Secondary Logo

Journal Logo


Comparison of Nagahara phaco-chop and stop-and-chop phacoemulsification nucleotomy techniques

Can, Iİzzet MD*; Takmaz, Tamer MD; Çakici, Ferda MD; Özgül, Meltem MD

Author Information
Journal of Cataract & Refractive Surgery: March 2004 - Volume 30 - Issue 3 - p 663-668
doi: 10.1016/j.jcrs.2003.06.006
  • Free

Many variations on phacoemulsification techniques have been described.1 The aim of all the techniques is to reduce the stress on the zonules and decrease the total ultrasound time and ultrasound energy used during nucleus emulsification. A method that protects intraocular tissues, especially the corneal endothelium, from surgical damage and has minimal complications rates is the objective. Among the techniques, stop-and-chop and phaco-chop are the most popular. The nucleus is divided mechanically into small fragments with a special instrument known as a chopper in both techniques. The main difference between the 2 is that at the beginning of the stop-and-chop procedure, ultrasound energy is used to produce a central groove. The cavity, which is produced by using more ultrasound power, helps the surgeon split the hard posterior plate, facilitating the procedure.

Only a few articles compare the phaco-chop and stop-and chop techniques using several parameters. In this study, we compared the efficiency and safety of the 2 techniques prospectively.

Patients and Methods

This prospective randomized study comprised 70 eyes of 70 patients with cataract who were randomly assigned (by a coin flip) to have phacoemulsification using the Nagahara phaco-chop technique or the stop-and-chop technique. Visual acuity, intraocular pressure, nuclear density, and ultrasound central corneal pachymetry were evaluated preoperatively. Nuclear density was graded by color using slitlamp biomicroscopy: 1 = gray or green–yellow, 2 = yellow, 3 = amber, 4 = brown–black.2 Exclusion criteria were corneal disease or opacity, glaucoma, uveitis, pupillary dilation problem, and previous ocular trauma or surgery.

Phacoemulsification was performed by the same surgeon (Iİ.C.), who was experienced in both techniques, with the Series 20000® Legacy® phacoemulsification unit (Alcon Laboratories). In all cases, surgery began with a clear corneal incision made with a 3.0 slit knife at the 9 o'clock meridian in right eyes and the 11 o'clock meridian in left eyes. Two side-port incisions were then made with the 20-gauge MVR knife 90 degrees from the main incision. Following the injection of chondroitin sulfate 4%–sodium hyaluronate 3% (Viscoat®) into the anterior chamber, a capsulorhexis was performed. Hydrodissection was done with a 27-gauge flat cannula, and phacoemulsification was performed. In all cases, a 0.9 mm flared, 30-degree, ABS Kelman microtip was used. The standard parameters used during phacoemulsification to create a groove were memory 1, vacuum 50 mm Hg, aspiration flow rate (AFR) 24 cc/min, phaco power 75%, bottle height 78 cm; and to perform quadrant emulsification, memory 2, vacuum 350 mm Hg, AFR 30 cc/min, phaco power 60%, and bottle height 110 cm.

In Group 1 (Nagahara phaco chop), phacoemulsification began with quadrant-removal parameters (memory 2). After the superficial cortex and epinucleus were aspirated, the phaco tip was buried in the center of the endonucleus with high vacuum with the footpedal (FP) in position 3. While the footpedal was in position 2, the Fine-Nagahara phaco chopper (Rhein Medical) was brought through the side-port incision and the equator of endonucleus was engaged by the chopper under the lower edge of the capsulorhexis and pulled toward the phaco tip. The 2 instruments were then separated laterally to produce a complete fracture of the nucleus (Figure 1). This process continued for both nuclear halves, and then the small fragments were emulsified and aspirated with phaco power.

Figure 1.
Figure 1.:
(Can) Nagahara phaco-chop nucleotomy technique. A: Burying the phaco tip in the center of the endonucleus and engaging the equator of the endonucleus with the chopper under the lower edge of the capsulorhexis. B, C: Pulling the chopper toward the phaco tip. D, E: Separating the phaco tip and the chopper laterally to produce a complete fracture of the nucleus.

In Group 2 (stop and chop), phacoemulsification began with groove-forming parameters (memory 1). After a groove that was 90% of the nucleus thickness was created, the nucleus was split with the Rosen chopper (Katena Products, Inc.) (Figure 2). After the nucleus was split, the phacoemulsification unit was set at memory 2 and the nuclear halves were cut into fragments and then emulsified and aspirated as in the phaco-chop group. Epinucleus and cortex removal were performed with bimanual infusion/aspiration (I/A) cannulas (+500 mm Hg vacuum and 25 cc/min AFR) in both groups. After this, sodium hyaluronate 1% (Healon®) was injected into the anterior chamber, the incision was enlarged to 5.5 mm, and an intraocular lens (IOL) (Crystal type-05 made of poly[methyl methacrylate] with a 5.5 mm optic and 12.0 mm overall length [Alcon]) was inserted in the capsular bag. The incision site was closed with a 10-0 monofilament single suture. The ophthalmic viscosurgical device was removed from the anterior chamber by I/A. After the side ports were closed by stromal hydration, the procedure was completed.

Figure 2.
Figure 2.:
(Can) Stop-and-chop nucleotomy technique. A: Aspirating the superficial cortex and epinucleus. B, C: Creating a groove. D, E: Nucleus splitting with the help of the chopper.

All procedures were uneventful. Intraoperative parameters—phaco time (minute), mean phaco power (average power) (%), and effective phaco time (calculated time required if 100% power had been used throughout)—were recorded. The effective phaco time was calculated with the following formula: phaco time (seconds) × mean phaco power (average power)/100.

The best corrected visual acuity, time to achieve best visual acuity, pachymetry, corneal thickness increase according to the preoperative values, and time to return to the preoperative values (±20 μm of the preoperative value) were recorded postoperatively. Patients were examined daily in the first week, at an interval of 2 or 3 days in the first month, and then every month. Two of us (T.T., M.Ö.) were masked to the randomization while performing the postoperative examinations.

The chi-square test and the independent-samples t test were used to compare the groups for statistical significance. All tests were 2-sided, and P values of 0.05 or less were considered statistically significant.


Seventy patients were evaluated in 2 groups of 35 each. The characteristics of the patients in both groups are shown in Table 1. There was no statistically significant between-group difference in any characteristic.

Table 1
Table 1:
Patients' characteristics.

All between-group differences in intraoperative and postoperative parameters except mean postoperative visual acuity were significant (Table 2). The results show that the postoperative healing period was shorter in the phaco-chop group.

Table 2
Table 2:
Intraoperative and postoperative parameters in the 2 groups.


Nagahara introduced the phaco-chop technique concept in 1993 (K. Nagahara, MD, “Phaco Chop,” presented as a video at the ASCRS Symposium on Cataract, IOL and Refractive Surgery, Seattle, Washington, USA, May 1993; “Phaco-Chop Technique Eliminates Central Sculpting and Allows Faster, Safer Phaco,” Ocular Surgery News, international edition, October 1993, pages 12–13). The phaco-chop procedure is a nucleus-separation process, which is performed in the natural cleavage planes of the lens. The human lens fibers are arranged as parallel lamellae, oriented much like the grain in a piece of wood. A natural cleavage plane occurs when the chopping forces are parallel to these lamellae. Nucleus separation is performed after the nucleus is pressed between the chopper and the phaco tip and the chopper is pulled toward the phaco tip.

The stop-and-chop technique introduced by Koch3 begins by creating a central groove, which provides space and facilitates separation of the posterior plate. After this, the cracking procedure is stopped and chopping of the remaining parts begins. The creation of a central groove at the beginning of the procedure is the main difference between phaco chop and stop and chop. During the creation of the groove, the cutting process is directed perpendicular to the lens lamellae, which resembles sawing through a log lying on its side. It requires multiple back-and-forth passes. In the phaco-chop procedure, a process that resembles chopping an upright log with an axe is performed. One strike, parallel to the grain, splits the log in half. Less phaco power and phaco time are needed, and stress on the zonules is minimized.4

A force to hold the nucleus, similar to a vise holding a piece of wood, is needed while the nucleus is separated. This force is the zonules and lens capsule in the stop-and-chop technique and the phaco tip buried in the nucleus in the phaco-chop technique. Centrifugal movements in the phaco-chop technique is farther from the zonules, whereas creating the groove in the stop-and-chop technique increases the stress on the zonules with movement toward them. As a result, the nucleus-separation process is done manually instead of by ultrasound energy as in the phaco-chop technique, which results in less damage to intraocular tissues.

Phacoemulsification has additional potential risks for corneal endothelial cell damage related with to ultrasound compared with extracapsular cataract extraction.5–8 These factors are mechanical (damage caused by turbulence); air bubble; release of free radicals; greater irrigation fluid volume; and direct trauma from surgical instruments, lens fragments, and the IOL.9–14 Hayashi and coauthors15 defined advanced age, small pupils, hard and large nucleus, greater infusion volume, and greater total ultrasound energy as the main risk factors for corneal endothelial damage during phacoemulsification. It is important to shorten the phaco time and reduce the phaco power to protect the corneal endothelium in phacoemulsification. We compared 2 techniques according to these parameters in this study. Our results showed that phaco time, phaco power, and effective phaco time were significantly lower in the phaco-chop group. In the postoperative follow-up period, corneal edema was significantly lower and the healing period (time to achieve best corrected visual acuity and time to return to the preoperative pachymetry values) was also shorter in this group.

Studies comparing the 2 techniques are rare. In a study by Vajpayee et al.,16 with 20 patients in each group, there were no significant differences between the phaco-chop and stop-and-chop groups in effective phaco time and endothelial loss; there were no data showing rehabilitation time. In a study of the divide-and-conquer and phaco-chop techniques by Wong and coauthors,17 there were significant between-group differences in phaco time and power in favor of the phaco-chop group. The authors stated there was no difference in complications, but there were no data showing with which technique visual rehabilitation was faster.

The corneal endothelial cell density and irrigation fluid volume used during surgery should be measured and the number of patients increased to have more specific results in our study. Since no complication was seen during the procedures, the results showed the negative effects of phaco time and power and also showed that these parameters affect the healing time directly. Phaco-chop technique was superior to the stop-and-chop technique as it decreased the phaco parameters and shortened the postoperative healing period.


1. Buratto L. Techniques of phacoemulsification. In: Buratto L, ed, Phacoemulsification: Principles and Techniques. Thorofare, NJ, Slack 1998; 71-170
2. Jaffe NS, Jaffe MS, Jaffe GF. Cataract Surgery and Its Complications, 5th ed. St Louis, MO, CV Mosby 1990; 264
3. Koch PS, Katzen LE. Stop and chop phacoemulsification. J Cataract Refract Surg 1994; 20:566-570
4. Chang DF. Converting to phaco chop: Why? Which technique? How? Ophthalmic Pract 1999; 17:202-210
5. Kreisler KR, Mortenson SW, Mamalis N. Endothelial cell loss following “modern” phacoemulsification by a senior resident. Ophthalmic Surg 1992; 23:158-160
6. Werblin TP. Long-term endothelial cell loss following phacoemulsification: model for evaluating endothelial damage after intraocular surgery. Refract Corneal Surg 1993; 9:29-35
7. Hayashi K, Nakao F, Hayashi F. Corneal endothelial cell loss after phacoemulsification using nuclear cracking procedures. J Cataract Refract Surg 1994; 20:44-47
8. Dçíaz-Valle D, Bençítez del Castillo Sánchez JM, Castillo A, et al. Endothelial damage with cataract surgery techniques. J Cataract Refract Surg 1998; 24:951-955
9. Olson LE, Marshall J, Rice NSC, Andrews R. Effects of ultrasound on the corneal endothelium: I. The acute lesion. Br J Ophthalmol 1978; 62:134-144
10. Dick HB, Kohnen T, Jacobi FK, Jacobi KW. Long-term endothelial cell loss following phacoemulsification through a temporal clear corneal incision. J Cataract Refract Surg 1996; 22:63-71
11. Beesley RD, Olson RJ, Brady SE. The effects of prolonged phacoemulsification time on the corneal endothelium. Ann Ophthalmol 1986; 18:216-219; 222
12. Krey HF. Ultrasonic turbulences at the phacoemulsification tip. J Cataract Refract Surg 1989; 15:343-344
13. Craig MT, Olson RJ, Mamalis N, Olson RJ. Air bubble endothelial damage during phacoemulsification in human eye bank eyes: the protective effects of Healon and Viscoat. J Cataract Refract Surg 1990; 16:597-602
14. Binder PS, Sternberg H, Wickham MG, Worthen DM. Corneal endothelial damage associated with phacoemulsification. Am J Ophthalmol 1976; 82:48-54
15. Hayashi K, Hayashi H, Nakao F, Hayashi F. Risk factors for corneal endothelial injury during phacoemulsification. J Cataract Refract Surg 1996; 22:1079-1084
16. Vajpayee RB, Kumar A, Dada T, et al. Phaco-chop versus stop-and-chop nucleotomy for phacoemulsification. J Cataract Refract Surg 2000; 26:1638-1641
17. Wong T, Hingorani M, Lee V. Phacoemulsification time and power requirements in phaco chop and divide and conquer nucleofractis techniques. J Cataract Refract Surg 2000; 26:1374-1378
© 2004 by Lippincott Williams & Wilkins, Inc.