, buprenorphine induction, naltrexone), and special populations (pediatrics, geriatrics, pregnancy, renal/hepatic).

Questions

200 scored questions

Time Limit

1-day computer-based exam

Passing Score

Criterion-referenced scaled score (typically ~75% correct)

Exam Fee

~$2,200 CAQ examination fee (ABR/ABA 2026) (American Board of Radiology (ABR) / American Board of Anesthesiology (ABA) / Pearson VUE)

ABR Pain Medicine Exam Content Outline

~13%

Image-Guided Interventional Procedures

Fluoroscopy and ultrasound technique, sterile prep, contrast confirmation under live fluoroscopy. Particulate (triamcinolone, methylprednisolone, betamethasone) vs non-particulate (dexamethasone) steroids — non-particulate REQUIRED for cervical and thoracic transforaminal injections to avoid catastrophic embolic spinal cord/brainstem infarct. Epidural steroid injections (interlaminar, transforaminal — Kambin's triangle, caudal). Facet joint injections and medial branch blocks (cervical/thoracic/lumbar) — diagnostic blocks require ≥80% pain relief on two separate occasions before proceeding to radiofrequency ablation. SI joint injection. Sympathetic blocks: stellate ganglion (C6-C7 anterior tubercle, C7 transverse process for ultrasound — for upper extremity CRPS, herpes zoster, hyperhidrosis), lumbar sympathetic (L2-L3 paravertebral for lower extremity CRPS), celiac plexus (T12-L1, transcrural or anterocrural; for pancreatic and upper abdominal cancer), superior hypogastric (L5-S1 anterior to vertebral body for pelvic cancer), ganglion impar (sacrococcygeal junction for perineal pain). Trigger point injections, peripheral nerve blocks (greater/lesser occipital, suprascapular, intercostal, ilioinguinal/iliohypogastric, lateral femoral cutaneous, genitofemoral, pudendal). Vertebral augmentation (vertebroplasty, kyphoplasty for osteoporotic VCF), epidural blood patch for PDPH (15-20 mL autologous blood).

~10%

Opioid Pharmacology & Prescribing Safety

Mu/kappa/delta opioid receptor pharmacology, full agonists (morphine, hydromorphone, oxycodone, fentanyl) vs partial agonists (buprenorphine — ceiling effect on respiratory depression but high mu affinity displaces full agonists). Morphine metabolites: M3G (neuroexcitatory, accumulates in renal failure causing myoclonus/hyperalgesia), M6G (active analgesic). Codeine — CYP2D6 prodrug; ultra-rapid metabolizers risk fatal respiratory depression (FDA boxed warning, contraindicated <12 yr and breastfeeding mothers). Tramadol (mu agonist + SNRI, lowers seizure threshold, serotonin syndrome risk), tapentadol (mu + NRI). Methadone — NMDA antagonism, QTc prolongation (baseline ECG, monitor at 30 days then annually), long variable half-life (8-59 hr), biphasic elimination, conversion ratios INCREASE at higher morphine equivalents (4:1 at <100 mg, up to 12:1 at >300 mg morphine). Fentanyl transdermal — onset 12-24 hr, lasts 72 hr, contraindicated opioid-naive. CDC 2022 guideline (no specific MME threshold; emphasize individualized risk-benefit, naloxone co-prescribing at MME ≥50 or with benzo co-use, PDMP query at every prescription). Urine drug screens — immunoassay screens followed by GC/MS confirmation; oxycodone, fentanyl, methadone, buprenorphine require specific assays (don't cross-react with standard opiate immunoassay). Opioid-induced hyperalgesia (paradoxical worsening with dose escalation), opioid-induced constipation (PAMORAs — methylnaltrexone, naloxegol, naldemedine).

~9%

Chronic Non-Cancer Pain

Low back pain — axial mechanical, facet-mediated (paramedian, worse with extension, relieved with flexion), discogenic (positive provocative discography — controversial), SI joint (Fortin finger test, multiple positive provocation tests), radicular (dermatomal, positive SLR), failed back surgery syndrome (epidural fibrosis, recurrent disc, adjacent segment disease, foraminal stenosis). Complex regional pain syndrome (Budapest criteria — 4 categories: sensory, vasomotor, sudomotor/edema, motor/trophic; ≥1 symptom in 3 categories AND ≥1 sign in 2 categories at evaluation; type I no nerve injury, type II with nerve injury). Fibromyalgia (2016 ACR criteria — Widespread Pain Index ≥7 + Symptom Severity ≥5, OR WPI 4-6 + SSS ≥9; symptoms ≥3 months; central sensitization, increased substance P, decreased descending inhibition). Myofascial pain with trigger points and twitch response. Osteoarthritis (knee, hip, hand). Chronic abdominal/pelvic pain (endometriosis, IBS, interstitial cystitis). Post-amputation phantom limb pain (mirror therapy, gabapentin, TCAs, peripheral/central techniques). Post-thoracotomy (intercostal neuritis), post-mastectomy (intercostobrachial nerve).

~8%

Pain Pathophysiology & Assessment

Nociceptive pain (somatic — well-localized; visceral — vague, referred), neuropathic pain (lesion of somatosensory system — burning, electric, allodynia, hyperalgesia), nociplastic pain (altered nociception without tissue damage — fibromyalgia, IBS). Peripheral sensitization (lower threshold of nociceptors), central sensitization (NMDA-mediated, wind-up, secondary hyperalgesia, allodynia). Ascending spinothalamic tract (lateral — discriminative; anterior — affective via medial thalamus to ACC and insula). Descending modulation (PAG → RVM → dorsal horn; serotonergic and noradrenergic — basis for TCA/SNRI efficacy). Gate control theory (Melzack-Wall). IASP 2020 revised definition: 'unpleasant sensory and emotional experience associated with, or resembling that associated with, actual or potential tissue damage.' Assessment scales: NRS 0-10, VAS, Verbal Rating, Faces Pain Scale Revised (3-7 yr), FLACC (preverbal/nonverbal), PAINAD (advanced dementia), CPOT/BPS (ICU intubated). Neuropathic screening: DN4 (≥4/10), LANSS, painDETECT. Multidimensional: Brief Pain Inventory (BPI severity + interference), McGill Pain Questionnaire, PROMIS pain measures.

~8%

Acute Pain Management

Postoperative multimodal analgesia (PROSPECT recommendations) — scheduled acetaminophen 1 g q6h, NSAIDs (ketorolac, ibuprofen, celecoxib), gabapentin/pregabalin (controversial — modest opioid-sparing but increased sedation in elderly per recent ASA guidance), low-dose ketamine infusion (0.1-0.5 mg/kg/hr), IV lidocaine infusion (1-2 mg/kg bolus then 1-3 mg/kg/hr), dexmedetomidine. Enhanced Recovery After Surgery (ERAS) — minimize opioids, regional techniques, early mobilization. Patient-controlled analgesia (PCA) — basal infusions in opioid-naive INCREASE respiratory depression risk; lockout intervals, 1-hr and 4-hr limits. Regional anesthesia: TAP (T10-L1 dermatomes for lower abdominal surgery), erector spinae plane (paraspinal at T5 for thoracic/breast surgery), PECS I/II (breast surgery), fascia iliaca/femoral (hip/knee surgery), brachial plexus (upper extremity), thoracic paravertebral. Neuraxial: epidural analgesia (continuous infusion or PCEA), intrathecal morphine for cesarean. Acute on chronic pain in opioid-tolerant patients (continue baseline opioid, add multimodal, increase PRN doses 50-100% above baseline). Sickle cell vaso-occlusive crisis — IV opioids within 30 min, hydration, NSAIDs unless contraindicated.

~8%

Neuropathic Pain

Postherpetic neuralgia (>90 days after herpes zoster rash; vaccine prevention with Shingrix recombinant zoster vaccine ≥50 yr — 90% effective). Diabetic peripheral neuropathy (length-dependent, stocking-glove, burning). Chemotherapy-induced peripheral neuropathy (CIPN): platinum (cisplatin, oxaliplatin — acute cold-triggered with oxaliplatin), taxanes (paclitaxel), vincristine (early-onset), bortezomib. Trigeminal neuralgia (V2/V3 most common, neurovascular conflict — superior cerebellar artery; carbamazepine first-line, oxcarbazepine alternative; refractory — microvascular decompression, gamma knife radiosurgery, percutaneous balloon/glycerol/RF rhizotomy). Painful HIV neuropathy. Central post-stroke pain (Dejerine-Roussy syndrome, thalamic). Spinal cord injury pain (above-level, at-level, below-level). Phantom limb pain. IASP/NeuPSIG algorithm — first-line: TCA (amitriptyline, nortriptyline — anticholinergic risk in elderly), SNRI (duloxetine, venlafaxine), gabapentinoids (gabapentin titrated to 1800-3600 mg/day; pregabalin 150-600 mg/day); second-line: lidocaine 5% patch (focal — PHN), capsaicin 8% patch (focal — PHN, painful diabetic peripheral neuropathy of the feet, HIV neuropathy), tramadol; third-line: opioids, botulinum toxin A (focal).

~8%

Cancer Pain Management

WHO analgesic ladder — Step 1: non-opioid (acetaminophen, NSAID) ± adjuvant; Step 2: weak opioid (codeine, tramadol) ± non-opioid ± adjuvant; Step 3: strong opioid (morphine, hydromorphone, oxycodone, fentanyl, methadone) ± non-opioid ± adjuvant. Recent revision considers Step 4 (interventional). Opioid rotation indicated for inadequate analgesia, intolerable side effects, opioid-induced hyperalgesia — use equianalgesic table and reduce by 25-50% for incomplete cross-tolerance (50-90% reduction for methadone). Methadone conversion ratios increase at higher morphine doses. Breakthrough pain — rapid-onset opioids (transmucosal fentanyl — buccal Fentora, sublingual Abstral, intranasal Lazanda; oral transmucosal Actiq lozenge); typically dosed at 10-20% of total daily morphine equivalent. Bone pain — NSAIDs, bisphosphonates (zoledronic acid IV q4 weeks), denosumab (RANK-L inhibitor), external beam radiation, bone-seeking radiopharmaceuticals (Sr-89, Sm-153 EDTMP, Ra-223 dichloride for castration-resistant prostate metastases). Intrathecal drug delivery (PACC guidelines — first-line morphine, ziconotide [non-opioid N-type calcium channel blocker, no tolerance, but psychiatric/cognitive side effects]; combinations with bupivacaine, clonidine, hydromorphone). Neurolytic blocks: celiac plexus (alcohol or phenol — pancreatic, upper abdominal), superior hypogastric (pelvic), ganglion impar (perineal). Cordotomy (anterolateral thoracic for unilateral lower-body cancer pain — historic). Palliative care integration.

~8%

Non-Opioid Analgesics & Adjuvants

Acetaminophen — 4 g/day max (3 g in chronic alcohol use, malnutrition, hepatic impairment); hepatotoxicity via NAPQI (treated with N-acetylcysteine). NSAIDs — nonselective COX-1/COX-2 inhibition; cardiovascular risk highest with diclofenac and rofecoxib (withdrawn), lowest with naproxen; GI risk (PPI co-prescription, avoid in active PUD), renal risk (avoid in CKD, volume depletion, ACE/ARB/diuretic co-use), cardiovascular contraindications (recent MI, CHF). Selective COX-2 (celecoxib) — lower GI risk, similar CV risk. Ketamine — non-competitive NMDA antagonist; sub-anesthetic infusion (0.1-0.5 mg/kg/hr) for acute, chronic, and CRPS; intranasal esketamine for treatment-resistant depression; dissociative side effects (emergence reactions, hallucinations, cystitis with chronic use). IV lidocaine infusion (1-2 mg/kg/hr) — perioperative and chronic neuropathic pain. Alpha-2 agonists — clonidine (oral, transdermal, intrathecal, epidural), tizanidine, dexmedetomidine (perioperative). Muscle relaxants — cyclobenzaprine (TCA-related, anticholinergic), baclofen (GABA-B agonist; oral and intrathecal for spasticity/dystonia — abrupt withdrawal causes severe rebound spasticity, hyperthermia, rhabdomyolysis), methocarbamol, tizanidine. Cannabinoids — CBD, dronabinol (THC), nabilone; modest evidence for chronic pain. Low-dose naltrexone (1.5-4.5 mg) — off-label for fibromyalgia and chronic pain. IV/oral magnesium.

~7%

Headache & Facial Pain

ICHD-3 classification — primary (migraine, tension-type, trigeminal autonomic cephalalgias, other) vs secondary. Migraine — with/without aura; chronic migraine ≥15 days/month for ≥3 months with ≥8 migraine days. Acute treatment: triptans (5-HT1B/1D — sumatriptan, rizatriptan, eletriptan; contraindicated in CAD, uncontrolled HTN, basilar/hemiplegic migraine), DHE, gepants (rimegepant, ubrogepant — CGRP receptor antagonists, no vasoconstriction), lasmiditan (5-HT1F — no vasoconstriction). Prophylaxis: beta-blockers (propranolol), TCAs (amitriptyline), topiramate, valproate, candesartan, CGRP monoclonal antibodies (erenumab, fremanezumab, galcanezumab, eptinezumab). Cluster headache — unilateral periorbital, autonomic features, circadian; acute: 100% O2 12-15 L/min via non-rebreather, subQ sumatriptan, intranasal zolmitriptan; prophylaxis: verapamil (high-dose with ECG monitoring), lithium, galcanezumab. TACs — paroxysmal hemicrania (indomethacin-responsive — diagnostic), SUNCT/SUNA, hemicrania continua (indomethacin-responsive). Trigeminal neuralgia — carbamazepine first-line (HLA-B*1502 screening in Asian patients for SJS risk). PREEMPT protocol for chronic migraine — onabotulinumtoxinA 155 units across 31 sites in 7 head/neck muscles q12 weeks. Medication overuse headache — withdraw offending agent (triptans, opioids, butalbital, NSAIDs). Occipital nerve stimulation, sphenopalatine ganglion block.

~6%

Psychological, Behavioral & Rehabilitation

Cognitive-behavioral therapy (CBT) for chronic pain — strongest evidence; targets catastrophizing, fear-avoidance, activity pacing, cognitive restructuring. Acceptance and commitment therapy (ACT) — psychological flexibility, values-based action despite pain. Mindfulness-based stress reduction (MBSR — Kabat-Zinn 8-week program). Biofeedback (EMG, thermal — for tension headache, migraine), hypnosis (IBS, procedural pain), relaxation training, guided imagery. Pain Catastrophizing Scale (PCS — rumination, magnification, helplessness). Fear-avoidance model (Vlaeyen) — pain-related fear leads to avoidance, deconditioning, disability. Tampa Scale for Kinesiophobia. Depression and anxiety comorbidities (PHQ-9, GAD-7) — bidirectional relationship with pain. Sleep disturbance (insomnia worsens pain via central sensitization). Pain self-efficacy (PSEQ). Physical therapy — graded activity, McKenzie method (directional preference), aquatic therapy. Manipulative therapy. Acupuncture (evidence for chronic LBP, knee OA, headache). TENS (high-frequency conventional gate control vs low-frequency endorphin-mediated). Interdisciplinary functional restoration programs (Mayday/Texas model — strongest evidence for chronic disabling LBP).

~5%

Neuromodulation & Advanced Techniques

Spinal cord stimulation (SCS) — indications include failed back surgery syndrome, painful diabetic neuropathy (SENZA-PDN trial — 10-kHz HF), CRPS, refractory angina, peripheral vascular disease. Trial period 5-7 days percutaneous lead with ≥50% pain relief required before permanent implant. Waveforms: tonic (paresthesia-based, traditional), burst (DeRidder — sub-perception), high-frequency 10-kHz (Nevro Senza — sub-perception, dorsal column), DTM (differential target multiplexed), closed-loop (Saluda Evoke — measures evoked compound action potentials, autoadjusts amplitude). MRI conditional considerations (1.5T or 3T conditional with manufacturer programming). Dorsal root ganglion stimulation (DRG-S — Abbott Proclaim) for focal lower extremity neuropathic pain (CRPS lower extremity, post-herniorrhaphy, post-knee/foot surgery — ACCURATE trial). Peripheral nerve stimulation (PNS) — temporary 60-day systems (SPRINT) and permanent implants (StimRouter, Bioness). Radiofrequency ablation: conventional thermal 80°C × 90 sec for medial branches (cervical TON, lumbar/thoracic), genicular nerves (knee OA — superior medial, superior lateral, inferior medial), SI joint lateral branch (L4 dorsal ramus, L5 dorsal ramus, S1-S3 lateral branches); pulsed RF 42°C (DRG, peripheral nerves — non-neurodestructive); water-cooled RF (larger lesions for SI joint). Cryoablation. Intrathecal drug delivery (programmable pumps — Medtronic SynchroMed, Flowonix Prometra) — PACC guidelines: first-line morphine and ziconotide; combinations include hydromorphone, bupivacaine, clonidine. Vertebroplasty/kyphoplasty for VCFs (VAPOUR trial — early intervention <6 weeks).

~5%

Addiction Medicine & SUD

DSM-5 substance use disorder criteria — 11 items across impaired control, social impairment, risky use, pharmacological criteria; severity: mild 2-3, moderate 4-5, severe ≥6. Distinguish tolerance (decreased effect with same dose), physical dependence (withdrawal on cessation — both expected with chronic opioids), and addiction (compulsive use, loss of control, continued use despite harm). Buprenorphine — partial mu agonist with high affinity, ceiling effect on respiratory depression; sublingual/buccal (Suboxone with naloxone, Subutex mono), transdermal (Butrans 5-20 mcg/hr for chronic pain), buccal film (Belbuca for chronic pain), monthly extended-release injection (Sublocade). DEA X-waiver ELIMINATED December 2022 (MAT Act in CAA 2023) — standard DEA registration sufficient to prescribe buprenorphine for OUD. Induction during mild-to-moderate opioid withdrawal (COWS ≥8-12) to avoid precipitated withdrawal; new low-dose/microdosing/Bernese method allows induction without withdrawal. Methadone for OUD restricted to federally certified opioid treatment programs (OTPs). Extended-release injectable naltrexone (Vivitrol IM monthly) — opioid antagonist; requires 7-10 days opioid-free, naloxone challenge. Naloxone — IM 0.4 mg, intranasal (Narcan 4 mg, Kloxxado 8 mg), autoinjector (Evzio); short half-life (30-90 min) often shorter than opioid, repeat dosing/infusion. Treating pain in patients on MOUD — split buprenorphine dosing, add short-acting opioids at higher than usual doses (mu antagonism), regional/multimodal preferred. Stimulant, alcohol (CIWA, benzodiazepines, naltrexone, acamprosate), benzodiazepine (gradual taper) use disorders.

~5%

Special Populations & Ethics

Pediatric pain — age-appropriate scales (FLACC <7 yr or nonverbal, Faces Pain Scale-Revised 3-7 yr, NRS ≥7 yr), weight-based dosing. FDA boxed warning: codeine and tramadol CONTRAINDICATED in <12 yr (and <18 yr for tonsillectomy/adenoidectomy) due to ultra-rapid CYP2D6 metabolism deaths; codeine contraindicated in breastfeeding. Intranasal fentanyl, intranasal/IM ketamine, sucrose for neonatal procedures, EMLA topical anesthetic, regional blocks (caudal, ilioinguinal). Geriatric pain — Beers criteria 2023: AVOID meperidine (normeperidine seizures), skeletal muscle relaxants (cyclobenzaprine, methocarbamol — anticholinergic), barbiturates, indomethacin, ketorolac >5 days; use lower acetaminophen dose; NSAIDs increase GI/renal/cardiac risk; gabapentinoid + opioid co-prescription increases respiratory depression. Pregnancy — acetaminophen first-line; AVOID NSAIDs after 30 weeks (premature ductus arteriosus closure, oligohydramnios; FDA 2020 warning at 20 weeks for renal effects); opioids increase risk of neonatal abstinence syndrome (NAS — Finnegan scoring, treat with morphine or methadone); MOUD in pregnancy — methadone or buprenorphine preferred over abstinence. Lactation — most opioids excreted in breast milk; codeine contraindicated; small doses of morphine, hydrocodone, oxycodone may be acceptable monitoring infant. Renal failure — AVOID morphine and codeine (M3G/M6G accumulation, normeperidine seizures with meperidine); preferred opioids include fentanyl, hydromorphone, methadone, buprenorphine. Hepatic failure — reduce dose/frequency of all opioids and acetaminophen. Sickle cell disease, end-of-life care, informed consent for chronic opioid therapy and high-risk interventions, controlled substance agreements.

How to Pass the ABR Pain Medicine Exam

What You Need to Know

  • Passing score: Criterion-referenced scaled score (typically ~75% correct)
  • Exam length: 200 questions
  • Time limit: 1-day computer-based exam
  • Exam fee: ~$2,200 CAQ examination fee (ABR/ABA 2026)

Keys to Passing

  • Complete 500+ practice questions
  • Score 80%+ consistently before scheduling
  • Focus on highest-weighted sections
  • Use our AI tutor for tough concepts

ABR Pain Medicine Study Tips from Top Performers

1Methadone is high-yield. Memorize: (1) NMDA antagonism in addition to mu agonism; (2) QTc prolongation requires baseline ECG, repeat at 30 days and annually, caution with co-prescription of QT-prolonging drugs (ondansetron, fluoroquinolones, antipsychotics); (3) long variable half-life (8-59 hr) with biphasic elimination and risk of accumulation/respiratory depression in first 5-7 days; (4) conversion from morphine is NON-LINEAR — ratios INCREASE at higher doses (start 4:1 at MEDD <100 mg, may reach 12:1 at MEDD >300 mg). Always reduce calculated dose by an additional 25-50% for incomplete cross-tolerance.
2Cervical and thoracic transforaminal epidural steroid injections require NON-PARTICULATE steroid (dexamethasone) ONLY. Particulate steroids (triamcinolone, methylprednisolone, betamethasone) can cause embolic stroke, brainstem infarct, or spinal cord infarct via radiculomedullary arteries (artery of Adamkiewicz typically T9-T12, but variable). Lumbar transforaminal can use either, though many centers use non-particulate as default. Real-time fluoroscopy with digital subtraction is recommended to detect intravascular uptake.
3Budapest criteria for CRPS — must have ALL FOUR: (1) continuing pain disproportionate to inciting event; (2) ≥1 SYMPTOM in 3 of 4 categories (sensory: hyperalgesia/allodynia; vasomotor: temperature asymmetry/skin color; sudomotor/edema: edema, sweating changes; motor/trophic: decreased ROM, motor dysfunction, trophic changes); (3) ≥1 SIGN at evaluation in 2 of 4 same categories; (4) no other diagnosis better explains. Type I = no nerve injury; Type II = with documented nerve injury (formerly causalgia).
4Spinal cord stimulation waveforms to know: (1) Tonic (traditional, paresthesia-based, ~50 Hz, dorsal column stimulation); (2) Burst (DeRidder, sub-perception, packets of high-frequency intra-burst at 40 Hz inter-burst, modulates medial pain pathway); (3) High-frequency 10-kHz (Nevro Senza, paresthesia-free, sub-perception, dorsal horn — SENZA-RCT showed superiority in chronic back/leg pain, SENZA-PDN for diabetic neuropathy); (4) DTM (differential target multiplexed, multiplexed waveforms targeting glia and neurons); (5) Closed-loop (Saluda Evoke, measures ECAPs and autoadjusts amplitude in real-time — EVOKE trial).
5IASP/NeuPSIG neuropathic pain algorithm — FIRST LINE: TCAs (amitriptyline, nortriptyline — anticholinergic risk in elderly, baseline ECG for QTc/conduction), SNRIs (duloxetine 60 mg, venlafaxine ≥150 mg for noradrenergic effect), gabapentinoids (gabapentin titrate to 1800-3600 mg/day, pregabalin 150-600 mg/day; both renally cleared, dose-adjust). SECOND LINE: lidocaine 5% patch (focal — PHN; up to 3 patches, 12 on/12 off), capsaicin 8% patch (single 60-min application, lasts 3 months; FDA-approved for PHN, painful diabetic peripheral neuropathy of feet, HIV neuropathy), tramadol. THIRD LINE: opioids, botulinum toxin A (focal). Note: gabapentin opioid co-prescription has FDA warning for respiratory depression in elderly/COPD.

Frequently Asked Questions

What is the ABR Pain Medicine CAQ?

The ABR Pain Medicine Subspecialty Certificate of Added Qualification (CAQ) is the multidisciplinary subspecialty certification examination for radiologists who completed an ACGME-accredited Pain Medicine fellowship. The exam is jointly developed and shared across the American Board of Anesthesiology (ABA), American Board of Radiology (ABR), American Board of Psychiatry and Neurology (ABPN), and American Board of Physical Medicine and Rehabilitation (ABPMR), reflecting the multidisciplinary nature of pain practice. It covers pain pathophysiology, acute and chronic pain, cancer pain, neuropathic pain, headache, opioid pharmacology, interventional procedures, neuromodulation, behavioral approaches, and addiction medicine.

Who is eligible to take the ABR Pain Medicine CAQ?

Candidates must hold ABR Diagnostic Radiology or IR/DR primary certification and must have satisfactorily completed a 1-year ACGME-accredited Pain Medicine fellowship. Candidates must maintain a valid unrestricted medical license, an active DEA registration, and their primary certification in good standing. Applications are submitted through the ABR within the designated eligibility window, and the fellowship program director must attest to satisfactory completion of training including required interventional procedure volumes.

What is the format of the ABR Pain Medicine CAQ exam?

The exam is a 1-day computer-based examination delivered at Pearson VUE test centers, containing approximately 200 single-best-answer multiple-choice questions. The exam is identical across the four boards offering Pain Medicine subspecialty certification (ABA, ABR, ABPN, ABPMR). Questions emphasize clinical reasoning across pain pathophysiology and assessment, pharmacology (especially opioids), interventional procedures with image interpretation, neuromodulation, multidisciplinary pain conditions (CRPS, fibromyalgia, headache, cancer pain, neuropathic pain), psychological approaches, addiction medicine, and special populations.

How much does the 2026 ABR Pain Medicine CAQ cost?

The 2026 ABR/ABA Pain Medicine CAQ examination fee is approximately $2,200. Cancellation and refund policies follow the ABR/ABA schedule with decreasing refunds as the exam date approaches. Candidates who fail may retake the exam in a subsequent administration within the eligibility window, subject to full re-registration and fee payment. Continuing Certification (OLA) participation has separate annual fees for maintaining the subspecialty designation.

When is the 2026 exam administered?

The Pain Medicine CAQ is typically offered once per year in a defined fall testing window (historically September). Applications open earlier in the year with a submission deadline well before the testing window. After application approval, candidates schedule specific Pearson VUE appointments at authorized test centers. Exact 2026 dates and application deadlines should be confirmed on the ABR Pain Medicine subspecialty page.

How is the CAQ exam scored?

The Pain Medicine subspecialty exam uses a criterion-referenced scaled scoring system with a passing standard set by the multidisciplinary Pain Medicine Examination Committee (representing all four sponsoring boards). Candidate pass/fail results depend on performance relative to the fixed cut-score rather than relative to other test-takers. Score reports include subdomain performance to guide future Continuing Certification module selection. Results are typically released several weeks after the testing window closes.

What are the highest-yield topics?

Highest-yield topics include: opioid pharmacology (mu/kappa/delta receptors; methadone QTc, conversion ratios that increase with dose, NMDA antagonism; codeine CYP2D6 ultra-rapid metabolism FDA boxed warning; buprenorphine partial agonism); CDC 2022 prescribing guidelines and naloxone co-prescribing; particulate vs non-particulate steroid choice for cervical/thoracic transforaminal injections (use only dexamethasone to avoid spinal cord/brainstem infarct); CRPS Budapest criteria; IASP/NeuPSIG neuropathic pain algorithm (TCAs, SNRIs, gabapentinoids first-line); ICHD-3 headache criteria, CGRP antagonists, PREEMPT botulinum protocol; spinal cord stimulation indications and waveforms (10-kHz, burst, DTM, closed-loop); buprenorphine induction during withdrawal (COWS ≥8-12) and X-waiver elimination 2022.

How should I study for the ABR Pain Medicine CAQ?

Use a structured 12-month plan during your fellowship year. Map to the multidisciplinary Pain Medicine content outline: lead with pain pathophysiology and assessment, then opioid and non-opioid pharmacology, interventional procedures (epidurals, facet/MBB, RFA, sympathetic blocks, vertebral augmentation), neuromodulation (SCS, DRG-S, intrathecal pumps), specific pain syndromes (CRPS, fibromyalgia, headache, cancer pain, neuropathic), addiction medicine, behavioral approaches, and special populations. Core resources include Bonica's Management of Pain, the Essentials of Pain Medicine textbook, the AAPM/ASRA practice guidelines, NeuPSIG recommendations, Pain Medicine board review courses, and 2-3 timed full-length practice exams.