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. 2014 Apr 25;49(3):227–232. doi: 10.1016/j.rboe.2014.04.008

Exposure of the surgical team to ionizing radiation during orthopedic surgical procedures☆☆

Exposição da equipe cirúrgica à radiação ionizante durante procedimentos cirúrgicos ortopédicos

Evandro Pereira Palácio 1,, André Araújo Ribeiro 1, Bruno Moreira Gavassi 1, Gabriel Guimarães Di Stasi 1, José Antônio Galbiatti 1, Alcides Durigam Junior 1, Roberto Ryuiti Mizobuchi 1
PMCID: PMC4511650  PMID: 26229805

Abstract

Objective

the aim of this study was to assess the degree of exposure of the orthopedic surgical team to fluoroscopic ionizing radiation.

Methods

the ionizing radiation to which the orthopedic surgical team (R1, R2 and R3) was exposed was assayed using thermoluminescent dosimeters that were distributed in target anatomical regions (regions with and without protection using a lead apron). This was done during 45 hip osteosynthesis procedures to treat transtrochanteric fractures that were classified as 31-A2.1 (AO).

Results

the radioactive dose received by R3 was 6.33 mSv, R2 4.51 mSv and R3 1.99 mSv (p = 0.33). The thyroid region received 0.86 mSv of radiation, the thoracic region 1.24 mSv and the gonadal region 2.15 mSv (p = 0.25). There was no record of radiation at the dosimeters located below the biosafety protectors or on the team members’ backs.

Conclusions

the members of the surgical team who were located closest to the fluoroscope received greater radiation doses than those located further away. The anatomical regions located below the waistline were the ones that received most ionizing radiation. These results emphasize the importance of using biosafety devices, since these are effective in preventing radiation from reaching the vital organs of the medical team.

Keywords: Ionizing radiation, Fluoroscopy, Orthopedic surgery

Introduction

Fluoroscopy is an important tool used during orthopedic surgery, which provides surgeons with better assessment of the anatomical structures operated and the synthesis materials implanted. It also considerably diminishes the duration of the operation and morbidity among patients. Although there are many advantages of using fluoroscopy devices, there is potential danger not only to the surgeon but also to all members of the surgical team: increased exposure to ionizing radiation.1, 2

Despite all the biosafety equipment available to medical teams, such as lead aprons, protective collars for the thyroid and goggles with lead film, the cumulative deleterious effects of radioactivity cannot be neglected. Fluoroscopes emit doses of approximately 5 rads per minute3 and minifluoroscopes can cause serious and irreversible damage to health.2, 3, 4, 5, 6 It is known that doses of 1 rad, when applied systematically to a given region, can cause damage to deoxyribonucleic acid (DNA) and consequently cancer, at proportions of approximately 1:100,000.5, 7 It is important to emphasize that, in the human organism, ionizing radiation inhibits cell mitosis and irreparably breaks the DNA double chain. Nuclear structural modifications produce severe alterations to cells and increase the chances of potential genetic transmission of such errors. The hands, thyroid, eyes, abdomen and genitals are critical target areas that should receive proper care.

Ionizing radiation and its negative effects take on greater gravity when the indiscriminate use of fluoroscopes by medical residents within orthopedics is taken into consideration. They are subjected to high doses of radiation from the start of their training, mainly because of lack of operative practice and/or knowledge of its dire consequences.

Taking into consideration the large number of orthopedic surgical interventions performed with the aid of fluoroscopes and the severe sequelae relating to ionizing radiation, along with the scarcity of literature on this topic, particularly in the main Brazilian databases, the present study was proposed with the objective of evaluating the degree of exposure of orthopedic surgical teams to fluoroscopic ionizing radiation, with or without the associated use of bioprotection equipment.

Materials and methods

In conformity with resolution no. 1595/2000 of the Federal Medical Council, the authors declare that they did not have assistance of any kind for this study. Moreover, the researchers did not have any conflicts of interest in relation to the present study.

The study protocol was approved by the Ethics Committee for Research involving Human Beings, under no. 474/2012. All the patients or the adults legally responsible for them agreed to participate in the study and signed a free and informed consent statement after having been given detailed information about the content and shape of the study.

The sample size was determined at the start of the study, by means of specific statistical tests. The α risk (5%) and β risk (20%) were taken into consideration, along with the diversity of the variables, and the minimum number of surgical procedures was calculated as 45.

The ionizing radiation to which the orthopedic surgical team (R1, R2 and R3) was exposed during surgical procedures of hip osteosynthesis (Richard dynamic hip screw (DHS) or sliding screw and plate) due to transtrochanteric fractures classified as 31-A2.1 (AO), performed between February 2012 and August 2012, was assayed. The inclusion criteria were that the patients should have a minimum age of 18 years and have proximal femoral fractures of type 31-A2.1. All patients whose operations required intraoperative radiographs, those with fractures of tumor origin and those who refused to sign the consent form were excluded. Seven patients were excluded from this study: five who required intraoperative radiographs and two who, at the time of admission to our service, were unconscious and unaccompanied and thus unable to sign the consent statement. In this manner, 48 surgical procedures were included in this study.

After arrival at the emergency service, the patients underwent the advanced trauma life support (ATLS) protocol and initial radiographs were produced, from which fractures in the proximal region of the femur were identified and classified. The patients were quickly thereafter taken to the surgical center to undergo osteosynthesis procedures, always performed by the same medical team (R1: technologist; R2: first surgeon; and R3: second surgeon) and using the same protocols and procedural times. All the surgical procedures were monitored in loco by the same preceptor, who was a specialist in hip surgery. The fluoroscopy device (Philips® BV Endura) (Fig. 1), which was calibrated within the specific technical standards,8, 9 was always operated by the same professional and under the same technical parameters.

Fig. 1.

Fig. 1

Fluoroscope (lateral view).

Protective lead aprons of thickness 5 mm (Konex®) were used by the surgical team as personal protection equipment. Throughout the time of the surgical procedure, the medical team used 21 thermoluminescent radiation dosimeters, distributed in different anatomical regions (Fig. 2 and Table 1), above and below the biosafety equipment, which had the function of measuring the ionizing radiation that was emitted by the fluoroscopy device and received by the orthopedic team.

Fig. 2.

Fig. 2

Anterior and posterior locations of the dosimeters on the team members (above and below the lead protector).

Table 1.

Anatomical distribution of the dosimeters according to the team members.

1st surgeon (R2) 2nd surgeon (R3) Technologist (R1)
Dorsal region (back) Dosimeter 1 Dosimeter 8 Dosimeter 15
Gonads (below the protector) Dosimeter 2 Dosimeter 9 Dosimeter 16
Gonads (above the protector) Dosimeter 3 Dosimeter 10 Dosimeter 17
Thyroid Dosimeter 4 Dosimeter 11 Dosimeter 18
Thorax (below the protector) Dosimeter 5 Dosimeter 12 Dosimeter 19
Thorax (above the protector) Dosimeter 6 Dosimeter 13 Dosimeter 20
Control Dosimeter 7 Dosimeter 14 Dosimeter 21

The dosimeters were kept packed in a lead box, from which they were removed by the surgical team only just before they performed their asepsis and antisepsis procedures. After the end of the operative procedure, the surgical team immediately placed the dosimeters back into the same container. Three dosimeters (controls) were kept permanently inside lead wrappings, protected from any external radiation that could compromise the results.

Information such as the length of time for which the fluoroscope was used and the quantity of kV and mSv emitted by the device were provided automatically by the computer of the device and were subsequently tabulated in an electronic spreadsheet. At the end of the study, the dosimeters were sent to the Department of Nuclear Physics of the Physics Institute, University of São Paulo, which analyzed the individual doses of radiation received by each dosimeter, without knowing the original anatomical location (blinding process).

Statistical methodology

The variables of duration of the surgery, individual dose of radiation and location where received, for each of the members of the surgical team, were analyzed by means of parametric and nonparametric descriptive statistical tests, in a fully randomized model, using the SigmaStat® software, version 3.5 (Systat Software Inc., 2006), and the Minitab® software, version 15 (Minitab Inc., 2007). For all the calculations, a significance level of 5% was used (p < 0.05).

The means, standard deviations, medians, frequencies, percentages and 95% confidence intervals (95% CI) were calculated (α = 5%).

Results

The total time for which the fluoroscope was used was 2 h and 55 min, and the mean length of use was 3 min and 53 s (±1 min 22 s) (minimum: 1 min 44 s; maximum: 6 min 45 s; 95% CI: 3 min 29 s to 4 min 18 s).

The effective radiation dose received by R3 was 6.33 mSv, by R2 4.51 mSv and by R1 1.99 mSv (p = 0.33) (Fig. 3). There were no statistical differences in total individual dose received between R3 and R2 (p = 0.58), R2 and R1 (p = 0.32) or R3 and R1 (p = 0.13).

Fig. 3.

Fig. 3

Total radiation dose (mSv) received by the team members.

In relation to the anatomical regions, the thyroid region received a mean radiation dose of 0.86 mSv (±0.3), the thoracic region 1.24 mSv (±0.8) and the gonadal region 2.15 mSv (±1.2) (p = 0.25) (Fig. 4).

Fig. 4.

Fig. 4

Total radiation dose (mSv) in the different anatomical areas of the team members.

The individual dose of radiation received by R3 in the thyroid region was 1.24 mSv, by R2 0.81 mSv and by R1 0.55 mSv (p = 0.87) (Fig. 5). There were no statistical differences in the doses received in the thyroid region between R3 and R2 (p = 0.76), R2 and R1 (p = 0.82) or R3 and R1 (p = 0.6).

Fig. 5.

Fig. 5

Radiation dose (mSv) received in the thyroid region of the team members.

The individual dose of radiation received by R3 in the thoracic region was 2.14 mSv, by R2 0.9 mSv and by R1 0.70 mSv (p = 0.61) (Fig. 6). There were no statistical differences in the doses received in the thoracic region between R3 and R2 (p = 0.47), R2 and R1 (p = 0.87) or R3 and R1 (p = 0.4).

Fig. 6.

Fig. 6

Radiation dose (mSv) received in the thoracic region of the team members.

The individual dose of radiation received by R3 in the gonadal region was 2.94 mSv, by R2 2.8 mSv and by R1 0.73 mSv (p = 0.5) (Fig. 7). There were no statistical differences in the doses received in the gonadal region between R3 and R2 (p = 0.95), R2 and R1 (p = 0.27) or R3 and R1 (p = 0.24).

Fig. 7.

Fig. 7

Radiation dose (mSv) received in the gonadal region of the team members.

The radiation levels detected in the control dosimeters, which were placed below the biosafety protectors (lead aprons) and on the backs of the team members, were less than 0.1 mSv. They were therefore considered to be zero.

Discussion

Studies conducted in the United States by the Department of Radiological Health and the Department of Health, Education and Wellbeing have indicated that the use of medical equipment that emits X-rays is the biggest source of exposure of the population to ionizing radiation of non-natural origin.10, 11, 12 In Brazil, the National Nuclear Energy Commission (CNEN) has recommended that the effective dose for individuals who are occupationally exposed to radiation should not exceed the mean limit of 20 mSv per year.13 The results from the present study demonstrate that, over a period of only six months, the residents in a medical residency program within orthopedics and traumatology received, on average, a quarter of the maximum permitted annual dose while only performing medium-complexity hip surgery, monitored by a specialist within the field. It can therefore be hypothesized that, if all the surgical procedures performed by these residents during their training were taken into consideration, the annual limit for the dose would certainly be exceeded.

Like other authors,14, 15, 16 we found that fluoroscopes generate large doses of ionizing radiation that affects the lower abdominal area, particularly the gonads (Fig. 4, Fig. 7). Reflected radiation, also known as scattered radiation, which is disseminated after it encounters the object of study, is one of the main agents responsible for increasing the incidence of radiation in these regions (Fig. 8). Reflected radiation also explains why the position of the fluoroscope should not be inverted when its radiation emission source is placed above the object of study.

Fig. 8.

Fig. 8

Reflected radiation (scattered radiation)

Source: Adapted from the AO Foundation.

The results also showed that, although there were no significant differences between R3, R2 and R1, there was a strong tendency toward diminished radioactive impact on the surgical team members, as their distance from the fluoroscope increased. In fact, several authors have recommended that the team should remain at a safe distance from the device, of at least one meter.11, 12, 13, 14, 15 It is also important to note that use of personal protection equipment (lead aprons, goggles, etc.) is essential for professionals who come into contact with this type of radiation.16, 17 In the present study, the dosimeters placed below the lead apron remained without registering any radiation, which proves the effectiveness of this protection for preserving the medical team. However, it needs to be emphasized that although the protection equipment is effective, the unprotected regions of the body, particularly the upper limbs, remain at risk of neoplasia development.

Orthopedic teams, whether composed of residents or trained orthopedic surgeons, should use fluoroscopes cautiously during their operative procedures. The time for which the devices are used should be kept as short as possible, the team members should remain at a distance from the ionizing source and, obviously, adequate protective equipment should be used. These are effective measures for preventing serious health problems among the team members.

Conclusions

Under the conditions of the present study, the members of the surgical team who remained closest to the fluoroscope (R3 and R2) received higher doses of radiation, particularly in anatomical regions below the waistline. The biosafety equipment (lead apron) was effective in preventing radiation from reaching the vital organs of the medical team members.

Conflicts of interest

The authors declare that there were no conflicts of interest.

Footnotes

Please cite this article as: Palácio EP, Ribeiro AA, Gavassi BM, Di Stasi GG, Galbiatti JA, Junior AD, et al. Exposição da equipe cirúrgica à radiação ionizante durante procedimentos cirúrgicos ortopédicos. Rev Bras Ortop. 2014;49:227–232.

☆☆

Work performed in the Department of Orthopedics and Traumatology, Faculdade de Medicina de Marília (FAMEMA), Marília, SP, Brazil.

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