UK National Clinical Guidelines in Paediatric Dentistry
UK National Clinical Guidelines in Paediatric Dentistry
Introduction
The twelfth National Clinical Guideline in Paediatric Dentistry is published here. The process of guideline
production began in 1994, resulting in first publication in 1997. Each guideline has a nominated main author
but the content is not a personal view; it represents rather a consensus of opinion of current best clinical
practice. Each guideline has been circulated to all consultants in paediatric dentistry in the UK, to the Council
of the BSPD, and to people of related specialities recognized to have expertise in the subject. The final version
of the guideline is produced from a combination of this input and thorough review of published literature.
The intention is to encourage improvement in clinical practice and to stimulate research and clinical audit
in areas where scientific evidence is inadequate. Evidence underlying recommendations is scored according
to the SIGN classification and guidelines should be read in this context. For those wishing further detail,
the process of guideline production in the UK is described in International Journal of Paediatric Dentistry
1997; 7: 267–268.
M. T. HOSEY
360 M. T. Hosey
1.1 General Dental Council definition 1.5 Patient information and consent [2]
A technique in which the use of a drug or drugs Grade C
produces a state of depression of the central nervous • Informed consent for a course of dental treatment
system enabling treatment to be carried out, but during under conscious sedation must be obtained from each
which verbal contact with the patient is maintained parent/guardian, and the child, where appropriate,
throughout the period of sedation. The drugs and tech- prior to the conscious sedation appointment.
niques used to provide conscious sedation for dental • An explanation of the sedation technique proposed
treatment should carry a margin of safety wide enough and of appropriate alternative methods of pain and
to render unintended loss of consciousness unlikely. anxiety control must be given.
The level of sedation must be such that the patient • In advance of the procedure, the child and their
remains conscious, retains protective reflexes, and parent or guardian must be given clear and com-
is able to understand and to respond to verbal prehensive pre- and postoperative instructions in
commands [2]. writing.
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Grade C
• Children who undergo all other forms of seda- 2.0 Choice of sedative agent for children
tion should be fasted prior to the procedure as undergoing dental treatment
follows: The drug groups used for paediatric dental sedation
• No solid food within 6 h include inhalational agents, benzodiazepines, other
• No milk within 4 h sedative hypnotics and psychosedatives.
• No clear fluid within 2 h
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362 M. T. Hosey
Grade C Grade B
• Dental operators should ensure that they comply • Is not recommended in children who have copious
with COSHH [6] in respect of N2O pollution and nasal secretions or who suffer from an upper res-
gas safety. piratory tract infection.
• Is not recommended for use outwith a hospital
environment.
2.1.4 Other inhalational agents
2.3.4
Grade C
• Although isoflurane and other inhalational agents Rectal midazolam:
such as sevoflurane have been reported, their use Grade A
in children should be limited until further research • Can facilitate restorative treatment in uncoopera-
emerges. tive children.
Grade C
2.2 Diazepam and temazepam • Should only be attempted in a hospital facility
with the assistance of a qualified anaesthetist.
2.2.1
2.3.5 Grade C
Grade B
Intramuscular midazolam:
• Oral benzodiazepines can be used to relax anxious
patients prior to dental treatment but their effects • Is not recommended for conscious sedation in
can be unpredictable in children. paediatric dentistry.
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• Repeated administration of chloral hydrate carries • Children who are given an oral sedative should
a theoretical risk of carcinogenesis. be placed in a quiet room facility together with
• These drugs are not recommended outwith a hos- their escort and a competent member of staff.
pital environment. • Sedated children should be monitored clinically
and electronically.
2.5.2 Grade C
• The use of narcotics such as pethidine is not rec-
ommended in the UK. 3.3 Intravenous conscious sedation
• Fentanyl and other potent opioids should only be
used by a qualified anaesthetist in a hospital setting. Grade C
• Intravenous sedation is not recommended in pre-
cooperative children. Dentists should consider
2.6 Common anaesthetic agents that are used as
whether the provision of an elective general
sedatives
anaesthetic might be preferable in such circum-
2.6.1 Propofol stances.
• Single drug intravenous sedation, e.g. midazolam,
Grade C
is recommended for adolescents who are psycho-
• The use of propofol in paediatric dentistry is still
logically and emotionally suitable.
experimental and requires the assistance of a qual-
• Intravenous sedation should only be administered
ified anaesthetist in a hospital environment.
by an experienced dental sedationist with a trained
dental nurse in an appropriate facility.
2.6.2 Ketamine
• A pulse oximeter, at least, should be used to aug-
Grade C ment alert clinical observation.
• Ketamine should only be administered by a qual- • Intravenous sedation for children below the age of
ified anaesthetist in a hospital environment. 14 years should be carried out in a hospital facility.
• Patient-controlled sedation may be of value for
3.0 Routes of administration anxious adolescents.
3.1 Inhalation
3.4 Rectal
Grade C
• This is the recommended route for conscious Grade C
sedation for paediatric dentistry • Rectal administration is not socially acceptable in
the UK.
Grade B
• It is currently not recommended outwith a hospital
• The inhalational route is the most reliable in terms
facility and requires the assistance of a qualified
of onset and recovery.
anaesthetist.
• Efficacy is reduced when children object to the nasal
hood or have difficulty breathing through the nose.
3.5 Intramuscular sedation
Grade C
• Only dedicated dental nitrous oxide inhalation Grade C
sedation delivery systems must be used. • This is not recommended.
• The operator should use a close-fitting scavenging • Operators should consider whether the alternative
nasal hood. An air-entrainment valve is not required. provision of a general anaesthetic might carry a
• The use of a rubber dam improves the effect of lower risk and give greater long-term psycholog-
the sedation and reduces atmospheric pollution. ical benefit to the child.
3.2 Oral
4.0 Polypharmacy
Grade C
• The oral sedative agent should only be prescribed Grade B
and administered by the operating dentist within the • The use of multiple drugs increases the risk of
facility where the dental procedure is to take place. complication and is not recommended.
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2.5.3 Pethidine
2.5 Chloral hydrate, hydroxyzine and promethazine
Pethidine has been reported to cause nausea,
hydrochlorate and pethidine
vomiting and oxygen desaturation [86].
2.5.1 Chloral hydrate Evidence to support the single use of Hydroxyzine
Chloral hydrate is a chlorinated derivative of ethyl Hydrochlorate, Promethazine Hydrochlorate or
alcohol that can act as an anaesthetic when Pethidine is poor. Their use should be restricted to
administered in high doses. It is a weak analgesic the hospital environment.
and psychosedative with an elimination half-life of
approximately 8 h. In small doses, mild sedation
2.6 Common anaesthetic agents that can also be
occurs and, in intermediate doses, natural sleep is
used as sedatives
produced. Although chloral hydrate has enjoyed
widespread use as a paediatric sedative agent for 2.6.1 Propofol
many years it can be ineffective in the management Propofol (Diprivan: 2,6 di-isopropophenol) is a fast
of the refractory child due to variable absorption and acting sedative with a narrower margin of safety
partial inactivation in the hepatic portal circulation than some other agents, i.e. the dose required to
[79]. Moreover, chloral hydrate depresses blood produce a sedative effect is close to that used to
pressure and respiratory rate and may cause oxygen induce anaesthesia. Infusion pumps are used to control
desaturation [80] and prolonged drowsiness [81]. the dose, and patient controlled systems are currently
Nausea and vomiting are also common complications, in development, which have been used with some
attributable to gastric irritation. In larger doses, success in adult patients [87–93]. Veerkamp et al.
myocardial depression and arrhythmia can occur. (1997) published an account of an exploratory study
The addition of nitrous oxide resulted in 27% of where children, mainly with nursing bottle caries,
children losing control of their airway [82]. Chloral had teeth removed using propofol administered by
hydrate is contraindicated in children with heart an anaesthetist. The authors reported that conscious
disease as well as those with renal or hepatic sedation was difficult to achieve in this age group and
impairment. Recently there has been concern that recommended further investigation [94]. Furthermore,
there is a risk of carcinogenesis, especially when the use of propofol to sedate children in intensive
used repeatedly [83]. It is rapidly becoming obsolete care units has lead to severe adverse reactions,
as a sedative agent in paediatric dentistry. related to hyperlipidaemia [95]. It is therefore
recommended that the use of propofol in children
2.5.2 Hydroxyzine hydrochloride and promethazine should be regarded as experimental and as such
hydrochloride confined to hospital facilities with the assistance
Hydroxyzine hydrochloride and Promethazine of a qualified anaesthetist until further research
hydrochloride are psychosedatives with an evidence emerges in this population.
antihistaminic, antiemetic and antispasmodic effect.
Common side-effects are dry mouth, fever and skin rash. 2.6.2 Ketamine
Hydroxyzine hydrochloride is a diphenylmethane Ketamine is a powerful analgesic, which, in small
which is usually given orally or intramuscularly, singly dosages, can produce a state of dissociation whilst
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maintaining the protective reflexes. Side-effects dose administered. Some sedationists prefer to use a
include hypertension, vivid hallucinations and (needleless) syringe placed in the buccal sulcus behind
physical movement although these are less prevalent the teeth or to mix the drug with a flavoured elixir.
in children [9]. Ketamine is also known to increase
secretions, including salivation, increasing the risk
3.3 Intravenous sedation
of laryngospasm [23,54,68,96]. Reinemer et al. (1996)
found that the combination of a benzodiazepine with The majority of studies where intravenous seda-
ketamine resulted in a statistically significant increase tion was performed have used adults, many of whom
in blood pressure, heart rate and a fall in oxygen were undergoing third molar surgery, as the study
saturation [97]. As such, advanced airway proficiency sample. The very few studies that reported the use of
was recommended [54]. This drug is not recommended intravenous sedation in children have used multiple
for use in paediatric dental sedation. drugs and have produced a deeper level of sedation
than is acceptable in the UK, and they have therefore
been excluded from this paper. Indeed, even paedi-
3.0 Routes of administration
atric dentists in the USA, who have deep sedation
techniques available, may prefer general anaesthesia
3.1 Inhalation
over parenteral sedation in their private (non-hospital)
The inhalation sedation technique that is com- practices [1,99–101].
monly used in dentistry refers to the administration
of a titrated dose of nitrous oxide in oxygen. In this
3.4 Rectal route
respect, the technique is different from the Entonox
(50 : 50 oxygen and nitrous oxide mixture) that is Although the rectal route has been reported to be
administered in maternity or medical A & E units. effective, predictable and safe, especially in relation
Only dedicated dental nitrous oxide inhalation seda- to diazepam [40,47], this route has not found wide-
tion delivery systems must be used. The standard spread acceptance in paediatric dental practice in the
delivery system is designed to prevent administra- UK, probably because an enema is required.
tion of nitrous oxide gas concentrations in excess of
70%, i.e. there is an assured minimum oxygen con-
3.5 Intramuscular
centration of 30%. There should be a fail-safe device
which shuts down nitrous oxide delivery should the Intramuscular administration of sedative agents is
oxygen supply fail. The dentist sets the flow depend- reliable but painful and was mainly used in the UK
ing on the calculated tidal volume of the patient and prior to induction of general anaesthesia. It is not
then uses a single valve to vary the percentage delivery recommended for paediatric dental management
of nitrous oxide against oxygen. Meanwhile, the [23,102].
dentist should encourage relaxation through semi-
hypnotic suggestion and reassurance as the psycho-
4.0 Polypharmacy
logical preparation by the operator exerts a beneficial
influence on the analgesic effect of the gas [98]. The use of drug combinations or premixed drug
cocktails is generally best avoided because of the
increased risk of side-effects [23,103–105].
3.2 Oral
Respiratory depression is more likely to occur
Oral agents have a slower and more variable onset when more that one sedative agent is administered.
of action and depth of sedation than sedatives Milgrom et al. reported that 63% of their anxious
administered by other routes. Compared to other young adult study group, sedated with a midazolam-
routes, onset of sedation is prolonged and duration fentanyl combination, suffered from apnoea (cessation
of action is unpredictable due to variable gastric of breathing) [106]. Barr and Wynn (1992) reported
absorption. Despite this, Nathan (1989), in a survey that 37% of children sedated with ketamine and
of USA pedodontists, reported that this was the fentanyl had either nausea or vomiting [107]. In a
preferred route even for difficult paediatric dental more recent study, almost 40% of children sedated
patients [1], even although children may spit out the with a combination of chloral hydrate, hydroxyzine
dose [59], leaving the clinician uncertain of the exact and pethidine suffered from apnoea [108].
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18 Crawford AN. The use of nitrous oxide-oxygen inhalation
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