The Prevalence of Contact Allergies for Wound Dressings In Patients With Diabetic Foot Ulcers (PAID Study)

Rijnstate Hospital

Status

Unknown

Conditions

Contact Allergy

Diabetic Foot

Treatments

Diagnostic Test: PATCH test

Study type

Observational

Funder types

Other

Identifiers

NCT04085705

PAID study

Details and patient eligibility

About

Rationale: Foot ulcers among diabetics are common. The presence of a contact allergy limits the healing process. Contact allergies for wound dressings are common among patients with ulcers caused by venous insufficiency but less is known about contact allergies in diabetic patients with ulcers.

Objective: To determine the prevalence of contact allergies for wound dressings in patients with diabetic foot ulcers.

Study design: A prospective multicenter study.

Study population: Patients (n=139) with diabetic foot ulcers caused by type 1 or 2 diabetes mellitus treated at Rijnstate Hospital Arnhem, the Netherlands.

Main study parameters/endpoints: The primary study parameter is the presence of contact allergies for wound dressings.

Nature and extent of the burden and risks associated with participation, benefit and group relatedness: An allergy test is standard procedure at Rijnstate Hospital, there is no direct technique-related burden or risk for the patient. In addition, wound dressings can be adjusted in patients where a contact allergy is determined which will benefit the prognosis of these patients. The data of this study will give insight in the prevalence of contact allergies for wound dressings in patients with diabetic foot ulcers.

Full description

Foot ulcers among diabetics are common. In 2015, around 20,000 patients in the Netherlands had a diabetic foot ulcer.1 A study using data from Dutch general practices found a prevalence rate of 0.50% and a 4-year prevalence rate of 2.85%.2 For Europe, Zhang et al. estimated a pooled prevalence of 5.1% (95%CI: 4.1-6.0%).3 Prevalence rates increase with age.

The underlying mechanism of diabetic foot ulcers is most often solely neuropathy (60 to 70%), 15 to 20% have peripheral artery disease (PAD) only, and 15 to 20% have a mixture of both.4 Diabetic foot is more prevalent in males and more prevalent in type 2 diabetes than in type 1 diabetes3. Ulcers in patients without diabetes are mostly caused by venous insufficiency.5

Ulcers have a slow healing tendency. Around 15 percent of diabetic patients with an ulcer eventually have to amputate (a part of) the leg.1 Good wound care is therefore important. However, wound care can be delayed in the presence of a contact allergy. Contact allergy (synonym for contact sensitivity) is defined as an altered immune status of an individual induced by a particular sensitizing substance, a contact allergen. An individual in whom contact allergy has been induced will develop a secondary immune response if there is skin exposure to the same (or cross-reacting) allergen. This process is called elicitation, and will manifest as allergic contact dermatitis (type IV hypersensitivity).6 Allergic contact dermatitis, also termed allergic contact eczema, is defined as an inflammatory skin reaction caused by direct contact with noxious agents in the environment as a result of contact allergy.

Among patients with venous leg ulcers contact allergies is seen in around 50 percent of which 10-20% for wound dressings.7-10 The prevalence of contact allergies is getting higher and also increasing with the duration of the ulcer. 8,10 Wound dressings can cause allergic contact eczema (allergic contact dermatitis).

At present, the prevalence of contact allergies for wound dressings in diabetic patients with foot ulcers is unknown. With this study we want to gain insight in the prevalence of contact allergies in patients with diabetic foot ulcers and investigate if the prevalence of contact allergies among diabetic patients is as high as the prevalence in patients with venous leg ulcers.

Objective of the study:

The primary objective of this study is to determine the prevalence of contact allergies in patients with diabetic foot ulcers.

Study design:

This is a prospective, multi-centre study.

Study population:

The study population are high risk diabetic patients with a foot ulcer visiting the multidisciplinary consultation hour for diabetics at the clinic.

Diabetic patients are patients diagnosed with type 1 or type 2 diabetes.

Primary study parameters/outcome of the study:

The presence of contact allergy for wound dressings

Secundary study parameters/outcome of the study (if applicable):

The following factors will be gathered at baseline:

Age
Gender
Diabetes type
Duration of diabetes
Medication use
Ulcer characteristics like type, size, duration, progress (TEXAS classification)
Number of past foot ulcers
Duration of past foot ulcers
Known allergies or atopy constitution
Presence of allergic contact dermatitis around the wound
Doses corticosteroid or antihistaminic therapy (not during PATCH testing)
History of eczema

Parameters to define if there are other mechanisms besides diabetics underlying the ulcer:

Ankle brachial index , toe pressure measurement or Transcutaneous oxygen pressure (TcPo2)
Venous insufficiency which is measured by a venous duplex, if applicable

Parameters related with contact allergy or parameters that can influence the development of a contact allergy:

Known allergy. If yes, which allergy/allergies?
Duration of current ulcus cruris
Number of past ulcers
Treatment with wound dressing(s) current episode:
- Duration of ulcer
Treatment with wound dressing(s) prior episode(s)
Prevalence of allergic contact dermatitis

Nature and extent of the burden and risks associated with participation, benefit and group relatedness (if applicable):

Not applicable

Enrollment

139 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Age of 18 years or older;
Diagnosed with type 1 or 2 diabetes mellitus;
Diagnosed with diabetic foot ulcer;
Provided written informed consent.

Exclusion criteria

Patient unwilling or unlikely to comply with the study procedures
Patient receiving systemic corticosteroid therapy during PATCH testing (patient should stop with corticosteroid therapy three days before PATCH testing, and may start when testing and reading is done)
Patient receiving antihistaminic therapy during PATCH testing (patient should stop with antihistaminic therapy three days before PATCH testing, and may start when testing and reading is done)