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Effect of dexmedetomidine premedication on the intraocular pressure changes after succinylcholine an

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Title: Effect of dexmedetomidine premedication on the intraocular pressure changes after succinylcholine an


1
Effect of dexmedetomidine premedication on the
intraocular pressure changes after
succinylcholine and intubation
BJA British Journal of Anaesthesia
  • British Journal of Anaesthesia 100 (4) 4859
    (2008) February 19, 2008
  • 2008.04.08 presentation ???

2
Background
  • Anaesthesia for patients with open globe injury
    who need emergency surgery may be hazardous.
  • Factors ? the intraocular pressure (IOP) may
    drain the aqueous humour or extrude the vitreous
    humour via the wound, which damage vision
    permanently.

3
Background
  • Succinylcholine is still recommended for some
    situations in open globe injuries.
  • However, the use of succinylcholine is associated
    with an ? intraocular pressure (IOP).
  • This may be deleterious in open globe injuries.
    No method has previously been shown to abolish
    completely this rise in the IOP.
  • We investigated whether dexmedetomidine, an
    alpha-2 agonist, could attenuate this increase in
    the IOP after succinylcholine and intubation.

4
Succinylcholine
  • Facilitate rapid tracheal intubation in high-risk
    patients for aspiration because of its fast onset
    time and excellent intubating conditions.
  • It is, however, associated with an increase in
    the IOP.
  • Durant NN, Katz RL. Suxamethonium. Br J Anaesth
    1982 54 195208
  • Edmondson L. Intraocular pressure and
    suxamethonium. Br J Anaesth 1997 79 146

5
Dexmedetomidine
  • Highly selective alpha-2 adrenergic agonist that
    has sedative and analgesic effects.
  • Dexmedetomidine an updated review. Ann
    Pharmacother 2007 41 24552
  • Intraoperative use of alpha2- adrenoceptor
    agonists. Best Pract Res Clin Anaesthesiol 2000
    14 33545

6
Method
  • Informed consent
  • 40 adult patients of ASA I or II.
  • Elective non-ophthalmic surgeries
  • General anaesthesia

7
Exclusion
  • gt 60 yr
  • Body weight more than 150 ideal body weight
    using Brocas index
  • acute or chronic Eye disease
  • Contraindication to the study drugs
  • Receiving any medication known to alter IOP.

8
www.randomizer.org
  • 2 equal groups (20 patients each)
  • Receive single bolus i.v. dose of dexmedetomidine
    (dexmedetomidine group)
  • Saline (control group)

9
Method
  • 40 patients with no pre-existing eye disease
    undergoing general anaesthesia were randomly
    premedicated by i.v. dexmedetomidine 0.6 mcg/kg,
    or saline.
  • Heart rate (HR), mean arterial pressure (MAP),
    and IOP (using Schioetz tonometer) were measured
  • Before premedication
  • after premedication
  • after thiopental,
  • after succinylcholine,
  • immediately after intubation,
  • and then every 2 min for 6 min.

10
Monitoring
  • Standard monitoring including ECG, pulse
    oximeter, capnometry, and non-invasive arterial
    pressure.
  • (Datex-Ohmeda S/5, ADU, Sweden).
  • IOP was measured with a Schioetz tonometer by an
    ophthalmologist
  • (For this procedure, topical oxybuprocaine
    hydrochloride 0.4 (BNX) was applied to the
    cornea before measurement.)

11
Premedication
  • Diluted 1 ml Dexmedetomidine 100 mg/ml with 49 ml
    normal saline to a concentration of 2 mg/ml.
  • Syringes containing solutions of either
    dexmedetomidine or saline were done in a
    Doubleblind fashion by a team member who was not
    in data recording.
  • Before induction, a single dose of
    dexmedetomidine 0.6 mg/kg was administered
  • i.v. syringe pump (Life Care 5000 Infusion
    System, Abbot) over 10 min.
  • Saline was given in the control group using the
    same pump.

12
Anaesthesia was standardized
  • Preoxygenation for 3 min,
  • induced with thiopental 5 mg/kg fentanyl 1
    mg/kg.
  • Succinylcholine 1.5 mg/kg.
  • When the fasciculations had ceased, tracheal
    intubated under direct vision laryngoscopy
  • correct position of the tracheal tube was
    verified by auscultation of the chest and by
    capnometry.

13
  • failed intubation at the 1st try, the patient was
    excluded.
  • Rocuronium provided the intraoperative
    neuromuscular block.
  • Anaesthesia was maintained with sevoflurane in a
    mixture of oxygen and air.
  • Fluid administration of lactated Ringer solution
    was standardized at 4 ml/kg/h.
  • If hypotension (MAP 30 from the baseline) or
    bradycardia (HR,40 beat/min) occurred, it was
    recorded and managed according to the preference
    of the attending anaesthetist.

14
  • Mean arterial pressure (MAP), heart rate (HR),
    and IOP were recorded at the following time
    points
  • T1 5 min after arrival to OR, before
    premedication (baseline).
  • T2 10 min after premedication.
  • T3 30 s after thiopental.
  • T4 30 s after succinylcholine.
  • T5 immediately after intubation.
  • T68 every 2 min for 6 min after intubation.

15
Results
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17
Heart Rate
  • No significant differences in HR between the two
    groups were recorded at any time.
  • HR ? significantly after injection of thiopental,
    succinylcholine, intubation in control group.
  • These ? in HR were not observed in the
    dexmedetomidine group.

18
Mean Arterial Pressure
  • The MAP increased significantly compared with the
    preoperative value after intubation in the
    control group and was significantly higher than
    the MAP in the dexmedetomidine group (P0.041).
  • In the dexmedetomidine group, the MAP was not
    significantly higher than the preoperative value
    at all times.
  • No incidence of hypotension or bradycardia
    requiring intervention was reported in both
    groups.

19
Intraocular Pressure
  • There was no significant difference in the
    baseline IOP between both groups.
  • After dexmedetomidine injection, there was a
    significant decrease in IOP, compared with
    baseline (P0.017).
  • Thiopental decreased IOP significantly in both
    groups (Plt0.001).
  • Succinylcholine and intubation increased IOP in
    both groups. However, IOP in the dexmedetomidine
    group after intubation was not significantly
    different from that at baseline (P0.65), unlike
    that in the control group (Plt0.001).

20
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21
Results
  • Succinylcholine and intubation increased IOP in
    both groups.
  • However, in the dexmedetomidine group, the IOP
    rise was not different from the baseline value
    (P0.65) and was significantly lower than in the
    saline group (P0.003).
  • After intubation, the MAP in the control group
    was higher than that in the dexmedetomidine group
    (P0.041) and exceeded the baseline value
    (Plt0.001).
  • The HR also showed less fluctuation in the
    dexmedetomidine group than in the saline group.

22
Disscusion
  • The main finding was that premedication with a
    dose dexmedetomidine 0.6 mg/kg over 10 min
    blunted the ?IOP caused by succinylcholine
    intubation.
  • Attenuated the haemodynamic response to
    laryngoscopy intubation.

23
  • Dexmedetomidine intraocular hypotensive effect is
    consistent with previous researches on alpha-2
    agonists.
  • Clonidine was effective in preventing the rise of
    the IOP in response to succinylcholine tracheal
    intubation.
  • The effects of clonidine on intraocular pressure,
    perioperative hemodynamics and anesthetic
    requirements. Anesthesiology 1988 68 70716
  • Oral clonidine premedication for elderly patients
    undergoing intraocular surgery. Acta Anaesthesiol
    Scand 1992 36 15964

24
  • Dexmedetomidine infusion adjunct to local
    analgesia in ophthalmic surgery was effective in
    ? IOP significantly.
  • Dexmedetomidine during local anesthesia. J Anesth
    2006 20 546
  • Intramuscular Dexmedetomidine reduces IOP in
    elderly during cataract surgery. (1.0mcg/kg) ?32
    IOP.
  • Dexmedetomidine as intramuscular premedication in
    outpatient cataract surgery a placebo-controlled
    dose-ranging study. Anaesthesia 1993 48 4827

25
  • Single i.v. dose of dexmedetomidine 0.6 mcg/kg ?
    IOP by 34.
  • The present study (0.6 mcg/kg) was based on a
    previous clinical study, where the selected dose
    resulted in a significant ? IOP and prevented IOP
    response to intubation.
  • Dexmedetomidine attenuates sympathoadrenal
    responses to tracheal intubation and reduces the
    need for thiopental and perioperative fentanyl.
    Br J Anaesth 1992 68 12631

26
  • Lee and colleagues infused dexmedetomidine as a
    supplement to isoflurane anaesthesia, they found
    no IOP lowering effect.
  • Dexmedetomidine infusion as a supplement to
    isoflurane anaesthesia for vitreoretinal surgery.
    Br J Anaesth 2007 98 47783
  • But, the loading dose of dexmedetomidine used in
    their study was lower. (0.4 mcg/kg)

27
mechanism
  • Dexmedetomidine on IOP effect may be due to
    direct vasoconstrictor effect on the afferent
    vessels of the ciliary body, which ? aqueous
    humour production.
  • Macri FJ, Cervario SJ. Clonidine. Arch Ophthalmol
    1978 96 21113
  • Dexmedetomidine ? outflow of the aqueous humour
    by reduce sympathetically mediated vasomotor tone
    of the ocular drainage system.
  • Dexmedetomidine-induced ocular hypotension in
    rabbits with normal or elevated intraocular
    pressures. Invest Ophthalmol Vis Sci 1992 33
    201923
  • Additionally, its associated haemodynamic
    response could contribute to the IOP lowering
    effect.
  • Sufentanil or clonidine for blunting the increase
    in intraocular pressure during rapid-sequence
    induction. Eur J Anaesthesiol 2002 13 51922

28
non-depolarizing neuromuscular blocking agents
  • Use of succinylcholine in open ocular trauma is
    controversial and an alternative anaesthetic
    management based on the use of nondepolarizing
    neuromuscular blocking agents, despite its slower
    onset, was suggested.
  • Various methods have been tried to speed up this
    onset, including priming, administering the
    non-depolarizing relaxant before the induction
    agent, and high-dose regimen.
  • J Clin Anesth 2004 16 837
  • Br J Anaesth 2007 98 60410

29
non-depolarizing neuromuscular blocking agents
  • Despite these strategies, non-depolarizing
    neuromuscular blocking agents can still result in
    non-ideal intubation conditions -
  • increases in the IOP from mask application and
  • longer time with insecure airway and
  • prolonged paralysis.
  • Despite this debate about the use of
    succinylcholine in open globe injury, most
    authors still agree on its use in difficult
    airway cases with salvageable eye situations.
  • Succinylcholine and the open eye. Ophthalmol Clin
    North Am 2006 19 27985

30
Limitations
  • Effect of dexmedetomidine on the IOP changes
    after succinylcholine intubation cannot be
    isolated from its action on the haemodynamics,
    since both effects are parallel and a causal
    relationship.
  • But, this limitation should not decline the
    advantage of dexmedetomidine to obtund the IOP
    changes of succinylcholine and intubation.

31
Conclusions
  • ? of IOP with succinylcholine endotracheal
    intubation can be blunted with i.v.
    dexmedetomidine premedication.
  • The haemodynamic stability is an additional
    advantage.
  • Dexmedetomidine could be a beneficial
    premedication in open globe injuries.

32
End of presentation
  • Thank you for your attention.

33
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35
  • Dexmedetomidine premedication administered in the
    present study (0.6 mcg/kg) was based on a
    previous clinical study, where the selected dose
    resulted in a significant reduction in IOP and
    prevented the rise in the IOP in response to
    intubation.
  • Dexmedetomidine attenuates sympathoadrenal
    responses to tracheal intubation.
  • Br J Anaesth 1992 68 12631

36
  • Several previous studies have reported the
    blunting effect of dexmedetomidine on the
    sympathetic response to laryngoscopy and
    intubation.
  • Hemodynamic and anesthetic advantages of
    dexmedetomidine, an alpha2-agonist, for surgery
    in prone position. Tohoku J Exp Med 2006 210
    15360
  • This could be due to the centrally mediated
    sympatholytic effects of alpha-2 agonists and by
    its decreasing norepinephrine release via
    peripheral presynaptic alpha-2 receptors.
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