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. 2020 Feb 14;117(7):108–115. doi: 10.3238/arztebl.2020.0108

eTABLE 3. Treatment for nausea and vomiting in patients with malignant bowel obstruction (MBO).

Drug class Medication Dosage Remarks
Prokinetics Metoclopramide 30–40* mg/day s.c.* Drug of choice when incomplete obstruction or functional disorder is suspected. Because it promotes GI motility, pain and vomiting may increase. Caution: This drug should be stopped if complete obstruction is present
Antipsychotics Haloperidol* 2.5–10 mg/day s.c.* or i.v.* Drug of choice when complete obstruction is present and no prokinetic antiemetic can be used
Levomepromazine* 1–5 mg oral/s.c.* at night Dose may be increased up to 25 mg/day, but this is rarely necessary
Olanzapine* 2.5 mg as initial dose, if needed, 5–10 mg oral/s.l. daily Use with caution in older patients and those with dementia, due to increased half-life and increased mortality risk
Antihistamines Dimenhydrinate 150 mg p.r. 62–400 mg/day s.c.* or i.v. Has a sedative effect
Setrons Ondansetron* 8 mg oral or s. l./ s.c.*/ i.v. 2–3× daily Increases constipation
Granisetron* 1–2 mg p.o./s.c.*/ i.v. 1× daily Increases constipation; dose may be increased up to 9 mg/day
Anticholinergics Butylscopolamine* 40–80 mg/day s.c./i.v. dose may be increased up to 120 mg* Used to reduce GI secretion; has no direct antiemetic effect. May increase oral dryness and thirst
Somatostatin analogs Octreotide* Initial dose 100 µg 12-hourly, dose may be increased up to 750 µg/day, further increase rarely has greater effect Used to reduce GI secretion; second-line drug (because expensive)
Lanreotide* 60 mg deep s.c. in upper outer quadrant of buttock every 3 months If necessary, 120 mg every 4 weeks
H2-blockers Ranitidine* 50 mg 2–4× daily, or continuously 100–200 mg/ 24 h i.v.
Proton pump inhibitors Omeprazole* 40–80 mg/day i.v, s.c.*
Corticosteroids Dexamethasone* 8–12 mg/day s.c.*/ i.v. Used to reduce peritumoral edema (may restore passage of bowel contents) and for antiemesis; fewer mineralocorticoid adverse effects than methylprednisolone

* * Off label use; GI, gastrointestinal; i.v., intravenous; p.o., orally; p.r., rectally; s.c., subcutaneously; s.l., sublingually

Source: “S3-Leitlinie Palliativmedizin für Patienten mit einer nicht-heilbaren Krebserkrankung” (2), adapted from Bausewein et al. (e8)