First-Pass Effect (2024)

Definition/Introduction

The first-pass effect is a pharmacological phenomenon in which a medication undergoes metabolism at a specific location in the body. The first-pass effect decreases the active drug's concentration upon reaching systemic circulation or its site of action. The first-pass effect is often associated with the liver, a major site of drug metabolism. However, the first-pass effect can also occur in the body's lungs, vasculature, gastrointestinal tract, and other metabolically active tissues. This effect can be increased by various factors such as plasma protein concentrations, gastrointestinal motility, and enzymatic activity.[1][2][3]The extent to which a patient may undergo the first-pass effect differs from patient to patient, and this must also be considered when determining appropriate dosing.[4][5]If the first-pass effect is significantly prominent in a patient, the medication may require administration via a different route or formulation to bypass the first-pass effect.[6]

Issues of Concern

A significant issue of concern with the first-pass effect is considering its variability among different individual patients. It is essential that pharmacological dosing considers these natural variations in human metabolism to ensure patients remain within the therapeutic window of the appropriate drug.[4]Also, differences in the first-pass effect have been noted based on gender and age.[7][8]

Clinical Significance

The clinical significance of the first-pass effect is crucial to the proper administration and maintenance of pharmacological therapy. Some drugs that undergo considerable first-pass metabolism include alprenolol, 5-fluorouracil, morphine, pentazocine, and mercaptopurine. When given orally, these drugs are quickly metabolized via the first-pass effect, requiring their oral dosages to be much larger than their intravenous dosages. The first-pass effect also impacts peak drug concentrations, which may result in drug concentration peaks occurring much earlier than they would in a parenteral dose.[5][9]

Sublingual nitroglycerin quickly relieves symptoms of angina due to its high lipid solubility and bypassing the first-pass effect before entering the systemic circulation.[10]Isosorbide mononitrate differs from nitroglycerin. ISMN undergoes minimal first-pass metabolism, leading to high bioavailability after oral administration. However, its onset of action is too slow for the acute treatment of angina.[11]Administering diazepam rectally in children with febrile seizures significantly bypasses first-pass metabolism, ensuring a rapid onset of anticonvulsant effects, which is particularly important in prehospital settings.[12][13]

Research has shown that monitoring blood concentrations of drugs that experience the first-pass effect is the most viable way to maintain therapeutic concentrations of these drugs.[14]Dextromethorphan, acting as a substrate for CYP2D6 and undergoing significant first-pass bioinactivation, exhibits potential in treating the pseudobulbar-affect. The co-administration of dextromethorphan with a minimal dose of quinidine effectively inhibits first-pass metabolism, resulting in increased systemic concentrations compared to monotherapy. This combination therapy is now FDA-approved for managing the pseudobulbar-affect.[15]

Nursing, Allied Health, and Interprofessional Team Interventions

The interprofessional healthcare team (eg, physicians, advanced practitioners, nurses, and pharmacists) must work together to ensure the safety and efficacy of pharmacotherapy. The healthcare team should monitor for signs of adverse drug reactions. The pharmacist should verify the dosing, perform medication reconciliation, and perform a drug interaction check.[16]Nurses can monitor adverse events and assess treatment effectiveness on subsequent visits. Applying basic pharmaco*kinetic concepts, eg, the first pass effect, can ensure the appropriate drug route of administration and dosing of the patient. Open communicationamong nurses, pharmacists, and the prescribing physician is crucial for reporting and discussing any concerns regarding pharmacotherapy. An interprofessional team approach with open communication is essential to optimize patient outcomes with minimal adverse events.

Nursing, Allied Health, and Interprofessional Team Monitoring

When monitoring patients taking drugs that experience the first-pass effect, it is critical to monitor the blood concentrations of these drugs to ensure that the patient's serum drug concentrations remain within their therapeutic windows. Implementing this approach will optimize the effectiveness of the treatment and enhance patient safety.[14]

References

1.

Doherty MM, Pang KS. First-pass effect: significance of the intestine for absorption and metabolism. Drug Chem Toxicol. 1997 Nov;20(4):329-44. [PubMed: 9433662]

2.

Wang X, Zheng M, Liu J, Huang Z, Bai Y, Ren Z, Wang Z, Tian Y, Qiao Z, Liu W, Feng F. Differences of first-pass effect in the liver and intestine contribute to the stereoselective pharmaco*kinetics of rhynchophylline and isorhynchophylline epimers in rats. J Ethnopharmacol. 2017 Sep 14;209:175-183. [PubMed: 28755970]

3.

Shen DD, Kunze KL, Thummel KE. Enzyme-catalyzed processes of first-pass hepatic and intestinal drug extraction. Adv Drug Deliv Rev. 1997 Sep 15;27(2-3):99-127. [PubMed: 10837554]

4.

Tam YK. Individual variation in first-pass metabolism. Clin Pharmaco*kinet. 1993 Oct;25(4):300-28. [PubMed: 8261714]

5.

Pond SM, Tozer TN. First-pass elimination. Basic concepts and clinical consequences. Clin Pharmaco*kinet. 1984 Jan-Feb;9(1):1-25. [PubMed: 6362950]

6.

Mattes RD, Shaw LM, Edling-Owens J, Engelman K, Elsohly MA. Bypassing the first-pass effect for the therapeutic use of cannabinoids. Pharmacol Biochem Behav. 1993 Mar;44(3):745-7. [PubMed: 8383856]

7.

Baraona E, Abittan CS, Dohmen K, Moretti M, Pozzato G, Chayes ZW, Schaefer C, Lieber CS. Gender differences in pharmaco*kinetics of alcohol. Alcohol Clin Exp Res. 2001 Apr;25(4):502-7. [PubMed: 11329488]

8.

Wynne H. Drug metabolism and ageing. J Br Menopause Soc. 2005 Jun;11(2):51-6. [PubMed: 15970015]

9.

Lalka D, Griffith RK, Cronenberger CL. The hepatic first-pass metabolism of problematic drugs. J Clin Pharmacol. 1993 Jul;33(7):657-69. [PubMed: 8366191]

10.

Divakaran S, Loscalzo J. The Role of Nitroglycerin and Other Nitrogen Oxides in Cardiovascular Therapeutics. J Am Coll Cardiol. 2017 Nov 07;70(19):2393-2410. [PMC free article: PMC5687289] [PubMed: 29096811]

11.

LiverTox: Clinical and Research Information on Drug-Induced Liver Injury [Internet]. National Institute of Diabetes and Digestive and Kidney Diseases; Bethesda (MD): Apr 27, 2018. Organic Nitrates. [PubMed: 31643263]

12.

Glauser T, Shinnar S, Gloss D, Alldredge B, Arya R, Bainbridge J, Bare M, Bleck T, Dodson WE, Garrity L, Jagoda A, Lowenstein D, Pellock J, Riviello J, Sloan E, Treiman DM. Evidence-Based Guideline: Treatment of Convulsive Status Epilepticus in Children and Adults: Report of the Guideline Committee of the American Epilepsy Society. Epilepsy Curr. 2016 Jan-Feb;16(1):48-61. [PMC free article: PMC4749120] [PubMed: 26900382]

13.

Eilbert W, Chan C. Febrile seizures: A review. J Am Coll Emerg Physicians Open. 2022 Aug;3(4):e12769. [PMC free article: PMC9396974] [PubMed: 36016968]

14.

Wargin WA, Sawchuk RJ, McBride JW, McCoy HG, Rylander ML. Variable first-pass elimination of propranolol following single and multiple oral doses in hypertensive patients. Eur J Drug Metab Pharmaco*kinet. 1982;7(3):183-9. [PubMed: 7173272]

15.

Fralick M, Sacks CA, Kesselheim AS. Assessment of Use of Combined Dextromethorphan and Quinidine in Patients With Dementia or Parkinson Disease After US Food and Drug Administration Approval for Pseudobulbar Affect. JAMA Intern Med. 2019 Feb 01;179(2):224-230. [PMC free article: PMC6439654] [PubMed: 30615021]

16.

Splawski J, Minger H. Value of the Pharmacist in the Medication Reconciliation Process. P T. 2016 Mar;41(3):176-8. [PMC free article: PMC4771087] [PubMed: 26957885]

Disclosure: Timothy Herman declares no relevant financial relationships with ineligible companies.

Disclosure: Cynthia Santos declares no relevant financial relationships with ineligible companies.

First-Pass Effect (2024)
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