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. 2020 Oct 19;2020(10):CD012859. doi: 10.1002/14651858.CD012859.pub2

Summary of findings 7. Summary of findings (extrapyramidal symptoms).

HARM
Patient or population: adults undergoing any type of surgery under general anaesthesia
Interventions: antiemetic drugs (monoprophylaxis and combination prophylaxis)*
Comparator (reference): placebo (or no treatment)
Outcome: extrapyramidal symptoms within 7 days postoperatively
Setting: inpatient and outpatient
Total studies: 64 RCTs
Total participants: 10,724
Number of treatments: 30
Geometry of the network**
Relative effect***
(95% CI)
Anticipated absolute effect **** (95% CI) Certainty of evidence Ranking *****
(P score)
Interpretation of findings
Without intervention With intervention Difference
5‐HT3 receptor antagonists
Dolasetron
(3 RCTs; 288 participants)
0.67
(0.10 to 4.38)
8 per 10001 5 per 1000 3 fewer per 1000
(7 fewer to 27 more)
⊕⊕⊖⊖
Low
Due to imprecision2
Rank 5
(0.5860)
Rank 3 of 16 single drugs
Dolasetron may reduce extrapyramidal symptoms
Granisetron
(5 RCTs; 330 participants)
0.90
(0.23 to 3.57)
8 per 10001 7 per 1000 1 fewer per 1000
(6 fewer to 21 more)
⊕⊖⊖⊖
Very low
Due to study limitations, imprecision3
Rank 12
(0.5109)
Rank 6 of 16 single drugs
We are uncertain whether granisetron reduces extrapyramidal symptoms
Ondansetron
(7 RCTs; 751 participants)
0.73
(0.39 to 1.38)
8 per 10001 6 per 1000 2 fewer per 1000
(5 fewer to 3 more)
⊕⊖⊖⊖
Very low
Due to study limitations, imprecision3
Rank 3
(0.6026)
Rank 1 of 16 single drugs
We are uncertain whether ondansetron reduces extrapyramidal symptoms
Palonosetron
(1 RCT; 60 participants)
1.00
(0.02 to 48.80)
8 per 10001 8 per 1000 0 fewer/more per 1000
(8 fewer to 382 more)
⊕⊖⊖⊖
Very low
Due to study limitations, imprecision3,4
Rank 18
(0.4885)
Rank 8 of 16 single drugs
We are uncertain whether palonosetron has no or minimal effect on extrapyramidal symptoms
Ramosetron
(no direct evidence, indirect evidence only)
0.73
(0.01 to 37.44)
8 per 10001 6 per 1000 2 fewer per 1000
(8 fewer to 292 more)
⊕⊖⊖⊖
Very low
Due to study limitations, imprecision, incoherence5
Rank 8
(0.5409)
Rank 5 of 16 single drugs
We are uncertain whether ramosetron reduces extrapyramidal symptoms
Tropisetron
(3 RCTs; 187 participants)
0.82
(0.43 to 1.58)
8 per 10001 7 per 1000 1 fewer per 1000
(5 fewer to 5 more)
⊕⊖⊖⊖
Very low
Due to study limitations, imprecision6
Rank 7
(0.5553)
Rank 4 of 16 single drugs
We are uncertain whether tropisetron reduces extrapyramidal symptoms
D2 receptor antagonists
Amisulpride
(1 RCT; 689 participants)
1.00
(0.02 to 50.11)
8 per 10001 8 per 1000 0 fewer/more per 1000
(8 fewer to 393 more)
⊕⊕⊖⊖
Low
Due to imprecision2,4
Rank 19
(0.4872)
Rank 9 of 16 single drugs
Amisulpride may have little or no effect on extrapyramidal symptoms
Droperidol
(22 RCTs; 3270 participants)
1.36
(0.89 to 2.08)
8 per 10001 11 per 1000 3 more per 1000
(1 fewer to 9 more)
⊕⊕⊖⊖
Low
Due to imprecision2
Rank 29
(0.3456)
Rank 15 of 16 single drugs
Droperidol may increase extrapyramidal symptoms
Haloperidol
(5 RCTs; 437 participants)
1.18
(0.37 to 3.73)
8 per 10001 9 per 1000 1 more per 1000
(5 fewer to 22 more)
⊕⊕⊖⊖
Low
Due to imprecision2
Rank 27
(0.4202)
Rank 14 of 16 single drugs
Haloperidol may increase extrapyramidal symptoms
Metoclopramide
(12 RCTs; 855 participants)
1.14
(0.59 to 2.20)
8 per 10001 9 per 1000 1 fewer per 1000
(3 fewer to 10 more)
⊕⊕⊖⊖
Low
Due to imprecision2
Rank 26
(0.4257)
Rank 13 of 16 single drugs
Metoclopramide may increase extrapyramidal symptoms
Perphenazine
(1 RCT; 115 participants)
1.03
(0.05 to 23.02)
8 per 10001 8 per 1000 0 fewer/more per 1000
(8 fewer to 176 more)
⊕⊖⊖⊖
Very low
Due to study limitations, imprecision3
Rank 23
(0.4774)
Rank 12 of 16 single drugs
We are uncertain whether perphenazine has no or minimal effect on extrapyramidal symptoms
NK1 receptor antagonists
Aprepitant
(0 RCTs; 0 participants)
NA NA NA NA NA NA No studies were found that looked at extrapyramidal symptoms
Casopitant
(0 RCTs; 0 participants)
NA NA NA NA NA NA No studies were found that looked at extrapyramidal symptoms
Fosaprepitant
(0 RCTs; 0 participants)
NA NA NA NA NA NA No studies were found that looked at extrapyramidal symptoms
Rolapitant
(0 RCTs; 0 participants)
NA NA NA NA NA NA No studies were found that looked at extrapyramidal symptoms
Corticosteroids
Dexamethasone
(4 RCTs; 1031 participants)
0.70
(0.17 to 2.80)
8 per 10001 6 per 1000 2 fewer per 1000
(7 fewer to 14 more)
⊕⊕⊖⊖
Low
Due to imprecision2
Rank 4
(0.5865)
Rank 2 of 16 single drugs
Dexamethasone may reduce extrapyramidal symptoms
Methylprednisolone
(0 RCTs; 0 participants)
NA NA NA NA NA NA No studies were found that looked at extrapyramidal symptoms
Antihistamines
Dimenhydrinate
(0 RCTs; 0 participants)
NA NA NA NA NA NA No studies were found that looked at extrapyramidal symptoms
Meclizine
(0 RCTs; 0 participants)
NA NA NA NA NA NA No studies were found that looked at extrapyramidal symptoms
Promethazine
(0 RCTs; 0 participants)
NA NA NA NA NA NA No studies were found that looked at extrapyramidal symptoms
Anticholinergics
Scopolamine
(0 RCTs; 0 participants)
NA NA NA NA NA NA No studies were found that looked at extrapyramidal symptoms
Comparator
Placebo Reference comparator Not estimable Not estimable Not estimable Reference comparator Rank 22
(0.4778)
Reference comparator
NMA‐SoF table definitions:
* Certainty of evidence was assessed only for single antiemetic drugs of direct interest.
** Geometry of the network is presented in Figure 18 (netgraph).
*** Network estimates are reported as risk ratio (RR) with confidence interval (CI).
**** Anticipated absolute effects. The anticipated absolute effect compares two risks by calculating the difference between risk of the intervention group and risk of the control group.
***** Ranking of treatments includes all single drugs and combinations of drugs and is based on the P score (a value on a continuous 0 to 1 scale), which measures the extent of certainty that a treatment is better than another treatment, averaged over all competing treatments (Supplementary Files‐6‐extrapyramidal symptoms). Larger P scores indicate better treatments. In addition, the rank of the treatment out of all single drugs is indicated.
GRADE working group grades of evidence (or certainty of the evidence).
High certainty: we are very confident that the true effect lies close to that of the estimate of the effect.
Moderate certainty: we are moderately confident in the effect estimate. The true effect is likely to be close to the estimate of the effect, but there is a possibility that it is substantially different.
Low certainty: our confidence in the effect estimate is limited. The true effect may be substantially different from the estimate of effect.
Very low certainty: we have very little confidence in the effect estimate. The true effect is likely to be substantially different from the estimate of effect.
Explanatory footnotes:
1 Baseline risks (assumed control risk) are based on the total events of all placebo groups included in the outcome extrapyramidal symptoms. The general incidence of extrapyramidal symptoms after surgery with placebo is about 0.79%.
2 Very serious concerns for imprecision.
3 Serious concerns for study limitations and very serious concerns for imprecision.
4 Poorly connected to the network. Only direct evidence available.
5 Serious concerns for study limitations and incoherence, and very serious concerns for imprecision.
6 Very serious concerns for study limitations and imprecision.