Health Expectations

Involving patients: representation or representativeness?
pp. 1-1(1)

Using disease risk estimates to guide risk factor interventions: field test of a patient workbook for self-assessing coronary risk
pp. 3-15(13)
Authors: Paterson J.M.; Llewellyn-Thomas H.A.; Naylor C.D.

The role of patients' meta-preferences in the design and evaluation of decision support systems
pp. 16-27(12)
Author: Dowie J.

Do Internet interventions for consumers cause more harm than good? A systematic review
pp. 28-37(10)
Authors: Bessell T.L.; McDonald S.; Silagy C.A.; Anderson J.N.; Hiller J.E.; Sansom L.N.

Consequences of surveying folate awareness
pp. 38-46(9)
Authors: Watson L.F.; Watson M.J.; Halliday J.L.; Bell R.J.

Deciding how NHS money is spent: a survey of general public and medical views
pp. 47-54(8)
Authors: Lees A.; Scott N.; Scott S.N.; MacDonald S.; Campbell C.

Whose priorities count? Comparison of community-identified health problems and Burden-of-Disease-assessed health priorities in a district in Uganda
pp. 55-62(8)
Authors: Kapiriri L.; Frithjof NorheimMD PhD O.

Improving communication between health professionals and women in maternity care: a structured review
pp. 63-83(21)
Authors: Rowe R.E.; Garcia J.; Macfarlane A.J.; Davidson L.L.

Appraising the quality of consumer health information leaflets
pp. 84-87(4)
Author: Shaddock J.

Promoting Accountable Managed Health-care: the Potential Role for Consumer Voice
pp. 88-89(2)
Author: Anderson W.

Too Ill to Talk? User Involvement and Palliative Care
pp. 89-90(2)
Author: Levvy G.

User Involvement in Cancer Care: Exclusion and Empowerment
pp. 90-91(2)
Author: Goodare H.