Pharmacokinetics in children
The following pharmacokinetic parameters have been found (Olkkola 1989, Barret 1993, Ng 2015):
| |
Administration route |
t½ (hours) |
Cl (l/hour/kg) |
Vd (l/kg) |
| Premature infants |
Intravenous |
20±8 |
0.23 ± 0.07 |
6.2 ± 2.1 |
| Neonates |
Sublingual |
11 |
3.5 |
- |
| 4-7 years |
Intravenous |
1 ± 0.2 |
3.6 ± 1.14 |
3.2 ± 2.0 |
dose recommendation of formulary compared to licensed use (on-label versus off-label)
No information is present at this moment.
Available formulations
No information is present at this moment.
Dosages
| Neonatal abstinence syndrome (NAS) |
- Sublingual
-
0 months
up to
1 month
- Initial dose:
15
microg./kg/day
in 3
doses.
- Maintenance dose:
15
- 60
microg./kg/day
in 3
doses.
- Directions for administration:
After 48 hours on an unchanged dose: reduce. Give 10% less of this ‘unchanged 48-hour dose’ every day until the initial dose is reached. After this, the administration can be stopped.
If there is insufficient effect, a rescue dose can be given (50% of the last dose) and the maintenance dose can be increased in steps of 25% per dose
|
| Moderate to severe pain |
- Transdermal
-
2 years
up to
18 years
and
<
30 kg
-
5
microg./hour
continuous release. Max: 140 microg./hour.
If there is insufficient effect after 24 hours, double the dose to a maximum of 140 mcg/hour..
-
2 years
up to
18 years
and
≥ 30 kg
-
10
microg./hour
continuous release. Max: 140 microg./hour.
If there is insufficient effect after 24 hours, double the dose to a maximum of 140 mcg/hour.
|
| Severe pain |
- Sublingual
-
≥ 6 years
and
≥ 45 kg
-
≥ 6 years
and
35
up to
45 kg
- Intramuscular
-
≥ 1 year
-
3
- 6
microg./kg/dose,
as required 3-4 times daily. Max: 9 microg./kg/dose.
- Intravenous
-
≥ 1 year
-
3
- 6
microg./kg/dose,
as required 3-4 times daily. Max: 9 microg./kg/dose.
|
Renal impaiment in children > 3 months
GFR ≥10 ml/min/1.73m2: Dose adjustment not required.
GFR <10 ml/min/1.73m2: A general recommendation on dose adjustment cannot be provided.
The complete list of all undesirable drug reactions can be found in the national Summary of Product Characteristics (SmPC) – click here
Side effects in children
Neonatal opioid withdrawal syndrome.
The complete list of all contra-indications can be found in the national Summary of Product Characteristics (SmPC) – click here
Contra-indications
No information available on specific contra indications in children.
The complete list of all warnings and precautions can be found in the national Summary of Product Characteristics (SmPC) – click here
Warnings & precautions in children
The patches sometimes become empty more rapidly in children; it is thought that this may be caused by a somewhat higher body temperature. The result of this is that the patches may have to be changed sooner than the manufacturer recommends.
Interactions
The complete list of all interactions can be found in the national Summary of Product Characteristics (SmPC) – click here
OPIOIDS
This pages provides a list of drugs from the same ATC class for comparison. This does not necessarily mean that these drugs are interchangeable.
| Natural opium alkaloids |
|
|
|
N02AA03
|
|
|
|
N02AA01
|
|
|
|
N02AA05
|
|
|
|
N02AA59
|
| Phenylpiperidine derivatives |
|
|
|
N02AB03
|
|
|
|
N02AB03
|
|
|
|
N02AB02
|
| Diphenylpropylamine derivatives |
|
|
|
N02AC06
|
|
|
|
N02AC03
|
| Morphinan derivatives |
|
|
|
N02AF02
|
| Other opioids |
|
|
|
N02AX06
|
|
|
|
N02AX01
|
|
|
|
N02AX02
|
| Opioids in combination with non-opioid analgesics |
|
|
|
N02AJ13
|
References
-
Barrett, D.A., et al, The pharmacokinetics and physiological effects of buprenorphine infusion in premature neonates. , Br J Clin Pharmacol, 1993, 36(3), 215-9.
-
Ng, C.M., et al, Population Pharmacokinetic Model of Sublingual Buprenorphine in Neonatal Abstinence Syndrome., Pharmacotherapy, 2015, 35(7), 670-80
-
Kraft, W.K., et al, Buprenorphine for the Treatment of the Neonatal Abstinence Syndrome., N Engl J Med, 2017, 376(24), 2341-2348
-
Kraft, W.K., et al, Revised dose schema of sublingual buprenorphine in the treatment of the neonatal opioid abstinence syndrome. , Addiction, 2011, 106(3), 574-80
-
Kraft, W.K., et al, Sublingual buprenorphine for treatment of neonatal abstinence syndrome: a randomized trial. , Pediatrics, 2008, 122(3), e601-7
-
Olkkola, K.T., et al, Pharmacokinetics of intravenous buprenorphine in children., Br J Clin Pharmacol, 1989, 28(2), 202-4
-
Ruggiero, A., et al., Efficacy and safety of transdermal buprenorphine in the management of children with cancer-related pain., Pediatr Blood Cancer, 2013, 60(3), 433-7
-
Indivior UK Limited, SmPC Temgesic SL (RVG 11872) 15-05-2016, www.geneesmiddelinformatiebank.nl
-
Disher T et al., Pharmacological Treatments for Neonatal Abstinence Syndrome: A Systematic Review and Network Meta-analysis, JAMA Pediatr, 2019, 173(3), 234-243
-
Hall ES et al., Comparison of Neonatal Abstinence Syndrome Treatment with Sublingual Buprenorphine versus Conventional Opioids., Am J Perinatol, 2018, 35(4), 405-412
-
Indivior Europe Limited, SmPC, Temgesic® sublingual/sublingual forte 0,2/0,4 mg Sublingualtablette (997.00.01/27138.00.00)
-
Indivior Europe Limited, SmPC, Temgesic® Ampullen 0,3 mg Injektionslösung (997.00.00), 01/2019
-
Barrett, D.A., et al, The pharmacokinetics and physiological effects of buprenorphine infusion in premature neonates., Br J Clin Pharmacol, 1993, 36(3), 215-9.
-
Kraft, W.K., et al, Sublingual buprenorphine for treatment of neonatal abstinence syndrome: a randomized trial., Pediatrics, 2008, 122(3), e601-7
-
Kraft, W.K., et al, Revised dose schema of sublingual buprenorphine in the treatment of the neonatal opioid abstinence syndrome., Addiction, 2011, 106(3), 574-80
Therapeutic Drug Monitoring
Overdose