Postoperative pain and risk of infection are the main concerns with surgery. Most studies testing postoperative pain are level 5 (case report) evidence or animal studies. There are no randomized studies on the matter, leading to prevalent skepticism in the medical and dental communities about whether the surgical technique used relates to postoperative pain. However, the plethora of case studies and the ever-increasing amount of anecdotal reports in the field of patient pain perception following CO2 laser surgery indicate that there is a basis for claiming reduced postoperative pain. This paper summarizes some of the existing research comparing postoperative pain and healing following CO2 laser surgery with conventional blade or scissors.
Healing, Myofibroblasts and Post- Operative Wound Contraction
Studies of the soft tissue response to CO2 laser surgery[1-25] have found reduced wound contraction (scarring) and delayed wound healing compared to scalpel surgeries.
Slower healing of laser wounds (during inflammation and proliferation stages[1,3,10]) has been attributed to the narrow zone of tissue denaturation at the margins and the coagulation of some connective tissue elements, and also to the temporary postponement of inflammation, phagocytic resorption, collagen production and re-epithelization in the early stages of repair. Since CO2 laser wounds are not as contracted as scalpel wounds, the larger surface area requires more time to re-epithelialize because cells have to migrate over a larger area. Zeinoun et al. reported a 3-day delay in re-epithelialization in CO2 laser wounds (the process was completed in 10 days in laser wounds vs. 7-days in scalpel wounds). Sanders et al. compared collagen thermal damage in pulsed and continuous-wave CO2 laser incisions and concluded that pulsing can reduce delay in healing. It has also been shown that delays in the early stages of the CO2 laser wound healing are normally overcome at later stages and do not appear to influence long-term outcomes. Minimizing thermal damage through lower power settings and active tissue cooling helps minimize delayed healing.[9,20,22-25]
Wound contraction and scarring during the remodeling phase of healing following CO2 laser surgery are reduced compared to scalpel surgery.[2,10,11] Myofibroblasts are stromal cells derived from fibroblasts and possess contractile features in common with smooth muscle cells. They are key factors in fibromatosis and granulation tissue contraction during wound healing.[26-28] Myofibroblasts have a specific capacity of developing cell-to-cell and cell-to-matrix connections thus acting on the whole tissue as a contractile network. It has been shown that reduced wound contraction correlates to the reduced number of myofibroblasts and connective tissue trauma.[30,31]
Zeinoun and colleagues analyzed the expression of myofibroblasts in healing CO2 laser excisions and control excisions made by scalpel in the dorsal tongue mucosa of 144 rats. This study found that myofibroblasts appeared and disappeared slower, and in significantly fewer numbers, in CO2 laser wounds. The lack of contractile myofibroblasts is suggested to be the reason for the minimal degree of contraction in healing CO2 laser excision wounds. Similar results were found by Fisher et al. and De Freitas et al.
Luomanen et al. compared healing scalpel wounds versus CO2 laser wounds by looking at the extracellular matrix (ECM) components (such as laminin, Type IV collagen, Type III collagen, and fibronectin) in laser-treated rat tongue mucosa. The study found that laser treatment caused extensive destruction of both epithelial and stromal cells but left much of the connective tissue matrix relatively intact. The regenerative processes with concomitant re-epithelialization occurred slower in laser-treated wounds. This study also noted that CO2 laser wounds differ drastically from burn wounds, which are characterized by the destruction of the connective tissue matrix, which results in notably more granulation tissue formation and wound contraction than is observed with the healing of CO2 laser wounds.[32-35] The study concluded that relative resistance of the ECM proteins to CO2 laser irradiation may account, at least partially, for the lack of contraction and scarring frequently observed in laser-treated areas. This may be another, less discussed reason for a less notable contraction of CO2 laser wound, in addition to the smaller number of myofibroblasts at the laser surgical site.
To summarize, the following generalizations can be made based on the existing research about CO2 laser wound healing and myofibroblasts that contract tissue during wound repair:[8,27,28]
- CO2 laser wounds have fewer myofibroblasts than scalpel wounds;[1,10,11]
- CO2 laser wounds display less contractility than scalpel wounds;[1,10,11]
- CO2 laser-wound healing results in less scarring;[1,5,10]
Post-Operative Pain, Healing and Return to Function
Many studies have reported lower levels of pain and discomfort following CO2 laser surgery in oral soft tissues, compared with scalpel surgery.[1,14,15,36,37]
In Haytac et al. 40 patients in need of frenectomy were randomly assigned to have treatment either with a scalpel or with a SuperPulse CO2 laser. The surgical wounds were left to heal by secondary intention. The postoperative pain and functional complications of each patient were recorded on days one and seven (a visual analog scale – VAS – was utilized). The CO2 laser frenectomy patients reported significantly less postoperative pain and fewer functional complications (e.g. speaking and chewing) and required fewer analgesics in comparison with scalpel group patients. The study concluded that “when used correctly, the CO2 laser offers a safe, effective, acceptable, and impressive alternative for frenectomy operations.”
In López-Jornet et al. study, 48 patients with oral leukoplakia were randomly assigned to receive treatment either with conventional scalpel surgery or with a CO2 laser. The site of scalpel surgery was sutured, while the laser wound was left to heal by secondary intention. A visual analog scale (VAS) was utilized to rate the intensity of pain and swelling at different postoperative time points. The patients reported that pain and swelling following scalpel surgery exceeded those with the CO2 laser (there were statistically significant differences between the two techniques during the first three days after surgery (p-value for related samples at 12 hours, 1, 2, and 3 days post-op ≤ 0.05). After that, the pain gradually decreased over one week in both groups. The study concluded CO2 laser surgery caused minimal pain and swelling and it may be an alternative to scalpel surgery in treating oral leukoplakia.
In another study, the CO2 laser was evaluated on 27 patients who underwent soft tissue pre-prosthetic surgery, including frenectomy, tuberosity reduction, hyperplasia removal, and sulcus deepening.4 The author pointed out that “it seems likely that discomfort is less after laser surgery than by more conventional techniques and it is definitely less than discomfort after conventional surgery with a secondary epithelialization technique. Swelling and edema were virtually nonexistent after laser surgery”. There was minimal swelling. The pain was moderate. A vestibular extension was created with mild-to-moderate discomfort, controlled with medium-strength analgesics. “For frenectomies, the main advantages appear to be speed and a clean, bloodless field… For palatal hyperplasia and soft tissue tuberosity reduction, the laser appears to be faster and cleaner with less discomfort than is normally associated with this form of surgery by other techniques”. A third of the patients did not need analgesics. Reduced wound contraction was observed.
Niccoli-Filho et al. described 15 cases where extensive epulis excision with maxillary or mandibular vestbuloplasty were carried out with a CO2 laser. Patients reported minimal discomfort during the first 24 hours after the surgery, in stark contrast with conventional surgery experience with complaints of significant pain, sialorrhaea, dysphonia, and dysphagia. For scalpel surgery patients, postoperative edema interfered with oral hygiene, further impairing healing. Overall, the study found that removal of epulis with the CO2 laser resulted in numerous notable improvements over conventional surgery, such as convenient removal of mucosa, lack of bleeding or need for sutures, and minimal postoperative pain and edema. In addition, the sites healed quickly, without complications, and both the esthetic and functional outcomes were excellent – all of the above allowed for more rapid placement of the final prosthesis.
Wlodawsky and Strauss presented several clinical cases showing CO2 laser applications in intraoral surgery, such as mucocele excision, sialolithotomy, frenectomy, gingival hyperplasia removal, vestibuloplasty, aphthous ulcer treatment, leukoplakia treatment, and others. One of their conclusions was that “the low morbidity and minimal pain generally associated with laser ablation makes it a valuable tool in the management of premalignant mucosal lesions.” Similarly, Mason et al. found low morbidity and minimal pain to be important post-operative outcomes following the removal of gingival fibromatosis. After the CO2 laser procedure, where the entire mouth was treated, no pressure packs were used and no sutures were placed. “Postoperative healing progressed with little discomfort or swelling and satisfactory improvement in gingival contour and aesthetics was achieved.”
In van der Hem et al., 39 oral lichen planus lesions in 21 patients were treated with a CO2 laser. Although this study was retrospective with no control group, the researchers pointed out the reduction in pain was an interesting result.
Ishii et al. assessed the usefulness of CO2 laser treatment of oral leukoplakia lesions in 116 patients. The study found laser excision suitable for leukoplakia lesions on non-keratinized epithelia, while laser vaporization can be used for the gingival cases of non-homogenous type leukoplakia. The authors reported damage to adjacent tissue is minimal (which reduces acute inflammatory reaction and postoperative pain, swelling, edema or infection); wound healing is excellent due to the limited contraction and scarring; and typically it is possible to leave the surgical defect to heal by secondary intention, which keeps functional disorders to a minimum because regeneration can occur without leaving postoperative cicatricial contractures. The study concluded CO2 laser surgery was an excellent procedure for the management of oral leukoplakia which can prevent recurrence, malignant transformation, and postoperative dysfunction.
To summarize, there are numerous reports of reduced postoperative pain, although not always predictable, following CO2 laser surgery.[4,11,15,38-42] It was speculated to be the result of microcoagulation or “sealing” of nerve endings while severed nerve endings in scalpel wounds cannot anastomose. It was also claimed that neuromas do not form.[36,43] However, Basu found neuronal hyperplasia and traumatic neuroma in all wounds. He rendered Carruth’s hypothesis about “sealing” of nerve endings postoperatively unlikely and suggested that some other mechanism might be involved. The “nerve-sealing” theory also contradicts later research showing that the number of intact peripheral nerve structures in laser-treated sites was similar to the numbers in cautery- and scalpel-treated sites. This, again, leaves the reasons for reduced postoperative pain unclear. Another proposed explanation is based on the finding that the CO2 laser induces a spinal inhibitory effect via peripheral nerve stimulation, in other words, the activation of peripheral inhibitory nerves decreases neural signals from the spine to the cortex (gate theory). Contrary to this, Tran et al. documented a central somatosensory cortical effect of peripheral dermal stimulation with the CO2 laser. Decreased pain is sometimes attributed to reduced mechanical trauma to the tissue (Gama et al., and others). In sum, while several possible explanations have been proposed over the years, the exact mechanism that is accountable for reduced postoperative pain in CO2 laser wounds compared to scalpel wounds is still unknown.
Recent Animal Studies on Post- and Intra-Operative Pain and Discomfort
Carreira et al. compared postoperative pain and healing after CO2 laser surgery and scalpel surgery. Laser group patients exhibited lower pain levels and higher post-op comfort than those in the scalpel group. The CO2 laser incisions were associated with lower white blood cell count (indicating reduced inflammatory response) and minor tissue trauma, because the endothelial wall does not incur as much injury as with scalpel incisions, thus decreasing the plasmatic protein total and serum albumin extravasation levels, and promoting healing.
Carreira et al. studied intra-operative hemodynamic responses (heart rate, various blood pressure parameters) in patients under general anesthesia and concluded that CO2 laser was perceived as less painful than scalpel surgery. By sealing blood and lymphatic vessels and nerve endings, laser surgery significantly reduces the local inflammatory response, leading to lower levels of glucocorticoids, epinephrine and norepinephrine, lowering the pain level.
Silva et al. compared the plasma C-Reactive Protein (CRP) level variation between CO2 laser surgery and scalpel surgery patients. CRP is an acute (inflammation) phase response protein. Peri-operatively, plasma CRP levels can help to monitor the level of tissue inflammation – the level of CRP correlates with the surgical trauma intensity in the patient. For CO2 laser surgery patients, lower plasma CRP levels were registered than for scalpel group patients, i.e. the CO2 laser in surgery was associated with lower inflammatory response, promoting a more comfortable peri-operative period for the patient.
Thus, all three above studies have shown that CO2 laser incisions are associated with reduced inflammatory response, less postoperative pain, and better healing.
Several studies have found the reduced presence of contractile myofibroblasts – cells accountable for postoperative scarring – in CO2 laser surgical wounds when compared to scalpel surgery. The authors of this review believe both the reduced production of myofibroblasts and reduced post-operative pain can be partially explained by the optimal depth of coagulation/hemostasis on CO2 laser surgical margins. Decreased extravasation of blood and lymphatic fluids into the CO2 laser wound space impedes the release of inflammatory mediators. This results in less edema around the wound than following conventional surgery and delayed minimal inflammatory response.[1,48] It may also account for the reduced immediate postoperative pain after CO2 laser surgery. Despite the abundant research and anecdotal reports regarding diminished pain following CO2 laser surgery, the exact mechanism behind it remains to be explained.
About the Authors
Anna (Anya) Glazkova, PhD, is the clinical continuing education coordinator at LightScalpel, LLC.
Peter Vitruk, PhD, MInstP, CPhys, is a member of The Institute of Physics, United Kingdom, and a founder of the American Laser Study Club, and LightScalpel, LLC, both in the United States. Dr. Vitruk can be reached at 1-866-589-2722 or email@example.com.
- Fisher SE, et al. A comparative histological study of wound healing following CO2 laser and conventional surgical excision of canine buccal mucosa. Arch. Oral Biol. 1983;28(4):287-291.
- Fisher SE, et al. The effects of the carbon dioxide surgical laser on oral tissues. Brit J Oral Maxillofac Surg. 1984;22:414-25.
- Basu MK, et al. Wound healing following partial glossectomy using the CO2 laser, diathermy and scalpel: a histological study in rats. J Laryngol Otol. 1988;102(4):322-7.
- Pogrel MA. The carbon dioxide laser in soft tissue preprosthetic surgery. J Prosthet Dent. 1989; 61:203-8.
- Luomanen M, et al. Extracellular matrix in healing CO2 laser incision wound. J Oral Pathol. 1987;16:322-31.
- Luomanen M. A comparative study of healing of laser and scalpel incision wounds in rat oral mucosa. Scand J Dent Res. 1987 Feb;95(1):65-73.
- Luomanen M, et al. Healing of laser and scalpel incision wounds of rat tongue mucosa as studied with cytokeratin antibodies. J Oral Pathol. 1987 Mar;16(3):139-44.
- Luomanen M, et al. Healing of rat mouth mucosa after irradiation with CO2, Nd:YAG, and CO2-Nd:YAG combination lasers. Scand J Dent Res. 1994;102(4):223-8.
- Wilder-Smith P, et al. Incision properties and thermal effects of three CO2 lasers in soft tissue. Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 1995; 79(6):685-91.
- Zeinoun T, et al. Myofibroblasts in healing laser excision wounds. Lasers Surg Med. 2001;28:74-79.
- de Freitas AC, et al. Assessment of the behavior of myofibroblasts on scalpel and CO2 laser wounds: an immunohistochemical study in rats. J Clin Laser Med Surg. 2002;20(4):221-225.
- Zaffe D, et al. Morphological histochemical and immunocytochemical study of CO2 and Er:YAG laser effect on oral soft tissues. Photomed Laser Surg. 2004;22(3):185-189.
- Ishii J, et al. Management of oral leukoplakia by laser surgery: relation between recurrence and malignant transformation and clinicopathological features. J Clin Laser Med Surg. 2004;22(1):27-33.
- Haytac M, et al. Evaluation of patient perceptions after frenectomy operations: a comparison of carbon dioxide laser and scalpel techniques. J Periodontol. 2006;77(11):1815-19.
- López-Jornet P, et al. Comparison of pain and swelling after removal of oral leukoplakia with CO2 laser and cold knife: A randomized clinical trial. Med Oral Patol Oral Cir Bucal. 2013;18(1):e38–e44.
- Carreira LM, et al. Comparison of the Influence of CO2-laser and scalpel skin incisions on the surgical wound healing process. ARC J Anesthesiol. 2016;1(3):1-8.
- Carreira LM, et al. Comparison of the hemodynamic response in general anesthesia between patients submitted to skin incision with scalpel and CO2 laser using dogs as an animal model. A preliminary study. ARC J Anesthesiol. 2017;2(1):24-30.
- Silva L, et al. Comparative Study on the Plasmatic CRP Level Variation in Dogs Undergoing Surgery with CO2 Laser and Scalpel Blade Incisions in a Pre- and Post-Surgical Time-Point. ARC J of Anesthesiol. 2018;3(4):3-11.
- Hendrick DA, et al. Wound healing after laser surgery. Otolaryngol Clin North Am. 1995;56:969–86.
- Sanders DL, et al. Wound healing and collagen thermal damage in 7.5-microsec pulsed CO(2) laser skin incisions. Lasers Surg Med. 2000;26(1):22-32.
- Fry TL, et al. Effects of laser, scalpel, and electrosurgical excision on wound contracture and graft “take”. Plast Reconstr Surg. 1980 Jun;65(6):729-31.
- Finsterbush A, et al. Healing and tensile strength of CO2 laser incisions and scalpel wounds in rabbits. Plast Reconstr Surg. 1982;70:360-2.
- Filmar S, et al. A comparative histologic study on the healing process after tissue transection: II: Carbon dioxide laser and surgical microscissors. Am J Obstet Gynecol. 1989;160:1068-72.
- Hall R. The healing of tissues incised by a carbon-dioxide laser. Br J Durg. 1971;58:222-5.
- Moreno R, et al. Epidermal cell outgrowth from CO2 laser- and scalpel-cut explants: Implications for wound healing. J Dermatol Surg Oncol. 1984;10:863-8.
- Hinz B, et al. Mechanical tension controls granulation tissue contractile activity and myofibroblast differentiation. Am J Pathol. 2001;159(3):1009–20.
- Darby IA, et al. Fibroblasts and myofibroblasts in wound healing. Clin Cosmet Investig Dermatol. 2014;7:301–11.
- Hinz B. Formation and function of the myofibroblast during tissue repair. J Invest Dermatol. 2007;127(3):526–37.
- Hinz B, et al. Myofibroblast development is characterized by specific cell-cell adherens junctions. Mol Biol Cell. 2004;15(9):4310–20.
- Schurch W, et al. The myofibroblast: a quarter century after its discovery. Am J Surg Pathol. 1998;22:141–7.
- Robbins SL, et al. Inflammation and Repair. Philadelphia: WB Saunders; 1984;40–84.
- Luomanen M, et al. Extracellular matrix in healing CO2 laser incision wound. J Oral Pathol. 1987;16:322-31.
- Ehrlich HP, et al. A comparative study of fibroblasts in healing freeze and burn injuries in rats. Am J Pathol. 1984 Nov;117(2):218-24.
- Fujikawa LS, et al. Fibronectin in healing rabbit corneal wounds. Lab Invest. 1981;45-120.
- Bertolami C, et al. The effect of full-thikness skin grafts on the actomyosin content of contracting wounds. Oral Surg. 1979; 37- 471.
- Carruth JAS. Resection of the tongue with the carbon dioxide laser. J of Laryn and Otol. 1982;96:529-43.
- Colvard M, et al. Managing aphthous ulcers: laser treatment applied. J Am Dent Assoc. 1991;122:51–3.
- Niccoli-Filho W, et al. Removal of epulis fissuratum associated to vestibuloplasty with carbon dioxide laser. Lasers in Medical Science. 1999;14(3):203–6.
- Wlodawsky RN, Strauss RA. Intraoral laser surgery. Oral Maxillofac Surg Clin North Am. 2004 May;16(2):149-63.
- Mason C, et al. The use of CO2 laser in the treatment of gingival fibromatosis: a case report. Int J Paediatr Dent. 1994;4(2):105-109.
- van der Hem PS, et al. CO2 laser evaporation of oral lichen planus. Int J Oral Maxillofac Surg. 2008 Jul;37(7):630-3. doi: 10.1016/j.ijom.2008.04.011. Epub 2008 Jun 6.
- Gama SK, et al. Benefits of the use of the CO2 laser in orthodontics. Lasers Med Sci. 2008 Oct;23(4):459-65.
- Holzer P, et al. Laser surgery of peripheral nerves. In: Kaplan I, ed. Laser Surgery III, part one. Tel-Aviv:OT-PAZ; 1979:149–53.
- Rocha EA, et al. Quantitative evaluation of intact peripheral nerve structures after utilization of CO2 laser, elecrocautery, and scalpel. J Clin Laser Med Surg. 2001;19:121–6.
- Weng HR, et al. Nociceptive inhibition of withdrawal reflex responses increases over time in spinalized rats. Neuroreport. 1996;7:1310–4.
- Tran TD, et al. Cerebral activation by the signals ascending through unmyelinated c-fibers in humans: a magnetoencephalographic study. Neuroscience. 2002;113: 375–86.
- Riek C, Vitruk P. Incision and Coagulation/Hemostasis Depth Control During a CO2 Laser Lingual Frenectomy, Dent Sleep Practice. Spring 2018:32-8.
- Pogrel M, et al. A comparison of carbon dioxide laser, liquid nitrogen cryosurgery, and scalpel wounds in healing. Oral Surg Oral Med Oral Pathol. 1990;69:269-73.