Next Article in Journal
Prospective Study of 4 Gy Radiotherapy for Orbital Mucosa-Associated Lymphoid Tissue Lymphoma (FORMAL)
Previous Article in Journal
Oncogenic and Stemness Signatures of the High-Risk HCMV Strains in Breast Cancer Progression
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Systematic Review

Complications of Immediate versus Delayed DIEP Reconstruction: A Meta-Analysis of Comparative Studies

Department of Plastic, Reconstructive, and Aesthetic Surgery, Geneva University Hospitals, Geneva University, 1205 Geneva, Switzerland
*
Author to whom correspondence should be addressed.
Cancers 2022, 14(17), 4272; https://doi.org/10.3390/cancers14174272
Submission received: 13 July 2022 / Revised: 23 August 2022 / Accepted: 29 August 2022 / Published: 1 September 2022
(This article belongs to the Section Cancer Therapy)

Abstract

:

Simple Summary

Although the deep inferior epigastric perforator flap (DIEP) has become the most frequent autologous flap in breast reconstruction, it remains unclear whether reconstruction should be performed at the same time as the mastectomy or delayed. Therefore, we conducted a meta-analysis to offer an overview of recipient site postoperative complications and help guide practicians toward the ideal timing for breast reconstruction. A pooled analysis using the Mantel and Haenszel methods with a fixed effect model provided results as an odd ratio with a 95% confidence interval. Among most complications including hematoma, infection, fat necrosis, and flap loss, no significant differences were observed. However, delayed wound healing was significantly higher for patients who underwent delayed breast reconstruction. This paper offers evidence that both surgical timings offer similar outcomes and are, therefore, valid surgical strategies.

Abstract

Purpose: The setting regarding the ideal timing for deep inferior epigastric perforator flap (DIEP) reconstruction remains unclear. Immediate breast reconstruction (IBR) is performed at the same time as mastectomy, while delayed breast reconstruction (DBR) is performed at any time after mastectomy except immediately. We compared both strategies to assess whether IBR or DBR should be performed to reduce postoperative adverse events. Methods: A systematic review of PubMed, Embase, Medline, Cochrane, and Web of Science was conducted, aiming at articles comparing the recipient site outcomes of IBR versus DBR with DIEP. We used the Mantel–Haenszel method with a fixed effects model. Results were expressed as the OR with a 95% CI. Results: Two retrospective and two prospective studies were identified involving 5784 DIEPs (1744 immediate and 4040 delayed). We showed a significant difference in favor of IBR for wound healing issues (OR = 0.57, 95% CI 0.41, 0.77; p = 0.0003). However, no significant differences for hematoma, infection, fat necrosis, partial flap loss, and total flap loss rate were seen. Conclusions: Despite variability in the choice of the ideal time for breast reconstruction and outcomes reported among studies, immediate DIEP surgery appears to be a reliable setting with less delayed healing issues.

1. Introduction

First used in 1989 [1] and then popularized in 1994 [2], the deep inferior epigastric perforator flap (DIEP) has become one of the most popular techniques for breast reconstruction [3]. This autologous procedure has many advantages compared to implant-based reconstruction such as no prothesis, no capsular contracture, a natural aesthetic shape, and a higher satisfaction rate [4]. Compared to other autologous flaps such as the transversus rectus abdominis muscle flap (TRAM) or the latissimus dorsi flap (LD), the DIEP carries many qualities including low donor site morbidity (fat necrosis, abdominal wall hernia) and less postoperative pain, at the price of longer operation time and microsurgical skill requirement [5,6,7]. Common postoperative complications such as abdominal bulging, wound dehiscence, seroma, infection, and hematoma have been reported either on the recipient site or on the donor site [8,9,10].
However, little attention has been focused on comparing complications in immediate versus delayed reconstruction. Two breast reconstruction strategies are possible after mastectomy, and the choice of the best setting depends on multiple factors. The first, immediate breast reconstruction (IBR), is performed at the same time as mastectomy, while the second, delayed breast reconstruction (DBR), is performed at any time after mastectomy except immediately (Figure 1). Delayed immediate reconstruction is also one strategy for breast reconstruction. It consists of tissue expander insertion before definitive breast reconstruction, sometimes preferred when adjuvant radiotherapy is necessary [11]. Because this strategy involves in most cases a distant definitive reconstruction, it was classified in the DBR group in the selected articles. IBR is known to have reduced recovery time, less psychological distress, and greater cost-effectiveness compared to DBR [12,13,14]. The last option is preferentially used in settings where adjuvant therapies such as radiation or chemotherapy are indicated, due to their association with potential flap complications (flap shrinkage and inconvenient scar formation) and morbidity rate in IBR [15]. Therefore, in daily practice, plastic surgeons frequently choose DBR for patients requiring adjuvant treatment.
Although breast reconstruction techniques have been widely investigated, there is a lack of evidence regarding how the appropriate timing for surgery affects postoperative adverse events. Therefore, the aim of this meta-analysis was to evaluate the quality and strengths of the current evidence regarding surgical complications on the recipient site between IBR and DBR with DIEP flaps. Both strategies were assessed to know whether IBR or DBR should be used to reduce postoperative adverse events.

2. Materials and Methods

We performed a meta-analysis of comparative studies in accordance with the PRISMA 2020 guidelines for reporting meta-analyses [16]. This meta-analysis was registered on Research Registry, ID: reviewregistry1437.

2.1. Search Strategy

A systematic review was conducted on 3 June 2022 using the following databases: PubMed, Embase, Medline, Cochrane, and Web of Science. Language was restricted to English. The keywords “immediate”, “delayed”, and “DIEP” were used as search strings.

2.2. Article Selection

All articles comparing the postoperative outcomes on the recipient site between immediate and delayed DIEP reconstruction after a mastectomy were selected for a qualitative analysis. No limitations were applied on the age of the patients or their ethnicity. Review articles, case reports, conference abstracts, simulation studies, and clinical studies in nonhuman subjects were not included. Studies involving patients who received other types of autologous reconstruction, implant-based reconstructions, or papers with no postoperative outcome measures were also removed. We decided to exclude studies where the overall population underwent radiotherapy to have a representation as close as possible to reality with the heterogenous group (Table 1).
Two authors (A.S.A. and V.T.) independently identified the relevant studies on the basis of the title and the abstract. Selected articles were then fully read. If they met all selection criteria, data were extracted independently by the two authors. In case of disagreement, it was solved after consultation with the senior author (C.M.O.).

2.3. Data Extraction

The following variables were extracted: the name of the study, the study design, the total number of DIEPs, the number of IBRs, the number of DBRs, and the minor and major complications. Two authors (A.S.A. and V.T.) independently identified these parameters, and disagreements were resolved after discussion with the senior author (C.M.O.).

2.4. Outcome of Interest

The mean interest of our study was to evaluate minor and major complications after IBR and DBR with the DIEP procedure. As minor complications, we selected wound healing issues (healing delayed, dehiscence, and superficial skin necrosis), hematoma, infection, and fat necrosis, while major complications were limited to partial or total flap loss.

2.5. Statistical Analysis

When two or more studies reported outcome data, these were pooled using Review Manager 5.4.1 software (The Cochrane Collaboration, The Nordic Cochrane Center, Copenhagen, Denmark). Odds ratios with 95% CI were used to evaluate dichotomous outcomes (reconstruction complications). Rates of each complication ((1) wound healing issues, (2) hematoma, (3) infection, (4) fat necrosis, and (5) partial or total flap loss) were compared for IBR and DBR.
Before performing the synthesized analysis, heterogeneity between studies was assessed in Review Manager 5.4.1 using the Higgins and Thompson I2 statistics. Levels of heterogeneity were defined as low and high heterogeneity if I2 < 50% and I2 ≥ 50%, respectively. In cases of low heterogeneity, we used the fixed effect Mantel–Haenszel model [17]. In the case of high heterogeneity, we applied the random effect DerSimonian and Laird model [18] assuming that part of the high heterogeneity was independent of fixe variables. Results of meta-analyses are shown as forest plots. Funnel plots were used to check the risk of publication bias. All statistical tests were two-sided, and statistical significance was defined as p < 0.05.

3. Results

3.1. Search Result

A total of 389 studies were identified. After deduplications and review of the title and abstract, 25 articles were selected for full-text review. Of these, two retrospective and two prospective studies met all the selection criteria and were analyzed [8,9,14,19] (Figure 2).
The four studies mentioned above were aimed at comparing several recipient site outcomes following DBR and IBR using the DIEP technique. Prantl et al. and Beugels et al. were both multicentric and national (Germany and the Netherlands) studies while Ochoa et al. and O’Connell et al. were monocentric. The meta-analysis covered a total of 5784 DIEPs, of which 1744 were immediate and 4040 were delayed [8,9,14,19] (Table 2). All studies were recent and covered a similar data collection period after 2009. Some adverse events differed in these studies but were always compared between IBR and DBR. All outcomes were reported if they happened after a follow-up period except for Prantl et al., which collected data on adverse events only if revision surgery was required. However, we considered that it was still relevant to include the latter study because the proportions of complications between both groups remained the same whether they required surgical revision or not. Our hypothesis proved to be relevant since our studies were comparable with an I2 equal or close to 0 for each outcome except for hematoma (Figure 3 and Figure 4). All studies except O’Connell et al. included unilateral and bilateral flap procedures. Population age was homogeneous across papers with adult women around the age of 50.

3.2. Minor Complications

This meta-analysis showed with all articles a significant difference in favor of IBR for wound healing (OR = 0.57, 95% CI 0.41, 0.77; p = 0.0003) but not for hematoma (OR = 1.46, 95% CI 0.45, 4.77; p = 0.53) or infection (OR = 0.81, 95% CI 0.52, 1.25; p = 0.34) [8,9,14,19]. Three studies reported fat necrosis, and no significant difference was found (OR = 0.71, 95% CI 0.47, 1.05; p = 0.09) [8,14,19]. Wound healing issues were defined in all studies as healing disturbances predisposing patients to delayed healing. For this outcome, Beugels et al. included patients with wound dehiscence and superficial skin necrosis. Ochoa et al. classified patients with wound problems if they required dressing changes, debridement, or vacuum-assisted or operative debridement. O’Connell et al. documented women with wound problems if the wound was not fully healed in 30 days or more after surgery. Lastly, Prantl et al. collected data of patients with wound-healing disturbances only if they required revision surgery. Concerning hematoma or infections, no description was made among studies except in Ochoa et al. where infection was classified depending on if patients required oral antibiotics, intravenous antibiotics, or surgical debridement. Three studies documented fat necrosis among other outcomes. Beugels et al. defined this outcome as a palpable firmness detected by physical examination or ultrasound. O’Connell et al. documented fat necrosis when excision surgery was required.

3.3. Major Complications

No significant differences were observed for partial flap loss (OR = 0.77, 95% CI 0.48, 1.24; p = 0.28) and total flap loss (OR = 1.04, 95% CI 0.69, 1.58; p = 0.85). Beugels et al. and Prantl et al. documented these last outcomes as a major complication requiring re-exploration for some patients.

3.4. Further Analysis

A funnel plot was established to assess possible publication bias for every subgroup. The standard error of log (OR) of each study was plotted against its log (OR), and no bias was found (Figure 5).

4. Discussion

The present meta-analysis, based on two retrospective and two prospective studies, reviewed all existing evidence on recipient site postoperative outcomes following IBR versus DBR with DIEP flap. This is the first meta-analysis of postoperative recipient site outcomes to our knowledge. No statistically significant difference was found in terms of hematoma, infection, fat necrosis, and partial or total flap loss. However, wound healing issues (healing delayed, dehiscence, and superficial skin necrosis) showed a significantly higher rate in DBR. Our findings suggest that adverse events do not seem to occur more frequently according to surgical timing except for delayed healing (wound healing issues).
The use of radiotherapy or chemotherapy as adjunctive oncological therapies could possibly explain some adverse events seen among DBR. Some patients with infiltrative breast cancer such as T3 to T4 with or without lymph node involvement are more likely to undergo radiotherapy before performing breast reconstruction [20,21,22]. Most patients requiring radiotherapy were found in the DBR group in relation to traditional guidelines. A few studies showed that DBR was preferable compared to IBR when multimodal treatment was required to reduce complications and increase aesthetic result [15,19,23]. Among other benefits, it has the advantage of replacing tissues damaged from radiation. In a delayed postradiotherapy setting, resection of irradiated skin between the mastectomy scar and the inframammary layer is commonly realized [24]. Even if DBR is preferably chosen in this case, wound healing problems such as wound dehiscence and superficial skin necrosis are still more frequent in DBR compared to IBR and could be due to radiation exposure. A sub-analysis of the association between surgical wound healing and the use of radiation therapy could help identify how the later affected cicatrization. However, radiation therapy was inconsistently reported in selected studies, not allowing this additional analysis. One article showed higher wound healing issues in IBR compared to DBR when patients received PMRT (17.2% vs. 7.6%, p < 0.01) [25]. In addition, surgical site infection might be favored by irradiation, but we only showed a trend in favor of IBR without statistical significance [26,27]. However, recent meta-analyses, one including patients with adjuvant radiotherapy and the other including all type of flaps, demonstrated no optimal evidence in terms of overall complications for immediate versus delayed reconstruction after postmastectomy radiotherapy [25,28].
As opposed to radiotherapy, chemotherapeutic agents such as tamoxifen are rather implicated in flap complications due to thrombotic effects that could potentially lead to flap loss [29,30]. Oncologic drugs could, therefore, affect surgical outcome in breast reconstructions. Even if it was not significant in our analysis, we showed a trend in favor of IBR concerning partial flap loss. This finding supports the fact that chemotherapy, which is more prevalent in DBR, may have an impact on the abovementioned outcome. Interestingly, some papers showed that, when IBR was performed even after neoadjuvant chemotherapy, no morbidity increase was found as opposed to DBR [31,32]. The need for oncologic treatment should, therefore, not be an obstacle to an IBR, as suggested by previous practice.
Mastectomy followed by breast reconstruction presents intraoperative circumstances that could increase hematoma development. Until now, no contributing factor has been clearly attributed to this outcome [33]. However, Seth et al. (2013) reported a preferential location of hematomas originating at the level of the pectoralis muscle and the axillary region. In our study, a trend was found in favor of delayed reconstruction, but it was not significant. This trend could perhaps be explained by the fact that IBR required generally extensive procedure with axillary node dissection during mastectomy, which increased the risk of active bleeding and hematoma formation [8]. Despite no risk factors being clearly associated with this outcome, perioperative measures could be introduced to reduce hematoma incidence. Plastic surgeons could prevent this outcome intraoperatively with intravenous tranexamic acid that has been associated with reduced risk of hematoma without increasing thromboembolic event [34]. Postoperatively, meticulous attention should be paid to the axilla region and surgical drains to monitor a bleed into the chest wall musculature.
The DIEP flap preparation could have a major impact on fat necrosis. A systematic review reported four principal factors increasing this outcome: perforator perfusion zones, perforator location, perforator number, and venous congestion [35]. They concluded that a minimum of two to three perforators of a sufficient caliber should be used, and Holm zones 3 and 4 should be spared to reduce fat necrosis. Computed tomographic angiography has become the current preoperative tool to evaluate vascular variability and quality [36]. Indocyanine green angiography provides intraoperative information to surgeons regarding tissue perfusion and the prevention of flap necrosis [37]. Our results did not show any significance regarding this adverse event but a trend in favor of IBR. A hypothesis could be due to radiotherapy which was more frequent in DBR than IBR, and which could lead to vessel damage and promote necrosis [38]. A study in a rat model demonstrated that ischemic preconditioning of the recipient site with deferoxamine could prevent flap graft necrosis by increasing angiogenesis, capillary neoformation, and vascular growth factor protein expression [39].
One of the most important aspects to discuss with patients is the aesthetic result with both techniques to reduce the psychological impact of the cancer. BREAST-Q is a valid scale that has been used into daily practice to evaluate the quality of life after breast surgery [40]. Unfortunately, selected articles did not report aesthetic satisfaction scores or reported them in a manner impeding meta-analysis of this outcome. Consequently, we could not include this variable in our analysis. Even though this aspect represents a limitation of the study, we found some articles discussing aesthetic outcome. Results showed that IBR is a better strategy in term of aesthetic outcome following 45 months after reconstructions [41]. For many patients, skin/nipple-sparing mastectomy and IBR result in a breast where it is difficult to tell there ever was a mastectomy [42]. However, similar satisfaction rates have previously been reported among patients undergoing IBR or DBR [14,43]. It seems that, in both settings, overall satisfaction with breast reconstruction improved over time since the procedure [44,45]. In situations where the patient will require PMRT, IBR with autologous tissue flaps can have quite problematic long-term outcomes. Therefore, DBR should be considered to not interfere with aesthetic outcomes. Minimizing the emotional impact and the best preservation of the natural aspect of the breast should be essential. In addition to complications, patient satisfaction should be considered in the balance.
Concerning the economic aspect, it is clearly stated that IBR is more cost-effective compared to DBR. An efficient healthcare system is a priority for any university hospital. It is known that cost-effectiveness is a key issue in the choice of medical treatments. A study compared the total cost between IBR and DBR with the DIEP procedure. This research highlighted a significant difference between both strategies with a financial cost of almost 35% less for IBR compared to DBR [12]. Delayed surgery was the costliest mostly due to the additional anesthetic drug, the costs of surgical materials, and the administrative paperwork. Another study showed no difference, but it also did not consider the abovementioned parameters that made the difference in the final cost [46].
The limitations of this meta-analysis are attributed to the small number of included studies. This is mostly explained by this topic only having recently been investigated. However, we believe that the quality of the selected studies offsets the number of papers. Moreover, it allowed comprehensive knowledge and statistical analysis of all available data to provide guidance in breast surgery reconstruction. All studies were published in the same period, and investigated outcomes presented a low heterogeneity (I2 = 0). Selected articles were placed toward the top of the funnel plot, indicating that they were large studies with high power. Moreover, our funnel plot was symmetrical, indicating a low probability of having highly heterogeneous results and differences in methodological quality [47]. We had large patient (n = 4904) and DIEP (n = 5784) samples. Lastly, the proportion of PMRT in the immediate (20%) and delayed (45%) groups was almost the same across studies.
In our articles, oncological outcomes such as tumor recurrence and overall survival (OS) were not reported. A previous study showed an increased risk of recurrence (1.7%) in women receiving delayed DIEP flap reconstruction compared with those who received an immediate reconstruction [48]. Regarding OS, IBR was associated with higher survival compared to DBR [25].

5. Conclusions

This meta-analysis provides new knowledge regarding adverse events depending on the time of procedure. This study revealed a higher prevalence of wound healing issues (healing delayed, dehiscence, and superficial skin necrosis) in delayed breast reconstruction, probably linked to complex care processes where radiation or chemotherapy are more frequent and could interfere in this setting. In times of health system efficiency, immediate breast reconstruction is known to be the best choice among both strategies in terms of total cost. However, plastic surgeons should also be aware of complications that may preferentially appear in one or the other setting. A shared decision-making process with patients should be essential to provide better insight into several complications.

Author Contributions

Conceptualization, A.S.A. and C.M.O.; methodology, A.S.A., V.T. and C.M.O.; validation, D.F.K. and C.M.O.; formal analysis A.S.A.; investigation, A.S.A. and V.T.; data curation, A.S.A. and V.T.; writing—original draft preparation, A.S.A.; writing—review and editing M.S., D.F.K. and C.M.O.; supervision, D.F.K. and C.M.O. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Koshima, I.; Soeda, S. Inferior Epigastric Artery Skin Flaps without Rectus Abdominis Muscle. Br. J. Plast. Surg. 1989, 42, 645–648. [Google Scholar] [CrossRef]
  2. Allen, R.; Treece, P. Deep Inferior Epigastric Perforator Flap for Breast Reconstruction. Ann. Plast. Surg. 1994, 32, 32–38. [Google Scholar] [CrossRef] [PubMed]
  3. Homsy, A.; Rüegg, E.; Montandon, D.; Vlastos, G.; Modarressi, A.; Pittet, B. Breast Reconstruction: A Century of Controversies and Progress. Ann. Plast. Surg. 2018, 80, 1. [Google Scholar] [CrossRef] [PubMed]
  4. Toyserkani, N.; Gustaf Jørgensen, M.; Tabatabaeifar, S.; Damsgaard, T.; Sørensen, J. Autologous versus Implant Based Breast Reconstruction: A Systematic Review and Meta-Analysis of Breast-Q Patient Reported Outcomes. J. Plast. Reconstr. Aesthetic Surg. 2019, 73, 278–285. [Google Scholar] [CrossRef] [PubMed]
  5. Blondeel, N.; Vanderstraeten, G.; Monstrey, S.; Van Landuyt, K.; Tonnard, P.; Lysens, R.; Boeckx, W.; Matton, G. The Donor Site Morbidity of Free DIEP Flaps and Free TRAM Flaps for Breast Reconstruction. Br. J. Plast. Surg. 1997, 50, 322–330. [Google Scholar] [CrossRef]
  6. Egeberg, A.; Rasmussen, M.; Sørensen, J. Comparing the Donor-Site Morbidity Using DIEP, SIEA or MS-TRAM Flaps for Breast Reconstructive Surgery: A Meta-Analysis. J. Plast. Reconstr. Aesthetic Surg. JPRAS 2012, 65, 1474–1480. [Google Scholar] [CrossRef]
  7. Futter, C.; Webster, M.; Hagen, S.; Mitchell, S. A Retrospective Comparison of Abdominal Muscle Strength Following Breast Reconstruction with a Free TRAM or DIEP Flap. Br. J. Plast. Surg. 2000, 53, 578–583. [Google Scholar] [CrossRef]
  8. Beugels, J.; Bod, L.; van Kuijk, S.M.J.; Qiu, S.S.; Tuinder, S.M.H.; Heuts, E.M.; Piatkowski, A.; van der Hulst, R.R.W.J. Complications Following Immediate Compared to Delayed Deep Inferior Epigastric Artery Perforator Flap Breast Reconstructions. Breast Cancer Res. Treat 2018, 169, 349–357. [Google Scholar] [CrossRef]
  9. Prantl, L.; Moellhoff, N.; von Fritschen, U.; Giunta, R.E.; Germann, G.; Kehrer, A.; Lonic, D.; Zeman, F.; Broer, P.N.; Heidekrueger, P.I. Immediate versus Secondary DIEP Flap Breast Reconstruction: A Multicenter Outcome Study. Arch. Gynecol. Obs. 2020, 302, 1451–1459. [Google Scholar] [CrossRef]
  10. Lindenblatt, N.; Gruenherz, L.; Farhadi, J. A Systematic Review of Donor Site Aesthetic and Complications after Deep Inferior Epigastric Perforator Flap Breast Reconstruction. Gland Surg. 2019, 8, 389–398. [Google Scholar] [CrossRef]
  11. Kronowitz, S.; Hunt, K.; Kuerer, H.; Babiera, G.; McNeese, M.; Buchholz, T.; Strom, E.; Robb, G. Delayed-Immediate Breast Reconstruction. Plast. Reconstr. Surg. 2004, 113, 1617–1628. [Google Scholar] [CrossRef] [PubMed]
  12. Neyt, M.J.; Blondeel, P.N.; Morrison, C.M.; Albrecht, J.A. Comparing the Cost of Delayed and Immediate Autologous Breast Reconstruction in Belgium. Br. J. Plast. Surg. 2005, 58, 493–497. [Google Scholar] [CrossRef]
  13. Yang, X.; Zhu, C.; Gu, Y. The Prognosis of Breast Cancer Patients after Mastectomy and Immediate Breast Reconstruction: A Meta-Analysis. PLoS ONE 2015, 10, e0125655. [Google Scholar] [CrossRef]
  14. Ochoa, O.; Garza, R.; Pisano, S.; Chrysopoulo, M.; Ledoux, P.; Arishita, G.; Ketchum, N.; Michalek, J.E.; Nastala, C. Prospective Longitudinal Patient-Reported Satisfaction and Health-Related Quality of Life Following DIEP Flap Breast Reconstruction: Effects of Reconstruction Timing. Plast. Reconstr. Surg. 2022, 149, 848e–857e. [Google Scholar] [CrossRef] [PubMed]
  15. Rogers, N.; Allen, R. Radiation Effects on Breast Reconstruction with the Deep Inferior Epigastric Perforator Flap. Plast. Reconstr. Surg. 2002, 109, 1919–1924, discussion 1925. [Google Scholar] [CrossRef] [PubMed]
  16. Page, M.; Mckenzie, J.; Bossuyt, P.; Boutron, I.; Hoffmann, T.; Mulrow, C.; Shamseer, L.; Tetzlaff, J.; Akl, E.; Brennan, S.; et al. The PRISMA 2020 Statement: An Updated Guideline for Reporting Systematic Reviews. Syst. Rev. 2020, 10, 89. [Google Scholar] [CrossRef]
  17. Mantel, N.; Haenszel, W. Statistical Aspects of the Analysis of Data From Retrospective Studies of Disease. J. Natl. Cancer Inst. 1959, 22, 719–748. [Google Scholar]
  18. Dersimonian, R.; Laird, N. Meta-Analysis in Clinical Trials. Control. Clin. Trials 1986, 7, 177–188. [Google Scholar] [CrossRef]
  19. O’Connell, R.L.; Di Micco, R.; Khabra, K.; Kirby, A.M.; Harris, P.A.; James, S.E.; Power, K.; Ramsey, K.W.D.; Rusby, J.E. Comparison of Immediate versus Delayed DIEP Flap Reconstruction in Women Who Require Postmastectomy Radiotherapy. Plast. Reconstr. Surg. 2018, 142, 594–605. [Google Scholar] [CrossRef]
  20. Recht, A.; Edge, S. Evidence-Based Indications of Postmastectomy Irradiation. Surg. Clin. North Am. 2003, 83, 995–1013. [Google Scholar] [CrossRef]
  21. Ragaz, J.; Olivotto, I.; Spinelli, J.; Phillips, N.; Jackson, S.; Wilson, K.; Knowling, M.; Coppin, C.; Weir, L.; Gelmon, K.; et al. Locoregional Radiation Therapy in Patients With High-Risk Breast Cancer Receiving Adjuvant Chemotherapy: 20-Year Results of the British Columbia Randomized Trial. J. Natl. Cancer Inst. 2005, 97, 116–126. [Google Scholar] [CrossRef] [PubMed]
  22. Dragun, A.; Huang, B.; Gupta, S.; Crew, J.; Tucker, T. One Decade Later: Trends and Disparities in the Application of Post-Mastectomy Radiotherapy (PMRT) since the Release of the American Society of Clinical Oncology (ASCO) Clinical Practice Guidelines. Int. J. Radiat. Oncol. Biol. Phys. 2012, 83, e591–e596. [Google Scholar] [CrossRef] [PubMed]
  23. Clemens, M.W.; Kronowitz, S.J. Current Perspectives on Radiation Therapy in Autologous and Prosthetic Breast Reconstruction. Gland Surg. 2015, 4, 222–231. [Google Scholar] [CrossRef] [PubMed]
  24. Greenall, M. Is There Any Argument for Delayed Breast Reconstruction after Total Mastectomy? Ann. R. Coll. Surg. Engl. 2007, 89, 754–756. [Google Scholar] [CrossRef] [PubMed]
  25. Heiman, A.J.; Gabbireddy, S.R.; Kotamarti, V.S.; Ricci, J.A. A Meta-Analysis of Autologous Microsurgical Breast Reconstruction and Timing of Adjuvant Radiation Therapy. J. Reconstr. Microsurg. 2021, 37, 336–345. [Google Scholar] [CrossRef] [PubMed]
  26. Fracol, M.; Basta, M.; Nelson, J.; Fischer, J.; Wu, L.; Serletti, J.; Fosnot, J. Bilateral Free Flap Breast Reconstruction After Unilateral Radiation: Comparing Intraoperative Vascular Complications and Postoperative Outcomes in Radiated Versus Nonradiated Breasts. Ann. Plast. Surg. 2015, 76, 311–314. [Google Scholar] [CrossRef]
  27. Araujo, T.; Xu, M.; Susarla, S.M.; Shmelev, K.; Jiang, W.; Pribaz, J.; Hergrueter, C.; Carty, M.; Caterson, S.; Chun, Y. Impact of Prior Unilateral Chest Wall Radiotherapy on Outcomes in Bilateral Breast Reconstruction. Plast. Reconstr. Surg. 2016, 138, 575e–580e. [Google Scholar] [CrossRef]
  28. Khajuria, A.; Charles, W.N.; Prokopenko, M.; Beswick, A.; Pusic, A.L.; Mosahebi, A.; Dodwell, D.J.; Winters, Z.E. Immediate and Delayed Autologous Abdominal Microvascular Flap Breast Reconstruction in Patients Receiving Adjuvant, Neoadjuvant or No Radiotherapy: A Meta-analysis of Clinical and Quality-of-life Outcomes. BJS Open 2020, 4, 182–196. [Google Scholar] [CrossRef]
  29. Kelley, B.P.; Valero, V.; Yi, M.; Kronowitz, S.J. Tamoxifen Increases the Risk of Microvascular Flap Complications in Patients Undergoing Microvascular Breast Reconstruction. Plast. Reconstr. Surg. 2012, 129, 305–314. [Google Scholar] [CrossRef]
  30. Beecher, S.M.; Woods, J.F.C. Tamoxifen Use in Microvascular Breast Reconstruction & Its Effect on Microvascular Complications: A Systematic Review & Meta-Analysis. Ann. Breast Surg. 2021, 5, 14. [Google Scholar] [CrossRef]
  31. Monrigal, E.; Dauplat, J.; Gimbergues, P.; Bouedec, G.; Peyronie, M.; Achard, J.-L.; Chollet, P.; Mouret-Reynier, M.A.; Nabholtz, J.-M.; Pomel, C. Mastectomy with Immediate Breast Reconstruction after Neoadjuvant Chemotherapy and Radiation Therapy. A New Option for Patients with Operable Invasive Breast Cancer. Results of a 20 Years Single Institution Study. Eur. J. Surg. Oncol. 2011, 37, 864–870. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  32. Song, J.; Zhang, X.; Liu, Q.; Peng, J.; Liang, X.; Shen, Y.; Liu, H.; Li, H. Impact of Neoadjuvant Chemotherapy on Immediate Breast Reconstruction: A Meta-Analysis. PLoS ONE 2014, 9, e98225. [Google Scholar] [CrossRef] [PubMed]
  33. Seth, A.K.; Hirsch, E.M.; Kim, J.Y.S.; Dumanian, G.A.; Mustoe, T.A.; Galiano, R.D.; Fine, N.A. Hematoma After Mastectomy With Immediate Reconstruction An Analysis of Risk Factors in 883 Patients. Ann. Plast. Surg. 2013, 71, 20–23. [Google Scholar] [CrossRef] [PubMed]
  34. Weissler, J.M.; Banuelos, J.; Jacobson, S.R.; Manrique, O.J.; Nguyen, M.-D.T.; Harless, C.A.; Tran, N.V.; Martinez-Jorge, J. Intravenous Tranexamic Acid in Implant-Based Breast Reconstruction Safely Reduces Hematoma without Thromboembolic Events. Plast. Reconstr. Surg. 2020, 146, 238–245. [Google Scholar] [CrossRef]
  35. Bhullar, H.; Hunter-Smith, D.J.; Rozen, W.M. Fat Necrosis After DIEP Flap Breast Reconstruction: A Review of Perfusion-Related Causes. Aesth. Plast. Surg. 2020, 44, 1454–1461. [Google Scholar] [CrossRef]
  36. Chae, M.P.; Hunter-Smith, D.J.; Rozen, W.M. Comparative Analysis of Fluorescent Angiography, Computed Tomographic Angiography and Magnetic Resonance Angiography for Planning Autologous Breast Reconstruction. Gland Surg. 2015, 4, 15. [Google Scholar]
  37. Lauritzen, E.; Bredgaard, R.; Bonde, C.; Jensen, L.T.; Damsgaard, T.E. Indocyanine Green Angiography in Breast Reconstruction: A Narrative Review. Ann. Breast Surg. 2022, 6, 6. [Google Scholar] [CrossRef]
  38. He, S.; Yin, J.; Robb, G.; Sun, J.; Zhang, X.; Li, H.; Liu, J.; Han, C. Considering the Optimal Timing of Breast Reconstruction With Abdominal Flaps With Adjuvant Irradiation in 370 Consecutive Pedicled Transverse Rectus Abdominis Myocutaneous Flap and Free Deep Inferior Epigastric Perforator Flap Performed in a Chinese Oncology Center: Is There a Significant Difference Between Immediate and Delayed? Ann. Plast. Surg. 2016, 78, 1. [Google Scholar] [CrossRef]
  39. Kim, J.; Park, M.; Jeong, W.; Lee, H.; Lee, G.; Lee, K.; Park, S.; Choi, J. Recipient-Site Preconditioning with Deferoxamine Increases Fat Graft Survival by Inducing VEGF and Neovascularization in a Rat Model. Plast. Reconstr. Surg. 2019, 144, 619e–629e. [Google Scholar] [CrossRef]
  40. Cano, S.; Pusic, A.L.; Klassen, A. The BREAST-Q: A New Patient-Reported Outcome Measure for Breast Surgery [abstract 1742]. 2009 International Society for Quality of Life meeting abstracts. QLR J. 2009, A-37. [Google Scholar] [CrossRef]
  41. Ménez, T.; Michot, A.; Tamburino, S.; Weigert, R.; Pinsolle, V. Multicenter Evaluation of Quality of Life and Patient Satisfaction after Breast Reconstruction, a Long-Term Retrospective Study. Ann. De Chir. Plast. Esthétique 2018, 63, 126–133. [Google Scholar] [CrossRef] [PubMed]
  42. Ho, A.Y.; Hu, Z.I.; Mehrara, B.J.; Wilkins, E.G. Radiotherapy in the Setting of Breast Reconstruction: Types, Techniques, and Timing. Lancet Oncol. 2017, 18, e742–e753. [Google Scholar] [CrossRef]
  43. Beugels, J.; Kool, M.; Hoekstra, L.; Heuts, E.; Tuinder, S.; van der Hulst, R.; Piatkowski, A. Quality of Life of Patients After Immediate or Delayed Autologous Breast Reconstruction: A Multicenter Study. Ann. Plast. Surg. 2018, 81, 523–527. [Google Scholar] [CrossRef]
  44. Fontein, D.B.Y.; Oros, M.; Held, L.; Giovanoli, P.; Pusic, A.L.; Lindenblatt, N. Patient-Reported Outcomes in Free-Flap Breast Reconstructive Surgery over Time (PRO-BREST). Breast Care 2022, 17, 272–278. [Google Scholar] [CrossRef] [PubMed]
  45. Billig, J.; Jagsi, R.; Qi, J.; Hamill, J.B.; Kim, H.M.; Pusic, A.L.; Buchel, E.; Wilkins, E.G.; Momoh, A.O. Should Immediate Autologous Breast Reconstruction Be Considered in Women Who Require Postmastectomy Radiation Therapy? A Prospective Analysis of Outcomes. Plast. Reconstr. Surg. 2017, 139, 1279–1288. [Google Scholar] [CrossRef]
  46. Cheng, M.-H.; Lin, J.-Y.; Ulusal, B.G.; Wei, F.-C. Comparisons of Resource Costs and Success Rates between Immediate and Delayed Breast Reconstruction Using DIEP or SIEA Flaps under a Well-Controlled Clinical Trial. Plast. Reconstr. Surg. 2006, 117, 2139–2142. [Google Scholar] [CrossRef]
  47. Sterne, J.A.C.; Sutton, A.J.; Ioannidis, J.P.A.; Terrin, N.; Jones, D.R.; Lau, J.; Carpenter, J.; Rucker, G.; Harbord, R.M.; Schmid, C.H.; et al. Recommendations for Examining and Interpreting Funnel Plot Asymmetry in Meta-Analyses of Randomised Controlled Trials. BMJ 2011, 343, d4002. [Google Scholar] [CrossRef]
  48. Joosen, M.E.M.; Schop, S.J.; Reinhoudt, L.L.; van Kuijk, S.M.J.; Beugels, J.; de Bruïne, A.P.; Goudkade, D.; Heuts, E.M.; van der Hulst, R.R.W.J.; de Grzymala, A.A.P. The Difference in Local, Regional and Distant Breast Cancer Recurrence between the Immediate and Delayed DIEP Flap Procedure; a Retrospective Cohort Study. Breast Cancer Res. Treat 2021, 188, 389–398. [Google Scholar] [CrossRef]
Figure 1. Time options for breast reconstruction. RT = radiotherapy; DIEP = deep inferior epigastric perforator flap.
Figure 1. Time options for breast reconstruction. RT = radiotherapy; DIEP = deep inferior epigastric perforator flap.
Cancers 14 04272 g001
Figure 2. Flow diagram of search for eligible studies.
Figure 2. Flow diagram of search for eligible studies.
Cancers 14 04272 g002
Figure 3. Combined ORs to assess effect of immediate versus delayed DIEP on adverse events for minor complication: (1.1) wound healing, (2.1) hematoma, (3.1) infections, and (4.1) fat necrosis [8,9,14,19]. Blue shapes correspond to individual studies. Squares size is proportional to the weight of the study while black diamonds shapes correspond to pooled studies.
Figure 3. Combined ORs to assess effect of immediate versus delayed DIEP on adverse events for minor complication: (1.1) wound healing, (2.1) hematoma, (3.1) infections, and (4.1) fat necrosis [8,9,14,19]. Blue shapes correspond to individual studies. Squares size is proportional to the weight of the study while black diamonds shapes correspond to pooled studies.
Cancers 14 04272 g003
Figure 4. Combined ORs to assess effect of immediate versus delayed DIEP on adverse events for major complications: (5.1) total flop loss, and (5.2) partial flap loss [8,9]. Blue shapes correspond to individual studies. Squares size is proportional to the weight of the study while black diamonds shapes correspond to pooled studies.
Figure 4. Combined ORs to assess effect of immediate versus delayed DIEP on adverse events for major complications: (5.1) total flop loss, and (5.2) partial flap loss [8,9]. Blue shapes correspond to individual studies. Squares size is proportional to the weight of the study while black diamonds shapes correspond to pooled studies.
Cancers 14 04272 g004
Figure 5. Funnel plot of comparison of adverse events for wound.
Figure 5. Funnel plot of comparison of adverse events for wound.
Cancers 14 04272 g005
Table 1. PICOS table features.
Table 1. PICOS table features.
PICOSInclusionExclusion
PopulationAdults who underwent breast reconstruction after mastectomyStudy where the overall population received radiotherapy
InterventionAutologous breast reconstruction with DIEP flapOther types of autologous reconstruction, implant-based reconstructions
ComparatorReconstruction timing (immediate versus delayed)
OutcomesRecipient site complicationsStudies that did not report recipient site complications
Study designComparative studiesReview articles, meta-analysis, case reports, conference abstracts, simulation studies, clinical studies in nonhuman subjects, and unpublished studies
Table 2. Characteristics of the included studies.
Table 2. Characteristics of the included studies.
AuthorYearStudy
Period
N° PatientsMean (SD) Age
IBR
Mean
(SD) Age
DBR
Total
of DIEP
Immediate
(IBR)
Delayed
(DBR)
PMRT before IBRPMRT before DBRFollow-Up
Beugels [8]20182010–201773750.7(9.4)51.0(8.6)91039751321.7%44.4%9–10 m
O’Connell [19]20182009–2014167§§1671085925.9%100.0%§
Prantl [9]20202011–2019392749.9(11.5)51.8(35.8)45771136344118.5%41.6%3 m
Ochoa [14]20222012–201673**1301032728.1%50.0%282–303 d
IBR = immediate breast reconstruction, DBR = delayed breast reconstruction, PMRT = post-mastectomy radiotherapy; * median age 52 (22–73) for IBR and 47.5 (41–61) for DBR; § data not reported for all IBR and DBR; m = months, d = days
Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Share and Cite

MDPI and ACS Style

Alves, A.S.; Tan, V.; Scampa, M.; Kalbermatten, D.F.; Oranges, C.M. Complications of Immediate versus Delayed DIEP Reconstruction: A Meta-Analysis of Comparative Studies. Cancers 2022, 14, 4272. https://doi.org/10.3390/cancers14174272

AMA Style

Alves AS, Tan V, Scampa M, Kalbermatten DF, Oranges CM. Complications of Immediate versus Delayed DIEP Reconstruction: A Meta-Analysis of Comparative Studies. Cancers. 2022; 14(17):4272. https://doi.org/10.3390/cancers14174272

Chicago/Turabian Style

Alves, André S., Vincent Tan, Matteo Scampa, Daniel F. Kalbermatten, and Carlo M. Oranges. 2022. "Complications of Immediate versus Delayed DIEP Reconstruction: A Meta-Analysis of Comparative Studies" Cancers 14, no. 17: 4272. https://doi.org/10.3390/cancers14174272

APA Style

Alves, A. S., Tan, V., Scampa, M., Kalbermatten, D. F., & Oranges, C. M. (2022). Complications of Immediate versus Delayed DIEP Reconstruction: A Meta-Analysis of Comparative Studies. Cancers, 14(17), 4272. https://doi.org/10.3390/cancers14174272

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop