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Controlled Clinical Trial
. 2016 May 23;11(5):e0156211.
doi: 10.1371/journal.pone.0156211. eCollection 2016.

The Lancet Weight Determines Wheal Diameter in Response to Skin Prick Testing with Histamine

Affiliations
Controlled Clinical Trial

The Lancet Weight Determines Wheal Diameter in Response to Skin Prick Testing with Histamine

Hjalte H Andersen et al. PLoS One. .

Abstract

Background: Skin prick test (SPT) is a common test for diagnosing immunoglobulin E-mediated allergies. In clinical routine, technicalities, human errors or patient-related biases, occasionally results in suboptimal diagnosis of sensitization.

Objective: Although not previously assessed qualitatively, lancet weight is hypothesized to be important when performing SPT to minimize the frequency of false positives, false negatives, and unwanted discomfort.

Methods: Accurate weight-controlled SPT was performed on the volar forearms and backs of 20 healthy subjects. Four predetermined lancet weights were applied (25 g, 85 g, 135 g and 265 g) using two positive control histamine solutions (1 mg/mL and 10 mg/mL) and one negative control (saline). A total of 400 SPTs were conducted. The outcome parameters were: wheal size, neurogenic inflammation (measured by superficial blood perfusion), frequency of bleeding, and the lancet provoked pain response.

Results: The mean wheal diameter increased significantly as higher weights were applied to the SPT lancet, e.g. from 3.2 ± 0.28 mm at 25 g to 5.4 ± 1.7 mm at 265 g (p<0.01). Similarly, the frequency of bleeding, the provoked pain, and the neurogenic inflammatory response increased significantly. At 265 g saline evoked two wheal responses (/160 pricks) below 3 mm.

Conclusion and clinical relevance: The applied weight of the lancet during the SPT-procedure is an important factor. Higher lancet weights precipitate significantly larger wheal reactions with potential diagnostic implications. This warrants additional research of the optimal lancet weight in relation to SPT-guidelines to improve the specificity and sensitivity of the procedure.

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Conflict of interest statement

Competing Interests: The authors have declared that no competing interests exist.

Figures

Fig 1
Fig 1. The setup of the SPT lancet attached to the SENSEBox Electronic von Frey weight transducer.
Fig 2
Fig 2
A) The mean wheal diameters on the forearms for each lancet weight; 25 g, 85 g, 135 g and 265 g. A higher lancet weight significantly increased the sizes of the wheal reactions. B) The mean wheal diameters on the back for each lancet weight; 25 g, 85 g, 135 g and 265 g. A higher lancet weight significantly increased the sizes of the wheal reactions. A significant difference was also observed when comparing the two histamine concentrations: 1 mg/mL and 10 mg/mL. For each condition; n = 20. * = p < 0.05, ** = p < 0.01. Mean ± SEM.
Fig 3
Fig 3
A) Changes in the mean superficial perfusion on the forearms according to the lancet weights: 25 g, 85 g, 135 g and 265 g. A difference in the mean superficial perfusion was seen from baseline to all the four applied lancet weights. B) On the back a difference in the mean superficial perfusion was seen from baseline to all the four applied lancet weights with both histamine concentrations (1 mg/mL and 10 mg/mL) and from baseline for the lancet weight of 265 g with saline as well. For each condition; n = 20. * = p < 0.05, ** = p < 0.01. Asterisks (*) or (**) placed just above the bars indicates significant difference from baseline superficial skin perfusion. Mean ± SEM.
Fig 4
Fig 4
The percentage distribution of bleeding incidents in response to individual SPTs when using the four lancet weights; 25 g, 85 g, 135 g and 265 g at A) the arm and B) the back, regardless of the applied solution (saline, 1 mg/mL histamine or 10 mg/mL histamine). A higher lancet weight caused increased incidents of bleeding. C) Peak pain intensity in response to the four lancet weights for both arm and back rated on a coVAS. The peak pain intensity increased significantly with increased weight. Notice that pain during SPT, regardless of weight, remains negligible, i.e. < 8 on a 0–100 VAS (N.B.: discrete x-axis is applied for graph C). For each condition; n = 20. * = p < 0.05, ** = p < 0.01. C) Mean ± SEM.
Fig 5
Fig 5
A) Shows individual lancet peak weight measurements from four different clinicians (no. 1–4). The horizontal lines denote the arithmetic mean for each individual. B) Shows intra-reliability and inter-reliability (dotted horizontal line) of applied weight expressed as the coefficient of variation (standard deviation expressed as % of the mean) for each of the four testees and between the four testees. CV% = Coefficient of variation (calculated as the ratio between the standard deviation and the mean in %).
Fig 6
Fig 6. Weighted SPT lancet device.
Depicts a suggested mechanical approach to a locked weight device allowing for SPT within a specific predetermined weight.

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