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ORIGINAL RESEARCH article

Front. Med., 18 November 2025

Sec. Ophthalmology

Volume 12 - 2025 | https://doi.org/10.3389/fmed.2025.1722973

This article is part of the Research TopicNew Concepts, Advances, and Future Trends in Clinical Research on Eye DiseasesView all 74 articles

Clinical effectiveness of scleral taping combined with perfluoropropane for complex retinal detachment

  • 1The First Clinical Medical College of Gannan Medical University, Ganzhou, China
  • 2The First Affiliated Hospital of Soochow University, Suzhou, China
  • 3First Affiliated Hospital of Gannan Medical University, Ganzhou, China

Purpose: This study evaluated the effectiveness of scleral taping combined with C3F8 gas filling for the management of complex retinal detachment (CRD) and to objectively assessed its clinical value.

Methods: Forty consecutive patients (40 eyes) with CRD who underwent surgical treatment were included. Patients were divided into two groups: the study group underwent scleral buckling (SB) combined with C3F8 gas filling, and the control group received scleral buckling alone. Each group comprised 20 patients (20 eyes). After anaesthesia, traction sutures were placed at the rectus muscle in all patients. Retinal breaks and degenerative areas were examined and treated with cryotherapy. A silicone sponge was positioned on the scleral surface, and the sutures were tightened to produce an indenting effect. Additionally, patients in the study group received an intravitreal injection of C3F8 gas.

Results: Both uncorrected visual acuity (UCVA) and best-corrected visual acuity (BCVA) improved in the study and control groups on the first post-operative day. However, the improvement was statistically significant only in the control group. Visual acuity in both groups improved significantly at 1 week, 1 month, and 3 months post-operatively compared with baseline and the first post-operative day. Intraocular pressure (IOP) in the study group was significantly elevated at 1 week, 1 month, and 3 months post-operatively compared with baseline. The retinal reattachment rate was 95% in the study group, significantly higher than 70% in the control group. The recurrence rate was 5% in the study group. No serious complications, including retinal incarceration, haemorrhage, anterior segment ischemia, or infection, were observed in either group.

Conclusion: Scleral buckling combined with C3F8 gas filling is a safe and effective treatment for CRD. It significantly improves post-operative visual acuity, enhances retinal reattachment, reduced the recurrence rate with minimal complications.

Introduction

Complex retinal detachment (CRD)—encompassing rhegmatogenous retinal detachment (RRD), tractional detachment secondary to proliferative diabetic retinopathy (PDR), and detachment following open-globe trauma—is a major cause of irreversible blindness. Without prompt intervention it may lead to phthisis bulbi and permanent vision loss (1, 2). The therapeutic goals are to seal retinal breaks, relieve vitreoretinal traction, achieve stable reattachment, and maximise visual recovery (35). Surgery remains the cornerstone of CRD management; timely intervention restores outer retinal anatomy and significantly improves visual outcomes (6, 7). Current surgical options comprise pars plana vitrectomy (PPV), scleral buckling (SB), and pneumatic retinopexy (PR) (8, 9).

SB creates an inward scleral indentation by suturing a silicone band or sponge to the episclera, thereby approximating the neurosensory retina to the retinal pigment epithelium. Being an extra-ocular procedure, SB avoids intra-ocular manipulation, carries a low complication profile, requires minimal specialised equipment, and is cost-effective (1012). SB is highly effective for uncomplicated detachments with a limited number of small breaks (13, 14). Anatomical success with a single SB procedure for CRD has been reported at about 80% (15). Nevertheless, SB alone is insufficient for complex RRD, which usually requires vitrectomy (16, 17). Studies indicate that vitrectomy achieves a retinal reattachment rate of 89% in the treatment of CRD (18). Vitrectomy necessitates prolonged face-down positioning and a second operation for silicone-oil removal about 6 months later. Even after oil extraction, recurrent detachment may occur, imposing additional psychological and economic burdens and exposing patients to higher complication rates (19, 20).

Intravitreal gas injection, introduced by Hilton in the mid-1980s (21, 22), yields an 85.2% single-operation success rate for uncomplicated RRD (23). The gas bubble tamponades retinal breaks by surface tension, preventing fluid flux into the sub-retinal space and facilitating closure (2426). No consensus exists regarding gas type or concentration. Low-concentration C3F8 is rapidly absorbed and may provide insufficient tamponade for complex detachments with multiple or large breaks (2729). In contrast, pure C3F8 is expansile and provides prolonged tamponade owing to its extended intra-ocular half-life (30). Combining SB with pure C3F8 avoids the adverse events associated with silicone-oil tamponade after vitrectomy. Most studies on SB combined with pure C3F8 have primarily focused on patients with uncomplicated retinal detachment, achieving a retinal reattachment rate of 77.6% (31). Research on SB combined with pure C3F8 for the treatment of CRD remains relatively scarce at present. For patients with CRD, intravitreal injection of an expansile gas combined with SB may enhance reattachment rates and maximise visual benefit through sustained internal tamponade. This study evaluates the anatomical and functional outcomes of SB combined with pure C3F8 injection for CRD, aiming to inform surgical decision-making.

Methods

Study subjects

This retrospective cohort study employed propensity score matching (PSM) to simulate randomisation. During the analysis phase, multivariable regression analysis was utilised to control for confounding factors including age, degree of proliferative vitreoretinopathy (PVR), number and size of retinal tears, and extent of retinal detachment. Included 40 patients (40 eyes) with CRD who underwent primary surgery at the First Affiliated Hospital of Gannan Medical University between January 2024 and December 2024. Assign patients to either the study group, which underwent SB combined with C3F8 gas filling, or the control group, which underwent SB alone. Each group comprised 20 patients (20 eyes).

Proliferative vitreoretinopathy (PVR) severity was graded according to the classification system established by the American Retinal Society in 1983. Eyes were eligible if they met all of the following: (1) PVR grade B–C; (2) ≥2 retinal breaks located at different meridians and involving more than one quadrant; (3) posterior pole breaks located 2–5 mm anterior to the equator; (4) giant retinal breaks spanning 70–130° circumference; and (5) all breaks distributed between the 8 and 4 o'clock meridians.

Exclusion criteria were: (1) contraindications to surgery; (2) history of prior vitrectomy; (3) significant media opacity precluding fundus examination; (4) failure to attend timely post-operative follow-up; and (5) pre-operative high intraocular pressure (IOP), glaucoma, diabetes, high myopia, or ocular trauma.

All patients were evaluated pre-operatively and at 1 day, 1 week, 1 month, and 3 months post-operatively. Data collected included uncorrected visual acuity (UCVA), best-corrected visual acuity (BCVA), and IOP, as well as enhanced OCT, fundus photography, and indirect ophthalmoscopy findings.

This study adhered to the principles of the Declaration of Helsinki and received approval from the Ethics Committee of the First Affiliated Hospital of Gannan Medical University. Ethical Approval No. : LLSC-2025-069.

Surgical methods and treatment plan

After comprehensive counselling, written informed consent was obtained from each patient. All operations were performed by the same surgeon. The patient is positioned supine, followed by retrobulbar anaesthesia. The eyelids are retracted using an eyelid speculum. The bulbar conjunctiva is dissected circumferentially 2 mm beyond the scleral-corneal junction to fully expose the scleral area. Retraction sutures are placed on the superior, inferior, medial, and lateral rectus muscles of the operative eye. Under binocular indirect ophthalmoscopy the fundus was systematically inspected; all breaks and clinically significant areas of degeneration were localised and marked on the sclera. Trans-scleral cryotherapy was applied around each break and degenerate retina until a uniform white frost (moderate-grade freeze) was observed. Perform scleral fixation around the tear. Perform scleral puncture drainage in the retinal detachment area, avoiding the retinal tear site. A silicone sponge explant was trimmed to size, positioned parallel to the limbus directly over the break, and secured with pre-placed 5-0 polyester sutures tightened to produce an inward scleral indentation. Following these steps, the experimental group underwent anterior chamber paracentesis at the superior temporal limbus to aspirate an appropriate volume of aqueous humour. Pure C3F8 inert gas (0.3–0.5 ml) was aspirated and injected intraocularly at the 10 o'clock position, 3.5 mm from the limbus, perpendicular to the ocular wall, slowly advancing the gas towards the ocular centre. The bulbar conjunctiva was sutured intermittently and irrigated with a gentamicin and dexamethasone mixture. Tobramycin-dexamethasone ophthalmic ointment was applied to the operated eye, and the patients were instructed to maintain a face-down position for 1–2 weeks and to avoid strenuous activity.

Statistical methods

Data were analysed using SPSS 27.0. After testing for normality, the mean and standard deviation of continuous variables were calculated. Quantitative variables (UCVA, BCVA, and IOP) were expressed as mean ± standard deviation (x ± s). For repeated measures (UCVA, BCVA, and IOP), repeated-measures analysis of variance (ANOVA) was performed. Independent-samples t-test were used to compare intergroup differences in UCVA, BCVA, and IOP between the study and control groups, while Fisher's exact test was used to compare intergroup differences in retinal reattachment rate. A P < 0.05 was considered statistically significant. Effect sizes are represented by Cohen's d, partial η2, and Odds Ratio (OR). Cohen's d ranges from 0 to 1, with values below 0.5 indicating a small effect, 0.5–0.8 denoting a medium effect, and above 0.8 signifying a large effect. The partial η2 ranges from 0 to 1, with values between 0.01 and 0.06 indicating a small effect, between 0.06 and 0.14 representing a medium effect, and greater than 0.14 signifying a large effect. OR = 1 indicates no association, OR < 1 denotes a negative association, OR > 1 signifies a positive association, and a higher OR value indicates a stronger association.

Results

General information

Forty patients with CRD were included in this study, comprising 22 males (55%) and 18 females (45%). Ages ranged from 44 to 84 years, with a mean of 57.2 ± 9.26 years. Twenty-nine patients (72.5%) had two lacunae, and 11 patients (27.5%) had three lacunae. PVR grade B was identified in 31 patients (77.5%)-−15 in the study group and 16 in the control group—while grade C was identified in nine patients (22.5%)—five in the study group and four in the control group. Regarding the extent of detachment, 22 patients (55%) had two quadrants involved, 17 patients (42.5%) had three quadrants involved, and one patient (2.5%) had four quadrants involved.

Comparative analysis of UCVA, BCVA and IOP before and after surgery

Comparative analysis of UCVA before and after surgery

(1) Study group: pre-operative, and 1 day, 1 week, 1 month, and 3 months post-operative mean UCVA values were (1.88 ± 0.37) logMAR, (1.55 ± 0.5) logMAR, (1.26 ± 0.37) logMAR, (0.97 ± 0.34) logMAR, and (0.6 ± 0.26) logMAR, respectively. At 1 day post-operatively, mean UCVA improved compared with pre-operative values, but the difference was not statistically significant (P > 0.05). UCVA at 1 week, 1 month, and 3 months was significantly better than at pre-operative and 1-day (P < 0.01). At 3 months, UCVA was also significantly better than at 1 week and 1 month (P < 0.01, η2 = 0.896).

(2) Control group: pre-operative, and 1 day, 1 week, 1 month, and 3 months post-operative mean UCVA values were (1.92 ± 0.34) logMAR, (1.57 ± 0.46) logMAR, (1.37 ± 0.45) logMAR, (1.0 ± 0.23) logMAR, and (0.64 ± 0.18) logMAR, respectively. At 1 day post-operatively, mean UCVA improved compared with pre-operative values, with the difference statistically significant (P < 0.05). UCVA at 1 month was significantly better than pre-operative, 1-day, and 1-week values (P < 0.05). At 3 months, UCVA was significantly better than pre-operative, 1-day, 1-week, and 1-month values (P < 0.01, η2 = 0.924).

Comparative analysis of BCVA before and after surgery

(1) Study group: pre-operative, and 1 day, 1 week, 1 month, and 3 months post-operative mean BCVA values were (1.76 ± 0.54) logMAR, (1.44 ± 0.59) logMAR, (1.1 ± 0.37) logMAR, (0.92 ± 0.35) logMAR, and (0.55 ± 0.27) logMAR, respectively. At 1 day post-operatively, mean BCVA improved compared with pre-operative values, but the difference was not statistically significant (P > 0.05). At 1 week, 1 month, and 3 months, BCVA was significantly better than at pre-operative and 1 day (P < 0.01). At 3 months, BCVA was also significantly better than at 1 week and 1 month (P < 0.01, η2 = 0.825).

(2) Control group: pre-operative, and 1 day, 1 week, 1 month, and 3 months post-operative mean BCVA values were (1.86 ± 0.38) logMAR, (1.39 ± 0.52) logMAR, (1.24 ± 0.49) logMAR, (0.87 ± 0.21) logMAR, and (0.53 ± 0.16) logMAR, respectively. At 1 day post-operatively, mean BCVA improved compared with pre-operative values, with the difference statistically significant (P < 0.05). At 1 month, mean BCVA was significantly better than at pre-operative, 1-day, and 1-week (P < 0.05). At 3 months, mean BCVA was significantly better than at pre-operative, 1-day, 1-week, and 1-month (P < 0.01, η2 = 0.908). Within-group differences in UCVA and BCVA at different time points in the control group are shown in Table 1. Within-group differences in UCVA and BCVA in the study group are presented in Table 2, and changes in UCVA and BCVA in both groups are shown in Figures 1, 2.

Table 1
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Table 1. Comparison of within-group differences in UCVA and BCVA at different times between pre-operative and post-operative periods in the control group (x¯±s).

Table 2
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Table 2. Comparison of within-group differences in UCVA and BCVA at different times between pre-operative and postoperative periods in the study group (x¯ ± s).

Figure 1
Line graph showing UCVA (logMAR) for study and control groups over time. Both groups show a decrease from pre-op to three months post-op. The study group data is represented by a blue line, and the control group by an orange line, with similar trends observed.

Figure 1. Changes in UCVA at various pre-operative and post-operative time points in the study and control groups.

Figure 2
Line graph comparing Best Corrected Visual Acuity (BCVA) in logMAR between study and control groups over five time points: pre-operation, one day, one week, one month, and three months post-operation. Both groups show a decreasing trend in BCVA, indicating improvement, with the study group showing slightly better outcomes at certain points.

Figure 2. Changes in BCVA at various pre-operative and post-operative time points in the study and control groups.

Comparative analysis of IOP before and after surgery

(1) Study group: before surgery, four patients (20%) had IOP < 10 mmHg, 16 patients (80%) had IOP 10–21 mmHg, and the mean IOP was (12.18 ± 4.33) mmHg. On the first post-operative day, one patient (5%) had IOP < 10 mmHg, 15 patients (75%) had IOP 10–21 mmHg, and four patients (20%) had IOP >21 mmHg, with a mean IOP of (16.8 ± 6.67) mmHg. At 1 week post-operatively, one patient (5%) had IOP < 10 mmHg, 19 patients (95%) had IOP 10–21 mmHg, and the mean IOP was (15.48 ± 3.35) mmHg. At 1 and 3 months after surgery, IOP in all patients was within the normal range, with mean values of (14.55 ± 1.99) mmHg and (14.3 ± 2.45) mmHg, respectively. Mean IOP at 1 day, 1 week, 1 month, and 3 months was slightly higher than the pre-operative value, with the increase most marked on the first post-operative day, followed by a gradual decline and stabilisation. The difference between IOP on day 1 and pre-operative IOP was not statistically significant (P > 0.05), whereas differences at 1 week, 1 month, and 3 months compared with pre-operative values were statistically significant (P < 0.05).

(2) Control group: before surgery, two patients (10%) had IOP < 10 mmHg, 18 patients (90%) had IOP 10–21 mmHg, and the mean IOP was (13.5 ± 3.85) mmHg. On the first post-operative day, one patient (5%) had IOP < 10 mmHg, 16 patients (80%) had IOP 10–21 mmHg, and three patients (15%) had IOP >21 mmHg, with a mean IOP of (16.6 ± 5.57) mmHg. At 1 week, 1 month, and 3 months after surgery, all patients' IOP values were within the normal range, with mean values of (15.35 ± 3.00) mmHg, (15.25 ± 2.43) mmHg, and (14.85 ± 2.43) mmHg, respectively. Mean IOP at each post-operative time point was slightly higher than the pre-operative value, with the rise most marked on the first post-operative day, after which IOP gradually decreased and stabilised. The difference in IOP between pre-operative and post-operative time points was not statistically significant (P > 0.05).

Comparison of intragroup differences in IOP between pre-operative and post-operative time points in the study and control groups is presented in Table 3, and changes in IOP in both groups are shown in Figure 3. Independent-samples t-test results for UCVA, BCVA, IOP, and other indices demonstrated no statistically significant intergroup differences at any post-operative time point (P > 0.05). Comparative analysis of intergroup differences in each index is presented in Table 4.

Table 3
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Table 3. Comparison of intragroup differences in IOP at different times between pre-operative and post-operative periods in the study and control groups (x¯ ± s).

Figure 3
Line graph depicting intraocular pressure (IOP) in millimeters of mercury (mmHg) for study and control groups at pre-op, 1 day, 1 week, 1 month, and 3 months post-op. Both groups show a peak at 1 day post-op, followed by a decline and stabilization.

Figure 3. Changes in IOP at various pre-operative and post-operative time points in the study and control groups.

Table 4
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Table 4. Comparative analysis of intergroup differences between the two groups on various indicators (x¯±s).

Post-operative retinal reset rate

On the 1st day, 1 week, 1 month, and 3 months after surgery, fundus examination showed that the fissures were located on the pressurised ridge, were well-closed, and that the retinas were reattached. In the study group, 19 patients (95%) achieved reattachment, whereas in the control group, 70% of patients achieved retinal reattachment. Post-operative recurrence of retinal detachment occurred in one patient (5%) in the study group and in six patients (30%) in the control group. The difference in retinal reset rate between the two groups was statistically significant (P < 0.05, OR = 8.14).

Comparison of fundus photography and OCT findings before and after SB combined with C3F8 surgery is shown in Figures 4, 5.

Figure 4
Five-panel medical image showing retinal and ultrasound views:
A. Posterior pole retinal detachment is visible.
B-C. Retinas with obscured details, suggesting disease.
D. Ultrasound image, possibly showing detachment or abnormality.
E. Wide view of retina with visible vessels and potential abnormalities.

Figure 4. (A–D) Fundus photography and ocular ultrasound demonstrated pre-operative total retinal detachment and proliferative retinal changes in the patient. (E) One month post-operative complete retinal reattachment in patients undergoing combined SB and pure C3F8 gas filling.

Figure 5
Preoperative OCT images A and B demonstrate retinal detachment, while postoperative images C and D show complete retinal reattachment.

Figure 5. (A, B) OCT revealed pre-operative separation of the retinal neuroepithelium from the pigment epithelium, with a subretinal fluid-filled area. (C, D) One month post-operatively, retinal reattachment was achieved with absorption of the subretinal fluid and no significant fluid accumulation observed.

Discussion

CRD presents a major challenge in ophthalmology and has a profoundly negative impact on patients' vision and quality of life. Vision loss not only limits daily activities but also delivers a heavy psychological burden, increasing anxiety and depression, while simultaneously imposing an economic strain on both families and society (32, 33). CRD is frequently associated with high-risk factors such as giant lacunae, multiple lacunae, and severe PVR. Among these, PVR is particularly important, as it arises from intraocular inflammation and fibroproliferative processes that drive retinal fibrosis (34, 35). Identifying safer and more effective treatment strategies, therefore, remains a key priority for both ophthalmologists and researchers.

Currently, there is no consensus on the optimal surgical modality for patients with CRD. Vitrectomy is an important treatment option, but it increases the risk of post-operative complications, whereas SB is associated with a comparatively lower complication rate and faster visual recovery (36, 37). C3F8 gas has favourable expansion properties and, when injected into the eye, can occupy space to exert a continuous tamponade effect on the retina, thereby facilitating reattachment (38). It also has good biocompatibility and does not provoke significant inflammatory or immune rejection responses within the eye (39). The expansion and absorption dynamics of C3F8 provide effective support for retinal repositioning over a sustained period. With appropriate post-operative positioning, the tamponade effect of C3F8 further accelerates retinal reattachment. In this study, all patients who underwent the combined surgical approach were instructed to maintain the foramen magnum position for 1–2 weeks after surgery, and to avoid strenuous activity, to ensure effective gas compression and stable retinal apposition. In contrast, other intraocular fillers may require a longer healing and recovery process. For example, patients who undergo silicone oil filling must remain in a specific position for a prolonged period, and subsequent silicone oil removal surgery can further extend the recovery phase and increase patient discomfort (40, 41). The volume of C3F8 gas injected is a critical determinant of surgical outcome. If the volume is insufficient, it cannot provide adequate tamponade on the retina, which may result in incomplete reattachment. Conversely, excessive volume may cause a marked rise in IOP, potentially damaging the optic nerve and retina and worsening visual impairment (42) Research indicates that axial length correlates positively with vitreous cavity volume. A longer axial length corresponds to a larger vitreous cavity volume, thus requiring a greater volume of gas to achieve equivalent filling (43). In clinical practise, the dosage of C3F8 gas injection should be adjusted according to the patient's axial length. For patients with shorter axial lengths (< 24 mm), 0.3–0.4 ml of C3F8 gas may be administered. For patients with longer axial lengths (≥24 mm), 0.4–0.5 ml of C3F8 gas may be administered. In this study, all patients received 0.3–0.5 ml of gas, tailored to their ocular condition, and no intraoperative spikes in IOP were observed.

The results of this study demonstrated that the study group achieved superior outcomes in promoting retinal reattachment. Post-operative funduscopic examination showed that fissures were located on the pressurised ridge, were well-closed, and the retina was flat in 14 patients in the control group, giving a reattachment rate of 70%. Six patients experienced recurrent retinal detachment after surgery, with a recurrence rate of 30%. In the study group, 19 patients achieved post-operative retinal reattachment, corresponding to a reattachment rate of 95%, which exceeded the retinal reattachment rate observed in vitrectomy procedures (18), only one patient experienced recurrent retinal detachment, giving a recurrence rate of 5%. This difference may be attributable to the effect of pure C3F8 gas injected into the vitreous cavity, which exerted an effective tamponade on the retina, compensating for the insufficient local pressure of simple SB and thereby stabilising larger retinal areas to reduce recurrence.

Among the seven patients with recurrence, two had PVR grade B and five had grade C. The recurrence rates in patients with PVR grade B and C were 6.4 and 55.6%, respectively. Among those with two retinal holes, three patients relapsed (recurrence rate 10.3%), whereas among those with three retinal holes, four patients relapsed (recurrence rate 36.3%). For detachments spanning two quadrants, recurrence occurred in two patients (9.1%); for three quadrants, four patients relapsed (23.5%); and for four quadrants, one patient relapsed (100%). These findings demonstrate that more severe PVR, a greater number of retinal breaks, and larger detachment extent are associated with higher recurrence rates and reduced surgical success (44).

In terms of visual acuity, no statistically significant difference was found between the two groups, yet a marked disparity in retinal reattachment rates was observed. This may indicate that the advantage of combined surgery lies in promoting retinal reattachment rather than in enhancing short-term visual acuity. At 1 day post-operatively, both uncorrected visual acuity (UCVA) and best-corrected visual acuity (BCVA) in the control group showed significant improvement compared to pre-operative levels, with statistically significant differences. In contrast, no significant improvement was observed in the study group. This may be attributed to the differing refractive indices of C3F8 gas and aqueous humour. This refractive index disparity causes significant refraction and scattering of light as it passes through C3F8 gas and aqueous humour, thereby impairing light focusing and imaging. Consequently, the image formed on the retina becomes blurred (24). Furthermore, studies indicate that following C3F8 gas filling, the a-wave and b-wave components of the electroretinogram (ERG) exhibit a decline in the immediate post-operative period. This suggests functional suppression of retinal photoreceptor and bipolar cells, leading to transient alterations in retinal function that subsequently impact short-term visual acuity improvement (45). In the study group, patients' mean UCVA improved from (1.88 ± 0.37) logMAR to (0.60 ± 0.26) logMAR, and mean BCVA improved from (1.76 ± 0.54) logMAR to (0.55 ± 0.27) logMAR. These results suggest that over time, combined procedure can lead to increasingly significant improvements in patients' vision, thereby contributing to better visual function and overall quality of life.

The mean IOP of patients in both groups at 1 day, 1 week, 1 month, and 3 months after surgery remained within the normal range and was slightly higher than the pre-operative values. The increase in mean IOP was most marked on the first post-operative day, after which it gradually decreased and stabilised. In this study, seven patients developed elevated IOP on the first post-operative day. In the control group, acute IOP elevation was likely related to short-term ocular inflammation and swelling. In the study group, IOP elevation was attributed not only to inflammation and swelling but also to intraocular volume increase from gas expansion and transient angle closure caused by forward displacement of the iris–lens diaphragm (24). In all cases, IOP normalised after administration of topical and systemic hypotensive medication. No other complications such as retinal incarceration, haemorrhage, anterior segment ischaemia, or infection occurred during follow-up.

Therefore, the combination of SB and C3F8 is clinically valuable in the management of CRD. SB provides external indentation on the retina, closing retinal breaks and reducing vitreoretinal traction, while C3F8 filling delivers continuous internal tamponade to promote retinal reattachment and apposition. Used together, these approaches complement one another, enhancing both external and internal support, thereby increasing the success rate of retinal reattachment and improving patients' long-term prognosis.

Although this study demonstrated favourable outcomes with SB combined with C3F8 in the treatment of CRD, several limitations should be acknowledged. This retrospective cohort study cannot entirely preclude the influence of confounding bias. Although we employed methods such as propensity score matching and multivariate regression analysis to control for known confounding factors, the possibility of residual confounding remains unavoidable. Further rigorous prospective cohort studies or randomised controlled trials will be required in the future to validate the conclusions of this research. While clinical data were collected and analysed in detail, uncontrollable factors such as inter-individual variability may have influenced the results, thereby limiting the generalisability and reliability of the conclusions. The study sample size was relatively small, with only 40 patients included, which may not fully represent the broader patient population and could reduce the ability to detect rare complications or less common clinical scenarios.

Furthermore, the follow-up period was relatively short. Longer-term studies are needed to evaluate the sustained effects of SB combined with C3F8, particularly with respect to the stability of visual acuity, durability of retinal reattachment, and the incidence of late complications over 5–10 years or more. Future research should therefore incorporate larger cohorts and extended follow-up to provide more robust evidence regarding the long-term safety and effectiveness of this combined surgical approach.

SB combined with C3F8 for CRD appears to be a safe and effective treatment, producing significant improvements in visual acuity, a higher rate of retinal reattachment, lower recurrence rates, and a reduced risk of complications.

Data availability statement

The raw data supporting the conclusions of this article will be made available by the authors, without undue reservation.

Ethics statement

The studies involving humans were approved by Ethics Committee of the First Affiliated Hospital of Gannan Medical University. The studies were conducted in accordance with the local legislation and institutional requirements. The participants provided their written informed consent to participate in this study. Written informed consent was obtained from the individual(s) for the publication of any potentially identifiable images or data included in this article.

Author contributions

XW: Software, Data curation, Methodology, Writing – original draft, Validation, Project administration, Writing – review & editing, Investigation, Formal analysis. CL: Validation, Writing – review & editing, Formal analysis, Supervision. LL: Formal analysis, Methodology, Supervision, Validation, Writing – review & editing. LX: Conceptualization, Writing – review & editing, Validation, Supervision, Methodology, Formal analysis. YJ: Validation, Investigation, Formal analysis, Conceptualization, Project administration, Writing – review & editing, Supervision, Methodology.

Funding

The author(s) declare that no financial support was received for the research and/or publication of this article.

Acknowledgments

Sincerely thank all colleagues and authors for their efforts in conceptualising, writing, and publishing the paper.

Conflict of interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Generative AI statement

The author(s) declare that no Gen AI was used in the creation of this manuscript.

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Abbreviations

CRD, complicated retinal detachment; UCVA, uncorrected visual acuity; BCVA, best-corrected visual acuity; IOP, intraocular pressure; RRD, rhegmatogenous retinal detachment; PVR, proliferative vitreoretinopathy; OCT, optical coherence tomography; PPV, pars plana vitrectomy; SB, scleral buckling; PR, pneumatic retinopexy; PSM, propensity score matching; ERG, electroretinogram; OR, odds ratio; logMAR, logarithm of the minimum angle of resolution (used as a visual acuity scale); C3F8, perfluoropropane gas.

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Keywords: scleral buckling, C3F8 gas, complex retinal detachment, clinical effectiveness, visual acuity outcomes, intraocular pressure, ophthalmic surgery

Citation: Wang X, Li C, Liu L, Xie L and Jiang Y (2025) Clinical effectiveness of scleral taping combined with perfluoropropane for complex retinal detachment. Front. Med. 12:1722973. doi: 10.3389/fmed.2025.1722973

Received: 11 October 2025; Accepted: 28 October 2025;
Published: 18 November 2025.

Edited by:

Weihua Yang, Southern Medical University, China

Reviewed by:

Ligang Jiang, Quzhou City People's Hospital, China
Minghui Zhao, Shanghai Municipal Hospital of Traditional Chinese Medicine, China

Copyright © 2025 Wang, Li, Liu, Xie and Jiang. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Yiping Jiang, c2hlbmdrYW5nQHNpbmEuY29t

These authors have contributed equally to this work

Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.