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Dive into the research topics where S.H. Ibbotson is active.

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Featured researches published by S.H. Ibbotson.


British Journal of Dermatology | 2004

An update and guidance on narrowband ultraviolet B phototherapy: a British Photodermatology Group Workshop Report.

S.H. Ibbotson; D.J. Bilsland; N H Cox; R.S. Dawe; B.L. Diffey; C. Edwards; P.M. Farr; James Ferguson; G Hart; J.L.M. Hawk; J. J. Lloyd; Christopher Martin; Harry Moseley; K.E. McKENNA; Lesley E. Rhodes; D.K. Taylor

Summary These guidelines for use of narrowband (TL‐01) ultraviolet B have been prepared for dermatologists by the British Photodermatology Group on behalf of the British Association of Dermatologists. They present evidence‐based guidance for treatment of patients with a variety of dermatoses and photodermatoses, with identification of the strength of evidence available at the time of preparation of the guidelines, and a brief overview of background photobiology.


British Journal of Dermatology | 2000

Guidelines for topical PUVA: a report of a workshop of the British Photodermatology Group

S.M. Halpern; Alexander Vincent Anstey; R.S. Dawe; B.L. Diffey; P.M. Farr; James Ferguson; J.L.M. Hawk; S.H. Ibbotson; Jane M. McGregor; G.M. Murphy; S.E. Thomas; Lesley E. Rhodes

Psoralen photochemotherapy [psoralen ultraviolet A (PUVA)] plays an important part in dermatological therapeutics, being an effective and generally safe treatment for psoriasis and other dermatoses. In order to maintain optimal efficacy and safety, guidelines concerning best practice should be available to operators and supervisors. The British Photodermatology Group (BPG) have previously published recommendations on PUVA, including UVA dosimetry and calibration, patient pretreatment assessment, indications and contraindications, and the management of adverse reactions .1 While most current knowledge relates to oral PUVA, the use of topical PUVA regimens is also popular and presents a number of questions peculiar to this modality, including the choice of psoralen, formulation, method of application, optimal timing of treatment, UVA regimens and relative benefits or risks as compared with oral PUVA. Bath PUVA, i.e. generalized immersion, is the most frequently used modality of topical treatment, practised by about 100 centres in the U.K., while other topical preparations tend to be used for localized diseases such as those affecting the hands and feet. This paper is the product of a recent workshop of the BPG and includes guidelines for bath, local immersion and other topical PUVA. These recommendations are based, where possible, on the results of controlled studies, or otherwise on the consensus view on current practice.


British Journal of Dermatology | 2006

Photopatch testing of 1155 patients: results of the U.K. multicentre photopatch study group

A.M. Bryden; Harry Moseley; S.H. Ibbotson; M.M.U. Chowdhury; M.H. Beck; John F. Bourke; John English; P.M. Farr; Iain S. Foulds; David J. Gawkrodger; S. George; David Orton; S. Shaw; J. McFadden; Pg Norris; P. Podmore; S. Powell; Lesley E. Rhodes; Jane E. Sansom; Mark Wilkinson; H. Van Weelden; James Ferguson

Background  Photoallergic contact dermatitis can be difficult to diagnose if not appropriately investigated. Currently, the most common U.K. photoallergens appear to be sunscreen chemicals. The investigation of choice is photopatch testing (PPT), which is probably underused. In part, this is due to differences in methodology and results interpretation.


British Journal of Dermatology | 1996

The relevance and effect of amalgam replacement in subjects with oral lichenoid reactions

S.H. Ibbotson; E.L. Speight; R. I. Macleod; E. R. Smart; C.M. Lawrence

In this study we examined the prevalence of mercury hypersensitivity in patients with oral lichenoid reactions (OLR) and the effect of amalgam replacement in subjects with amalgams adjacent to OLR irrespective of their mercury sensitivity status. One hundred and ninety‐seven patients with oral problems were examined: 109 with OLR. 22 with oral and generalized lichen planus. and 66 with other oral diagnoses, including aphthous ulcers and orofacial granulomatosis. Nineteen per cent of patients with OLR reacted to mercury on patch testing, significantly more than in those with generalized lichen planus (0%) and in those with other oral diagnoses (3%). Twenty‐two patients with OLR and adjacent amalgams had amalgam replacement and. in 16 of 17 mercury‐positive subjects and three of four mercury‐negative subjects, the OLR resolved after amalgam removal. In conclusion, we found a significantly increased prevalence of mercury hypersensitivity in patients with localized OLR in comparison to subjects with other oral problems. Amalgam replacement resulted in resolution of OLR in the majority of patients with amalgams adjacent to OLR irrespective of their mercury sensitivity status.


British Journal of Dermatology | 1995

The effect of aspirin on haemostatic activity in the treatment of chronic venous leg ulceration

S.H. Ibbotson; A.M. Layton; J.A. Davies; M.J.D. Goodfield

An increased rate of venous ulcer healing with the use of oral enteric‐coated aspirin (300mg) daily has been reported.1 Whether the effect of aspirin in this condition is related to its action on the haemostatic mechanism is unclear, and therefore this study aimed to assess the effect of aspirin on some haemostatic parameters in patients with chronic venous leg ulcers. A double‐blind, randomized, placebo‐controlled, parallel‐group study of haemostatic activity and the effect of aspirin was implemented over a 4‐month period.


British Journal of Dermatology | 1994

Follicular keratoses at amputation sites

S.H. Ibbotson; N.B. Simpson; N.C.M. Fyfe; C.M. Lawrence

We describe two patients with painful follicular keratoses at lower limb amputation sites. Subsequent examination of 31 amputees revealed evidence of keratoses in four of 28 patients with lower limb stumps. Two of the four affected subjects experienced stump pain exacerbated by weight‐bearing. This problem is not well documented. Local treatment measures may be ineffective. Painful stump follicular keratoses many be a cause of significant morbidity in lower limb amputees, and may be the result of an ill‐fitting prosthesis.


British Journal of Dermatology | 1996

The effect of topical indomethacin on ultraviolet-radiation-induced erythema

S.H. Ibbotson; B.L. Diffey; P.M. Farr

Summary Indomethacin inhibits UVB erythema but is thought not to influence UVA erythema. We have examined the wavelength dependence of the effect of indomethacin on ultraviolet radiation (UVR) erythema. Duplicate sites on the back were irradiated with a series of doses at 300 and 320 nm, or single doses at 330, 340, 350 or 370 nm. Indomethacin 1% was applied to sites on one side of the back after irradiation, occluded for 2 h and erythema measured at 24h with a reflectance instrument. Indomethacin inhibited 300 and 320nm (UVB) erythema, had no effect at 330 and 340 nm (UVA2), but augmented 350 and 370 nm (UVA1) erythema. There appears to be a varied response of UVR erythema to cyclo‐oxygenase inhibition at different wavelengths across the UVR spectrum. This mechanism may be deranged in certain photosensitive disorders.


British Journal of Dermatology | 1994

Plasminogen activator inhibitor 1 (PAI-1) levels in patients with chronic venous leg ulceration

S.H. Ibbotson; A.M. Layton; J.A. Davies; M.J.D. Goodfield

1 Ofuji S, Ogino A, Horio T, Ohseko T. Eosinophllic pustular folliculitis. Acta Derm Venereol (Stockh) 1970; 50: 195-203. 2 Malanin G, Helander I. Eosinophllic pustular folliculitis (Ofujis disease): response to dapsone but not to isotretinoin therapy. / Am Acad Dermatol 1989; 20: 1121. 3 Lee ML. Tham SN, Ng SK. Eosinophilic pustular folliculitis (Ofujis disease) with response to indomethacin. Dermatx)Iogy 1993; 186: 210-12. 4 Harris DWS, Ostlere L, Buckley C et al. Eosinophilic pustular folliculitis in an HIV-positive man; response to cetirizine. Br J Dermatol 1992; 126: 392-4. 5 Berbis P, Janovici E, Lebreuil G et al. Eosinophilic pustular folliculitis (Ofujis disease); efficacy of isotretinoin. Dermatologka 1989; 179:214-16. 6 Pomeuf M, Gulllot B. Bameon G. Guilhou JJ. Eosinophilic pustular folliculitis responding to UVB therapy. / Am Acad Dermatol 1993; 29: 259-60. 7 Thomson AW, Milton JI, Aldridge RD et al. Inhibition of drugInduced eosinophiUa by cyclosporin A. Scand J Immunol 1986; 24: 163-70. 8 Shupack JL, Kenny C, Jondreau L et al. Decreased peripheral blood eosinophll counts in severe psoriatic patients treated with lowdose cyclosporin A. Dermatology 1992; 185: 202-4. 9 Andreano ]M, Kantor GR, Bergfeld WF ef al. Eosinophllic cellulitis and eosinophllic pustular folliculitis. /Am Acad Dermatol 1989; 20: 934-6. 10 Horiguchl Y. Mltani T, Ofuji S. The ultrastructural histopathology of eosinophllic pustular folliculitis. / Dermatol 1992; 19: 201-7. to leg ulceration complicating Klinefelters syndrome, but also occur in association with chronic venoushypertension. Impairment of fibrinolysis in the quiescent phase of venous leg ulceration may indicate that it plays a role in the pathogenesis of the condition, and perhaps sheds further light on the factors involved in the aetiology of this disorder.


Journal of Investigative Dermatology | 1999

The time-course of psoralen ultraviolet A (PUVA) erythema

S.H. Ibbotson; P.M. Farr


Journal of Investigative Dermatology | 2001

The effect of Methoxsalen dose on ultraviolet-A-induced erythema

S.H. Ibbotson; P.M. Farr; R.S. Dawe

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P.M. Farr

Royal Victoria Infirmary

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Lesley E. Rhodes

Manchester Academic Health Science Centre

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C.M. Lawrence

Royal Victoria Infirmary

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