Skip to main content
. 2021 May 18;2021(5):CD007579. doi: 10.1002/14651858.CD007579.pub3

Abdel‐Aleem 2012.

Study characteristics
Methods RCT.
Participants Inclusion criteria:
  • Women undergoing elective CS at term were eligible

  • N = 173 but 53 (31%) were excluded because of intraoperative nausea and vomiting, leaving 120 for analysis


Exclusion criteria:
  • Any contraindication to spinal, contraindication/allergy to IT morphine, GI condition causing vomiting, hyperemesis, obesity, previous PONV, migraine, skin allergy causing itching, psych.

  • Also excluded post‐enrolment if suffered intraoperative nausea and vomiting.

Interventions Intervention: corticosteroid (Comparison 3)
  • Dexamethasone (8 mg IT).

  • N = 60.


Comparator: placebo
  • Normal saline (IT).

  • N = 60.

Outcomes Nausea, vomiting, number of vomiting attacks, need for anti‐emetics, sedation, itch, respiratory depression, pain, satisfaction (retching classified as vomiting).
Notes Setting: Assiut University Hospital, Egypt.
Dates: February 2008 to December 2009.
Funding source: not reported
Declaration of interest: none declared.
We wrote to authors for clarification on whether the 53 women were excluded pre or post randomisation as it is unclear from the text of the publication.
Spinal with bupivacaine and 200 mcg IT morphine
Risk of bias
Bias Authors' judgement Support for judgement
Random sequence generation (selection bias) Low risk Quote: "computer based random allocation table"
Allocation concealment (selection bias) Low risk Quote:“sealed opaque envelopes consecutively numbered and coded”
Blinding of participants and personnel (performance bias)
All outcomes Low risk the patient ... was unaware of which intervention had been received
Blinding of outcome assessment (detection bias)
All outcomes Low risk Those assessing the outcomes were also unaware of which intervention had been received.
Incomplete outcome data (attrition bias)
All outcomes Unclear risk 53 patients were excluded enrolment although it is unclear if this was before or after randomisation.
Selective reporting (reporting bias) Unclear risk We were unable to assess the trial protocol.
Other bias Low risk Similar baseline characteristics