Predictability of refraction following immediate sequential bilateral cataract surgery (ISBCS) performed under general anaesthesia
© Guber et al. 2015
Received: 19 March 2015
Accepted: 30 July 2015
Published: 20 August 2015
To evaluate the predictability of refraction following immediate sequential bilateral cataract surgery (ISBCS) performed under general anaesthesia.
This is a retrospective review of all ISBCS performed at Kantonsspital Winterthur, Switzerland, between April 2000 and September 2013. The case notes of 250 patients were reviewed. Patients having full refraction reported (110 patients/220 eyes) were included. 210 (95 %) eyes had a straight forward phacoemulsification with posterior chamber intraocular lens implantation, seven eyes had a planned extracapsular cataract extraction (ECCE); three eyes had an intracapsular cataract extraction.
Both eyes of 110 patients (64 women, 46 men) with a mean age of 79.0 years, standard deviation (SD) ±11.4 (range 26 to 97 years) were included. Median preoperative best corrected visual acuity (BCVA) was 0.5 LogMAR in the first eye, the interquartile range (IQR) was [0.4, 1.2]; 0.7 LogMAR in the second eye with IQR [0.4, 1.8]. At one month, the median BCVA was 0.2 LogMAR, IQR [0.1, 0.3] in the first eye, median BCVA was 0.1 LogMAR and IQR [0.0, 0.5] in the second eye. There were 3 eyes (3 %) that lost 3 lines or more in BCVA at one month (control vs. pre-operatively). In all three cases, poor visual acuity had been recorded pre-operatively (>1 LogMAR). Achieved refraction was within ±1.0 D of the target in 83 % of eyes. There were only 5 % (n = 6) of cases where if delayed sequential bilateral extraction had been performed could potentially intraocular lens (IOL) choice have been adjusted, in four of these cases, target refraction was within ±1.0 D in the second eye.
ISBCS performed under general anaesthesia achieves target refraction in 83 % of eyes after consideration of complications, ocular co-morbidities and systemic restrictions. In the majority of cases where IOL power calculation could be considered, the achieved refraction of the second surgical eye was within ±1.0 D of intended refraction. This undermines the utility of IOL power adjustments in the second surgical eye.
KeywordsCataract Cataract surgery Immediate sequential bilateral cataract surgery
While refractive bilateral surgery is nowadays standard practice, the widespread implementation of immediate sequential bilateral cataract surgery (ISBCS) has remained a subject of controversy . A survey of the members of the American Society of Cataract and Refractive Surgeons in 2012 revealed that less than 1 % of surgeons routinely perform ISBCS . There is unfounded fear of intraocular infection associated with ISBCS [3–5], which continues to be cited as the primary reason why this procedure has not been implemented as standard practice. To a lesser extent, reluctance is due to the occasional significant intraocular lens (IOL) power calculation errors in the first eye that can potentially be refined and thereby prevented in the second eye .
On the other hand, there are important considerations for the patient in terms of cost and for healthcare services due to the resources required—ISBCS approximately halves the number of required post-operative appointments. In particular, this eases the demand on support infrastructure for mobility restricted patients [7, 8]. With an aging population these considerations will be of increased importance particularly in an era where healthcare is obliged to focus on cost efficiency. Due to the rapid visual rehabilitation and obvious practicalities for elderly patients, some surgeons will perform it on request in the absence of contraindications . Therefore ISBCS is growing in popularity worldwide; some regions such as the Canary Islands have adopted ISBCS as a standard procedure, now 80 % of all cataract surgeries are performed in this way .
The very low risk of bilateral complications following ISBCS has been well documented, and will in time erode resistance to the widespread adoption of ISBCS in this respect. This article focuses on the secondary perceived impediment i.e., the possible adjustment of IOL power in the second surgical eye. Therefore, the aim of this study was to calculate the percentage of eyes where adjustments might have proved beneficial in terms of the visual outcome, refractive error and difference from target refraction for the first and second surgical eye.
The retrospective study followed the tenets of the Declaration of Helsinki and was reviewed by the internal ethics committee of Kantonsspital of Winterthur, the Canton of Zurich, Switzerland.
Patient charts of all consecutive ISBCS performed at the Kantonsspital of Winterthur, Switzerland, performed between April 2000 and September 2013 were reviewed. There were 250 patients in total, only those with refraction available pre- and post-operatively were included in this study (n = 110). In general, indication for ISBCS was defined as the need for bilateral cataract surgery (reduced visual acuity with evidence of lens opacity as observed at the slit lamp) and where surgery under local anaesthesia was not feasible due to general health restrictions.
Calculating IOL power
Biometry was performed with the IOL Master (Carl-Zeiss AG, Oberkochen, Germany). However, in cases of high lens opacity, patients had axial length measured with an A-scan ultrasound (Ocuscan, Alcon, Hünenberg, Switzerland). In five cases, where patients were unable to cooperate, the biometry measurements were completed under general anaesthesia (e.g. Trisomy 21, Parkinson’s disease). Where biometry was completed successfully with the IOL master, the Haigis formula was used to calculate IOL power, elsewhere, the SRK II/SRK T formula was used.
Pre and post-operative visual outcomes
0.52 (0.39, 1.15)
0.40 (0.15, 0.70)
2.97 ± 0.46
2.98 ± 0.47
23.5 ± 1.6
23.6 ± 1.75
−1.29 ± 4.79
−0.93 ± 4.59
−0.72 ± 4.77
−0.34 ± 4.51
−1.30 ± 1.30
−1.27 ± 1.25
Target SE (D)
−1.00 ± 1.13
−0.78 ± 1.40
Zeiss Asphina CT409MP
Ophtec PC292Y (PMMA)
0.22 (0.10, 0.35)
0.13 (0.01, 0.52)
−1.00 ± 1.13
−0.99 ± 1.40
−0.36 ± 1.09
−0.34 ± 1.39
−1.40 ± 1.11
−1.41 ± 1.34
Difference between target and achieved (D)
The postoperative regimen included Tobradex® (tobramycin 1 mg/dexamethasone 3 mg) eye drops qid. The eye drops were tapered over four weeks. Postoperative controls were one day, one week and one month postoperatively. This is a retrospective review of patient case notes. Patients operated under general anaesthesia normally have the day one follow-up visit performed at the hospital. In Switzerland, the primary eye care providers are ophthalmologists rather than optometrists, therefore, week 1 and month 1 follow-up visits were more often performed by the referring ophthalmologist. In this way, only the more complicated cases and those in close proximity to the hospital continued post-operative follow-up at the hospital. All follow-up visits were performed by ophthalmologists. Details on post-operative complications but not refractive outcomes were available for all patients.
In this retrospective study, 250 patient files were reviewed, of which 110 patients (64 women, 46 men) with a mean age of 79.0 years, SD ± 11.4 (range 26 years to 97 years) had suitable data available and were included. In all but two patients, surgeries were performed under inpatient conditions. To date, in this centre, ISBCS is non-standard, reserved only for those cases where it was not possible to perform straightforward cataract surgery under topical anaesthesia, due to the general health condition of the patient (e.g. reduced mobility, nervous system disorders).
Baseline characteristics and ocular co-morbidities
- Distance vision target (0 D, -1 D)
88 (80 %)
- Near vision target (less than -2 D)
22 (10 %)
First operated eye R/L
Primary open angle glaucoma
Angle closure glaucoma
Retinal vein occlusion
Previous retinal detachment
Corneal scar due to herpes
Asymptomatic cornea guttata
Chronic anterior uveitis
One patient had no systemic co-morbidity, 109 patients had at least one systemic comorbidity, but on average patients had 3.4 co-morbidities (1–7). Twenty-five (23 %) patients were receiving oral anticoagulation, 53 patients (48 %) had heart problems (arrhythmia, heart failure, or cardiovascular disease), 66 patients (60 %) had high blood pressure. Thirty-six (33 %) patients had diabetes mellitus. Twenty-seven (25 %) patients had reduced renal function. Nineteen (17 %) patients had reduced respiratory function. Forty (36 %) patients had reduced mobility (e.g. paraplegia), 21 patients were morbidly obese (body mass index (BMI) > 30). Twenty patients (18 %) had suffered cerebral vascular insult. Fifty-five patients had a history of psychological disorder/impairment. Seven patients had a history of cancer.
There was no difference observed in myopic eyes (spherical equivalent (SE) < −4.00 D) from the rest of the group (SE > −4.00D) in terms of pre-operative visual acuity, divergence from SE or post-operative visual acuity.
Eighty-four patients had both eyes measured with optical biometry and the Haigis formula was used to calculate the target SE, this included 88/110 first eyes and 94/110 second eyes measured with optical biometry successfully measured using optical biometry. In the remaining eyes, ultrasound was used with either the SRKII formula (n = 20, 13 first eyes/7 second eyes) or SRKT formula (n = 18, 9 first eyes/9 second eyes) to calculate the target SE. There was a significant difference in the pre-operative LogMAR BCVA of eyes measured with biometry and ultrasound (0.5 logMAR vs. 1.7 logMAR) and the average difference between target SE and achieved (0.42 D vs 0.73 D).
Examining the subgroup of patients with both eyes that had pre-operative optical biometry and simple lens IOL exchange (n = 78 patients), the postoperative refraction was within ±0.5 D of the target in 63 % (n = 49 patients) of first surgical eyes and 54 % (n = 42) for the second eye. The postoperative refraction was within ±1.0 D in 86 % (n = 67) for the first eye and 91 % (n = 71) for the second eye, and it was within ±2.0 D in 99 % (n = 77) for the first eye and 97 % (n = 76) for the second eye (Fig. 2b).
Twenty patients had post-operative refraction greater than 1.0 D from target SE in their first operated eye. Two of these eyes had intraoperative complications; in three eyes, biometry could only be achieved under general anaesthesia; one eye developed choroidal neovascularisation postoperatively. Pre-operatively, one eye had choroidal neovascularisation, four had age related macular degeneration (AMD), one had strabismus. Two patients had dementia thus resulting in unreliable refraction results. Therefore, there were 6 patients who based on the visual outcome of the first eye, could have considered adjustments to the IOL power calculation. In 4 of these 6 patients, the refractive outcome of the second eyes was within ±1.0 D.
In 98 patients, there were no intraoperative or postoperative complications observed in either eye. In the remaining 12 patients, one or more complications were observed unilaterally, there were no cases of bilateral complications.
In one eye, an accidental sulcus implantation led to a rhexis fixated optic. An intraoperative conversion to ICCE because of total zonula dialysis was performed in three eyes (1 %). One IOL implant broke during insertion, and consequently was replaced intraoperatively. In 18 eyes of ten patients (9 %), an intraoperative floppy-iris syndrome (IFIS) was noted, and in one of these eyes, an iris prolapse occurred intraoperatively requiring a sectorial iridectomy.
Postoperative hypertony (IOP > 30 mmHg) was observed in 3 eyes (1 %), ICCE has been performed in two of these eyes. One eye after ECCE had a postoperative wound dehiscence with iris incarceration (due to eye rubbing). One eye (1 %) had a corneal decompensation (preoperatively Fuchs dystrophy had not been observed but known PEX glaucoma patient). Following uncomplicated phacoemulsification, postoperative conversion from a dry AMD to a wet AMD was observed in one eye. One eye had reactivation of herpes keratitis. One eye suffered from a prolonged anterior chamber inflammation (toxic anterior segment syndrome (TASS) suspect).
In most countries, ISBCS is done as the exception rather than the rule, ophthalmic surgeons state that the fear of bilateral sight-threatening complications is the limiting factor, in reality there is a very low risk of bilateral complications . The second and lesser reservation of surgeons when performing ISBCS is the loss of the ability to adjust their IOL calculation for the second eye following the visual outcome of first eye. This study demonstrated the relatively small deviation from target spherical equivalence in the majority of cases of ISBCS, in particular, these results highlighted the small percentage of cases where IOL calculation could be practically employed. These results combined with the good final visual acuity of patients who underwent ISBCS, adds further evidence to support a more general acceptance of ISBCS clinically.
Deviation from target spherical equivalence and postoperative BCVA outcomes reported here agree well with earlier retrospective studies [15, 16]. Johansson et al. reported similar predictability: within 1.0 D was achieved in 71 % of eyes in comparison to the 83 % reported here, any difference may be due to inconsistencies between IOL calculation methodologies (optical vs ultrasound) . Our results were also in line with the results reported from prospective large studies [17, 18], however, it is worth noting that unlike these prospective studies, the group reported here had no eligibility criteria. The results of this article are more representative of the general cataract population, with multiple ocular and systemic co-morbidities. In a subgroup of these patients, where optical biometry was available bilaterally pre-operatively and where simple crystalline lens-IOL exchange was performed, we observed that predictability increased, surpassing results reported in the other studies .
Olsen et al. suggested a correction of the IOL calculation of left eye based on the outcomes of the right eye that may be beneficial. This correction could theoretically increase the predictability in the second eye (increasing the number of eyes within ±1.0 D) . In our study group, only 20 patients had a refraction that was greater than 1.0 D from target SE in their first operated eye. Examining these patients in detail, we observed that many patients had additional considerations that would have inhibited the adjustment of IOL power calculations. Finally, there were only 6 patients who based on the visual outcome of the first eye, could have considered adjustment to the IOL power calculation. In four of these six patients, the second eye achieved a refraction that was within ±1.0 D of the target (with no adjustment based on achieved refraction of the first eye), therefore there were two eyes that could have potentially benefitted from such an adjustment, and four that potentially could have resulted in a worse result due to any such adjustment. This suggests that IOL calculation adjustment based on the surgical outcome of the first eye is not advisable as a rule.
As a retrospective study, the available data is not directly comparable to those reported in prospective studies. For example, the preoperative measurements, the surgical techniques/surgeon, and the formulas chosen to calculate the implanted IOL are not uniform; these inconsistencies will inevitably influence the postoperative refraction. Moreover, there was no pre-screening of patients for inclusion or exclusion criteria, therefore the patients included here are likely more complex. On the other hand, a group of senile patients with a multitude of ocular and general comorbidities is more typical of general clinical case mix. Lastly, since the refraction was measured in the clinic, it can be assumed that a proportion of visual acuity measures were sub-optimal. These factors will impact the reproducibility of our results.
There is a potential bias in the patient selection, as only 110 patients had pre- and post-operative refraction available from the full consecutive series of 250 ISBCS surgeries. Unlike other countries, the operating policy in Switzerland is to return the patient immediately to the referring ophthalmologist, with only the more complicated cases and those in close proximity to the hospital returning to the tertiary centre for post-operative follow-up. This could potentially have influenced our results negatively, for example here we observed three conversions to ICCE intraoperatively, however in all the 250 patients notes reviewed, there were no additional cases of conversion to ICCE.
The formulas used here were the Haigis, SRKT and SRKII. It is likely that the universal choice (where available) of the Haigis formula for IOL power calculation, was suboptimal for longer or shorter eyes. In this study, there was significant difference in the improvement from pre- to post-operative BCVA, and it achieved refraction between the eyes calculated with Haigis and SRK formulae. However, this was likely due to the more complicated cases estimated with the ultrasound rather than any unsuitability of formula choice. There was no significant difference in the divergence from target SE with myopia, indicating that this was not a highly significant contributing factor.
This retrospective study demonstrates that ISBCS is a safe surgical option in terms of refraction. The good predictability of SE observed here, indicates that only in a small proportion of eyes could IOL calculation be beneficial between surgery of the first and second eye. This suggests that there is little merit to delaying the second surgery with this aim.
No author has a financial or proprietary interest in any material or method mentioned.
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