Skip to main content
Journal of Breast Cancer logoLink to Journal of Breast Cancer
. 2024 Jul 27;27(4):248–259. doi: 10.4048/jbc.2024.0045

Unveiling the Potential of Drain Tip Cultures: Impact on Surgical Site Infections in Implant-Based Breast Reconstruction

Ji-Young Kim 1,2, I Zhen Ma 1, Ki Yong Hong 1,✉
PMCID: PMC11377939  PMID: 39069783

Abstract

Purpose

Surgical site infections (SSIs) remain a concern after implant-based breast reconstruction, despite preventive measures. These infections can have serious consequences. This study evaluated the correlation between drain tip culture results and SSIs in this patient population.

Methods

We analyzed data from patients who underwent implant-based breast reconstruction between July 2021 and May 2023. Drain tip cultures were collected, and any SSIs occurring within one month of surgery were documented. We then compared clinical data with the culture results.

Results

A total of 263 drain tip cultures were included. Notably, none of the 61 patients who underwent tissue expander removal and implant insertion had positive cultures. However, among the 202 patients who received tissue expanders or direct-to-implant procedures, 11 (5.45%) had positive cultures, with a total of 12 SSIs identified. Importantly, five of the 11 culture-positive wounds developed SSIs. Multivariate analysis revealed a significant two-way association between infection and positive drain tip cultures. For Staphylococcus aureus specifically, drain tip cultures showed excellent predictive value: sensitivity (33.33%), specificity (100%), positive predictive value (100%), and negative predictive value (95.96%).

Conclusion

Drain tip cultures from immediate implant-based breast reconstructions significantly correlated with SSIs. Close monitoring is crucial, especially when S. aureus is identified in the culture.

Keywords: Bacteria, Breast Implants, Infections, Suction, Tissue Expansion Devices

INTRODUCTION

Implant-based breast reconstruction, a popular choice for breast cancer patients who have undergone mastectomy [1], is not without its drawbacks. While the number of procedures is increasing, complications like capsular contracture, implant malposition, and infection can occur. Infection is particularly concerning because it can lead to implant loss, additional surgeries, and disruptions in a patient’s treatment plan. Various studies have explored preventive measures like skin decolonization, prophylactic antibiotics, and sterile techniques [2,3]. However, despite these efforts, the reported incidence of infection in implant-based reconstruction varies widely, ranging from 1% to 30% [2,4,5,6,7,8].

Closed-suction drainage plays a vital role in various surgeries by effectively reducing dead space and preventing postoperative seroma formation. However, this benefit comes with a potential downside: the drain may create a pathway for bacteria to travel from the external environment to the sterile implant pocket, leading to infection [9,10,11]. The debate regarding drain management continues. Some advocate for early drain removal to minimize the risk of infection, while others believe closed-suction drains are crucial for preventing seroma and hematoma formation and promoting wound healing [12]. Additionally, studies have shown limited effectiveness of prolonged antibiotic use until drain removal [13,14]. Therefore, establishing a standardized protocol for drain management is essential.

Several studies in other surgical fields suggest drain tip cultures might be useful for early detection of surgical site infections (SSIs), particularly those caused by methicillin-resistant bacteria in spinal surgery [15]. However, their routine use is not universally recommended, as seen in total hip arthroplasty [16]. In implant-based breast reconstruction, leaving the drain in for a longer period has been linked to a higher infection risk [12]. Analysis of bacterial profiles in suction drain fluid showed a 26% positive culture rate, with coagulase-negative Staphylococci being the most common bacteria, followed by Staphylococcus aureus. The study reported promising clinical value with sensitivity (85.71%), specificity (81.48%), positive predictive value (PPV) of 37.50%, and negative predictive value (NPV) of 97.79% [17]. However, the drainage fluid might not accurately reflect the bacteria within the implant cavity due to the potential contamination of the suction drain bottles. Therefore, no prior studies have explored the usefulness of drain tip cultures for early SSI detection in implant-based breast reconstruction. This study aims to address this gap by investigating whether a positive drain tip culture predicts SSIs in patients who underwent implant-based breast reconstruction. The secondary aim is to gain a deeper understanding of the bacterial profile to provide clinical guidance for interpreting drain tip culture results in this context.

METHODS

We conducted a retrospective chart review of patients who underwent implant-based breast reconstruction at Seoul National University Hospital between July 2021 and May 2023. Patients were divided into two cohorts. The first cohort included patients who underwent breast reconstruction with tissue expander insertion (TEI) or direct-to-implant (DTI) after mastectomy. The second cohort included patients whose previously inserted tissue expanders were removed and replaced with implants. Patients who underwent reconstruction using both implants and autologous tissue, such as a latissimus dorsi flap or fat graft, were excluded.

Perioperative management

All patients received prophylactic antibiotics to prevent infection. They received their first intravenous dose of cefazolin (1 g) at least 30 minutes before surgery. Subsequent doses were administered every eight hours for a total of 24 hours after surgery. Patients whose antimicrobial susceptibility testing showed resistance to cefazolin were switched to moxifloxacin (400 mg/day). The drain insertion site was disinfected with povidone-iodine every other day and dressed with a polyurethane foam (BETAfoam T®; Genewel, Seongnam, Korea) containing 3% povidone-iodine and covered with a transparent film. This dressing remained in place until the drain was removed.

During outpatient follow-up, additional oral antibiotics (cefixime 100 mg twice daily) were prescribed for patients experiencing mastectomy skin flap congestion or necrosis, or if drainage persisted beyond one week. For patients with positive drain tip cultures, the decision to prescribe oral antibiotics or conduct a short-term follow-up was based on the results of the antibiotic resistance test, regardless of whether the patient met the criteria for an SSI. Patients scheduled for adjuvant chemotherapy or radiotherapy had to wait at least one month after surgery to ensure complete healing of the surgical site.

Surgical procedures

TEI or DTI procedures

An acellular dermal matrix (ADM) was used above the pectoralis major muscle to create a pocket for the implant, leaving an opening for implant insertion. For subpectoral reconstruction, a pocket was created for the expander/implant along with the ADM after elevation of the pectoralis major muscle flap. Before inserting the expander/implant, the surgical field was irrigated with a povidone-iodine solution followed by a mixture of cefazolin (2 g) and gentamicin (160 mg) in 1 L of normal saline. Following irrigation, the skin was disinfected again with povidone-iodine, and gloves were changed.

The expander/implant was placed directly into the implant pocket, and the window was closed. An ADM was used in all cases. Two closed-suction drains were placed: one in the subcutaneous (outer pocket) plane and another in the periprosthetic plane (subADM or submuscular). Once the drain output decreased to less than 30 mL over a 24-hour period, the drain was removed. Upon removal, approximately 2 cm from the innermost end of the drain was aseptically cut, placed in a sterile tube, and sent for culture testing.

Tissue expander removal and implant insertion

The skin incision followed the existing scar from the previous TEI procedure. The tissue expander was carefully exposed and removed. A single closed-suction drain was placed in the periprosthetic plane. An implant of the appropriate size was then inserted into the pocket. It is important to note that other sterile techniques employed during this surgery mirrored those used in TEI or DTI reconstruction.

SSIs

SSIs were defined according to criteria established by the Centers for Disease Control and Prevention. These criteria require at least one of the following signs or symptoms to be present within one month of surgery: purulent drainage from the wound, positive culture results from a sterile sample of fluid or tissue collected from the wound, fever greater than 38°C (100.4°F), or localized pain or tenderness in the wound area. Any SSIs that developed post-operatively were identified through clinical examinations and medical record reviews.

For patients diagnosed with an SSI, treatment involves incision and drainage of the wound. The collected material was then sent for culture testing. This procedure was performed when an open wound with purulent drainage was present, or when significant fluid collection occurred within the implant pocket without an open wound. It is important to note that incision and drainage are also indicated for specific types of seromas that develop after surgery, including large seromas, those resistant to repeated aspiration, and those complicated by infection [18]. For patients with an expander and fluid collection but no open wound, aspiration of the fluid could be performed using a port on the expander. The expander/implant should then be removed from the pocket and subsequently washed repeatedly with a povidone-iodine solution.

Statistical analysis

Continuous variables are presented as means with standard deviations. Categorical variables are presented as counts and percentages. Based on the type and distribution of the variables, statistical analyses were conducted using an independent sample t-test for continuous variables and Fisher’s exact test for categorical variables. To account for multiple tip culture results per patient and their association with SSIs, generalized estimating equation models were employed. These models helped identify statistically significant variables associated with both tip culture results and SSIs. Further analysis was then performed for clinical factors with a p-value of ≤ 0.1. For all statistical tests, a p-value < 0.05 was considered statistically significant. All analyses were performed using the SPSS version 26.0 (IBM Corp., Armonk, USA).

Ethical standards

All procedures involving human participants performed in this study were in accordance with the ethical standards of the Institutional Review Board (IRB) of Seoul National University Hospital, which approved the study (IRB No. H-2302-079-1404) and the 1964 Helsinki Declaration and its later amendments or comparable ethical standards. Due to the retrospective nature of the study, the requirement for informed consent was waived.

RESULTS

Patient characteristics

A total of 263 drain-tip cultures were collected during the study period. In the first cohort, involving 119 patients who underwent TEI or DTI reconstruction, 202 drain tip cultures were performed. Out of these, 11 (5.45%) yielded positive results (Figure 1). Patient demographics and characteristics are presented in Table 1.

Figure 1. The flow of patients included in the study and tip culture results compared with clinical outcomes in the two cohorts.

Figure 1

IV = intravenous; tid = three times a day; PO = per os; bid = twice a day; TEI = tissue expander insertion; DTI = direct-to-implant; TER & II = tissue expander removal and implant insertion; MSSA = methicillin-sensitive Staphylococcus aureus; MSSE = methicillin-sensitive Staphylococcus epidermidis; SSI = surgical site infection.

Table 1. Patient characteristics in the first cohort.

Variables Negative culture Positive culture p-value
No. of drain 191 (94.6) 11 (5.4)
Side 0.536
Right 110 (57.6) 5 (45.5)
Left 81 (42.4) 6 (54.5)
Age (yr) 48.27 ± 8.15 46.91 ± 7.41 0.590
BMI (kg/m2) 23.33 ± 4.08 23.06 ± 5.89 0.832
Comorbidity
Hypertension 12 (6.3) 1 (9.1) 0.528
Smoking 5 (2.6) 1 (9.1) 0.288
Diabetes 5 (2.6) 2 (18.2) 0.049

Values are presented as number (%) or mean ± standard deviation.

BMI = body mass index.

The average age in the first cohort was 48.19 ± 8.10 years at surgery (p = 0.590), and the average body mass index (BMI) was 23.32 ± 4.18 kg/m2 (p = 0.832). There were no significant differences between the culture-positive and culture-negative groups in terms of hypertension (p = 0.528) or smoking history (p = 0.288). Importantly, the proportion of patients with positive cultures was significantly higher in the culture-positive group compared to the culture-negative group (p = 0.049).

Interestingly, none of the 61 drain tip cultures obtained from the second cohort of patients who underwent expander removal and implant insertion showed positive results (Supplementary Table 1).

Operation-related characteristics

There were no significant differences between the culture-negative and culture-positive groups regarding the type of mastectomy performed (Table 2). Most patients underwent skin-sparing mastectomies (69.8%, n = 141), while nipple-sparing mastectomies accounted for 30.2% (n = 61). Nearly all patients (96.9%, n = 196) underwent immediate breast reconstruction, with only a small portion (3.1%, n = 6) undergoing delayed reconstruction. Interestingly, no positive cultures were observed in the delayed-reconstruction group. The distribution of reconstruction methods was similar across both groups, with TEI being used in almost half of the cases (49.5%, n = 100) and the other half (50.5%, n = 102) utilizing DTI. The prepectoral plane was the preferred choice for implant placement in the vast majority of cases (87.6%, n = 177), with only 12.4% (n = 25) utilizing the subpectoral plane. Preoperative radiotherapy was uncommon (5.9%, p > 0.999), while neoadjuvant chemotherapy was administered to 31.7% of patients (p = 0.330). No statistically significant differences were observed between the groups in terms of these preoperative treatments. While no significant differences were found concerning surgical characteristics, the rate of postoperative infections differed significantly between the groups (p < 0.001). Overall, 12 (5.9%) patients experienced infections. However, in the culture-positive group, the infection rate was significantly higher (45.5%, n = 5) compared to the culture-negative group (3.7%, n = 7).

Table 2. Operation-related characteristics in the first cohort.

Variables Negative culture Positive culture p-value
No. of drains 191 (94.6) 11 (5.4)
Type of mastectomy 0.737
NSM 57 (29.8) 4 (36.4)
SSM 134 (70.2) 7 (63.6)
Timing of reconstruction > 0.999
Immediate 185 (96.9) 11 (100)
Delayed 6 (3.1) 0 (0)
Type of reconstruction 0.214
Tissue expander 97 (50.8) 3 (27.3)
Direct-to-implant 94 (49.2) 8 (72.7)
Implant insertion plane 0.141
Prepectoral 169 (88.5) 8 (72.7)
Subpectoral 22 (11.5) 3 (27.3)
Axillary lymph node dissection 29 (15.2) 3 (27.3) 0.386
Mastectomy flap necrosis 16 (8.4) 2 (18.2) 0.255
Neoadjuvant therapy
Radiotherapy 12 (6.3) 0 (0) > 0.999
Chemotherapy 59 (30.9) 5 (45.5) 0.330

Values are presented as number (%).

NSM = nipple-sparing mastectomies; SSM = skin-sparing mastectomies.

Prognosis of SSIs

All patients received antibiotic treatment. The outcomes included implant removal in four cases, implant change in three cases, and improvement after incision and drainage, or aspiration in three cases (Table 3). Among the patients who developed SSIs, four required implant removal. Tissue cultures confirmed S. aureus infection in three of these cases. In the remaining case, although final tissue culture results were unavailable, the tip culture revealed S. aureus. This finding suggests a poorer prognosis when S. aureus is associated with SSIs.

Table 3. Epidemiological and microbiological characteristics of surgical site infections.

Patient Age (yr) Subcutaneous drain Peri-prosthetic drain Tissue Cx (within postop 3 mo) Treatment
Removal POD Cx result Removal POD Cx result
1 51 26 MSSA 13 NG MSSA Abx
Implant removal
2 36 NA 14 MSSA NA Abx
Expander removal
3 59 NA 17 NG Staphylococcus lugdunensis Abx
I & D
4 59 NA 8 NG MRSA[A], NG[T] Abx
Expander removal
5 41 NA 12 Corynebacterium NG[A] Abx
Aspiration
6 51 NA 15 NG MSSA Abx
I & D
7 39 NA 10 NG Pseudomonas aeruginosa Abx
Implant change
8 52 5 NG 14 MSSA MSSA Abx
Expander change
9 45 NA 8 MRSA MRSA Abx
Implant change
10 52 NA 13 NG MSSA Abx
Expander removal

POD = postoperative day; Cx = culture; MSSA = methicillin-sensitive Staphylococcus aureus; NG = no growth; Abx = antibiotics; NA = not available; I & D = incision and drainage; MRSA = methicillin-resistant Staphylococcus aureus; [A] = aspiration specimen; [T] = tissue specimen.

Among the five patients with positive tip cultures, four showed S. aureus infection. Interestingly, salvage surgery was successful in 50% of these cases. In contrast, among the five cases with negative tip culture results, three patients eventually had S. aureus cultured from tissue or aspiration samples, and salvage surgery was successful in only one case (33%).

It is important to note that no SSIs were associated with positive tip cultures from drains removed within the first week of surgery. Additionally, the average time to drain removal differed between culture-positive and culture-negative SSI patients. Patients with positive cultures had drains removed slightly earlier (14.8 ± 6.72 days) compared to those with negative cultures (11.57 ± 4.16 days). Furthermore, the average time to symptom onset differed between these groups. Culture-positive patients showed symptoms earlier (14.6 ± 8.17 days) compared to culture-negative patients (22 ± 7.78 days). This finding, along with drain removal timing, suggests that tip cultures might be more informative for SSI detection when the drain is removed closer to the typical timeframe for symptom onset.

Some patients with negative results from the first drain culture eventually showed bacterial growth in subsequent cultures. This highlights that early tip cultures, particularly those obtained shortly after surgery, are not reliable indicators for completely ruling out infection.

Drain information

Of all drains, 68 (33.7%) were in the subcutaneous plane and 134 (66.3%) were in the periprosthetic plane, with no significant difference between the two groups (p = 0.513) (Table 4). The average duration of all drains was 10.22 ± 4.23 days, and the duration was significantly longer in the culture-positive group, lasting 12.82 ± 6.06 days, compared to 10.07 ± 4.07 days in the culture-negative group (p = 0.036).

Table 4. Drain information in the first cohort.

Variables Negative culture Positive culture p-value
No. of drains 191 (94.6) 11 (5.4)
Plane of drains 0.513
Subcutaneous 63 (33.0) 5 (45.5)
Peri-prosthetic 128 (67.0) 6 (54.5)
Average drain duration (days) 10.07 ± 4.07 12.82 ± 6.06 0.036

Values are presented as number (%) or mean ± standard deviation.

Factors influencing infection and positive tip culture

Univariate analysis was conducted to identify factors influencing infection and positive tip culture results. Skin necrosis (p = 0.020), drain duration (p = 0.021), smoking history (p = 0.003), and positive tip culture results (p < 0.001) were all found to be significant factors influencing the development of infection. Similarly, diabetes (p = 0.001) and the presence of infection itself (p < 0.001) significantly influenced positive tip culture results.

Multivariate analysis, focusing on clinical factors with a p-value ≤ 0.1 in the univariate analysis (Table 5), revealed that smoking (p = 0.021) and positive tip culture results (p < 0.001) remained independent predictors of infection. Likewise, infection (p = 0.002) remained a significant factor influencing positive tip culture results (Table 6).

Table 5. Generalized estimating equations to analyze factors influencing infection.

Variables Regression coefficient B Standard error p-value
BMI 0.122 0.0741 0.101
Comorbidity
Diabetes 1.160 2.5000 0.643
Smoking 2.749 1.1850 0.020
Culture result 3.072 0.9448 0.001
Average drain duration (days) −0.016 0.0724 0.827
Mastectomy flap necrosis 1.070 1.4090 0.448

BMI = body mass index.

Table 6. Generalized estimating equations to analyze factors influencing positive culture result.

Variables Regression coefficient B Standard error p-value
Comorbidity
Diabetes 1.627 1.035 0.116
Infection 2.184 0.701 0.002
Implant insertion plane 0.700 0.807 0.385
Average drain duration (days) −0.139 0.093 0.137

These findings highlight a strong correlation between infection and positive tip culture results. This suggests that tip cultures have the potential to serve as an early diagnostic tool for predicting SSIs in implant-based breast reconstruction.

Microbiological profile of positive tip culture samples

Drain tip cultures were positive for bacteria in 11 patients (5.78%). The most common bacteria identified were S. aureus and Staphylococcus epidermidis, with four cases each (Table 7). Additionally, two Corynebacterium spp. and one Bacillus spp. were detected. Of the 11 patients with positive cultures, only five developed SSIs.

Table 7. Microbiological profiles of positive drain tip cultures and postoperative surgical site infection.

Gram-positive bacteria No. SSI
Concordant Discordant NA Total
Staphylococcus aureus 3 (MSSA) 2 0 1 3
1 (MRSA) 1 0 0 1
Staphylococcus epidermidis 1 (MSSE) 0 0 0 0
3 (MRSE) 0 0 0 0
Bacillus spp. 1 0 0 0 0
Corynebacterium spp. 2 0 1(A) 0 1
Total 11 3 1 1 5

SSI = surgical-site infection; NA = not available; MSSA = methicillin-sensitive Staphylococcus aureus; MRSA = methicillin-resistant Staphylococcus aureus; MSSE = methicillin-sensitive Staphylococcus epidermidis; MRSE = methicillin-resistant Staphylococcus epidermidis; A = aspiration specimen.

Analyzing the first cohort’s data for all bacterial strains, drain tip cultures demonstrated a sensitivity of 41.67%, specificity of 96.84%, NPV of 96.34%, and PPV of 45.45%.

Notably, all four cases (100.0%) where S. aureus was detected in the tip culture resulted in SSIs. Excluding one case without final tissue culture results, all S. aureus cases showed consistent findings between the final tissue and tip culture results. For S. aureus, drain tip cultures demonstrated a sensitivity of 33.33%, specificity of 100.0%, PPV of 100.0%, and NPV of 95.96%. In contrast, among the seven cases where bacteria other than S. aureus were detected, only one patient developed an SSI. This translates to a low PPV (14.29%) for predicting SSIs with these bacteria.

One patient with a Corynebacterium spp. SSI presented with fever, erythema, and swelling. However, the infection resolved with antibiotics, and no bacteria were found in the aspirated sample. No SSIs occurred in patients where S. epidermidis or Bacillus spp. were detected in the tip cultures. These findings highlight the importance of considering the specific bacteria identified in tip cultures when interpreting results. The presence of S. aureus showed a significantly higher accuracy in predicting SSIs compared to other bacteria.

DISCUSSION

The drain tip serves as a direct connection between the internal body and the external environment, prompting research into its potential for detecting early signs of infection [15,16]. However, previous studies on implant-based breast reconstruction have not fully explored the usefulness of tip cultures, and lack sufficient statistical data for interpreting results. This study collected drainage tips directly from the implant pocket for bacterial culture analysis. This is a more targeted approach compared to previous research that analyzed drainage fluid from suction drain bottles [17]. This method is expected to provide new insights and improve our understanding of tip culture results in breast implant surgery.

Direct examination of the drain tip yielded a lower culture-positivity rate (5.4%) compared to the 26% reported in a previous study using drainage fluid from the drain bottle [17]. This decrease is likely due to reduced contamination during the culture process, leading to a higher predictive value for specific bacterial species. Notably, S. aureus demonstrated a strong correlation with SSIs, with a sensitivity of 33.33%, specificity of 100.0%, PPV of 100.0%, and NPV of 95.96%. This emphasizes the importance of considering bacterial species when interpreting culture results. Studies have shown that individuals colonized with S. aureus on their skin have a 7.1-fold increased risk of SSIs regardless of surgery type [19]. In this study, S. aureus accounted for 60.0% of the bacteria identified in SSIs. Although S. epidermidis was identified in tip cultures as frequently as S. aureus, none of these cases developed SSIs. This suggests that S. epidermidis is less harmful than S. aureus. Unlike S. aureus, which produces toxins that facilitate infections, S. epidermidis has fewer virulence factors and typically does not cause invasive infections in healthy individuals [20].

When interpreting culture results, it is crucial to consider the surgical approach (performed independently by plastic surgery or in collaboration with another department) and the timing of reconstruction (immediate vs. delayed or secondary). Studies have shown a slightly higher incidence of SSIs and non-infectious wound complications in immediate implant-based reconstruction compared to delayed or secondary procedures [21]. This increased risk might be due to the longer surgery duration in immediate reconstruction, which often involves consecutive mastectomies and reconstructions. Additionally, the placement of the implant in an area with significant dead space and reduced vascularization during immediate reconstruction can contribute to complications like infection, hematoma, or seroma [22]. Culture positivity also reflects these findings. In our study of patients undergoing second-stage surgery (tissue expander removal and implant insertion), all 61 tip cultures were negative. Conversely, all culture-positive drains were observed in patients who underwent immediate reconstruction. These results suggest that drain tip cultures might be more informative for predicting SSIs in immediate reconstruction compared to delayed procedures.

Several factors are known to be associated with SSIs in implant-based breast reconstruction, including BMI, smoking, diabetes, radiation therapy, mastectomy technique, skin flap necrosis, seroma, and hematoma [8,23]. In our study, smoking and positive culture results were identified as the only factors influencing infection development. Concerning the culture results, no other factors affected the outcomes beyond the occurrence of SSI. The risk of infection can vary depending on a center’s protocols for preoperative and postoperative antibiotics, as well as patient management practices. In our study, even patients not meeting the standard criteria for SSIs received oral antibiotics on an outpatient basis if deemed at risk based on clinical experience. While antibiotic use after implant-based breast reconstruction has been shown to reduce infection rates [8], recent studies suggest that prolonged use does not significantly decrease SSIs or implant loss [24]. Similarly, oral antibiotics are not effective in preventing infection or implant loss after immediate prosthetic reconstruction [25]. Interestingly, in our study, all patients with SSIs received oral antibiotics regardless of negative culture results, and these antibiotics did not prevent the infections. This aligns with recent findings and highlights the need for further investigation into alternative interventions, potentially including intravenous antibiotics.

This study has some limitations. First, the relatively small number of culture-positive cases and SSIs limited our ability to comprehensively analyze the influence of clinical factors and specific bacterial species. Second, although our center identified S. aureus as the primary causative agent in implant-related infections, the varying distribution of bacterial species in SSIs across different institutions could affect how drain tip culture results are interpreted [26,27,28,29]. Finally, the study had limitations in proposing a strategy to prevent SSIs when S. aureus is detected in tip cultures. Some patients developed SSIs despite receiving antibiotics based on positive cultures. This suggests that multiple factors may contribute to SSIs, and antibiotic resistance is a crucial clinical consideration. Additionally, since tip cultures and subsequent treatment often occur on an outpatient basis, interventions beyond oral antibiotics may be necessary. This aligns with previous research [24]. Large-scale studies are warranted to investigate these factors and potential antibiotic resistance. Despite these limitations, the study has several strengths. To our knowledge, it is the first to explore the importance of drain tip cultures after breast reconstruction surgery. Previously, no research existed on tip cultures in this context. Providing information on tip culture results can be valuable for guiding future research. Furthermore, the 0.0% positivity rate in delayed reconstructions or procedures performed solely by plastic surgeons suggests such surgeries with low positivity rates may not need further investigation.

This study explored the effectiveness of drain tip cultures in implant-based breast reconstruction and provided new insights into culture outcomes. Tip culture results in patients undergoing TEI or DTI procedures showed a significant correlation with SSIs. Among infectious species, S. aureus emerged as a major contributor to SSIs, highlighting the importance of considering this bacterium when interpreting culture results. This is especially true when S. aureus is cultured, as it warrants close monitoring.

Footnotes

Funding: This research was supported by the National Research Foundation of Korea (NRF-2022R1C1C1010912 to Ki Yong Hong) grant funded by the Korea government (MSIT) and the Technology Innovation Program (Grant No. 20022828; Research and development of micronized human acellular dermal matrix preserving collagen and growth factor for soft tissue filling) funded by the Ministry of Trade, Industry & Energy (MOTIE, Korea).

Conflict of Interest: The authors declare that they have no competing interests.

Data Availability: In accordance with the ICMJE data sharing policy, the authors have agreed to make the data available upon request.

Author Contributions:
  • Conceptualization: Hong KY.
  • Supervision: Hong KY.
  • Writing - original draft: Kim JY.
  • Writing - review & editing: Kim JY, Ma IZ.

SUPPLEMENTARY MATERIAL

Supplementary Table 1

Patient and operation-related characteristics in the second cohort

jbc-27-248-s001.xls (28KB, xls)

References

  • 1.American Society of Plastic Surgeons. 2017. Plastic Surgery Statistics Report. [Accessed August 20th, 2021]. https://www.plasticsurgery.org/news/plastic-surgery-statistics?sub=2017+Plastic+Surgery+Statistics .
  • 2.Dassoulas KR, Wang J, Thuman J, Ndem I, Schaeffer C, Stovall M, et al. Reducing infection rates in implant-based breast reconstruction: impact of an evidence-based protocol. Ann Plast Surg. 2018;80:493–499. doi: 10.1097/SAP.0000000000001407. [DOI] [PubMed] [Google Scholar]
  • 3.Khansa I, Hendrick RG, Jr, Shore A, Meyerson J, Yang M, Boehmler JH., 4th Breast reconstruction with tissue expanders: implementation of a standardized best-practices protocol to reduce infection rates. Plast Reconstr Surg. 2014;134:11–18. doi: 10.1097/PRS.0000000000000261. [DOI] [PubMed] [Google Scholar]
  • 4.Gabriel SE, Woods JE, O’Fallon WM, Beard CM, Kurland LT, Melton LJ., 3rd Complications leading to surgery after breast implantation. N Engl J Med. 1997;336:677–682. doi: 10.1056/NEJM199703063361001. [DOI] [PubMed] [Google Scholar]
  • 5.Brand KG. Infection of mammary prostheses: a survey and the question of prevention. Ann Plast Surg. 1993;30:289–295. doi: 10.1097/00000637-199304000-00001. [DOI] [PubMed] [Google Scholar]
  • 6.Olsen MA, Nickel KB, Fox IK, Margenthaler JA, Ball KE, Mines D, et al. Incidence of surgical site infection following mastectomy with and without immediate reconstruction using private insurer claims data. Infect Control Hosp Epidemiol. 2015;36:907–914. doi: 10.1017/ice.2015.108. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 7.Wilkins EG, Hamill JB, Kim HM, Kim JY, Greco RJ, Qi J, et al. Complications in postmastectomy breast reconstruction: one-year outcomes of the Mastectomy Reconstruction Outcomes Consortium (MROC) Study. Ann Surg. 2018;267:164–170. doi: 10.1097/SLA.0000000000002033. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 8.Hu Y, Zhou X, Tong X, Chen X, Wang M, Wu X, et al. Postoperative antibiotics and infection rates after implant-based breast reconstruction: a systematic review and meta-analysis. Front Surg. 2022;9:926936. doi: 10.3389/fsurg.2022.926936. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 9.Xue DQ, Qian C, Yang L, Wang XF. Risk factors for surgical site infections after breast surgery: a systematic review and meta-analysis. Eur J Surg Oncol. 2012;38:375–381. doi: 10.1016/j.ejso.2012.02.179. [DOI] [PubMed] [Google Scholar]
  • 10.Murray JD, Elwood ET, Jones GE, Barrick R, Feng J. Decreasing expander breast infection: a new drain care protocol. Can J Plast Surg. 2009;17:17–21. [PMC free article] [PubMed] [Google Scholar]
  • 11.Patel VP, Walsh M, Sehgal B, Preston C, DeWal H, Di Cesare PE. Factors associated with prolonged wound drainage after primary total hip and knee arthroplasty. J Bone Joint Surg Am. 2007;89:33–38. doi: 10.2106/JBJS.F.00163. [DOI] [PubMed] [Google Scholar]
  • 12.Hanna KR, Tilt A, Holland M, Colen D, Bowen B, Stovall M, et al. Reducing infectious complications in implant-based breast reconstruction: impact of early expansion and prolonged drain use. Ann Plast Surg. 2016;76(Suppl 4):S312–S315. doi: 10.1097/SAP.0000000000000760. [DOI] [PubMed] [Google Scholar]
  • 13.Phillips BT, Fourman MS, Bishawi M, Zegers M, O’Hea BJ, Ganz JC, et al. Are prophylactic postoperative antibiotics necessary for immediate breast reconstruction? Results of a prospective randomized clinical trial. J Am Coll Surg. 2016;222:1116–1124. doi: 10.1016/j.jamcollsurg.2016.02.018. [DOI] [PubMed] [Google Scholar]
  • 14.Wang F, Chin R, Piper M, Esserman L, Sbitany H. Do prolonged prophylactic antibiotics reduce the incidence of surgical-site infections in immediate prosthetic breast reconstruction? Plast Reconstr Surg. 2016;138:1141–1149. doi: 10.1097/PRS.0000000000002737. [DOI] [PubMed] [Google Scholar]
  • 15.Kobayashi K, Imagama S, Ito Z, Ando K, Yagi H, Hida T, et al. Is a drain tip culture required after spinal surgery? Clin Spine Surg. 2017;30:356–359. doi: 10.1097/BSD.0000000000000326. [DOI] [PubMed] [Google Scholar]
  • 16.Takada R, Jinno T, Koga D, Hirao M, Muneta T, Okawa A. Is drain tip culture prognostic of surgical site infection? Results of 1380 drain tip cultures in total hip arthroplasty. J Arthroplasty. 2015;30:1407–1409. doi: 10.1016/j.arth.2015.02.038. [DOI] [PubMed] [Google Scholar]
  • 17.Yoon J, Chung JH, Hwang NH, Lee BI, Park SH, Yoon ES. Bacterial profile of suction drains and the relationship thereof to surgical-site infections in prosthetic breast reconstruction. Arch Plast Surg. 2018;45:542–549. doi: 10.5999/aps.2018.00437. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 18.Meshkin DH, Firriolo JM, Karp NS, Salibian AA. Management of complications following implant-based breast reconstruction: a narrative review. Ann Transl Med. 2023;11:416. doi: 10.21037/atm-23-1384. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 19.Kluytmans J, van Belkum A, Verbrugh H. Nasal carriage of Staphylococcus aureus: epidemiology, underlying mechanisms, and associated risks. Clin Microbiol Rev. 1997;10:505–520. doi: 10.1128/cmr.10.3.505. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 20.Sabaté Brescó M, Harris LG, Thompson K, Stanic B, Morgenstern M, O’Mahony L, et al. Pathogenic mechanisms and host interactions in Staphylococcus epidermidis device-related infection. Front Microbiol. 2017;8:1401. doi: 10.3389/fmicb.2017.01401. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 21.Olsen MA, Nickel KB, Fox IK, Margenthaler JA, Wallace AE, Fraser VJ. Comparison of wound complications after immediate, delayed, and secondary breast reconstruction procedures. JAMA Surg. 2017;152:e172338. doi: 10.1001/jamasurg.2017.2338. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 22.Matar DY, Wu M, Haug V, Orgill DP, Panayi AC. Surgical complications in immediate and delayed breast reconstruction: a systematic review and meta-analysis. J Plast Reconstr Aesthet Surg. 2022;75:4085–4095. doi: 10.1016/j.bjps.2022.08.029. [DOI] [PubMed] [Google Scholar]
  • 23.Long C, Sue GR, Chattopadhyay A, Huis In’t Veld E, Lee GK. Critical evaluation of risk factors of infection following 2-stage implant-based breast reconstruction. Plast Reconstr Surg Glob Open. 2017;5:e1386. doi: 10.1097/GOX.0000000000001386. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 24.Sisco M, Kuchta K, Alva D, Seth AK. Oral antibiotics do not prevent infection or implant loss after immediate prosthetic breast reconstruction. Plast Reconstr Surg. 2023;151:730e–738e. doi: 10.1097/PRS.0000000000010073. [DOI] [PubMed] [Google Scholar]
  • 25.Sergesketter AR, Langdell HC, Shammas RL, Geng Y, Atia AN, Rezak K, et al. Efficacy of prophylactic post-operative antibiotics in tissue expander-based breast reconstruction: a propensity score-matched analysis. Plast Reconstr Surg. 2024;153:496e–504e. doi: 10.1097/PRS.0000000000010825. [DOI] [PubMed] [Google Scholar]
  • 26.Ahn CY, Ko CY, Wagar EA, Wong RS, Shaw WW. Microbial evaluation: 139 implants removed from symptomatic patients. Plast Reconstr Surg. 1996;98:1225–1229. doi: 10.1097/00006534-199612000-00016. [DOI] [PubMed] [Google Scholar]
  • 27.Dobke MK, Svahn JK, Vastine VL, Landon BN, Stein PC, Parsons CL. Characterization of microbial presence at the surface of silicone mammary implants. Ann Plast Surg. 1995;34:563–571. doi: 10.1097/00000637-199506000-00001. [DOI] [PubMed] [Google Scholar]
  • 28.Cohen JB, Carroll C, Tenenbaum MM, Myckatyn TM. Breast implant-associated infections: the role of the National Surgical Quality Improvement Program and the local licrobiome. Plast Reconstr Surg. 2015;136:921–929. doi: 10.1097/PRS.0000000000001682. [DOI] [PubMed] [Google Scholar]
  • 29.Seng P, Bayle S, Alliez A, Romain F, Casanova D, Stein A. The microbial epidemiology of breast implant infections in a regional referral centre for plastic and reconstructive surgery in the south of France. Int J Infect Dis. 2015;35:62–66. doi: 10.1016/j.ijid.2015.04.010. [DOI] [PubMed] [Google Scholar]

Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Supplementary Materials

Supplementary Table 1

Patient and operation-related characteristics in the second cohort

jbc-27-248-s001.xls (28KB, xls)

Articles from Journal of Breast Cancer are provided here courtesy of Korean Breast Cancer Society

RESOURCES