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21 Apr 2008 : Column 1784W—continued



21 Apr 2008 : Column 1785W
Table Two: Proportion male and female screened for chlamydia by NCSP programme area for the period 1 April 2006 to 31 March 2007
Programme area Percentage male Percentage female Total( 1)

Ashfield

46

54

28

Bedfordshire and Hertfordshire

23

77

2,009

Berkshire East

45

55

2,645

Birmingham

12

88

6,736

Bournemouth and Poole

34

66

693

Bradford and Airedale

17

83

1,048

Brent and Harrow

22

78

2,253

Brighton

17

83

5,736

Buckinghamshire

21

79

14

Cambridge and Peterborough

30

70

1,506

Camden and Islington

7

93

3,404

Central Lancashire

13

87

1,378

City and Hackney

0

100

(2)

Cornwall

35

65

8,076

Coventry

18

82

1,908

Cumbria

0

100

(2)

Dorset

61

39

594

Durham and Teeside

53

47

7,132

East Cheshire

14

86

3,922

East Kent

18

82

3,200

East Lancashire

22

78

482

East Yorkshire

37

63

757

Enfield and Haringey

19

81

1,874

Greater Manchester

17

83

7,866

Halton, St. Helens and Warrington

0

100

(2)

Hampshire

39

61

5,791

Hastings

20

80

532

Hounslow

25

75

234

Hull

17

83

3,668

Lambeth and Southwark

16

84

9,463

Leeds

27

73

5,509

Leicester

21

79

211

Lewisham

18

82

6,498

Liverpool

14

86

11,456

Mid Essex

0

100

(2)

Milton Keynes

19

81

2,793

Norfolk and Waveney

22

78

2,539

North Staffordshire

15

85

4,236

Northern Lincolnshire

32

68

132

Northumberland, Tyne and Wear

37

63

1,205

Nottingham

12

88

6,775

Plymouth

33

67

(2)

Portsmouth

12

88

4,797

Sheffield

16

84

5,036

South East Essex

11

89

2,403

South Staffordshire

12

88

349

Southampton

26

74

392

Suffolk

13

87

1,193

Tower Hamlets

0

100

(2)

Wakefield District and Dewsbury, Batley

14

86

336

West Cheshire

8

92

1,777

West Kent

17

83

1,779

West Sussex

40

60

43

Wirral

14

86

5,242

York

30

70

3,572

Boots Pathfinder

22

78

11,729

Total

21

79

162,961

(1) Total number screened excluding screens with sex marked as unknown and unspecified.
(2) Cell sizes between 1 and 4 (and totals that would allow for them to be deduced) have been masked to prevent deductive disclosure in accordance with ONS guidelines.
Notes:
1. Data as of 27 February 2008.
2. The data from the NCSP are for screens outside of GUM clinics only and include screens from the Boots pathfinder project.
3. The data available from the NCSP are the number of screens done and not the number of patients screened. The number of screens is assumed to be a close proxy of the number of people screened.
4. The data only include those aged 13-24 years.
5. The data are for 1 April 2006 to 31 March 2007 because the NCSP receives data on a quarterly basis and follows the financial year.
6. The data provided are based on NCSP programme areas, not postcode of residence. The programme areas are geographically distinct areas formed by one or more primary care trusts and are responsible for coordinating local screening.
Source:
HPA-NCSP.

Chronic Fatigue Syndrome: Research

Mr. Maude: To ask the Secretary of State for Health if he will establish an independent scientific committee to oversee research into myalgic encephalomyelitis/chronic fatigue syndrome. [199903]

Ian Pearson: I have been asked to reply.

There are currently no plans to establish an independent scientific committee to oversee research into myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS). However, the Medical Research Council (MRC) is planning to set up a panel of experts from different disciplines to look more closely at the area. The panel will come from varied fields including neuroscience, immunology, toxicology and imaging, and will involve interested parties and focus on the subtypes and causes of ME/CFS.

Mr. Maude: To ask the Secretary of State for Health if he will take steps to ensure that Government funding for biomedical research on ME/CFS is equal to Government funding for psychological research on Myalgic Encephalomyelitis/Chronic Fatigue Syndrome. [199904]

Ian Pearson: I have been asked to reply.

The Medical Research Council (MRC) is committed to funding scientific research into all aspects of myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) including evaluations of other treatments and studies into the biological and psychological basis of the condition. The amount provided by the MRC to each type of research depends on the quality and number of proposals received.


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