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    Lasers in Surgery and Medicine 37:144148 (2005)

    In Vivo Animal Trials With a ScanningCO2 Laser Osteotome

    Mikhail Ivanenko,1* Robert Sader,2,3 Said Afilal,1 Martin Werner,1 Martina Hartstock,3

    Christian von Hanisch,5 Stefan Milz,4 Wolf Erhardt,5 Hans-Florian Zeilhofer,2,3 and Peter Hering1,6

    1center of advanced european studies and research, 53175 Bonn, Germany2Division of Cranio-Maxillo-Facial Surgery, Clinic for Reconstructive Surgery, University Hospital,

    4031 Basel, Switzerland3Center of Advanced Studies in Cranio-Maxillo-Facial Surgery, Klinikum Rechts der Isar,

    University Hospital, 81675 Munich, Germany4Anatomical Institute, LMU University of Munich, 80336 Munich, Germany5Institute of Experimental Oncology and Therapy Research, Klinikum Rechts der Isar,

    University Hospital, 81675 Munich, Germany6Institute of Laser Medicine, University of Duesseldorf, 40225 Duesseldorf, Germany

    Background and Objectives: We report first results of

    animaltrialsusing an improved laser osteotomy technique.

    This technique allows effective bone cutting without the

    usual thermal tissue damage.

    Study Design/Materials and Methods: A comparative

    invivostudy onmandibles ofseven canines was donewitha

    mechanical saw and a CO2 laser based osteotome with a

    pulse duration of 80 microseconds. The laser incisions were

    performed in a multipass mode using a PC-controlled

    galvanic beam scanner and an assisting water spray.

    Results: A complete healing through a whole bony rear-

    rangement of the osteotomy gap with newly build lamellar

    Haversian bone was observed 22 days after the laseroperations under optimal irradiation conditions.

    Conclusions: An effective CO2 laser osteotomy without

    aggravating thermal side effects and healing delay is

    possible using the described irradiationtechnique. It allows

    an arbitrary cut geometry and may result in new advanta-

    geous bone surgery procedures. Lasers Surg. Med. 37:144

    148, 2005. 2005 Wiley-Liss, Inc.

    Key words: laser osteotomy; CO2 laser; animal trials

    INTRODUCTION

    Noncontact cutting of bone tissue without mechanical

    stress is an old dream of surgeons and a laser beam is an

    instinctive choice for this. It can be tightly focused and itsposition controlled electronically, so that precise narrow

    cuts with sophisticated geometry can be exactly planned

    and performed. Early attempts to cut bones with lasers

    have failed, however, because of strong thermal sideeffects

    in case of continuous wave (cw) and long-pulsed carbon

    dioxide (CO2) lasers [15] or very low cutting rate with

    excimer lasers [6 9]. One third of the compact bone tissue

    volume consists of hard minerals, which melt only above

    1,0008C [10,11]. The minerals are embedded on the other

    side in a sensitive collagen matrix, which will be charred

    after evaporation of the internal bone liquid and tempera-

    ture rise above 1508C. Living bone cells will be irreparably

    damaged at even lower temperatures. The common laser

    cutting, as known from material processing, is therefore

    unsuitable for bone surgery.

    A successful laser osteotomy has to be based on an effec-

    tive tissue ablation process, which does not takes place at

    very high temperatures and is much faster than the heat

    diffusion in the bone. Little thermal damage has been

    demonstrated, for example, in ex vivo studies with short

    CO2 laser pulse durations of 0.12 microseconds [1214].

    With an additional use of an air-water spray, the collateral

    thermal damage remains small even after prolonged tissue

    irradiation with such laser systems [15]. The ablation rateis, however, not high for such short pulses (510 mm/pulse,

    see refs. above).

    A relatively fast and clean tissue removal (up to 100mm/

    pulse) is possible with 100500 microseconds pulses of an

    Er:YAG laser at the wavelength of 2.94mm [1620]. A zone

    of thermal necrosis after Er:YAG laser incision in cortical

    bone is small, 2050 mm, according to [2123], so that

    healing observed in animal trials is similar to one after the

    use of a mechanical saw [22].

    Essential details of the bone ablation mechanism are

    probably similar for Er:YAG and CO2 lasers. At high in-

    tensity of the light pulse, the energy will be accumulated

    very quickly in the tissue and confined initially in the form

    of heat in a very thin absorption layer. That overheatedlayer explodes after high internal pressure is built up

    (ultimate tensile strength is about 1,000 bar for compact

    Robert Saders present address is University of Frankfurt,Klinikum fur Kiefer- und Plastische Gesichtschirurgie, Theodor-Stern-Kai 7, 60596 Frankfurt am Main, Germany.

    *Correspondence to: Dr. Mikhail Ivanenko, caesar, Ludwig-Erhard-Allee 2, 53175 Bonn, Germany.E-mail: [email protected]

    Accepted 20 May 2005Published online 29 August 2005 in Wiley InterScience(www.interscience.wiley.com).DOI 10.1002/lsm.20207

    2005 Wiley-Liss, Inc.

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    bone [24]). If the pressure built-up time is shorter than

    thermal relaxation time of the tissue, then most of the

    energy is consumed for this thermomechanical ablation

    process and removed from the tissue together with the hot

    ablation products. The water spray prevents tissue parch-

    ing and cools it additionally.

    A very promising way to avoid an accumulation of a restheat in the bone tissue is the multipass cutting. A fast

    repeated motion of the focused beam along a predefined

    cut trajectory can be realized conveniently using a PC-

    controlled galvanic beam scanner. We use this technique,

    since it allows an effectivecleanosteotomywith relatively

    long (about 100 microseconds) powerful CO2 laser pulses,

    at pulse repetition rates of several hundreds hertz and

    average laser power of several tens of watts [25]. For

    example, at the pulse energy of 68 mJ, every laser pulse

    removes up to 500 mm of compact tissue, so that at

    the average laser power of 40 W, we reach a cut rate of

    40 mm/minute for a 6-mm deep and 0.2-mm broad incision.

    Ex vivo incisions with such a laser system have previously

    been examined histologically [26]. The incisions were notaccompanied with carbonization. At thecut border, a 50-mm

    broad zone with in part empty cell lacunae and damaged

    osteocytes was presented. Intact osteocytes were, however,

    observed also very near to the cut surface. Polarized light

    microscopy showed no alterations in the inorganic struc-

    ture of the bone at the cut borders.

    In the present report, we describe first experience of

    in vivo application of this scanning laser osteotomy tech-

    nique and preliminary results of the operations on seven

    beagle canines. A complete report on the healing process

    and a detailed evaluation of the histological examinations

    will be given later.

    MATERIALS AND METHODS

    In the animaltrials, a prototype CO2 laser osteotome was

    used, which was developed by the center of advanced

    european studies and research (caesar) in Bonn. The

    laser osteotome is based on a RF-excited slab CO2 laser

    system with wavelength of 10.6 mm. Laser pulses of 80 mJ

    energyand of 80 microseconds duration aredeliveredto the

    application site through an articulated mirror-arm with an

    action radius of 1.5 m. The preoperative planning of

    the incision and control over all the functions of the

    osteotome are done with a PC. Exact positioning and

    motion of the beam is fulfilled with a PC-controlled galvanic

    X-Y-scanner. The scanner is mounted on a 5-axis mechan-ical adjustment unit, which is fixed at the operation stand

    near patient. The unit is used for initial manual focus

    positioning andcut orientation relative to thebone.Two red

    pilot beams are helped by the adjustment: one of them is

    collinearwith theCO2 laser beam; theotherone crosses it in

    the focus plane 159 mm below the scanner. The focusing

    optic provides a spot diameter of about 200mm on the tissue

    (1/e2 intensity level) and is protected against ablation

    products, blood, and water droplets with a pressurized

    airflow. Two fine spray-nozzles are mounted sideward to

    irrigate the incision continuously with isotonic NaCl solu-

    tion during the osteotomy (throughput about 3 ml/minute

    by every spray). The velocity of the beamfocus on the tissue

    in the multipass osteotomy was 480 mm/second.

    To assess the in vivo healing of bone in response to the

    laser osteotomy versus a conventional mechanical saw, we

    carried out a comparative study on the mandibles of seven

    beagle canines. The mechanical incisions were done with aOsseoscalpel micro saw with oscillating hub according to

    Sachse and blades of 0.35-mm thickness (Medicon eG,

    Tuttlingen, Germany).

    The canines were chosen, because their mandible con-

    tains, like in humans, a central artery with centripetal

    nutrition and homogenous spongiosa architecture. Fromits

    size, form, and hardness, the bone is comparable with the

    human one. Also the physiological reaction is similar, as

    secondary osteons can be detected during bone healing

    process.

    At the beginning of the study, four male and three

    female canines, from breeding facilities of the German

    National Research Center for Environment and Health,

    were between 2 and 8 years old and 12.519 kg heavy.The canines were accommodated in groups of up to three

    animals in 12 m2 large ventilated double boxes. Also an

    access to walking area was granted to them. The tempera-

    ture in the areas was 19238C and relative air humidity

    50 70%. The illumination changed automatically between

    day and night phases. The animals were inoculated,

    dewormed, and free from specific pathogens. Feeding took

    place once daily. There was no feeding 18 hours prior to the

    operation.

    The animal head was fixed during the operation with

    non-invasive headrest pad and tape. A 58 mm long laser

    incision and similar in geometry saw incision were made in

    pairs in the ventral aspect of the lower margin of both leftand right mandibles of each canine under general anesthe-

    sia. Thedistance between thelaser andsaw incision at each

    mandible side was about 10 mm. To avoid laser damage

    of the soft tissue, a metal shield was placed behind

    the bone during the irradiation. Two animal groups were

    built randomly to evaluate different irradiation settings. A

    special scan procedure [27] has been applied to dilate the

    laser cut and so to increase the cutting efficiency in the first

    group. The beamfocus was positioned 6 mmbelow the front

    bone surface in this case. The pulse repetition rate was

    400 Hz and the duration of the irradiation varied between

    45 and 90 seconds, depending on the cut length and

    thickness of mandibles (710 mm). In the second group,

    narrow cuts without the dilatation at the repetition rate of200 Hz and the focus position 2 mm below the bone surface

    were done. The cut duration was 60155 seconds. Seven

    laser incisions were done in every group: three canines

    belong to the first group, three to the second and one animal

    became dilated laser incision at the left mandible side

    and narrow incision at the right one (e.g., belongs to both

    groups). Both types of laser cutting procedure were at first

    carefully tested and optimized in ex vivo models. The used

    slit dilation technique allows to shorten the cut time about

    1.5 times for 8-mm thick mandible and to fulfill deeper

    incisions. The optimal positioning of the beam focus

    SCANNING CO2 LASER OSTEOTOME 145

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    beneath the bone surface brings further improvement in

    the cut rate. There was no difference between the two

    animal groups in relation to saw incisions.

    During the healing period, three different intra-

    vital stains were injected one after the other to mark

    the surface of new-bone growth for fluorescence micro-

    scopy. By this, after the animals were sacrificed 22 daysfollowing the surgery, the tissue response was examin-

    ed by polychrome sequential labeling and undecalcifi-

    ed paragon-stained ground sections. In addition, contact

    radiographic and micro-radiographic examinations were

    performed.

    The study met the requirements of the German law for

    the animal protection and was approved from the District

    Government of Upper Bavaria.

    RESULTS

    The laser osteotomy was in general unproblematic. Small

    bleeding did not prevent the cutting, while the blood was

    blown out of the incision with the spray and due to theexplosion-like action of repetitive laser pulses. Only a

    relativelystrong bleeding hasled once to the fail of thelaser

    procedure. In one other case, the lasing has been inter-

    rupted, because the canine twitched.

    In the first group, the dilated incisions, like in Figure 1a,

    with an entry width of 1 mm were performed. They were

    wedge-shaped, that is, the cut slit at the exit site was 3

    4 times narrower as at the entry site. By the very first

    incision, a carbonization at the medial end of the cut

    channel occurred. The thickness of the carbonized zone

    amounted to about 300 mm. It was caused by a strong back

    light reflection from the dorsal metal shield, which was

    positioned in direct contact with the jaw. To avoid this, weused in further operations, in both animal groups, metal

    plates with enhanced absorption and more homogeneous

    light scattering, which were positioned 2 3 mm apart from

    the bone. No carbonization was found in this case. As an

    interesting subsidiary result, it was observed that it did not

    come to a callus formation by the first laser group. It can be

    interpreted as a missing induction of a secondary fracture

    healing and associated with relatively large width of the

    dilated laser incisionsas compared to thesaw incisions with

    0.5 mm width.

    In the second group, we have reduced the laser cut width

    down to 0.20.3 mm at the entry side (Figs. 1b and 2a).

    The duration of the cuts increased up to 70%. There were

    no visible traces of tissue carbonization immediately afterthe irradiation. Theincision boarders were clean and plain.

    Twenty-two days post-operative, the histological speci-

    mens did not show any noticeable thermal damage at the

    border of the laser cuts (Fig. 2). A complete healing through

    a whole bony rearrangement of the osteotomy gap with

    newly build lamellar Haversian bone was observed in this

    laser group. Scanning acoustic microscopy of the laser

    incision (Fig. 1c) confirmed that the newly built bone pos-

    sessed elastomechanical properties, which are very similar

    to the neighboring bone tissue. Contrary to this, the sawed

    mandibles demonstrated persistent superficial defect at

    Fig. 1. a: Examples of 1-mm broad laser incisions in canine

    mandible (ex vivo) with a special cut slit dilatation procedure.

    b: Narrow (0.25 mm) in vivo incision in canine mandible with

    the scanning CO2 laser osteotome. c: Scanning acoustic

    microscopy of the laser incision (b) 22 days postoperative.

    Arrowsindicate the cut margins. The incision gap is completely

    bridged, its acoustic properties indicate that the newly built

    bone is similar to neighboring bone tissue.

    146 IVANENKO ET AL.

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    the impact site and steady delay of the healing process. The

    saw-osteotomy gaps were not completelybony bridged after

    the 22 days.

    DISCUSSION

    The results of these trials prove that effective osteotomywithout aggravating thermal side effects is possible with

    a pulsed CO2 laser under optimal irradiation conditions.

    These conditions include pulse duration of 80 microse-

    conds, use of an air-water spray, and fast multipass beam

    scanning along the cut trajectory. The scanning velocity

    hastobehighenoughtoshiftthebeamfocusonthetissueat

    half of its diameter or more in the time between consequent

    laser pulses. Such a multipass cutting cannot be done per

    hand because of the fastness and very high demands on the

    reproducibility of the beam focus position and beam orien-

    tation at the every pass.

    In most other in vivo experiments with CO2-lasers re-

    ported so far, carbonization and an extended necrosis zone

    in the treated bones have been described. For example

    Horch et al. stated early that the CO2 laser osteotomy is not

    promising because of the collateral thermal damage [4,28].

    They worked with a continuous cw CO2 laser with 34 W of

    average power. A gas jet has been used for cooling. Severecarbonization has led to an impairment of the healing

    process of more than 12weeks. The bad results of these and

    other authors [15] were responsible for the fact that most

    research groups were looking for a new laser system for

    osteotomy. Actually, more understanding of the ablation

    process and careful optimization of the irradiation para-

    meters were necessary. By this, the average laser power

    used before was quite similar to that we used now. The

    reported irradiation technique provides, however, more

    effective ablation and prevents accumulation of the rest

    heat in the tissue.

    The experiences of this trial also show that further

    improvements are necessary to grant an acceptance of the

    laser in the field of osteotomy. One important goal will be aprevention of the laser action on tissue behind the bone. In

    the present study, it was done with a small shielding metal

    plate. An optimal way, however, is recognition of a bone-

    soft-tissue interface by changes in the acoustical signal

    [29,30] or by changes in optical emission accompanying the

    ablation process. Theentire laser systemhas also to become

    more surgeon-friendly and compact. Special surgeon-

    oriented software and combination with robotic or haptic

    guidance and computer-assisted navigation will make the

    positioning of the beam on the tissue much easier. The

    absence of a tactile feedback with the present laser tech-

    nique makes this especially important. If these improve-

    ments are done, the laser osteotomy may result in new

    Fig. 2. Typical histological slices of (a) laser incision (10) and

    (b) saw osteotomy (2.5). Canine 4, right mandible side,

    undecalcified, paragon-stained.

    Fig. 3. An example of a self-stabilizing laser incision in

    compact bone tissue (ex vivo).

    SCANNING CO2 LASER OSTEOTOME 147

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    advanced bone surgery techniques, for example, a self-

    stabilizing osteotomy in Figure 3. Such a complicated and

    precise incision would never be possible with a hand-held

    system.

    REFERENCES1. Clayman L, Fuller T, Beckman H. Healing of continuous-

    wave and rapid superpulsed, carbon dioxide, laser-inducedbone defects. J Oral Surg 1978;36(12):932937.

    2. Small IA, Osborn TP, Fuller T, Hussain M, Kobernick S.Observations of carbon dioxide laser and bone bur in theosteotomy of the rabbit tibia. J Oral Surg 1979;37(3):159166.

    3. Tauber C, Farine I, Horoszowski H, Gassner S. Fracturehealing in rabbits after osteotomy using the CO2 laser. ActaOrthop Scand 1979;50(4):385390.

    4. Horch HH, Keiditsch E. Morphological findings on the tissuelesion and bone regeneration after laser osteotomy. DtschZahnarztl Z 1980;35(1):2224.

    5. Gertzbein SD, deDemeter D, Cruickshank B, Kapasouri A.The effect of laser osteotomy on bone healing. Lasers SurgMed 1981;1(4):361373.

    6. Lustmann J, Ulmansky M, Fuxbrunner A, Lewis A. 193 nmexcimer laser ablation of bone. Lasers Surg Med 1991;11(1):5157.

    7. Yow L, Nelson JS, Berns MW. Ablation of bone andpolymethylmethacrylate by an XeCl (308 nm) excimer laser.Lasers Surg Med 1989;9(2):141147.

    8. Sarkar R, Fabian RL, Nuss RC, Puliafito CA. Plasma-mediated excimer laser ablation of bone: A potential micro-surgical tool. Am J Otolaryngol 1989;10(2):7684.

    9. Dressel M, Jahn R, Neu W, Jungbluth KH. Studies in fiberguided excimer laser surgery for cutting and drilling boneand meniscus. Lasers Surg Med 1991;11(6):569579.

    10. Corcia JT, Moody WE. Thermal-analysis of human dentalenamel. J Dent Res 1974;53(3):571580.

    11. Newesely H. High temperature behaviour of hydroxy- andfluorapatite. Crystalchemical implications of laser effects ondental enamel. J Oral Rehabil 1977;4(1):97104.

    12. Forrer M, Frenz M, Romano V, Altermatt H, Weber H,

    Silenok A, Istomyn M, Konov V. Bone-ablation mechanismusing CO2 lasers of different pulse duration and wavelength.

    Appl Phys B 1993;56:104 112.13. Ertl TP, Mueller GJ. Hard-tissue ablation with pulsed CO2

    lasers. Proc SPIE 1993;1880:176181.14. Ivanenko MM, Hering P. Wet bone ablation with mechani-

    cally Q-switched high-repetition-rate CO2 laser. Appl Phys1998;B 67:395397.

    15. Ivanenko MM, Fahimi-Weber S, Mitra T, Wierich W, HeringP. Bone tissue ablation with sub-ms pulses of a Q-switch CO2laser: Histological examination of thermal side effects. LasersMed Sci 2002;17(4):258264.

    16. Bonner R, Smith P, Leon M, Esterowitz L, Strom M, Levin K,Tran D. Quantification of tissue effects due to a pulsedEr:YAG laser at 2.94 mm with beam delivery in a wet field viazirconium fluoride fibers. Proc SPIE 1986;713:25.

    17. Nuss RC, Fabian RL, Sarkar R, Puliafito CA. Infrared laserbone ablation. Lasers Surg Med 1988;8(4):381391.

    18. Nelson JS, Yow L, Liaw LH, Macleay L, Zavar RB, OrensteinA, Wright WH, Andrews JJ, Berns MW. Ablation of bone andmethacrylate by a prototype mid-infrared erbium:YAG laser.Laser Surg Med 1988;8(5):494500.

    19. Waisn J, Jr., Deuiscn IP. Er:YAG laser ablation of tissue:Measurement of ablation rates. Lasers Surg Med 1989;9(4):327337.

    20. Hibst R, Keller U. Experimental studies of the applicationof the Er:YAG laser on dental hard substances: I. Measure-ment of the ablation rate. Lasers Surg Med 1989;9:338344.

    21. Nelson JS, Orenstein A, Liaw LH, Berns MW. Mid-infrared erbium:YAG laser ablation of bone: The effect oflaser osteotomy on bone healing. Lasers Surg Med 1989;9(4):362374.

    22. Scholz C. Neue Verfahren der Bearbeitung von Hartgewebein der Medizin mit dem Laser. In: Muller G, editor. Advancesin Laser Medicine, Vol. 7. Landsberg, Lech: Ecomed. 1992.203p.

    23. Kautzky M, Susani M, Leukauf M, Schenk P. [Holmium:YAGand erbium:YAG infrared laser osteotomy]. Langenbecks

    Arch Chir 1992;377(5):300 304.24. Duck FA. Physical properties of tissue. London: Academic

    Press. 1990.25. Afilal S, Ivanenko M, Werner M, Hering P. Osteotomie mit

    80 ms CO2-Laserpulsen. Fortschritt-Berichte VDI 2003;17(231 Biotechnik/Medizintechnik):164169.

    26. Frentzen M, Gotz W, Ivanenko M, Afilal S, Werner M,Hering P. Osteotomy with 80-ms CO2 laser pulses-histologicalresults. Laser Med Sci 2003;18(2):119124.

    27. Hering P, Mitra T, Ivanenko M; Laserschneiden. PatentDE10133341A1; 2001.

    28. Horch HH. Laser-Osteotomie. Habilitationsschrift. Munich;1978.

    29. Rupprecht S, Tangermann-Gerk K, Wiltfang J, Neukam FW,Schlegel A. Sensor-based laser ablation for tissue specificcutting: An experimental study. Lasers Med Sci 2004;19(2):8188.

    30. Ratzer-Scheibe A, Klasing M, Werner M, Ivanenko M,Hering P. Akustische Kontrolle der Knochenablation mitkurzgepulstem CO2-Laser. Aktuelle Methoden der Laser-undMedizintechnik. Berlin: VDE Verlag; 2005. pp 281286.

    148 IVANENKO ET AL.