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. Author manuscript; available in PMC: 2015 Jul 29.
Published in final edited form as: Clin Biochem. 2012 Sep;45(0):1012–1032. doi: 10.1016/j.clinbiochem.2012.08.002
Bibliographic information
Overall rating
Study*
Category (points deducted)
Practice*
Category (points deducted)
Outcome measures*
Category (pts deducted)
Results/findings*
Category (points deducted)
Author(s): Marcus EH Ong; Yiong Huak Chan; Chin Siah Lim.
 – Year: 2008
 – Publication: Ann Acad Med Singapore
 – Affiliations: Singapore General Hospital, Singapore
 – Funding: Internal
 – Author(s): Marcus EH Ong; Yiong Huak Chan; Chin Siah Lim.
 – Year: 2009
 – Publication: Am J Med
 – Affiliations: Singapore General Hospital, Singapore
 – Funding: Internal
Design: (0)
Cross-Sectional with follow-up
Facility/setting: (0)
No description. Estimated an average of 200 UE samples collected daily
Time period: (1)
Not described.
Population/sample: (0)
Convenience population of 227 patients.
All patients requiring blood urea and electrolytes (UE) during study time period were eligible. No requirements put upon personnel drawing blood
Comparator: (0)
1) Straight needle vs. IV start
2)Syringe vs. vacuum tube
3) =21 vs. >21 gauge needle
Other comparisons not being evaluated: operator, blood flow, difficulty of draw, source (venous vs. arterial)
Study bias: (1)
None observed — only used UE samples.
Did not control for other parameters (but did state no statistical influence by operator).
-Description: (1)
Scanty protocol provided. No description of patients selection (N seemed small) or time period. No controls put on methods or participation of operators.
Follow-up study evaluated change in numerous practices parameters and overall hemolysis rates, but did not provide rates by practice parameters.
Duration: (0)
Not specified.
Training: (0)
None in Phase 1 — Education in phase 2.
Staff/other resources: (0)
Minimal
Cost: (0)
Not specified.
Description: (0)
Hemolysis defined using standard laboratory procedure — not defined.
Recording method: (0)
Questionnaire on blood draw parameters with patient label matched to reported laboratory outcomes (hemolysis
Type of findings: (0)
Rates of hemolysis
Findings/effect size: (0)
Phase 1: N=227.
Straight needle vs. IV start:
4 (6.8%) vs. 41 (24.4%)
OR=4.4 (1.5–13.0)
Syringe vs. Vacuum tube:
Insufficient control
≤21 gauge needle vs. >21 gauge:
Insufficient control
Logistic regression analysis has inadequate data to provide much information.
Phase 2: N=204
Significant changes in practices including straight needle vs. IV starts and syringe vs. vacuum tube resulted in reduction of hemolysis rates for 19.8% before to 4.9% after. However, no rates by practice provided
Statistical significance/test(s): (0)
ORs and CIs provided.
Results/conclusion biases: (1)
Convenience sample with little description and no data provided to control for other practice parameters.
Quality rating: 6 (fair)
Effect rating: SubstantialRelevance: Direct
Study (3 max): 1
No description of study time period, hospital, etc. Lack of cross-parameter analyses.
Practice (2 max): 1
Very minimal description of study
Outcome (2 max): 2 Results/findings (3 max): 2
Lack of control for other practice parameters and sample size does not support logistic regression
*

Numbers in () by category headings reflect the number of points deducted from the maximum points for that column domain.