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Antibiotikaprofylax vid kirurgiska ingrepp - SBU

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Table 4.4.10 Hysterectomy, duration of prophylaxis.<br />

Author<br />

Year<br />

Reference<br />

Country<br />

Study<br />

design<br />

Population<br />

characteristics<br />

Intervention<br />

Method<br />

Number indi<strong>vid</strong>uals<br />

Control<br />

Number indi<strong>vid</strong>uals<br />

Results<br />

Withdrawal<br />

Drop outs<br />

Study quality<br />

and relevance<br />

Comments<br />

Kocak<br />

2005<br />

[46]<br />

Turkey<br />

RCT<br />

Elective abdominal<br />

hysterectomy.<br />

n=1 020<br />

I: Single dose 1st generation<br />

cephalosporin 2 g (n=500)<br />

C: 2 g per day for 7 days<br />

1st generation cephalosporin<br />

(n=520)<br />

Total number<br />

of infections<br />

I: 32/500<br />

(6.4%)<br />

C: 41/520<br />

(7.8%) ns<br />

Moderate<br />

Very large, no power<br />

calculation, not blinded,<br />

side effects not reported<br />

Su<br />

2005<br />

[6]<br />

Taiwan<br />

RCT<br />

Elective vaginal or<br />

abdominal hysterectomy.<br />

n=531<br />

I: Cefazolin 1 g iv pre-op<br />

(n=267)<br />

C: Cefazolin 1 g iv pre-op<br />

+ 1 g every 6 h for 1 day<br />

(=3 doses post-op)<br />

(n=264)<br />

Serious<br />

infections<br />

I: 1 pt (0.37%)<br />

C: 1 pt (0.37%)<br />

17/548 Moderate<br />

Large study. Infections<br />

= vaginal cuff infections,<br />

wound infections<br />

C = Control group; h = Hours; I = Intervention group; iv = Intravenous; n = Number<br />

of patients; RCT = Randomised controlled trial<br />

Table 4.4.11 Hysterectomy, administration.<br />

Author<br />

Year<br />

Reference<br />

Country<br />

Study<br />

design<br />

Population<br />

characteristics<br />

Intervention<br />

Method<br />

Number indi<strong>vid</strong>uals<br />

Control<br />

Number<br />

indi<strong>vid</strong>uals<br />

Results<br />

Withdrawal<br />

Drop outs<br />

Study quality<br />

and relevance<br />

Comments<br />

Hemsell<br />

1990<br />

[43]<br />

USA<br />

RCT<br />

Hysterectomy, abdominal<br />

(n=539), vaginal (n=207)<br />

(772 patients)<br />

I: Cefazolin 1 g im pre-op<br />

(n=365)<br />

C: Cefazolin 1 g iv<br />

pre-op (n=381)<br />

Major infections<br />

I: Abdominal 20/264<br />

(7.6%)<br />

Vaginal 8/101 (7.9%)<br />

C: Abdominal 21/275<br />

(7.6%)<br />

Vaginal 5/106 (4.7%) ns<br />

26 (3.4%) after<br />

informed consent,<br />

listed per reason<br />

Moderate<br />

Large, no power<br />

calcualtion, probably<br />

not blinded, side<br />

effects not reported<br />

C = Control group; I = Intervention group; im = Intramuscular; iv = Intravenous;<br />

n = Number of patients; ns = Non significant; RCT = Randomised controlled trial<br />

246 antibiotikaprofylax <strong>vid</strong> <strong>kirurgiska</strong> <strong>ingrepp</strong> KAPITEL 4 • den systematiska litteraturöversikten<br />

247

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