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Journal of Contemporary Brachytherapy logoLink to Journal of Contemporary Brachytherapy
. 2015 Jun 8;7(3):197–202. doi: 10.5114/jcb.2015.52071

A novel perineal shield for low-dose-rate prostate brachytherapy

Joseph P Weiner 1,2,, David Schwartz 1,2, Joseph Safdieh 1,2, Alex Polubarov 1, Tejas Telivala 1, Matthew Worth 1, David Schreiber 1,2
PMCID: PMC4499515  PMID: 26207107

Abstract

Purpose

To study the impact on radiation exposure to staff through the use of an original perineal shield during low-dose-rate prostate brachytherapy.

Material and methods

We designed a 1 mm thick stainless steel shield that duplicates and is able to slide directly over a standard commercialized prostate brachytherapy grid. We then analyzed the post-procedure exposure in 15 consecutive patients who underwent Iodine-125 seed placement. Measurements were performed with and without the shield in place at fixed locations relative to the grid template. Endpoints were analyzed using the paired two-sample t-test, with statistical significance defined as a p-value < 0.05.

Results

The exposure at the midline grid template ranged from 0.144-0.768 mSv/hr without the shield, and 0.038-0.144 mSv/hr with the shield (p < 0.0001). The exposure 10 cm left of the grid template was 0.134-0.576 mSv/hr without the shield, and 0.001-0.012 mSv/hr with the shield (p < 0.0001). The exposure 10 cm right of the grid template was 0.125-0.576 mSv/hr without the shield, and 0.001-0.012 mSv/hr with the shield (p < 0.0001). The median reduction of exposure at the grid was 76% midline, 98.5% left, and 99% right. Similarly, each individual dose rate was recorded at 25 cm from the perineum, both with and without shield. The median reduction of exposure 25 cm from the perineum was 73.7% midline, 77.7% left and 81.6% right (p < 0.0001).

Conclusions

Our novel shield took seconds to install and was non-restrictive during the procedure, and provided at least a four-fold reduction in radiation exposure to the brachytherapist.

Keywords: ALARA, brachytherapy, iodine-125, prostate cancer, seeds, shield

Purpose

Prostate cancer remains the most common non-cutaneous malignancy diagnosed in the United States, with an estimated 220 800 new diagnoses and 27 540 deaths expected in 2015 [1]. Over 80% of these men will present with localized, curative disease, for which the 5-year relative survival rate approaches 100% [2]. Men with a high probability of organ-confined disease can be offered brachytherapy as monotherapy, while men with a significant risk of extraprostatic extension can be offered brachytherapy with supplemental external beam radiation therapy [35].

It is estimated that as many as 50 000 men are treated with interstitial brachytherapy in the United States per year with the vast majority of these implants utilizing low-dose-rate (LDR) [6]. Additionally, patterns of care studies suggest increasing prostate brachytherapy use in Europe as well [7]. A recent survey of current clinical practice in prostate brachytherapy revealed that the mean number of LDR implants per year per brachytherapist was 39, but the range extended up to 200 implants [6]. Despite advances from earlier techniques of prostate brachytherapy, the use of LDR poses inherent risks to both the practitioner performing the implant as well as those in close proximity of the patient [8]. This risk to the practitioner is exacerbated by the lack of mechanized after-loading, which has been employed in high-dose rate (HDR) brachytherapy [9]. Numerous articles reporting data about radiation exposure to the general public exist [1012]. In addition, the literature also includes practical and effective methods of reducing exposure to the general public. Such examples of this include minimizing time of exposure and increasing distance to the patient's pelvis [13, 14]. Additional examples include dedicated shielding in the form of lead-lined underwear [15, 16].

In contrast, less data is available about radiation exposure to personnel performing the implant [17]. When such information is discussed in the literature, it is usually limited and involves one site of interest, such as the eye or hand [18, 19]. Despite this, even fewer articles discuss techniques or materials that can help reduce exposure to the medical staff performing the implant. In this study, we analyzed the results of our newly created brachytherapy shield that has minimal to no impact on the set-up time or the ability to perform the brachytherapy procedure but is able to significantly reduce radiation exposure.

Material and methods

Shield design

A novel shield model system was constructed to enable sufficient dose reduction to medical personal (Fig. 1). The overall design of the system was a 1 mm thick stainless steel shield with duplicate holes and markings to a standard, commercially available prostate brachytherapy grid (Civco Medical Solutions, Disposable Template Grid, Orange City, Iowa, USA). Stainless steel was chosen for shield as this material provides significant attenuation of the radiation and is also able to safely undergo autoclaving after use, allowing for repeated use of the shield. The thickness of 1 mm was similarly chosen in order to provide radiation shielding with the minimal width shield, in order to make the shield as lightweight and unobtrusive to the procedure as possible. The shield was designed to be taller and wider in dimensions than the grid (21 cm by 21 cm in size) and was constructed to be compatible with our ultrasound stepper system (Civco Medical Solutions, Classic Stepper) but easily adaptable to other systems.

Fig. 1A-D.

Fig. 1A-D

A) Perineal shield: B) oblique anterior view, C) oblique posterior view, D) posterior view

Two stainless steel latches on the back of the shield allows it to slide over the grid and lock into place. Once in place, the openings of the shield and the grid are aligned flush against one another. Therefore, the brachytherapist is able to easily insert the needles through both the shield and grid openings, directly into the perineum. During the procedure, the device is easily installed within seconds and remains in place for the entire duration of the implant. At the conclusion of the procedure, the device is removed and sent to our sterile processing department where it undergoes steam autoclave prior to use in the next case.

Exposure analysis

We analyzed the post-procedure exposure in 15 consecutive patients who underwent permanent LDR Iodine-125 seed placement for prostate cancer from October 2013 to January 2014. Measurements were performed utilizing a Ludlum Model 14C S/N 80047 air ionization chamber survey meter calibrated yearly against Iodine-125, both with and without the shield in place. Measurement locations were at the grid template, which is flush to the perineum, and at the stepper dial, which was 25 cm from the perineum. At both of these locations, three measurements were taken at the midline, left lateral, and right lateral. At the grid, the lateral measurements were 10 cm off central axis, and at the stepper dial, the lateral measurements were 25 cm off central axis. Endpoints were analyzed using the paired two-sample t-test with statistical significance defined as a p-value < 0.05.

Results

The prescription dose, individual seed activity, number of seeds, and total implant activity were recorded for each patient (Table 1). Each individual dose rate for all patients at the grid, both with and without shield, was recorded (Table 2). The exposure at the midline grid template ranged from 0.144-0.768 mSv/hr without the shield, and 0.038-0.144 mSv/hr with the shield (p < 0.0001). The exposure 10 cm left of the grid template was 0.134-0.576 mSv/hr without the shield, and 0.001-0.012 mSv/hr with the shield (p < 0.0001). The exposure 10 cm right of the grid template was 0.125-0.576 mSv/hr without the shield, and 0.001-0.012 mSv/hr with the shield (p < 0.0001). The median reduction of exposure at the grid was 76% midline, 98.5% left and 99% right.

Table 1.

Patient and seed data

Patient Rx (Gy) Activity (mCi) No seeds Total activity (mCi)
1 108 0.47 55 25.85
2 108 0.47 41 19.27
3 108 0.47 38 17.86
4 108 0.434 39 16.926
5 108 0.475 34 16.15
6 108 0.512 57 29.184
7 108 0.481 40 19.24
8 108 0.471 57 26.847
9 108 0.461 40 18.44
10 108 0.47 47 22.09
11 108 0.402 42 16.884
12 108 0.47 43 20.21
13 108 0.475 37 17.575
14 108 0.475 54 25.65
15 108 0.47 38 17.86
Mean 108 0.467 44.1 20.67

Table 2.

Dose rate in mSv/hr at the template grid

Patient At central grid % Reduction 10 cm left of midline % Reduction 10 cm right of midline % Reduction
Shield No shield Shield No shield Shield No shield
1 0.096 0.432 77.8 0.010 0.384 97.4 0.010 0.336 97.0
2 0.144 0.384 62.5 0.007 0.384 98.2 0.004 0.288 98.6
3 0.048 0.144 66.7 0.002 0.134 98.5 0.001 0.125 99.2
4 0.096 0.288 66.7 0.005 0.288 98.3 0.005 0.288 98.3
5 0.144 0.576 75.0 0.004 0.480 99.2 0.004 0.480 99.2
6 0.067 0.288 76.7 0.004 0.240 98.3 0.002 0.192 99.0
7 0.048 0.144 66.7 0.002 0.134 98.5 0.002 0.134 98.5
8 0.048 0.192 75.0 0.002 0.173 98.8 0.001 0.192 99.5
9 0.096 0.384 75.0 0.003 0.336 99.1 0.003 0.336 99.1
10 0.115 0.480 76.0 0.012 0.384 96.9 0.012 0.384 96.9
11 0.038 0.192 80.2 0.002 0.144 98.6 0.001 0.144 99.3
12 0.067 0.384 82.6 0.001 0.240 99.6 0.001 0.240 99.6
13 0.058 0.768 92.4 0.005 0.576 99.1 0.005 0.576 99.1
14 0.067 0.576 88.4 0.005 0.384 98.7 0.005 0.384 98.7
15 0.016 0.192 91.7 0.004 0.144 97.2 0.004 0.144 97.2
Mean 0.077 0.362 76.9 0.004 0.295 98.4 0.004 0.283 98.6

Each individual dose rate for all patients at the stepper dial, located 25 cm from the perineum, both with and without shield, was also recorded (Table 3). The exposure at the midline, 25 cm from the perineum, ranged from 0.013-0.058 mSv/hr without the shield, and 0.004-0.019 mSv/hr with the shield (p < 0.0001). The exposure 25 cm from the perineum and left of midline was 0.013-0.058 mSv/hr without the shield, and 0.002-0.012 mSv/hr with the shield (p < 0.0001). The exposure 25 cm from the perineum and right of midline was 0.013-0.048 mSv/hr without the shield, and 0.002-0.012mSv/hr with the shield (p < 0.0001). The median reduction of exposure 25 cm from the perineum was 73.7% midline, 77.7% left, and 81.6% right.

Table 3.

Dose rate in mSv/hr at stepper dial (25 cm from perineum)

Patient At central % Reduction 25 cm left of midline % Reduction 25 cm right of midline % Reduction
Shield No shield Shield No shield Shield No shield
1 0.019 0.048 60.4 0.008 0.058 86.2 0.008 0.058 86.2
2 0.013 0.048 72.9 0.012 0.038 68.4 0.012 0.038 68.4
3 0.012 0.058 79.4 NA NA NA NA NA NA
4 0.010 0.038 73.7 0.012 0.038 68.4 0.012 0.038 68.4
5 0.011 0.038 71.1 0.010 0.038 73.7 0.010 0.038 73.7
6 0.010 0.038 73.7 0.007 0.029 75.9 0.007 0.038 81.6
7 0.005 0.019 73.7 0.004 0.024 83.3 0.004 0.024 83.3
8 0.005 0.019 73.7 0.003 0.019 84.2 0.003 0.019 84.2
9 0.012 0.038 68.4 0.007 0.038 81.6 0.007 0.038 81.6
10 0.005 0.029 82.8 0.009 0.038 76.3 0.007 0.038 81.6
11 0.005 0.014 64.3 0.004 0.012 66.7 0.004 0.014 71.4
12 0.007 0.029 75.9 0.005 0.019 73.7 0.005 0.029 82.8
13 0.010 0.048 79.2 0.007 0.048 85.4 0.005 0.048 89.6
14 0.010 0.038 73.7 0.008 0.038 79.0 0.008 0.038 79.0
15 0.004 0.013 69.2 0.002 0.013 84.6 0.002 0.013 84.6
Mean 0.009 0.034 72.8 0.007 0.032 77.7 0.006 0.034 79.7

Discussion

Principles of radiation safety during brachytherapy implantation include limiting time of exposure, increasing distance from the source, avoiding unnecessary exposure and shielding with protective materials. While in the clinical setting, the first three concepts may be challenging to quickly enact meaningful change, the latter-most idea of shielding can be implemented without significant cost or time commitment. The benefit of the perineal shield presented in this paper is a four-fold reduction in radiation exposure to the brachytherapist. This device takes seconds to install and is non-restrictive during the procedure.

A review of the existing literature reveals no previously described perineal shield designed with the purpose of protecting staff during brachytherapy implant. Most existing radiation safety literature describes exposure with respect to the community or family of the patient rather than the practitioner [11, 12]. One such study investigating dose to the performing staff determined that with the use of personal lead, body doses were near negligible but hands received the highest doses, an average of 420 microSv per implant [20]. Recently, another study described post-implant surface dose after brachytherapy with and without the use of 0.1 mm thickness lead-lined underwear [15]. The magnitude of radiation exposure attenuation was > 90%, and confirmed that such shielding is effective in the post-brachytherapy setting to reduce exposure to the community. These two studies, though with different purposes, exemplify the ability of shielding to reduce exposure.

In our study we found that the perineal shield reduced the radiation exposure by a median of 76% at the grid and 98-99% lateral to the grid. However, prior studies of the attenuation of stainless steel for Iodine 125 have revealed that 1 mm of stainless steel should reduce exposure by > 99% [21], differing from our findings. We believe this is likely related to the needle holes in the grid, which are left unprotected by the shield in order to allow for needle placement, and therefore remain exposed, leading to higher radiation exposure detection than would be expected with a solid shield without any exposed holes.

Though personal shielding is not a new concept in radiation therapy, as is evident by the vast market full of leaded aprons, thyroid shields, gloves, glasses, and even underwear, this is, to our knowledge, the first published device with the intention of reducing radiation exposure to the performing physician via a perineal shield. This approach has several theoretical benefits. First, as with all protection devices, they are only useful if they are actually used. Universal compliance with standard leaded personal shielding is less than ideal [2224]. These personal articles tend to be heavy and uncomfortable, encumbering the brachytherapist for the duration of the case. Our shield does not burden the practitioner during implant and is easy to use. Second, various personal protective devices are worn adjacent to the intended site or organ of protection. Thus, protection is only afforded to a specific site. By placing our shielding closer to the source, we are able to effectively reduce exposure to a wider area due to shielding at a point with less divergence from the source. Third, personal protective shielding, particularly leaded gloves, have been shown to reduce manual dexterity [25]. No such problem exists with this device, as it is fully compatible with a commercially available template grid, and is non-restrictive with respect to needle placement. A final benefit of this device is that it is able to be used in combination with the above mentioned protective devices, in order to afford even greater protection to the brachytherapist. This is in agreement with the “As-Low-As-Reasonable-Achievable (ALARA)” concept, which was first introduced as an innovative recommendation by the National Council on Radiation Protection and Measurements (NCRP) in 1954 [26, 27].

While our shield is highly effective in reducing radiation exposure during brachytherapy, the actual clinical relevance of further reducing such already low exposure rates remains unknown. Per the International Commission on Radiological Protection (ICRP), the occupational exposure of a radiation worker is to be limited to not more than 50 mSv per any one year, and to average not more than 20 mSv per year over a five year period [28]. In our study, the average dose measured at the midline grid was 0.362 mSv/hr without the shield, and 0.077 mSv/hr with the shield in place. If one were to make a conservative estimate that for every brachytherapy case, there is an average of 15 minutes of exposure to this dose, then for the brachytherapist performing 50 cases per year there would be an exposure of approximately 4.5 mSv without the shield and 1 mSv with the shield. While quantitatively, both of these exposures are low and well below ICRP recommendations, there is no known “safe” exposure. A recent article Sutlief et al. reviewed the stochastic effects of radiation at low exposure and the subsequent development of secondary malignancy [29]. The authors argue that the validity and applicability of the commonly used linear non-threshold model is not verified at such low doses, thus limiting the ability to draw conclusions about the risks of low rate exposure. A recent multinational, retrospective cohort study of over 400 000 nuclear industry workers revealed that low dose chronic occupational exposure to external radiation did result in an excess risk of cancer, likely accounting for 1-2% of cancer deaths in this population [30]. Thus, even the seemingly low doses of radiation the brachytherapist is exposed to during each case, could potentially cause devastating events such as radiation induced carcinogenesis.

Conceivable detriments to the use of the device are limited. Increased dose to the patient due to backscatter is possible. However, prior studies attempting to quantify backscatter exposure with Iridium-192, a higher energy source than Iodine-125 have revealed that the backscatter dose is essentially negligible at > 1 mm [31]. For our shield, it is practically difficult to measure the radiation exposure on the patient's side of the shield due to the radiation emitted directly from the sources inside the prostate. However, between the shield and the patient is the template grid itself, which measures 1 cm in width, and therefore likely provides more than enough distance to make the risk from backscatter inconsequential.

Conclusions

This novel shield is easy to use, installs in seconds, and doesn't interfere at all with the brachytherapy procedure. In agreement with the ALARA principle, it allows for at least a four-fold reduction in radiation exposure to the brachytherapist performing the seed implant without any credible harm to the patient or medical staff.

Disclosure

Authors report no conflict of interest.

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