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Table 1 Assessment of risks to bias in non-randomised studies

From: Clinical effectiveness and cost-effectiveness of pegvisomant for the treatment of acromegaly: a systematic review and economic evaluation

Study

Were eligibility criteria explicit?

Was sample source/selection described?

Were patients assembled at same time?

Was a method of diagnosis stated?‡

Were clinical details described?

Was individual patient data reported?

Was outcome assessment blinded?

Was blinding method adequately described?

Was follow up time stated?Φ

Were withdrawals stated?

Were reasons for withdrawal stated?

Barkan 2005[24]

Y

N

CT

N

Y

N

N

NA

Y

Y

Y

Jorgensen 2005[19]

Y

Y

CT

N

Y

N

N

NA

Y

Y

Y

Feenstra 2005[18]

Y

N

CT

N

Y

N

N

NA

Y

N

NA

Van der Lely 2001[8]

Y

N

N

N

Y

N

N

NA

Y

Y

Y

Sesmilo 2002[9]

Y

N

CT

Y

Y

N

N

NA

Y

Y

Y

Fairfield 2002[10]

N

N

CT

N

Y

N

N

NA

Y

N

NA

Parkinson 2002[22]

N

N

CT

N

Y

Y†

N

NA

N

N

NA

Parkinson 2003a[15]

Y

N

CT

N

Y

N

N

NA

N

N

NA

Parkinson 2003b[23]

N

N

CT

N

Y

Y†

N

NA

Y

N

NA

Parkinson 2004[14]

N

N

CT

N

N

Y†

N

NA

N

N

NA

Jehle 2005[17]

N

N

CT

N

Y

Y

N

NA

Y

Y

Y

Paisley 2006[13]

N

N

CT

N

Y

Y

N

NA

N

N

N

Biering 2006[11]

CT

Y

NA

N

N

Y a

N

NA

N

Y

Y

Colao 2006[16]

Y

Y

Y

Y

Y

Y

N

NA

Y

Y

Y

Pivonello 2007[20]

Y

N

CT

Y

Y

Y

Y

Y

Y

Y

N

Schreiber 2007[21]

N

Y

N

N

Y

N

N

NA

Y

Y

N‡‡

Parkinson 2007[12]

Y

N

CT

N

Y

Y

Y

N

N

N

NA

  1. a for subgroup of patients. ‡ in most studies this was implicit ("patients with established diagnosis") rather than explicit. † in graphs. Φ where patient follow up varied but group value only provided N is entered. ‡‡ for adverse events only.
  2. Y = yes; N = no; CT = can't tell; NA = not applicable. Assessment used recommendations in the CRD handbook 2'edition [6]