All procedures involving human participants were reviewed and approved by the Medical Ethics Committee of the First Affiliated Hospital of Guangxi Medical University (Approval No.: 2026-E0435; date of approval: 13 May 2026). Ethics approval was obtained for the retrospective use of these data. Written informed consent for the surgical procedures, the use of clinical data, and the publication of identifiable photographs was obtained from all participants. This study was conducted in accordance with the Declaration of Helsinki.
General clinical data
Clinical data were collected from 121 patients who underwent treatment with an orbital septum fascial flap combined with orbital fat release at the outpatient clinic of the Department of Plastic and Reconstructive Surgery, First Affiliated Hospital of Guangxi Medical University. All procedures were performed by the same surgeon between December 2019 and March 2025. All patients presented with lower eyelid bags accompanied by pronounced tear trough deformity, and their preoperative evaluations met the surgical indications for orbital fat release.
A total of 121 cases (242 eyes) were included in this study. Among these, 53 cases underwent a transcutaneous approach, comprising 50 females (94.3%) and 3 males (5.7%), with a median age of 45 years (IQR, 41–49). One case in this subgroup had undergone lower eyelid surgery 4 years prior to enrollment; because the exclusion criterion specifies no lower eyelid or periorbital plastic surgery within the past 2 years, this patient was not excluded. The remaining 52 transcutaneous cases and all 68 transconjunctival cases were primary surgeries. The transconjunctival group comprised 64 females (94.1%) and 4 males (5.9%), with a median age of 28 years (IQR 25–33; mean 29.03 ± 5.49). Comprehensive clinical records, including standardized photographs, were complete for all patients. Patients with severe underlying diseases, surgical contraindications, infectious diseases, or psychiatric disorders were excluded preoperatively.
Inclusion and exclusion criteria
Inclusion criteria: Patients diagnosed with Type II or Type III lower eyelid bags, according to the Summary of the First Academic Conference on Ophthalmic Plastic and Orbital Diseases of the Ophthalmological Society of the Chinese Medical Association; Patients aged > 18 years, with complete clinical data and the ability to tolerate surgery; Patients with clear consciousness and normal communication capabilities; Patients and their families who provided informed consent.
Exclusion criteria: Presence of malignant tumors, severe organ dysfunction, or severe systemic diseases; Drug addiction or dependence on alcohol/tobacco; History of lower eyelid or periorbital plastic surgery within the past 2 years; History of ocular or periocular trauma within the past six months.
Surgical technique (Figure 2 and Figure 3)
Preoperative preparation and anesthesia
All procedures were performed under local anesthesia on an outpatient basis. Anesthesia consisted of 2% lidocaine hydrochloride injection combined with epinephrine at a 1:500,000 concentration, administered via infraorbital nerve block, zygomaticofacial nerve block, and local infiltration anesthesia. The surgical field was prepared with povidone-iodine solution (0.5%) applied three times, and the head and face were draped to expose the full facial region while maintaining a sterile field. Preoperative marking with methylene blue delineated the tear trough, the lower eyelid fat herniation, and the midfacial depression to be corrected.
For the transconjunctival approach, the patient was instructed to keep the eyes closed, and a small square gauze was placed to protect the upper eyelid and cornea. For the transcutaneous approach, the patient was instructed to keep the eyes open to facilitate assessment of eyelid contour and protect the globe. Sharp dissection was performed using a single-use monopolar needle-tip electrocautery electrode, which also provided intraoperative hemostasis.
In the transconjunctival group, the distal fat flap was fixated to the skin at the pre-marked points using 6-0 nylon sutures, secured externally with a petrolatum gauze bolster. In the transcutaneous group, the distal flap was fixated to the periosteum using 5-0 polydioxanone (PDS) absorbable sutures. Postoperatively, ofloxacin eye drops (0.3%) were instilled four times daily. The external bolster was maintained until suture removal, and the transcutaneous incision was cleansed daily. Patients were advised to avoid strenuous activity and bending for 1 week, and skin sutures were removed at 7 days. Standardized follow-up evaluations were scheduled at postoperative day 30, and at 3, 6, and 12 months.
Surgical technique for the Type II study group
The patient was instructed to keep their eyes closed. The conjunctiva was exposed, and a small square gauze was used to protect the upper eyelid. A transconjunctival incision of approximately 15 mm was made at the lower margin of the tarsal plate using a needle-tip electrocautery. Dissection was performed closely along the deep surface of the orbicularis oculi muscle using mosquito forceps. While keeping the orbital septum intact, the dissection proceeded to just above the arcus marginalis, and an eyelid retractor was applied to expose the orbital rim. Using needle-tip electrocautery, the tear trough ligament and the orbicularis retaining ligament were sharply released from medial to lateral up to the preoperatively marked position. This loosened the orbicularis oculi muscle, exposed the levator labii superioris alaeque nasi, and provided access to the prezygomatic space. A nerve dissector was then used to dissect the area according to the preoperatively marked fat fixation sites. To ensure adequate release, the endpoint of this dissection was approximately 7 mm above the nasal ala. After achieving meticulous hemostasis, the orbital septum was opened at the arcus marginalis and dissected to form a complete fan-shaped orbital septum fascial flap (as shown in Figure 3). The preoperatively marked protruding fat, specifically the medial and central compartments of orbital fat, was fully released to create a fan-shaped orbital fat flap measuring approximately 2 cm to 2.5 cm. The entire procedure was performed delicately to avoid injury to the inferior oblique muscle, and care was taken to ensure the harvested fat flap retained its vascular pedicle, which was carefully preserved at the base to maintain perfusion from the infraorbital artery branches.
The orbital septum fascial flap was laid flat on the inner side of the fat flap to reinforce the middle-layer structure, and then sutured into place. The distal portion of the fat flap was engaged using a 6-0 nylon suture. The fat flap, now covered by the orbital septum fascial flap, was pulled down into the premaxillary space. The sutures were passed through the skin at the pre-marked fixation points. After confirming a satisfactory aesthetic appearance of the midface, the sutures were secured externally with a petrolatum gauze bolster.
Surgical technique for the Type III study group
The patient was instructed to keep their eyes open. The skin was incised at the designed incision site, 2 mm below the lower margin of the tarsal plate. Using ophthalmic scissors, a skin flap was undermined between the skin and the orbicularis oculi muscle down to 4–5 mm from the lower eyelid margin. A needle-tip electrocautery was used to incise the orbicularis oculi muscle to enter the preseptal space. Dissection was performed closely along the deep surface of the orbicularis oculi muscle (i.e., the preseptal space) using mosquito forceps. While keeping the orbital septum intact, the dissection proceeded to just above the arcus marginalis, and an eyelid retractor was applied to expose the orbital rim. Using needle-tip electrocautery, the tear trough ligament and the orbicularis retaining ligament were sharply released from medial to lateral to loosen the orbicularis oculi muscle, forming a muscle flap. Entry was gained into the premaxillary space and prezygomatic space. A nerve dissector was used for dissection within these spaces, with the endpoint of dissection approximately 7 mm above the lower margin of the nasal ala. After achieving meticulous hemostasis, the orbital septum was opened at the arcus marginalis and dissected to form a complete fan-shaped orbital septum fascial flap (as shown in Figure 3). The medial, central, and lateral compartments of orbital fat were fully released to create a fan-shaped orbital fat flap measuring approximately 2 cm to 2.5 cm. The orbital septum fascial flap was laid flat on the inner side of the fat flap and sutured into place. The fat flap was positioned to cover the midface depression. After confirming a satisfactory aesthetic result, the distal portion was fixated to the periosteum using 5-0 PDS absorbable sutures. The patient was instructed to open their mouth and look straight ahead to evaluate the amount of excess skin to be excised. The excess skin (approximately 2–4 mm) was marked with methylene blue and removed using ophthalmic scissors. The orbicularis oculi muscle flap was retracted upward to lift the midface, and the main ligament was sutured and fixated to the orbital rim. The orbicularis oculi muscle and skin were then sutured in precise anatomical alignment.
Outcome measures
Comparison of baseline data and objective intraoperative and perioperative parameters between the two groups
The operative duration, length of the prepared fat flap, and recovery time of the ocular appearance were recorded for patients in both groups. Criteria for normal recovery of ocular appearance: The periorbital skin exhibited no erythema, edema, or inflammation; the eye contour maintained a normal, natural curvature; there was no obvious scarring in the periorbital or adjacent areas; eyelid dynamics during blinking were natural; there was no alteration in the palpebral fissure size during facial expressions, and patients reported no sensation of pulling or heaviness around the eyes.
Assessment of tear trough deformity (Barton grading) and inter-rater reliability
Tear trough deformity was graded using the Barton classification preoperatively and at postoperative day 30. Grading was performed independently by two certified oculoplastic surgeons (with 12 and 8 years of experience, respectively), neither of whom had participated in the index surgeries or the initial assessments. Both assessors were fully blinded to surgical approach, postoperative time point, patient demographics, and the original scores. Standardized clinical photographs (frontal, 45-degree oblique, and lateral views) were de-identified and presented in random order using REDCap (version 13.0). Inter-rater reliability was formally evaluated in a stratified random subsample of 25 patients (20.7% of the cohort). Agreement was quantified using the weighted kappa coefficient with bootstrap-estimated 95% confidence intervals, interpreted according to Landis and Koch benchmarks. Preoperative weighted kappa was 0.78 (95% CI 0.62–0.91) and postoperative weighted kappa was 0.82 (95% CI 0.69–0.94), indicating substantial agreement.
Intra-group and inter-group evaluation of surgical efficacy (complete resolution rate of the tear trough)
The Barton grading system for tear troughs was utilized to evaluate the tear trough condition of patients in both groups preoperatively and postoperatively (at day 30). Grade 0: No obvious demarcation line from the medial to the lateral orbital rim; the contour at the lid-cheek junction is smooth, without a transitional outline. Grade I: Mild depression or shadowing is visible at the medial orbital rim, while the contour of the lid-cheek junction at the lateral orbital rim remains smooth. Grade II: A discernible demarcation line is present at the lid-cheek junction, with moderate fat bulging observed above the line. Grade III: An obvious demarcation line is present at the lid-cheek junction, and the area between the orbit and the cheek exhibits a step-like bulging deformity. A higher Barton grade indicates a more pronounced tear trough deformity.
Postoperative safety and complication assessment
Complication data were recorded up to 6 months postoperatively and included incidences of incisional hematoma, incisional infection, and lower eyelid ectropion, which were the three complications systematically captured by a pre-specified protocol. In addition, the following events were reviewed through clinical follow-up records: diplopia, sensory nerve injury, enophthalmos, and fat necrosis or displacement. None of these four events was observed during the follow-up period.
Beyond the 30-day and 6-month endpoints (Figure 4 and Figure 5), selected cases with extended follow-up illustrated the durability of the combined technique. A representative 45-year-old male patient who underwent the transcutaneous approach maintained a smooth lower eyelid contour, resolved eye bags, and an effaced tear trough at 18 months postoperatively (Figure 6). A representative 35-year-old female patient who underwent the transconjunctival approach showed comparable, stable restoration of the lid-cheek junction at 36 months postoperatively (Figure 7). These observations are consistent with the overall cohort, in which standardized comparative photographs were available up to 36 months (Figure 8), supporting the short- to mid-term stability of the procedure. Nevertheless, because standardized comparative photographs at ≥2 years were not available for the majority of patients, long-term durability remains to be confirmed in prospective studies with structured long-term follow-up.
Statistical methods and data processing
Study groups: Data were extracted and compared as two independent samples: the transconjunctival approach group (n = 68) and the transcutaneous approach group (n = 53), yielding a total cohort of 121 cases. Given that many patients presented with bilateral involvement, totaling 242 eyes across 121 patients, all analyses were conducted at the patient level, yielding 121 independent observations. For efficacy evaluation, the worse eye, defined as the higher-grade eye according to the Barton classification, was used to represent the patient-level outcome, adhering to the worst-eye principle. For safety evaluation, complications were coded on a binary basis at the patient level, meaning a patient was recorded as having a specific complication if it occurred in either eye.
Handling of missing data: Variables such as "aesthetic satisfaction" and some postoperative follow-up evaluations were recorded in only a small subset of the sample (validity rate < 10%), indicating severe non-random missingness. In accordance with statistical standards for this analysis, these variables were excluded from quantitative inter-group hypothesis testing to avoid introducing strong selection bias.
Normality testing and descriptive statistics: The Shapiro-Wilk test indicated that all continuous variables (age, operative duration, fat flap length, and recovery time) exhibited non-normal distributions (P < 0.05). Consequently, continuous quantitative data are uniformly expressed as the median and interquartile range M (P25, P75). Categorical and ordinal data are expressed as frequencies and percentages n (%).
Statistical tests: Inter-group comparisons of independent continuous and ordinal variables were performed using the Mann-Whitney U test. Intra-group comparisons of ordinal data before and after surgery (rating downgrades) were evaluated using the Wilcoxon signed-rank test. For inter-group comparisons of nominal categorical variables, Fisher's exact test was uniformly applied due to the presence of expected frequencies < 5.
Significance level and software: All statistical tests were two-sided, with the significance level set at α = 0.05. P-value < 0.05 was considered to indicate a statistically significant difference. Continuous and ordinal comparisons were performed using IBM SPSS Statistics (version 26.0). Inter-rater reliability was analyzed using R software (version 4.3.0) with the irr package. Effect sizes for the primary outcome are reported as absolute risk differences with 95% confidence intervals.