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. 2004 Apr 9;4(2):107–108. doi: 10.1159/000210541

Shoulder Strain Caused by Mammary Prostheses – an Experimental Comparison of Different Forms of Epicutaneous Prostheses

Andreas Hackethal 1,*, Karsten Münstedt 1
PMCID: PMC2931070  PMID: 20847888

Summary

Background

In the case of breast cancer, removal of the breast can not always be avoided. The use of external prostheses, however, can lead to discomfort for the patients through shoulder pain and muscle hardening. It can be assumed that this is caused by strain on the shoulder due to the weight of the prosthesis. This study was to identify the possibilities to objectively assess patients' complaints associated with this type of supportive treatment.

Subjects and Methods

In this pilot study, varying types and sizes of prostheses were tested on male subjects, quasi as if they were women amputated on both sides. The strain caused by the prostheses and distributed via the straps of the brassiere were measured by electronic pressure sensors and statistically evaluated.

Results

Weight-reduced prostheses significantly decreased the resulting average pressure amplitude (p < 0.01) compared to normal weight prostheses. Furthermore, heavy contact prostheses, which are attached to the chest wall, have a significant advantage (p < 0.01) compared to normal prostheses of the same size. Moreover, evidence was found that contact prostheses have advantages with respect to pressure on the shoulder during physical exercise, e.g. running.

Conclusion

Currently, weight-reduced contact prostheses present optimal treatment after breast amputation.

Key Words: Breast cancer, Epicutaneous breast prostheses, Shoulder pressure

Introduction

Apart from the possibilities of breast-preserving and reconstructive surgery, supplying women with epicutaneous prosthetics still plays an integral role in the medical care of female patients after mammectomy. For women dependent on epicutaneous provisions, optimal counselling is of paramount importance in order to supply them with the best possible prosthesis. Deciding on a specific prosthesis depends on different factors, many of which are completely subjective (e.g. comfort, naturalness).

To date, studies only focussed on subjective complaints of patients. Therefore, the aim of this paper is to investigate the shoulder strain through objective measures, thereby assessing possible advantages of epicutaneous prostheses, especially regarding adhesive appliances.

Subjects and Methods

The pressure beneath the straps of the brassiere was measured by pressure sensors (9800 series, consisting of 8 × 16 single sensor fields; Tekscan, South Boston, MA, USA) placed beneath the straps. Subsequently, the sensors lying directly beneath the straps were identified. In order to simulate the strain generated by movement, the measurements were taken on a treadmill (Trimline 7150.3E; DF Hebb Industries, Tyler, TX, USA) during walking and running. Thus, it was possible to generate a time-pressure curve for each side, whereupon maximum and minimum values were obtained by administering periodical oscillations. The oscillation amplitude was calculated and correlated to either walking or running.

In order to compare different forms of breast prostheses, the subjects were all male volunteers (simulating bilaterally ablated female patients). Subject 1 (age 30, 178 cm, 82 kg) was given a corsage size 90B (brand Virginia; Amoena, Raubling, Germany) and tested prostheses of size 7. Subject 2 (age 34, 185 cm, 78 kg) was given a bra of the same trademark size 90D and prostheses of size 10. Each subject underwent 9 iterations. Each result represents the mean value of >50 individual measurements. Measurements were repeated to assure accuracy. Characterisation of the prostheses is shown in table 1. Statistical analyses consisted of Student's t-test for independent samples.

Table 1.

Characterisation of the tested pros-theses

Name Type of prosthesis Weight size 7, g Weight size 10, g
Tria II two-layered prosthesis 456 732
Tria basic one-layered prosthesis 448 710
Tria II light weight-reduced two-layered prosthesis 346 552
Tria basic light weight-reduced one-layered prosthesis 309 511
Tria contact normal weight contact prosthesis 490 751
Tria contact light weight-reduced contact prosthesis 372 585

Results

No significant differences between one-layer and two-layer prostheses regarding shoulder strain were found.

Contact adhesive prostheses of size 10 showed significantly smaller pressure amplitudes during running compared to normal prostheses (t = 3.67, p < 0.005; fig. 1).

Fig. 1.

Fig. 1

Contact prostheses compared to normal prostheses during running (∗ p < 0.05).

It was shown that lower weight led to a lower pressure amplitude in both conventional and adhesive prosthetics. Exemplary data are shown in figure 2. Even though the small sample size does not allow generalisations, it can still be said that both subjects reported the highest comfort wearing light contact prostheses.

Fig. 2.

Fig. 2

Light weight prostheses compared to normal weight prostheses during walking. The results are shown for 3 types of size 7 prostheses (∗ p < 0.05).

Discussion

The results clearly show that light adhesive prostheses cause the least pressure amplitudes beneath the straps of the brassiere. These can be viewed as a correlative of the shoulder discomfort reported by patients, as it can be assumed that higher pressure amplitudes lead to microtraumata within the underlying tissue in these regions during motion. Both the adhesion of the prosthesis to the skin as well as the weight reduction absorbs a part of the pressure. These findings adequately explain patients reporting lesser shoulder complaints after the transition to adhesive prostheses and explain why most women in the aforementioned studies preferred self-adhesive breast forms [1,2,3].

It may be concluded from studies on reduction mammoplasty and discomfort caused by too heavy breasts that better external breast prostheses may also positively influence lung function and the vegetative nervous system [4,5,6]. Thus, weight-reduced, self-adhesive breast forms should be considered as the standard care for women after mammectomy without immediate breast reconstruction, especially in women with larger breasts.

Conflict of Interest

This study was supported by Amoena GmbH, Raubling, Germany. Apart from this support the authors have no conflict of interest to disclose.

Acknowledgement

We would like to thank Amoena GmbH, Raubling, Germany, as well as Dr. Klaus J. Dimde and Mr. Phillip Grant for their support.

References

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