BNF for Children (BNFC) 2018-2019

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local anaesthetic effect may also be reduced by altered
local pH.
lCAUTIONSAcute porphyrias p. 603 .cardiovascular
disease.children (consider dose reduction).debilitated
patients (consider dose reduction).epilepsy.
hypovolaemia.impaired cardiac conduction.impaired
respiratory function.myasthenia gravis.shock


lINTERACTIONS→Appendix 1 : anaesthetics, local


lSIDE-EFFECTS
▶Common or very commonArrhythmias.back pain.chills.
dizziness.headache.hypertension.hypotension.nausea
.sensation abnormal.urinary retention.vomiting
▶UncommonAnxiety.dyspnoea.hypothermia.
neurotoxicity.syncope
▶Rare or very rareCardiac arrest
▶Frequency not knownDyskinesia


SIDE-EFFECTS, FURTHER INFORMATIONToxic effects after
administration of local anaesthetics are a result of
excessively high plasma concentrations; severe toxicity
usually results from inadvertent intravascular injection.
The systemic toxicity of local anaesthetics mainly involves
the central nervous and cardiovascular systems. The onset
of toxicity can be unpredictable and delayed. Monitor as
per local protocol for at least 30 minutes after
administration.

lALLERGY AND CROSS-SENSITIVITY
▶Hypersensitivity and cross-sensitivityHypersensitivity
reactions occur mainly with the ester-type local
anaesthetics, such as tetracaine; reactions are less
frequent with the amide types, such as articaine,
bupivacaine, levobupivacaine, lidocaine, mepivacaine,
prilocaine, and ropivacaine. Cross-sensitivity reactions
may be avoided by using the alternative chemical type.


lPREGNANCYNot known to be harmful. Do not use for
paracervical block in obstetrics.


lBREAST FEEDINGNot known to be harmful.


lHEPATIC IMPAIRMENTUse with caution in severe
impairment.
lRENAL IMPAIRMENTCaution in severe impairment.
Increased risk of systemic toxicity in chronic renal failure.


lMEDICINAL FORMS
There can be variation in the licensing of different medicines
containing the same drug.
Solution for injection
ELECTROLYTES:May contain Sodium
▶Ropivacaine hydrochloride (Non-proprietary)
Ropivacaine hydrochloride 2 mg per 1 mlRopivacaine 20 mg/ 10 ml
solution for injection ampoules| 10 ampouleP£ 16. 50 (Hospital
only)
Ropivacaine hydrochloride 7.5 mg per 1 mlRopivacaine
75 mg/ 10 ml solution for injection ampoules| 10 ampouleP
£ 25. 00 (Hospital only)
Ropivacaine hydrochloride 10 mg per 1 mlRopivacaine
100 mg/ 10 ml solution for injection ampoules| 10 ampouleP
£ 30. 00 (Hospital only)
▶Naropin(Aspen Pharma Trading Ltd)
Ropivacaine hydrochloride 2 mg per 1 mlNaropin 20 mg/ 10 ml
solution for injection ampoules| 5 ampouleP£ 12. 79
Ropivacaine hydrochloride 7.5 mg per 1 mlNaropin 75 mg/ 10 ml
solution for injection ampoules| 5 ampouleP£ 15. 90
Ropivacaine hydrochloride 10 mg per 1 mlNaropin 100 mg/ 10 ml
solution for injection ampoules| 5 ampouleP£ 19. 22
Infusion
ELECTROLYTES:May contain Sodium
▶Ropivacaine hydrochloride (Non-proprietary)
Ropivacaine hydrochloride 2 mg per 1 mlRopivacaine
400 mg/ 200 ml infusion bags| 10 bagP£ 137. 00 (Hospital only)
▶Naropin(Aspen Pharma Trading Ltd)
Ropivacaine hydrochloride 2 mg per 1 mlNaropin 400 mg/ 200 ml
infusion Polybags| 5 bagP£ 86. 70


Tetracaine


(Amethocaine)


lINDICATIONS AND DOSE
Anaesthesia before venepuncture or venous cannulation
▶TO THE SKIN
▶Neonate:Apply contents of tube (or appropriate
proportion) to site of venepuncture or venous
cannulation and cover with occlusive dressing; remove
gel and dressing after 30 minutes for venepuncture and
after 45 minutes for venous cannulation.

▶Child 1 month–4 years:Apply contents of up to 1 tube
(applied at separate sites at a single time or appropriate
proportion) to site of venepuncture or venous
cannulation and cover with occlusive dressing; remove
gel and dressing after 30 minutes for venepuncture and
after 45 minutes for venous cannulation
▶Child 5–17 years:Apply contents of up to 5 tubes
(applied at separate sites at a single time or appropriate
proportion) to site of venepuncture or venous
cannulation and cover with occlusive dressing; remove
gel and dressing after 30 minutes for venepuncture and
after 45 minutes for venous cannulation

lUNLICENSED USENot licensed for use in neonates.
lCONTRA-INDICATIONSShould not be applied to damaged
skin
lINTERACTIONS→Appendix 1 : anaesthetics, local
lSIDE-EFFECTSOedema.skin reactions
SIDE-EFFECTS, FURTHER INFORMATIONThe systemic
toxicity of local anaesthetics mainly involves the central
nervous system; systemic side effects unlikely as minimal
absorption following topical application.
lALLERGY AND CROSS-SENSITIVITY
▶Hypersensitivity and cross-sensitivityHypersensitivity
reactions occur mainly with the ester-type local
anaesthetics, such as tetracaine; reactions are less
frequent with the amide types, such as articaine,
bupivacaine, levobupivacaine, lidocaine, mepivacaine,
prilocaine, and ropivacaine. Cross-sensitivity reactions
may be avoided by using the alternative chemical type.
lBREAST FEEDINGNot known to be harmful.
lPATIENT AND CARER ADVICE
Medicines for Children leaflet: Tetracaine gel for local
anaesthesiawww.medicinesforchildren.org.uk/tetracaine-gel-
for-local-anaesthesia

lMEDICINAL FORMS
There can be variation in the licensing of different medicines
containing the same drug.
Gel
EXCIPIENTS:May contain Hydroxybenzoates (parabens)
▶Ametop(Alliance Pharmaceuticals Ltd)
Tetracaine 40 mg per 1 gramAmetop 4 % gel| 1. 5 gramp£ 1. 08

BNFC 2018 – 2019 Local anaesthesia 831


Anaesthesia

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