What is the prophylactic dosing of tinzaparin (a low molecular weight heparin) for Deep Vein Thrombosis (DVT) prophylaxis, specifically 75 units/kilogram?

Medical Advisory BoardAll articles are reviewed for accuracy by our Medical Advisory Board
Educational purpose only • Exercise caution as content is pending human review
Article Review Status
Submitted
Under Review
Approved

Last updated: March 30, 2025View editorial policy

Personalize

Help us tailor your experience

Which best describes you? Your choice helps us use language that's most understandable for you.

From the Guidelines

The standard DVT prophylaxis dose for tinzaparin is 4500 units subcutaneously daily, or 75 units/kg subcutaneously daily, with the fixed dose being the preferred option. For prophylaxis in surgical patients, tinzaparin should be administered 2 hours before surgery and then continued once daily for 7-10 days or until the patient is fully mobile. In high-risk orthopedic surgery patients, prophylaxis may be extended up to 28-35 days. Dosage adjustments are needed for patients with severe renal impairment (creatinine clearance <30 mL/min), and monitoring of anti-Xa levels may be considered in these cases 1. Tinzaparin should be administered subcutaneously, preferably in the anterolateral or posterolateral abdominal wall. The medication works by binding to antithrombin, which enhances its inhibitory effect on factor Xa, thereby preventing thrombin formation and clot development. Common side effects include injection site bruising and minor bleeding. Contraindications include active major bleeding, thrombocytopenia associated with positive in vitro tests for anti-platelet antibodies, and hypersensitivity to tinzaparin.

Some key considerations for tinzaparin dosing include:

  • Significant renal clearance; avoid in patients with creatinine clearance <35 ml/min or adjust dose based on antifactor Xa levels 1
  • Tinzaparin should be avoided in patients aged >70 y with renal insufficiency, as stated by the FDA Website, and fondaparinux is contraindicated in patients with creatinine clearance <30 mL/min 1
  • LMWHs, including tinzaparin, should be used with caution in patients with renal dysfunction, and dose adjustments and anti-Xa monitoring may be required 1

It's essential to follow institutional standard operating procedures (SOP) for dosing schedules, and if no SOP is available, use the American College of Chest Physicians (ACCP) recommendations, as outlined in the guidelines by Kahn et al. and Garcia et al. 1.

From the Research

DVT Prophylaxis Tinzaparin Dosing

  • The dosing for tinzaparin in DVT prophylaxis is not explicitly stated as 75 units/kg in the provided studies 2, 3, 4, 5, 6.
  • However, one study mentions that tinzaparin is administered subcutaneously, but does not specify the dose for prophylaxis 2.
  • Another study compares the efficacy of tinzaparin with other low-molecular-weight heparins, but also does not provide a specific dose for prophylaxis 6.
  • It is worth noting that the provided studies primarily focus on the treatment of DVT rather than prophylaxis, and the dosing information for prophylaxis is not clearly stated.

Comparison of Tinzaparin with Other Low-Molecular-Weight Heparins

  • Tinzaparin has been compared with other low-molecular-weight heparins, such as dalteparin, in terms of efficacy and safety for the treatment of DVT and pulmonary embolism 6.
  • The study found that tinzaparin and dalteparin are safe and effective for the outpatient treatment of DVT or pulmonary embolism, with no significant differences between the two drugs in terms of major clinical end points 6.

Administration and Monitoring

  • Tinzaparin can be administered subcutaneously once daily, which may facilitate self-administration in the outpatient setting 2.
  • The studies suggest that tinzaparin requires little or no monitoring, which can be beneficial for patients 2, 3.

Related Questions

What is the role of Innohep (tinzaparin) in managing anticoagulation for patients with active bleeding on apixaban?
What is the prophylactic dosing of tinzaparin (a low molecular weight heparin) for Deep Vein Thrombosis (DVT) prophylaxis, specifically 75 units/kilogram?
How soon can tinzaparin (low molecular weight heparin) for Deep Vein Thrombosis (DVT) prophylaxis be restarted after an Esophagogastroduodenoscopy (EGD) with biopsy?
Is it okay to change the administration time of tinzaparin (low molecular weight heparin) from 10:00 to 21:00?
What anticoagulants are recommended after procedures with high risk of thromboembolic events?
What is the treatment for a 6-month-old baby with acute diarrhea (loose motions) 4 to 5 times a day, characterized by mucous and frothy stools with a foul odor?
What is the optimal treatment plan for cystic fibrosis (CF) infants experiencing recurrent bacterial lung infections, specifically with Staphylococcus aureus and Pseudomonas aeruginosa, utilizing pulmonary nebulizers, systemic antibiotics, inhaled antibiotics, and pulmonary hygiene, including chest physiotherapy (CPT), hypertonic saline nebulizers, Xopenex (levalbuterol), Pulmicort (budesonide) nebulizer, and Pulmozyme (dornase alfa)?
What is the prophylactic dosing of tinzaparin (a low molecular weight heparin) for Deep Vein Thrombosis (DVT) prophylaxis, specifically 75 units/kilogram?
What is the comparative efficacy and side effect profile of available oral Glucagon-Like Peptide-1 (GLP-1) receptor agonist drugs, such as Victoza (liraglutide), Trulicity (dulaglutide), and Rybelsus (semaglutide), for weight loss?
What is the comparative efficacy and side effect profile of available injectable Glucagon-Like Peptide-1 (GLP-1) receptor agonist drugs, such as Victoza (liraglutide), Trulicity (dulaglutide), and Ozempic (semaglutide), for weight loss?
What is the comparative efficacy and side effect profile of available injectable Glucagon-Like Peptide-1 (GLP-1) receptor agonist drugs, such as Victoza (liraglutide), Trulicity (dulaglutide), and Ozempic (semaglutide), for weight loss?

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

Have a follow-up question?

Our Medical A.I. is used by practicing medical doctors at top research institutions around the world. Ask any follow up question and get world-class guideline-backed answers instantly.