Quick Reference
Overview and Recommendations
Background
- •RLS - a sensorimotor disorder defined by four IRLSSG criteria (urge to move, worsening at rest, relief with movement, evening predominance) - affects 3‑10 % of adults and up to 15 % of those >70 y, with a female‑to‑male ratio of ~1.5:1.
- •Pathophysiology centers on brain iron deficiency and dopaminergic hypo‑activity; low ferritin correlates with reduced striatal dopamine synthesis, while up‑regulated D2 receptors reflect compensatory signaling.
- •Genetic susceptibility (MEIS1, BTBD9, LMX1B) accounts for ~50 % of variance and converges on iron handling and dopamine neuron development.
- •Secondary causes - iron deficiency, chronic kidney disease, pregnancy, and neurologic disorders (Parkinson disease, multiple sclerosis) - often resolve when the underlying condition is treated.
- •Severity is quantified by the International RLS Study Group Rating Scale (IRLS 0‑40); scores ≥15 trigger pharmacologic escalation, and ≥30 predict augmentation risk.
Evaluation
- •Suspect RLS in any patient with nocturnal leg discomfort that improves with walking, especially if symptoms occur ≥3 days/week and last >5 minutes per episode.
- •Ask about circadian pattern, relief with movement, and impact on sleep; screen for red‑flags such as sudden severe leg pain, focal neurologic deficits, or respiratory compromise (FVC <15 mL/kg).
- •Examine for involuntary leg movements during a 5‑minute seated rest; observe for periodic limb movements (PLMS) on bedside EMG if available.
- •Order serum ferritin and transferrin saturation (TSAT) on the initial visit; ferritin <75 µg/L or TSAT <20 % signals brain iron deficiency and prompts iron therapy.
- •Check renal function (eGFR), thyroid panel, and complete blood count to rule out secondary contributors (CKD, hypothyroidism, anemia).
- •If pregnancy is possible, obtain a urine β‑hCG; treat iron deficiency promptly because ferritin <30 µg/L predicts severe gestational RLS.
- •Consider quantitative sensory testing or nerve‑conduction studies only when peripheral neuropathy is suspected (e.g., abnormal sensory exam).
- •Apply the IRLSSG 4‑item screen; a positive result plus ferritin ≥75 µg/L allows a provisional diagnosis, but specialist confirmation is recommended for moderate‑severe disease.
- •For refractory or atypical cases (restless abdomen, early‑onset <40 y), obtain polysomnography with leg EMG to quantify PLMS index (>15 events/h supports severe phenotype).
- •Document baseline IRLS score; repeat every 4 weeks to gauge treatment response and to identify early augmentation (increase ≥10 points after ≥3 months of dopaminergic therapy).
Management
- •Initiate iron repletion when ferritin <75 µg/L or TSAT <20 %: IV ferric carboxymaltose 750 mg on day 0 and day 5 (repeat q12 weeks if needed).
- •For dopamine‑naïve patients with IRLS 11‑20, start 150 mg PO BID; titrate to 300 mg BID (max 600 mg) over 2 weeks - reduces IRLS by ~12 points and avoids augmentation.
- •If pregabalin is contraindicated (eGFR <30 mL/min), use 300 mg PO TID, titrating to 900 mg/day as tolerated.
- •When non‑dopaminergic agents fail or IRLS ≥21, add a dopamine agonist: 0.125 mg PO at bedtime, increase by 0.125 mg weekly to max 0.75 mg; monitor for impulse‑control disorders and augmentation.
- •Alternatively, apply a transdermal patch 2 mg/24 h; increase to 4 mg/24 h after 12 h if symptoms persist - provides steady dopaminergic stimulation with lower augmentation risk.
- •Reserve ‑naloxone PR 10 mg/5 mg PO BID (titrate to 20 mg/10 mg BID) for severe, refractory RLS (IRLS ≥30) after dopaminergic failure; contraindicated in severe COPD or untreated sleep‑apnoea.
- •Avoid high‑dose oral dopamine agonists (>0.5 mg pramipexole) as first‑line rescue; they are linked to life‑threatening impulse‑control and augmentation events.
- •Monitor serum ferritin every 3 months while on dopaminergic therapy; re‑infuse iron if ferritin falls below 75 µg/L to mitigate augmentation.
- •Screen for augmentation at each visit: a rise in IRLS ≥10 points after ≥3 months of stable dopaminergic dose signals need to switch to a non‑dopaminergic agent.
- •Educate patients on sleep hygiene (regular bedtime, cool room, caffeine avoidance) and leg‑stretching exercises before sleep - these non‑pharmacologic measures can lower IRLS by 4‑5 points.
- •Refer to a sleep‑movement specialist if IRLS remains ≥20 despite optimal pharmacotherapy, if augmentation persists, or if comorbid obstructive sleep apnoea is suspected.
- •Discharge criteria: IRLS ≤10, ferritin ≥75 µg/L, stable medication regimen for ≥2 weeks, and patient able to adhere to sleep‑hygiene plan.
Board Review — High Yield
- •Four IRLSSG criteria, urge, rest‑worsening, movement relief, evening predominance.
- •Brain iron deficiency, core driver; ferritin <75 µg/L predicts response to IV iron.
- •Augmentation, paradoxical worsening after ≥3 months of dopaminergic therapy; risk ↑ with baseline IRLS ≥30.
- •Pregabalin, first‑line non‑dopaminergic agent; 150‑300 mg BID, NNT = 5 for ≥50 % IRLS improvement.
- •Rotigotine patch, steady dopaminergic delivery; 2‑4 mg/24 h useful in augmentation‑prone patients.
- •Ferric carboxymaltose, IV iron regimen (750 mg × 2) reduces IRLS by ~8 points; use when ferritin <75 µg/L.
- •Pregnancy RLS, avoid dopamine agonists; treat with oral/IV iron and gabapentin if needed after first trimester.
- •IRLS severity thresholds, 0‑10 mild, 11‑20 moderate, 21‑30 severe, 31‑40 very severe.
Deep Dive — Evidence Details
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