Environmental sustainability of ultrasound-guided core-needle breast biopsy: a survey on current practices by the European Society of Breast Imaging (EUSOBI)
Andrea Cozzi, Serena Carriero, Maria Adele Marino, Simone Schiaffino, Fleur Kilburn-Toppin, Matthew G. Wallis, Paola Clauser, Michael H. Fuchsjäger, Elisabetta Giannotti

TL;DR
This study surveyed European breast imaging experts to assess how ultrasound-guided breast biopsy practices affect environmental sustainability.
Contribution
The study identifies opportunities to reduce resource use and environmental impact without compromising infection control in breast biopsies.
Findings
Most respondents used minimal disposable materials per procedure, but few used recycling bins.
No significant link was found between perceived hygiene levels and post-procedural infections.
Resource-intensive communication methods for benign results are commonly used.
Abstract
In the context of a global appraisal of the environmental impact of radiology, this survey among members of the European Society of Breast Imaging (EUSOBI) investigated procedural aspects of ultrasound-guided core-needle breast biopsy that may impact its environmental sustainability. A 25-item online questionnaire, developed by a panel of nine breast imaging experts, was distributed from September 25th to December 25th, 2024, within the EUSOBI mailing list and social media platforms. The survey investigated materials routinely used for ultrasound-guided core-needle biopsies, waste disposal practices, the relationship between perceived procedural hygiene levels and self-reported frequency of post-procedural infectious complications, and results’ communication methods. Replies were analysed with descriptive and non-parametric statistics. Among the 787/823 respondents (95.6%) who…
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Taxonomy
TopicsBreast Lesions and Carcinomas · Digital Radiography and Breast Imaging · Radiation Dose and Imaging
Introduction
While the industry and energy sectors have traditionally been the focus of research and practical interventions for environmental sustainability [1, 2], the healthcare sector—responsible for an estimated 5% of global greenhouse gas emissions—is now recognised both as a contributor to environmental degradation and as a potential leader in driving change [3–5]. Across different medical specialities, including radiology, there is a growing imperative to rethink daily clinical activities through the lens of environmental responsibility [4–10].
Within this context, breast imaging has a particularly relevant position, as it combines high patient volumes, standardised workflows, and frequent use of disposable materials. Ultrasound-guided core-needle biopsy is one of the most performed procedures in breast care, having largely replaced surgical biopsy by offering a safe, minimally invasive, and cost-effective option [11, 12].
There is substantial variability in how ultrasound-guided core-needle biopsy is performed across different centres [11, 12]. Despite it being a low-risk procedure with minimal bleeding [13–15] and an extremely low infection rate—reported to be less than 0.3% [16], pre-procedural and peri-procedural hygiene practices vary widely, with some operators adopting fully sterile techniques and others opting for aseptic or clean procedures. There is often limited awareness of the rationale that underpins the choice between these different hygienic approaches, also considering that several socioeconomic factors—including the availability and cost of disposable materials—might influence this choice at national, regional, and even institutional levels [11, 13, 16, 17].
Although no robust evidence has ever been presented to support the necessity of rigorous sterile precautions for core-needle breast biopsy [11, 13], the procedure commonly involves an abundant and non-standardised use of single-use disposable materials, such as gloves, sterile drapes, syringes, needles, ultrasound probe covers, gauze swabs, plasters, and bandages. All these materials, especially in interventional procedures, represent a major source of biomedical waste [18–20], with far-reaching environmental implications [21, 22].
This survey, promoted by the European Society of Breast Imaging (EUSOBI), aims to provide a comprehensive overview—both from a qualitative and quantitative point of view—of several aspects of ultrasound-guided core-needle breast biopsy that carry a potential environmental impact, in order to identify opportunities to minimise waste and prepare for future recommendations on sustainable breast imaging.
Materials and methods
As this online survey was fully anonymous and implied voluntary consent from the participants, the Ethics Committee of the institution of the senior author (Cambridge University Hospital NHS Foundation Trust, Cambridge, United Kingdom) required no specific approval. The questionnaire (reported in the Supplementary Material) was developed by a panel of nine experts in breast cancer imaging (S.C., A.C., S.S., M.A.M., F.K.-T., M.G.W., P.C., M.H.F., and E.G.) representing different experience levels and scopes of activity in breast imaging (e.g., public, private and university hospitals) across Europe. The panellists discussed and agreed upon questions about materials and practices that were deemed to be common for ultrasound-guided core-needle breast biopsy across different practice settings and countries, while also aiming to build a questionnaire that could be completed in about 10 minutes to encourage participation and minimise incomplete responses. Ultimately, the questionnaire comprised 25 questions divided into two main sections: the first focusing on demographics and clinical practice settings of the respondents, and the second on their specific experience with ultrasound-guided core-needle breast biopsy, including procedural habits and resource utilisation. Two different pathways were designed, one for respondents who declared they performed core-needle breast biopsy and one for those who claimed they did not perform any. For those responders who indicated they did not perform biopsies, the questionnaire ended, while the full questionnaire was accessible only to those who performed core-needle breast biopsies in their daily practice. The survey was conducted anonymously.
First, the respondents who declared to perform ultrasound-guided core-needle breast biopsies were asked to express their opinion on how they would define their way of performing core-needle biopsy according to three different scenarios: (i) sterile, i.e., performed in a completely sterile environment; (ii) aseptic, i.e., using aseptic techniques (including sterile gloves) to minimise contamination; (iii) clean, i.e., maintaining basic cleanliness without attaining the levels required by asepsis or sterility.
Then, the survey explored the type and amount of material used during core-needle breast biopsy, accounting for their total number (per operator and assistant, if any, whose presence was the focus of a specific question) across all procedural steps, from operator preparation to sample collection and post-procedural care. Specific materials assessed were: sterile and non-sterile gloves, sterile keyboard covers for ultrasound systems, probe covers, sterile drapes, sterile gowns, hair caps, sterile gel, sterile and non-sterile gauze swabs, local anaesthetic vials, scalpels, plastic trays (used for disinfectant, gauzes, or sharp materials) and biopsy kits.
In addition to procedural details, the survey examined waste disposal practices, the self-reported and self-estimated perceived frequency of post-procedural infectious complications, and the methods used to communicate benign and malignant results to the patients.
The survey was disseminated through the EUSOBI official mailing list and made available on Google Forms (Google LLC) from September 25th 2024, to December 25th 2024. Two reminders were sent to all contacts in the mailing list on November 25th 2024, and on December 15th 2024. In addition to email dissemination, the survey was promoted on the official EUSOBI Instagram page through stories containing a direct link to the questionnaire. This social media promotion occurred on five separate occasions between September 25th and November 25th, 2024.
After the closure of the survey, data were exported in spreadsheets, coded wherever appropriate for multiple-choice or open-ended questions, then analysed and reported through descriptive statistics, presenting categorical data as counts and percentages. The Fisher’s exact test was used to evaluate potential associations between procedural hygiene practices and the occurrence of post-procedural infectious complications. Due to the very small number of missing replies (< 1.5% of respondents in each question), no correction for missing data was applied. All analyses were conducted with R (version 4.5.0, The R Foundation for Statistical Computing).
Results
Responses to the survey
The survey was completed by 823 respondents, most of whom (787/823, 95.6%) perform US-guided core-needle breast biopsy in their clinical practice. As the complete questionnaire was only available for respondents who declared to effectively perform US-guided core-needle breast biopsy, all analyses focused on these 787 respondents. Most of the respondents came from Europe (491/787, 62.4%), followed by respondents from Asia (131/787, 16.6%), the Americas (67/787, 8.5%), Africa (14/787, 1.8%), and Oceania (11/787, 1.4%), while geographic origin was not declared by 73/787 respondents (9.3%).
Most respondents (560/787, 71.2%) declared to perform US-guided core-needle biopsy only in one of the five practice settings indicated in the survey, with public hospitals being the most common single setting (217/787, 27.6%), followed by university hospitals (178/787, 22.6%). Overall, considering multiple replies, 362/787 respondents (46.0%) declared to perform core-needle biopsies in public hospitals, 321/787 in university hospitals (40.8%), 237/787 in private hospitals (30.1%), and 145/787 (18.4%) in private outpatient settings (Fig. 1).Fig. 1. Upset plot of practice settings among respondents
Most respondents declared that they aimed to perform core-needle biopsies in aseptic conditions (460/787, 58.4%), 147/787 in sterile conditions (18.7%), and 178/787 (22.6%) while maintaining only basic cleanliness without attaining sterility or asepsis; only 2/787 of respondents (0.3%) were effectively unsure about how the different choices of materials and procedural steps qualified their usual procedural pathway in one of the aforementioned categories.
More than 90% of respondents declared to perform core-needle biopsy in the presence of an assistant, who was always present in 572/787 cases (72.7%) and often present in 152/787 cases (19.3%). Only 32/787 respondents perform core-needle biopsies alone (4.1%), while the other 31/787 (3.9%) replied that an assistant was “almost never” present. If present, the assistant was involved in saving the images in 548/787 cases (69.6%), being the sole responsible for this task in 442/787 cases (56.1%). The radiologist performing the core-needle biopsy was instead involved in saving images, either with foot-switches (89/787 respondents, 11.3%) or directly touching the keyboard of the ultrasound system in 213/787 cases (27.1%). Of note, only 43 of the latter 213 respondents (20.2%) reported using at least one sterile keyboard cover.
Materials used in ultrasound-guided core-needle breast biopsies
As shown in Tables 1–3, across all surveyed disposable materials, most respondents used no more than one item or packet for the whole procedure, also considering the presence of an assistant. In particular, only 236/787 (30.0%) respondents used more than one pair of sterile gloves, while 500/787 respondents (63.5%) used less than two pairs of non-sterile gloves. Two pairs of non-sterile gloves were used by 247/787 respondents (31.4%), among whom only 14/247 (5.7%) declared to perform the procedure alone. As already mentioned, the use of sterile keyboard covers was reported by a minority of respondents (165/787, 21.0%), with only 21/787 (2.7%) respondents using more than one (Table 1). Among the 665/787 respondents (84.5%) using a probe cover, only 58/787 (7.4%) use more than one of these items. Of note, most of these 665 respondents (447/665, 67.2%) cover the probe with sterile items (specific sterile probe covers in 381 cases and a sterile glove in 66 cases), while the remaining 218/665 respondents (32.8%) use non-sterile disposables (specific non-sterile probe covers in 190 cases and a non-sterile glove in 28 cases). At least one sterile drape is used by 65.6% of the respondents (516/787), but only 134/787 respondents (17.0%) indeed use more than one (Table 2). Conversely, the majority of respondents do not routinely use sterile gowns (562/787, 71.4%) or hair caps (614/787, 78.0%). The use of sterile gel was declared by 438/787 respondents (55.7%), but only 41/438 (9.4%) use more than one packet per procedure, with a further 16/438 respondents (3.7%) declaring to conserve opened sterile gel packets for use in multiple procedures (Table 1). Sterile gauze emerged as the most widely used type of gauze (733/787 respondents, 93.1%), with 532/787 respondents (67.6%) consuming between one and three swabs per procedure. Conversely, while 263/787 respondents use at least one swab of non-sterile gauze (33.4%), only 36/263 (13.7%) consume more than three swabs (Table 3). Finally, while the use of scalpels was frequently reported (607/787 respondents, 77.1%; Table 1), only 16 of these 607 respondents used more than one scalpel per procedure (2.6%).Table 1. Amount of disposable material used for a single ultrasound-guided core-needle breast biopsy0123> 3One for more than one procedureNo replyPairs of sterile gloves137 (17.4%)414 (52.6%)197 (25.0%)31 (3.9%)8 (1.0%)—0 (0.0%)Pairs of non-sterile gloves109 (13.9%)391 (49.7%)247 (31.4%)25 (3.2%)13 (1.6%)—2 (0.2%)Keyboard covers621 (78.9%)144 (18.3%)14 (1.8%)3 (0.4%)4 (0.5%)—1 (0.1%)Probe covers122 (15.5%)607 (77.1%)33 (4.2%)15 (1.9%)10 (1.3%)—0 (0.0%)Sterile gowns562 (71.4%)136 (17.3%)65 (8.3%)11 (1.4%)9 (1.1%)—4 (0.5%)Hair caps614 (78.0%)62 (7.9%)72 (9.1%)39 (5.0%)——0 (0.0%)Sterile gel packets348 (44.2%)381 (48.4%)35 (4.5%)3 (0.4%)3 (0.4%)16 (2.0%)1 (0.1%)Plastic trays150 (19.1%)388 (49.3%)129 (16.4%)40 (5.1%)20 (2.5%)56 (7.1%)4 (0.5%)Scalpels178 (22.6%)591 (75.1%)9 (1.1%)7 (0.9%)^§^——2 (0.3%)^§^ More than two scalpels per procedureTable 2Number of sterile drapes used for a single ultrasound-guided core-needle breast biopsySterile drapesRespondents0269 (34.2%)1382 (48.5%)293 (11.8%)326 (3.3%)49 (1.1%)54 (0.5%)> 52 (0.3%)No reply2 (0.3%)Table 3. Number of sterile and non-sterile gauze swabs used for a single ultrasound-guided core-needle breast biopsySterile gauzeNon-sterile gauze0 swabs51 respondents (6.5%)515 respondents (65.4%)1–3 swabs532 respondents (67.6%)227 respondents (28.8%)3–5 swabs129 respondents (16.4%)20 respondents (2.5%)5–8 swabs54 respondents (6.9%)11 respondents (1.4%)8–10 swabs11 respondents (1.4%)4 respondents (0.5%)> 10 swabs7 respondents (0.9%)1 respondent (0.1%)No reply3 respondents (0.4%)9 respondents (1.1%)
As shown in Fig. 2, 5 mL anaesthetic vials resulted in being the most commonly used (403/787 respondents, 51.2%), followed by 10 mL vials (260/787 respondents, 33.0%) and 2 mL vials (167/787 respondents, 21.2%). The use of more than one vial of anaesthetic was reported by 145/787 respondents (18.4%), with only 42/787 respondents (5.4%) effectively employing—i.e., opening vials, regardless of the effectively injected quantity—more than 10 mL of anaesthetic for a single procedure.Fig. 2. Upset plot of the respondents’ preferences for the use of anaesthetic vials for ultrasound-guided core-needle breast biopsy
During and after the procedure, the use of plastic trays (i.e., containers for disinfectants, garments, cutters, etc., excluding the specimen containers) remains common (633/787 respondents, 80.4%), but confined to one per procedure in 388/633 cases (61.3%) and one for more than one procedure in 56 further cases (8.8%; Table 1). However, the number of respondents declaring the use of more than one plastic tray (189/633 cases, 29.9%) remains higher than the number of respondents who do not use them (150/787, 19.1%). Finally, most respondents declared not using a recycling bin for the disposal of non-sharp tools (404/787, 51.3%) and not to routinely use prepackaged biopsy kits (424/787, 53.9%).
Post-procedural infectious complications and communication of results
Among the 776 respondents who answered the question about the occurrence of infectious complications after ultrasound-guided core-needle biopsy, 549 (70.7%) declared that they had never seen any, and another 224/776 (28.9%) reported that they “almost never” saw any infectious complications. Only 3/776 respondents (0.4%) “often see” post-procedural infectious complications. Among these 776 respondents, 774 were able to categorise their procedures as clean, aseptic, or sterile (Fig. 3), without any significant association between the grade of sterility and the occurrence of post-procedural infectious complications (Fisher’s exact test p = 0.334).Fig. 3. Mosaic plot and contingency table for the association between procedural conditions and the occurrence of infectious complications after ultrasound-guided core-needle breast biopsy
Finally, for the communication of benign biopsy results (Fig. 4), resource-intensive modalities such as in-person communication and communication by letter were used by 68.0% (535/787) and 11.6% (91/787) of respondents, respectively.Fig. 4. Upset plot of the respondents’ preferences for the communication of benign results after ultrasound-guided core-needle breast biopsy. Categories shaded in red indicate resource-intensive modalities
Discussion
Over the last few years, radiology as a discipline and as a professional community has begun to devise and implement a framework to recognise, evaluate, and address its impact on the environment [8, 9, 23]. Arguably, ultrasound-guided core-needle breast biopsy represents one of the most common interventional procedures across the world, and constitutes one of the most resource-intensive acts performed in the preoperative phase of breast cancer care [11, 17]. Surprisingly, only a loose procedural framework exists for core-needle breast biopsy, which is known to be performed with widely varying protocols, especially concerning the choice of pre-procedural and peri-procedural hygiene practices and the use (and the amount) of disposable materials. This represents a paradox in a field where highly detailed quality standardisations and evaluations have been developed and enforced for diagnostic techniques such as mammography [24, 25] and indeed for the entire breast cancer care pathway [26, 27]. Moreover, this lack of procedural standardisation contributes to waste generation, which in turn results in increased expenses for waste management and for the procurement of disposable material [28].
This scenario must be accurately and consistently taken into account when interpreting and contextualising the results of this survey. As in other surveys promoted or endorsed by EUSOBI [25, 29–32], the 787 respondents who declared to routinely perform ultrasound-guided core-needle breast biopsy (out of a total 823 respondents to the survey) came from all continents and represented a broad spectrum of practice settings, from private outpatient clinics to public hospitals and academic tertiary care centres. This adds several institutional and national layers of heterogeneity to the known and expected intra-individual protocol variations. In particular, as this survey aimed to map several facets of the core-needle biopsy workflow that entail environment-related consequences—such as the use of disposable materials—resource constraints (or excessive abundance) due to country-specific or institution-specific economic conditions may have played a part in defining how breast imaging professionals effectively perform this procedure. Overall, most respondents used no more than one unit (or prepackaged bundles) of most disposable materials for each procedure: while we could not ascertain whether this indeed derives from individual consciousness about the economic costs of these materials, it indirectly translates into a resource-savvy approach.
However, a more complicated and less favourable scenario emerged when considering some aspects where personal preferences of the operators play a greater part in defining resource use and some other aspects where an active role of the operator is needed to achieve sustainable practices. For instance, while no significant association between the level of procedural sterility and the occurrence of post-procedural infectious complications (which were self-reported as practically non-existent by 70.7% of respondents) was found, up to 77.1% of respondents declared to prepare a self-reported aseptic (58.4%) or even sterile (18.7%) working environment. This is a crucial point for two reasons: first, because percutaneous core-needle biopsy is classifiable as a low-risk procedure even in basic cleanliness conditions [13, 16], therefore positioning aseptic or sterile environments as overly prudent approaches that are not supported by robust evidence; second, and most importantly, because subsequent declarations of the type and quantity of disposable materials used during the procedure point to the fact that properly defined sterility (and most likely also properly defined aseptic conditions) was most likely not attained even if it was self-reported, resulting in sizable and repeated waste of materials and also effectively nullifying the efforts towards attaining higher levels of procedural hygiene, however superfluous they might be. Likewise, several steps of the core-needle biopsy procedure where the operator must deliberately take action to ensure sustainable practices showed less favourable trends, as for instance more than a half (51.3%) of respondents declared not to use a recycle bin for the disposal of non-sharp tools, a little more than a half (53.9%) declared to avoid using prepackaged biopsy kits, and only about a fifth of the respondents (163/787, 20.7%) declared to avoid resource-intensive options for communicating negative biopsy results, such as letters or in-person appointments, thus helping to reduce unnecessary hospital visits and the associated carbon emissions from patient travel.
Aside from the geographic heterogeneity of the respondents, which might reflect differences in training and in economic conditions that directly influence the availability of materials, three main limitations of this work must be acknowledged. First, although comprising almost 800 single replies from respondents routinely performing breast biopsy, our sample undoubtedly still offers a partial representation of current practice and is likely mostly composed by EUSOBI members, who might have a relatively higher degree of acquaintance with the discourse revolving around the environmental impact of radiology, which has been widely promoted in scientific journals and international congresses over the last few years [3, 4, 8, 9, 23]. Second, this survey focused only on ultrasound-guided core-needle biopsy: while this procedure remains by far the most widely performed type of breast biopsy, the emerging role of other minimally-invasive breast interventions, such as vacuum-assisted breast biopsy and vacuum-assisted excision, deserves to be considered in future studies, as the evidence-based higher required level of hygiene for these procedures implies a correspondingly higher use of disposable materials. Third, no analyses could be conducted on how institutional factors beyond the control of each respondent directly influence their decision to use a specific amount of a disposable material during the core-needle biopsy procedure: these factors include—but are not limited to—institutional procurement contracts, standardised packaging and stockage of supplies, and local regulations about the use of pharmaceutical products or devices.
In conclusion, this survey provides a first mapping of current practices of ultrasound-guided core-needle breast biopsy that carry an environmental impact. This survey highlights wide variability in these procedural aspects, reveals that some economically driven sustainable behaviours are already in place, and shows substantial opportunities to reduce material use and waste. The absence of significant associations between sterility levels and post-procedural infectious complications suggests that resource-intensive habits—that result in avoidable waste of materials without any proven benefit for the patients—might be safely streamlined with the help of high-quality evidence and of standardised guidance.
Supplementary information
ELECTRONIC SUPPLEMENTARY MATERIAL
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