Abstract
Background:
The deep inferior epigastric perforator (DIEP) procedure is regarded a safe option for autologous breast reconstruction. Reoperations, however, may occur, and there is no consensus in the literature regarding the risk factors. The aim of this study was to identify factors associated with reoperations in DIEP procedure.
Patients and Methods:
A retrospective study of consecutive patients undergoing DIEP breast reconstruction 2007 to 2014 was performed and included a review of 433 medical charts. Surgical outcome was defined as any unanticipated reoperation requiring return to the operating room. Multivariate regression analysis was utilized to identify predictors of reoperation. The following factors were considered: age, body mass index, comorbidity, childbearing history, previous abdominal surgery, adjuvant therapy, reconstruction laterality and timing, flap and perforator characteristics, and number and size of veins.
Results:
In total, 503 free flaps were performed in 433 patients, 363 (83.8%) unilateral and 70 (16.2%) bilateral procedures. Mean age was 51 years; 15.0% were obese; 13.4% had hypertension; 2.3% had diabetes; 42.6% received tamoxifen; 58.8% had preoperative radiotherapy; 45.6% had abdominal scars. Reoperation rate was 15.9% (80/503) and included flap failure, 2.0%; partial flap loss, 1.2%; arterial thrombosis, 2.0%; venous thrombosis, 0.8%; venous congestion, 1.2%; vein kinking, 0.6%. Other complications included bleeding, 2.2%; hematoma, 3.0%; fat necrosis, 2.8%, and infection, 0.2%. Factors negatively associated with reoperation were childbearing history (odds ratio [OR]: 3.18, P = 0.001) and dual venous drainage (OR: 1.91, P = 0.016); however, only childbearing remained significant in the multivariate analyses (OR: 4.56, P = 0.023).
Conclusions:
The history of childbearing was found to be protective against reoperation. Number of venous anastomoses may also affect reoperation incidence, and dual venous drainage could be beneficial in nulliparous patients.
The deep inferior epigastric perforator (DIEP) flap is a workhorse for autologous breast reconstruction worldwide. The DIEP procedure is regarded a safe option with high success rate and satisfactory outcomes; however, the learning curve is steep, and complications and reoperations may occur. Perioperative factors associated with complications after abdomen-based microsurgical procedures have been addressed in numerous studies, but the conclusions vary among the institutions and series. Apart from the generally accepted risk factors such as smoking, diabetes, and obesity, some studies also identified associations between flap complications and flap characteristics (eg, perforator selection and number, number of veins and their size) or adjuvant treatment (eg, radiotherapy).1–10 Despite missing consensus and insufficient evidence on the predictors of complications, data on potential risk factors are helpful for patient selection and preoperative planning.
Optimizing the results and standardizing the procedure by reducing risks are essential as the request for autologous reconstruction is increasing.11 Overall, the majority of articles addressing surgical outcomes in larger series of abdomen-based breast reconstructions show low incidence of total flap failures and partial flap necrosis (0%–3% and 0%–11%, respectively).2,5,9,12–14 Complications such as venous congestions and/or fat necrosis are seen to a higher extent, and the reasons for these events are often difficult to explain, being partly related to the flap vascularity and perfusion.5,15,16 The substantial impact of the revision procedures on patients’ well-being and also healthcare burden call for further research to minimize the need of these reoperations.
The aim of this study was to critically evaluate perioperative predictors of complications and reoperations in DIEP breast reconstruction.
PATIENTS AND METHODS
A retrospective analysis of a consecutive series of patients undergoing DIEP breast reconstruction at Uppsala University Hospital between October 2007 and December 2014 was performed. Patients were identified through the local operation registry where all surgical procedures performed at the Department of Plastic and Maxillofacial Surgery are registered prospectively. All relevant data were retrieved into a study-specific database manually by 2 independent doctors from the hospital-based medical chart system where all preoperative, operative, and postoperative notes are maintained. In total, 436 medical charts were evaluated and the following demographic and preoperative information was collected: date of birth, body mass index (BMI), active smoking, medical comorbidities (hypertension, diabetes, obesity, and others), childbearing, previous abdominal surgery, preoperative radiotherapy, chemotherapy, and tamoxifen treatment.
The operative and reconstructive characteristics included date of the procedure, timing of reconstruction (immediate vs delayed), side of reconstruction, flap (perforator) side, perforator(s) number and row, number of veins, venous drainage, coupler size, flap weight, ischemic time, length of surgery, and number of operating microsurgeons. The postoperative and follow-up data comprised surgical and systemic complications, date and type of reoperation(s), perioperative medications, and date of discharge.
Complication was defined as any unanticipated event requiring return to the operating room and general anesthesia. Anticipated reoperations due to asymmetry (eg, scar correction, lipofilling, liposuction) and also nipple–areola reconstructions were excluded from the analyses. All complications were further divided into flap circulation–related and others (eg, hematoma, bleeding). Fat necroses were considered clinically significant and registered in the study if they were treated with reoperation. Reoperations due to fat necrosis and other aesthetic adjustments were offered to all patients who would opt for the corrections.
All systemic complications were registered and described separately.
The study was approved by the Regional Research Ethics Committee in Uppsala (2014/354).
Surgical Procedure
All patients scheduled for the DIEP breast reconstruction routinely undergo computed tomography (CT) angiography to identify and assess deep inferior epigastric artery perforator vessels. CT scans are further reviewed by the members of the microsurgical team. Candidates for autologous reconstruction should strictly comply with perioperative smoking cessation (6 wk before and after the surgery) according to the routines of the department.
The harvest of the DIEP flap begins with the identification and preservation of the superficial inferior epigastric veins (SIEVs). The internal mammary vessels are the first-choice recipient vessels at our institution. The use of the SIEV as an extra vein is at the discretion of the operating surgeon. An implantable Cook-Swartz probe was used in most cases to monitor the flap postoperatively.10 Flap monitoring is performed according to the local guidelines including clinical evaluation, invasive Doppler and hand-held Doppler.10 A single dose of antibiotics (cloxacillin 2 g, intravenously) is given perioperatively. Anticoagulation therapy includes a prophylactic dose of dalteparin 2500 IU subcutaneously the night before surgery and 5000 IU/d 10 days after surgery. In addition, 75 mg/d acetylsalicylic acid orally is prescribed 30 days postoperatively.
Routinely, the patient is seen back 1 week, 6 weeks, and 3 months postoperatively at the department (first 2 visits are to a specialist nurse). All patients are offered nipple–areola reconstruction and/or symmetrizing surgery of the contralateral breast as an outpatient procedure at a later stage.
Statistical Analyses
All available data were collected into a study-specific database that was designed before variables collection and further transferred to STATA 13.1 for Mac OS (StataCorp; College Station, Tex.) for statistical analyses.
Reoperation was chosen as an appropriate outcome variable because of its statistical robustness and major clinical relevance compared with other surgical outcome endpoints as, for example, complication or readmission to the hospital.
All reoperations were registered and analyzed per flap. For the purpose of data analyses, all bilateral reconstructions were considered as 2 separate flaps. In cases with more than 1 reoperation (repeated events), only 1 reoperation was included in the regression model to avoid statistical dependence. Pearson’s chi-square or Student’s t test, when appropriate, was utilized for the assessment of possible differences in cases with and without reoperation.
Univariate and multivariate logistic regression models were performed to test the association of reoperation after DIEP flap procedures and potential confounders. In the univariate models, reoperation (yes vs no) was analyzed in relation to the following patient characteristics: age at procedure, BMI: <25 versus ≥25 kg/m2; hypertension: no versus yes; diabetes: no versus yes; smoking: no versus yes; laterality: unilateral versus bilateral; childbearing history: yes versus no; abdominal scars: no versus yes and treatment variables [calendar year: 2011–2014 vs 2007–2010; preoperative radiotherapy: no vs yes; preoperative chemotherapy: no vs yes; tamoxifen: no vs yes; operating microsurgeons: team vs one; number of perforators; flap weight; number of veins: one vs >one; vein (coupler) size: <median vs ≥median].
For the purpose of the analyses, the following variables were dichotomized at the mean after they were tested as continuous variables with no marked differences: age, flap weight, flap ischemia time, operative time, and length of surgery. Coupler size and length of stay were dichotomized at the median.
The associations between reoperation and potential categorical risk factors were presented as odds ratios (OR) with 95% CI and P value. Reported P values from these models refer to the Wald test. A 2-tailed P < 0.05 was considered significant in all statistical tests.
RESULTS
In total, 436 patients underwent breast reconstruction with a free flap procedure during the study period and were considered eligible. Two patients with the superior gluteal artery perforator flap technique were excluded, and also 1 woman with a complex bipedicled DIEP chest wall reconstruction for breast sarcoma. Thus, 433 patients were included in the study as undergoing either unilateral (n = 363, 83.8%) or bilateral (n = 70, 16.2%) procedure, accounting for 503 flaps in total. The mean follow-up was 5.2 years (range: 1.1–8.3).
Patients’ mean age was 51 years (range: 27–72) and BMI = 26.2 kg/m2 (range: 19.5–40.0). The distribution of comorbidities in the whole group (n = 433) was obesity (n = 65, 15%), hypertension (n = 58, 13.4%), and diabetes (n = 10, 2.3%). Three patients (0.7%) were smokers, 184 (42.6%) received tamoxifen, 254 (58.8%) had preoperative radiotherapy, and 197 (45.6%) had abdominal scars.
The other relevant demographic and clinical characteristics are presented per flap in Table 1 and stratified for 2 groups: flaps with no reoperation (n = 423) and with reoperation (n = 80). There were no significant differences in patient characteristics between the 2 groups, except for history of childbearing where the reoperation group was nulliparous more often (25.4% vs 10.7%, P = 0.002).
Table 1.
Demographic and Patient Characteristics Stratified for Reoperation

Of the total of 503 flaps, 484 (96.2%) were DIEPs and 19 (3.8%) were superficial inferior epigastric artery (SIEA) flaps, with more frequent use of the SIEA flap in the reoperation group (Table 2). The majority of reconstructions were delayed (n = 401, 79.9%). Mean operative time was 302.4 minutes (range: 132–558) with mean flap ischemic time of 56 minutes (range: 14–124). Mean flap weight was 622 g (range: 150–1700), and more than one vein was used in 218 (43.4%) flaps as shown in Table 2.
Table 2.
Flaps and Technical Characteristics of the Procedure Stratified for Reoperation

Median length of stay after the procedure was 7 days (range: 3–18). Systemic complications included 2 cases of pulmonary embolism and 1 case of deep venous thrombosis. All were diagnosed and treated during the early postoperative period.
Data on complications and reoperations are presented in Table 3. Among the 80/503 flaps with reoperation, 10 (2.0%) total flap failures were observed. In 6 cases, a latissimus dorsi reconstruction was performed at the time of flap removal; 2 other cases were managed with delayed expander-implant reconstructions. Two remaining patients refused any secondary reconstruction.
Table 3.
Complications Requiring Reoperation and Number of Reoperations per Flap

In the univariate analyses of the DIEP flaps (n = 484), factors negatively associated with reoperation were childbearing history (OR: 3.18, 95% CI: 1.62–6.26, P = 0.001) and dual venous drainage (OR: 1.91, 95% CI: 1.12–3.25, P = 0.016), Table 4. Only childbearing remained a negative predictor of reoperation in the multivariate analyses (OR: 4.56, 95% CI: 1.23–16.9, P = 0.023).
Table 4.
Univariate and Multivariate Regression Analyses for Reoperation in DIEP Flaps (n = 484)*

From the available data on childbirth (n = 298), 216 (72.5%) had vaginal delivery and 82 (27.5%) had a cesarian section, and no statistically significant difference in flap reoperation was revealed between the groups (13.9% vs 15.9%, P = 0.666, respectively).
The presence of the Pfannenstiel incision (n = 93) did not correlate with the reoperation incidence, flap weight, vein size, or operational time (all P > 0.05, data not shown).
In the nulliparous subgroup (n = 51), there was a trend toward lower probability of reoperation in DIEP flaps with more than 1 vein (31.3% vs 68.8%, P = 0.946), although the difference did not reach statistical significance.
No association between the incidence of fat necrosis and flap weight, number of veins, vein size, or abdominal scars was found in the subset analyses of the flaps with fat necrosis (data not shown).
DISCUSSION
The findings of this study suggest previous childbearing to be a protective factor against reoperations in patients undergoing DIEP flap procedures.
The implications of childbearing for patients opting for abdominal flap procedures have been sparsely discussed in the literature. A study by Santanelli et al7 was the first to include data on previous childbearing in their review of the DIEP flaps. The authors found an association between nulliparity and perfusion-related flap complications, explaining their findings by a potentially favorable superficial abdominal perfusion in pluriparous women. This assumption is also in line with the published articles that show that venous drainage of the lower abdominal wall mainly relies on the superficial venous system17,18 and that the venous territory of the SIEV is different from that of deep inferior epigastric vein.19,20
To the best of our knowledge, there are no studies specifically addressing changes in the abdominal wall associated with pregnancy. In the light of our findings, we consider that previous childbearing leads to complex anatomic and physiologic changes in the abdominal wall and its hemodynamics, which could be beneficial in abdomen-based free flap procedures. Apart from the known expansion-related changes in tissues,21–23 pregnancy might lead to certain rearrangements in arterial and venous hemodynamics.
The growing abdominal pressure may increase perfusion via perforators, extending the axiality of the blood flow and creating connections between the adjacent perforators by activation of the linking vessels.24 According to the study by Saint-Cyr et al, perforators give off vertical and oblique branches to the subdermal plexus, and recurrent flow to adjacent perforasomes is possible through the oblique branches. Theoretically, this pathway of blood flow could be activated at later stages of pregnancy leading to potential perfusion changes in the superficial system compared with a nonpregnant abdomen.
Veins of the abdominal wall, being capacitance vessels, represent one of the largest reservoirs of blood in the human body. During the pregnancy, blood volume expansion may rise up to 50% in the third trimester, leading to an increased cardiac output, venous pressure, and vasodilation.25,26
The influence of estrogens and progesterone on the superficial venous system is also well documented in the literature and confirmed in the studies on the veins of the lower extremities.27,28 Interestingly, an imaging study on pregnancy-induced changes in the superficial veins of the lower limbs showed that the veins do not seem to return to their initial diameter after the pregnancy.27
In some cases, later gestational changes in the circulation may be caused by the growing uterus resulting in the compression of the inferior vena cava, the iliac veins, and the inferior epigastric veins. In this scenario, the development of the collateral circulation in the deep and superficial systems of the epigastric veins may take place. The importance of collateral venous pathways of the abdominal wall was demonstrated in a comprehensive anatomic CT angiography review of compressions of the inferior vena cava caused by pathologic conditions.29 An involvement of the superficial tributaries of the paraumbilical veins may also play a role thus potentially improving the vascularity in certain parts of the future flaps.17,18
Finally, an increase of the BMI and the amount of abdominal fat during childbearing may also lead to vasculature rearrangements. Studies on patients after massive weight loss confirmed that the superficial veins in obese population were significantly larger than in the control group.30 Our study could not reveal any differences in the SIEV size between the groups stratified for childbearing or for BMI (data not shown). Yet, measurements of the vein diameter were indirect and relied upon the venous coupler dimensions.
The selection of perforators required to adequately perfuse the DIEP flap is judgmental and the decision is taken intraoperatively along with the decision to augment the venous drainage.
The beneficial role of a second vein anastomosis to improve venous drainage and reduce the incidence of venous congestion was first demonstrated by Enajat et al.12 A recent systematic review on the perfusion-related complications in DIEP flaps supercharged with SIEV confirmed a significant decrease in postoperative flap congestion in the superdrainage group. There was also a trend toward decreasing of the incidence of partial flap loss and fat necrosis, but the difference was not statistically significant.31 In our study, the SIEV was used in almost half of the DIEP flaps, and the dual venous drainage was associated with lesser probability of reoperation. In fact, when analyzing the subset of nulliparous women, there was a clear trend toward lower probability of reoperation in the subgroup of DIEPs with more than 1 vein—31.3% versus 68.8%, although the difference did not reach statistical significance. This finding could have an important clinical implication, suggesting the advantage of dual venous drainage in nulliparous patients and should be addressed in a larger series.
The results of our reoperation analyses also indicated that the presence of the additional routes of venous drainage could be more critical than the single vein caliber, which is also supported by other studies.12,32
SIEA flap was anecdotally used at our institution (19 of 503 flaps, 3.8%) and has predominantly been performed by one of the experienced microsurgeons in selected bilateral reconstructions. Higher complication rates in this subgroup however are in line with other publications from the centers where SIEA flaps are not performed regularly33–35 and may be attributed to vessel caliber and flap thrombosis.
The role of scars and previous incisions in the lower abdomen for the future abdomen-based microsurgical breast reconstruction was addressed in several articles.2,4,36,37 Patients with prior abdominal and/or gynecological surgery do not seem to have an increased risk for the DIEP flap–related complications. These studies, however, have a retrospective design and are not specific to scar location in relation to flap perfusion zones or other CT angiography landmarks. A recent anatomic CT imaging study38 showed that the presence of the Pfannenstiel scar was associated with the larger deep inferior epigastric artery perforator size (0.96 vs 0.85 mm). Clinical implication of this subtle difference seems uncertain. In fact, the analysis would benefit from an adjustment for childbearing, which could shed light on if it is the pregnancy per se or the cesarian section that is associated with larger perforator size.
The strengths of this study include its detailed data collection, robust statistical analysis, and sample size, where all consecutive patients operated at the same institution were included in the study with no patients lost to follow-up. The same local guidelines were used in all abdomen-based microsurgical breast reconstructions over the study period of 7 years. Furthermore, we were able to analyze the role of the traditional childbearing and also the scar after cesarian section on the surgical outcomes of DIEP breast reconstruction.
The limitation of the study may lie in its retrospective nature, where some of the data in the medical charts were not available. Thus, we could not incorporate the data on multiple pregnancies, and some other intraoperative information was not recorded. The majority of the patients in this study had had a history of one or more childbearing, and the generalization to other patient populations would require confirmation. Another methodological weakness could be the low number of negative outcomes (ie, complications), which might result in a lower statistical power to detect differences. This could also partially explain why no more associations between reoperations and other potential risk factors have been identified in the regression analysis.
CONCLUSIONS
In our study, the history of childbearing was found to be a protective factor against complications in abdomen-based microsurgical breast reconstruction. These findings require further evaluation, but we consider that pregnancy leads to complex anatomic and physiologic changes in the abdominal wall and its hemodynamics, which could be beneficial in abdomen-based flap procedures. According to the study results, the usage of the dual venous drainage could be favorable in nulliparous patients undergoing DIEP breast reconstruction.
Footnotes
Disclosure: The authors have no financial interest to declare in relation to the content of this article. This study was supported by Uppsala County Council (ALF grant). The Article Processing Charge was paid for by the authors.
REFERENCES
- 1.Broer PN, Weichman KE, Tanna N, et al. Venous coupler size in autologous breast reconstruction–does it matter? Microsurgery. 2013;33:514–518. doi: 10.1002/micr.22169. [DOI] [PubMed] [Google Scholar]
- 2.Gill PS, Hunt JP, Guerra AB, et al. A 10-year retrospective review of 758 DIEP flaps for breast reconstruction. Plast Reconstr Surg. 2004;113:1153–1160. doi: 10.1097/01.prs.0000110328.47206.50. [DOI] [PubMed] [Google Scholar]
- 3.Hofer SO, Damen TH, Mureau MA, et al. A critical review of perioperative complications in 175 free deep inferior epigastric perforator flap breast reconstructions. Ann Plast Surg. 2007;59:137–142. doi: 10.1097/01.sap.0000253326.85829.45. [DOI] [PubMed] [Google Scholar]
- 4.Laporta R, Longo B, Sorotos M, et al. Tips and tricks for DIEP flap breast reconstruction in patients with previous abdominal scar. Microsurgery. 2015 doi: 10.1002/micr.22457. Epub ahead of print. [DOI] [PubMed] [Google Scholar]
- 5.Riot S, Herlin C, Mojallal A, et al. A systematic review and meta-analysis of double venous anastomosis in free flaps. Plast Reconstr Surg. 2015;136:1299–1311. doi: 10.1097/PRS.0000000000001791. [DOI] [PubMed] [Google Scholar]
- 6.Rogers NE, Allen RJ. Radiation effects on breast reconstruction with the deep inferior epigastric perforator flap. Plast Reconstr Surg. 2002;109:1919–1924. doi: 10.1097/00006534-200205000-00022. discussion 1925. [DOI] [PubMed] [Google Scholar]
- 7.Santanelli F, Longo B, Cagli B, et al. Predictive and protective factors for partial necrosis in DIEP flap breast reconstruction: does nulliparity bias flap viability? Ann Plast Surg. 2015;74:47–51. doi: 10.1097/SAP.0b013e31828d994d. [DOI] [PubMed] [Google Scholar]
- 8.Scheer AS, Novak CB, Neligan PC, et al. Complications associated with breast reconstruction using a perforator flap compared with a free TRAM flap. Ann Plast Surg. 2006;56:355–358. doi: 10.1097/01.sap.0000201549.83738.42. [DOI] [PubMed] [Google Scholar]
- 9.Seidenstuecker K, van Waes C, Munder BI, et al. DIEAP flap for safe definitive autologous breast reconstruction. Breast. 2016;26:59–66. doi: 10.1016/j.breast.2015.12.005. [DOI] [PubMed] [Google Scholar]
- 10.Rozen WM, Chubb D, Whitaker IS, et al. The efficacy of postoperative monitoring: a single surgeon comparison of clinical monitoring and the implantable Doppler probe in 547 consecutive free flaps. Microsurgery. 2010;30:105–110. doi: 10.1002/micr.20706. [DOI] [PubMed] [Google Scholar]
- 11.Kadle R, Cohen J, Hambley W, et al. A 35-year evolution of free flap-based breast reconstruction at a large urban academic center. J Reconstr Microsurg. 2016;32:147–152. doi: 10.1055/s-0035-1563702. [DOI] [PubMed] [Google Scholar]
- 12.Enajat M, Rozen WM, Whitaker IS, et al. A single center comparison of one versus two venous anastomoses in 564 consecutive DIEP flaps: investigating the effect on venous congestion and flap survival. Microsurgery. 2010;30:185–191. doi: 10.1002/micr.20712. [DOI] [PubMed] [Google Scholar]
- 13.Saint-Cyr M, Chang DW, Robb GL, et al. Internal mammary perforator recipient vessels for breast reconstruction using free TRAM, DIEP, and SIEA flaps. Plast Reconstr Surg. 2007;120:1769–1773. doi: 10.1097/01.prs.0000287132.35433.d6. [DOI] [PubMed] [Google Scholar]
- 14.Gosseringer N, Mani M, Cali-Cassi L, et al. Benefits of two or more senior microsurgeons operating simultaneously in microsurgical breast reconstruction: Experience in a Swedish medical center. Microsurgery. 2016 doi: 10.1002/micr.30039. Epub ahead of print. [DOI] [PubMed] [Google Scholar]
- 15.Bui DT, Cordeiro PG, Hu QY, et al. Free flap reexploration: indications, treatment, and outcomes in 1193 free flaps. Plast Reconstr Surg. 2007;119:2092–2100. doi: 10.1097/01.prs.0000260598.24376.e1. [DOI] [PubMed] [Google Scholar]
- 16.Lie KH, Barker AS, Ashton MW. A classification system for partial and complete DIEP flap necrosis based on a review of 17,096 DIEP flaps in 693 articles including analysis of 152 total flap failures. Plast Reconstr Surg. 2013;132:1401–1408. doi: 10.1097/01.prs.0000434402.06564.bd. [DOI] [PubMed] [Google Scholar]
- 17.Rozen WM, Pan WR, Le Roux CM, et al. The venous anatomy of the anterior abdominal wall: an anatomical and clinical study. Plast Reconstr Surg. 2009;124:848–853. doi: 10.1097/PRS.0b013e3181b037a2. [DOI] [PubMed] [Google Scholar]
- 18.Imanishi N, Nakajima H, Minabe T, et al. Anatomical relationship between arteries and veins in the paraumbilical region. Br J Plast Surg. 2003;56:552–556. doi: 10.1016/s0007-1226(03)00207-8. [DOI] [PubMed] [Google Scholar]
- 19.Carramenha e Costa MA, Carriquiry C, Vasconez LO, et al. An anatomic study of the venous drainage of the transverse rectus abdominis musculocutaneous flap. Plast Reconstr Surg. 1987;79:208–217. doi: 10.1097/00006534-198702000-00010. [DOI] [PubMed] [Google Scholar]
- 20.Schaverien M, Saint-Cyr M, Arbique G, et al. Arterial and venous anatomies of the deep inferior epigastric perforator and superficial inferior epigastric artery flaps. Plast Reconstr Surg. 2008;121:1909–1919. doi: 10.1097/PRS.0b013e31817151f8. [DOI] [PubMed] [Google Scholar]
- 21.Leighton WD, Russell RC, Marcus DE, et al. Experimental pretransfer expansion of free-flap donor sites: I. Flap viability and expansion characteristics. Plast Reconstr Surg. 1988;82:69–75. [PubMed] [Google Scholar]
- 22.Argenta LC, Marks MW, Pasyk KA. Advances in tissue expansion. Clin Plast Surg. 1985;12:159–171. [PubMed] [Google Scholar]
- 23.Kim KH, Hong C, Futrell JW. Histomorphologic changes in expanded skeletal muscle in rats. Plast Reconstr Surg. 1993;92:710–716. doi: 10.1097/00006534-199309001-00022. [DOI] [PubMed] [Google Scholar]
- 24.Saint-Cyr M, Wong C, Schaverien M, et al. The perforasome theory: vascular anatomy and clinical implications. Plast Reconstr Surg. 2009;124:1529–1544. doi: 10.1097/PRS.0b013e3181b98a6c. [DOI] [PubMed] [Google Scholar]
- 25.Edouard DA, Pannier BM, London GM, et al. Venous and arterial behavior during normal pregnancy. Am J Physiol. 1998;274:H1605–H1612. doi: 10.1152/ajpheart.1998.274.5.H1605. [DOI] [PubMed] [Google Scholar]
- 26.Gelman S. Venous function and central venous pressure: a physiologic story. Anesthesiology. 2008;108:735–748. doi: 10.1097/ALN.0b013e3181672607. [DOI] [PubMed] [Google Scholar]
- 27.Pemble L. Reversibility of pregnancy-induced changes in the superficial veins of the lower extremities. Phlebology. 2007;22:60–64. doi: 10.1258/026835507780346196. [DOI] [PubMed] [Google Scholar]
- 28.Vin F, Allaert FA, Levardon M. Influence of estrogens and progesterone on the venous system of the lower limbs in women. J Dermatol Surg Oncol. 1992;18:888–892. doi: 10.1111/j.1524-4725.1992.tb02922.x. [DOI] [PubMed] [Google Scholar]
- 29.Miranda Orella L, Mellado Santos JM, Yanguas Barea N, et al. Collateral pathways of the abdominal wall: anatomical review and pathologic findings at 64-slice multidetector CT angiography. 2010. Available from: dx.doi.org/10.1594/ecr2010/C-3062.
- 30.Gusenoff JA, Coon D, De La Cruz C, et al. Superficial inferior epigastric vessels in the massive weight loss population: implications for breast reconstruction. Plast Reconstr Surg. 2008;122:1621–1626. doi: 10.1097/PRS.0b013e31818cbf80. [DOI] [PubMed] [Google Scholar]
- 31.Lee KT, Mun GH. Benefits of superdrainage using SIEV in DIEP flap breast reconstruction: a systematic review and meta-analysis. Microsurgery. 2015 doi: 10.1002/micr.22420. Epub ahead of print. [DOI] [PubMed] [Google Scholar]
- 32.Smit JM, Audolfsson T, Whitaker IS, et al. Measuring the pressure in the superficial inferior epigastric vein to monitor for venous congestion in deep inferior epigastric artery perforator breast reconstructions: a pilot study. J Reconstr Microsurg. 2010;26:103–107. doi: 10.1055/s-0029-1243294. [DOI] [PubMed] [Google Scholar]
- 33.Coroneos CJ, Heller AM, Voineskos SH, et al. SIEA versus DIEP arterial complications: a cohort study. Plast Reconstr Surg. 2015;135:802e–807e. doi: 10.1097/PRS.0000000000001150. [DOI] [PubMed] [Google Scholar]
- 34.Spiegel AJ, Khan FN. An intraoperative algorithm for use of the SIEA flap for breast reconstruction. Plast Reconstr Surg. 2007;120:1450–1459. doi: 10.1097/01.prs.0000270282.92038.3f. [DOI] [PubMed] [Google Scholar]
- 35.Masoomi H, Clark EG, Paydar KZ, et al. Predictive risk factors of free flap thrombosis in breast reconstruction surgery. Microsurgery. 2014;34:589–594. doi: 10.1002/micr.22250. [DOI] [PubMed] [Google Scholar]
- 36.Parrett BM, Caterson SA, Tobias AM, et al. DIEP flaps in women with abdominal scars: are complication rates affected? Plast Reconstr Surg. 2008;121:1527–1531. doi: 10.1097/PRS.0b013e31816b14a5. [DOI] [PubMed] [Google Scholar]
- 37.Mahajan AL, Zeltzer A, Claes KE, et al. Are Pfannenstiel scars a boon or a curse for DIEP flap breast reconstructions? Plast Reconstr Surg. 2012;129:797–805. doi: 10.1097/PRS.0b013e3182450a8f. [DOI] [PubMed] [Google Scholar]
- 38.Niumsawatt V, Chow K, Shen X-Y, et al. The Pfannenstiel scar and its implications in DIEP flap harvest: a clinical anatomic study. Eur J Plast Surg. 2016;39:1–8. [Google Scholar]
