Parecoxib - analgesia guidelines for acute pain management in adults

Warning

Parecoxib

Patients at high risk of NSAID-induced GI adverse events or surgical/traumatic bleeding

Parecoxib is a parenteral pro-drug for valdecoxib, a highly selective cyclo-oxygenase-2 (COX-2) inhibitor. COX-2 is the inducible isoform of cyclo-oxygenase whose expression is markedly increased in response to inflammatory stressors. In contrast, COX-1 is the constitutive isoform whose activity predominates during normal physiological conditions. The therapeutic and anti-inflammatory activity of NSAIDs results primarily from their inhibition of COX-2 whereas their toxicity, antiplatelet activity and adverse effects result mainly from COX-1 inhibition.

  • similar analgesic efficacy to ketorolac 30mg IV or 60mg IM, a conventional non-selective parenteral NSAID
  • has a significant opioid-sparing effect, therefore reducing opioid side effects
  • causes significantly less erosion and ulceration of the gastroduodenal mucosa and fewer clinical gastrointestinal adverse events than ketorolac
  • has no antiplatelet activity and therefore, unlike ketorolac, it does not affect peri-operative or traumatic blood loss
  • has a rapid onset (13 minutes) and long duration of action (more than 15 hours IV)
  • It is indicated for short-term management of acute postoperative pain and should be considered for parenteral short-term management of acute pain of moderate severity in patients:
    • for whom oral medication is inappropriate
    • who would be at high risk of gastrointestinal adverse events if prescribed ketorolac
    • in whom any antiplatelet effect must be minimised

Contraindications

Contraindications include:

  • hypersensitivity to aspirin or any other NSAID, or sulphonamide hypersensitivity
  • active peptic ulcer disease (i.e. patients on treatment) or GI bleeding
  • established ischaemic heart disease or cerebrovascular disease
  • mild to severe heart failure
  • peripheral arterial disease
  • inflammatory bowel disease

Cautions

Caution should be observed in:

  • patients with dehydration
  • renal impairment
  • hepatic impairment or predisposed to fluid retention
  • oedema
  • the elderly
  • hypertension
  • left ventricular dysfunction
  • cardiac impairment
  • following coronary artery bypass surgery
  • allergic disorders
  • coagulation defects and alternative therapy considered.
  • avoid in pregnancy, breast feeding, severe liver disease.

Rare but potentially serious or fatal hypersensitivity and severe skin reactions are possible with COX II inhibitors – this risk is increased in patients with a history of drug allergy. The drug should be immediately discontinued if an adverse drug reaction of this type occurs.

Editorial Information

Last reviewed: 28/02/2022

Next review date: 28/02/2025

Author(s): Smith S.

Version: 2

Author email(s): shona.smith@borders.scot.nhs.uk.

Approved By: Acute Pain Service

Reviewer name(s): Smith S.

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