REVIEW PAPER / OBSTETRICS

Ginekologia Polska

2023, vol. 94, no. 9, 754–758

Copyright © 2023 PTGiP

ISSN 0017–0011, e-ISSN 2543–6767

DOI 10.5603/GP.a2023.0043

Optimization of the cosmetic appearance of skin scar after caesarean section — part I: obstetric practice

Daniel P. Wolder1Grzegorz M. Swiercz2Agata Michalska2Justyna Pogorzelska2
1Clinic of Obstetrics and Gynaecology, Provincial Combined Hospital, Kielce, Poland
2Jan Kochanowski University in Kielce, Poland
ABSTRACT
Caesarean section (CS) is a surgical way of child delivery by cutting the abdomen and uterus. Although compared to natural childbirth, it carries a greater risk of complications, the percentage of performed cuts is still increasing. The consequence of this procedure is the surgical skin scar. The appearance of this scar depends on many factors, including appropriate pre- and intraoperative procedure, operator skills and experience. The aim of the work is to present actions aimed at increasing the aesthetics of the skin scar after CS including pre-, intra- and postoperative procedures.
Keywords: skin scar; caesarean section; wound healing
Ginekologia Polska 2023; 94, 9: 754758

Corresponding author:

Daniel P. Wolder

Clinic of Obstetrics and Gynaecology, Provincial Combined Hospital, 45 Grunwaldzka St, 25736 Kielce, Poland

e-mail: d.wolder@wp.pl

Received: 8.02.2023 Accepted: 15.03.2023 Early publication date: 17.04.2023

This article is available in open access under Creative Common Attribution-Non-Commercial-No Derivatives 4.0 International (CC BY-NC-ND 4.0) license, allowing to download

articles and share them with others as long as they credit the authors and the publisher, but without permission to change them in any way or use them commercially.

INTRODUCTION

The surgical wound after a caesarean section is a cut wound, leaving a linear scar. Initially, a sterile wound is surgically sutured with edges of the wound placed close together, healing by primary intention. Wounds with infection or significant tissue loss heal by secondary intention, resulting in larger scars. Scars differ in appearance and structure from skin, and changes in their appearance reflect remodeling and maturation processes. Immature scars are characterized by a disorganized collagen fiber system and the presence of blood vessels (up to 6 months after injury). They are red, slightly raised scars. Mature scars are characterized by a pale color (usually lighter than the surrounding tissue), lack of pigmentation, lack of hair, and less elasticity (replacement of type III collagen with type I collagen thicker fibers arranged in an orientation corresponding to the lines of skin tension). The maturation process of scars leads to a significant increase in mechanical strength. It can last up to 12 months after injury or even up to 2 years. Despite these intense remodeling processes, scars never reach the strength of unharmed skin [1, 2]. Maturation disorders can lead to uncontrolled scar growth, which becomes hard, thickened, less elastic and strongly reddened (keloid, hypertrophic scar) or lack of filling the entire tissue defect (the bottom of the scar lies below the skin surface atrophic scar). Such forms of scars not only disfigure, but can also provoke pain, burning and can lead to body deformities. Women with hypertrophic skin scares and depressed hypopigmented scars are more likely to have adhesions in the abdominal region [3, 4]. The process of proper wound healing depends on many factors: the patient’s age, nutritional status, the presence of diabetes (weakened expression of cytokines, delayed epithelialization), the presence of obesity [healing disorders with a body mass index (BMI) > 3035 kg/m2 or subcutaneous tissue thickness > 3 cm], smoking, individual tendencies to keloid scars. Factors that are independent of the patient include the technique used for the procedure, the duration of the procedure, and postoperative care that includes wound care [5, 6].

Disturbed wound healing after CS can be result of partial or total wound dehiscence, hematoma within the wound, tissue necrosis due to ischemia, increased abdominal pressure or wound infection. A common complication that significantly affects cosmetic appearance of the scar is surgical site infection (SSI). This results in abnormal wound healing, often accompanied by separation of wound edges. It prolongs hospitalization and can be the cause of re-suturing the wound. There are significant differences in the frequency of SSI after CS (1.811.3% even up to 15%), as well as wound dehiscence (0.41.2%) [2]. Based on 3-year observations conducted in five Polish hospitals, the frequency of SSI was determined to be 0.5% (differences between facilities ranging from 0.1% to 1.8%), with a predominance of deep infections (61.5%) [7]. Delayed wound healing is observed more frequently in case of emergency CS [8]. Preventing SSI requires implementing appropriate perioperative procedures. Postoperative factors have been considered to play a relatively minor role in causing SSI. The aims of this review were to appraise actions aimed at increasing the cosmetic appearance of the skin scar after CS with regard to pre-, intra- and postoperative procedures. To identify the risk factors and preventive strategies, a literature search with no date restrictions was conducted using the terms: scar, wound care, wound management, surgical site infections, C-section.

PREOPERATIVE CARE

Preoperative care aims to minimize risk of wound infection by implementing procedures to protect the continuity of skin, and the and reduce the bacterial flora present on the patient’s skin. It is not recommended to shave or remove pubic hair at least one week before the surgery, as it may cause skin microdamage (Tab. 1). If hair removal is required, it is recommended to use an electric clipper with a single-use head, and shaving should be done as close to the procedure as possible, but outside the operating room [5, 9]. Using a razor increases the risk of SSI [10]. At the latest, the day before the surgery and on the day of the surgery, it is recommended to wash the entire body, including head, with special attention to areas characterized by significant bacterial colonization (skin folds, armpits, navel, groin, and perineum). Using mild, regular soap, wiping patient’s body with a fresh towel, and avoiding moisturizers or oily cosmetics is a common practice. There are no recommendations for shower or bath optimal time, and the amount or type of cleaning agents used [8]. It is acceptable to use soap and antiseptic solution, usually chlorhexidine. However, there is no evidence of their greater effectiveness in reducing SSI [5, 11, 12]. Heavy smokers are also advised to quit or reduce smoking at least 30 days before the procedure [10]. Smoking increases the risk of complications after surgical procedures. Nicotine impairs blood flow through tissues, which disrupts the wound healing process.

Table 1. Procedures aimed at optimizing wound healing process and postoperative skin scar cosmetic appearance (compiled by this review authors)

Preoperative care

Intraoperative care

Postoperative care

  • Proper hygiene (shower, bath)
  • Prohibition of shaving pubic hair 7 days before surgery
  • Shaving pubic hair with clippers as close to the surgery as possible
  • Giving up or limiting smoking (at least 30 days before surgery)
  • Providing single-use hospital underwear during surgery
  • Antibiotic prophylaxis
  • Skin preparation (chlorhexidine)
  • Preoperative vaginal irrigation (optional)
  • Maintaining appropriate body temperature and saturation
  • Glucose control
  • Localization and length of the incision
  • Subcutaneous tissue suturing in case of thickness above 2 cm
  • Skin closure (non-absorbable sutures), avoiding excessive tension on the wound edges
  • Dressing application
  • Dressing removal after 2448 hours following the procedure
  • Proper hygiene and wound care
  • Appropriate ways of changing body position (without tensing the abdominal muscles)
  • Stabilizing the wound during activities that cause abdominal pressure (coughing, sneezing, laughing, pushing)
  • Wound healing process evaluation

An important element of preoperative prevention is antibiotic therapy. According to the guidelines in every case of CS (elective, emergency), a single dose of cefazolin in a dose adjusted to the patient’s body weight (80 kg — 1 g, above 80 kg — 2 g) should be administered within 30 minutes before skin incision. Prolonging perioperative prophylaxis beyond 24 hours does not reduce the risk of infectious complications but may increase the risk of antibiotic resistance and side effects. Prophylactic antibiotic therapy in women undergoing CS reduces the frequency of wound and endometrium infections and serious infectious complications by 6070% [13, 14]. However, this method of drug administration raises concerns due to their potential impact on the newborn (disruption of intestinal microflora formation, disruption of immune system development, development of antibiotic resistance, masking of infections). In both methods of administration Jyothirmay et al. [15] found no differences in the condition of newborns. The long-term impact of antibiotics administered before CS on the child’s body has not yet been analyzed.

INTRAOPERATIVE CARE

Intraoperative care aimed at minimizing the risk of SSI includes skin disinfection, ensuring hemostasis, avoiding prolonging anesthesia, avoiding hypothermia (maintaining body temperature above 36°C), controlling blood glucose levels in patients with diabetes (< 11 mmol/L) [5, 6, 9, 16]. Operator- related factors: experience and technical ability are essential for wound healing process. The skin scar aesthetics also depend on the choice of incision localization, tools and suture materials selection and appropriate sutu­ring technique. World Health Organization recommends using alcohol solutions of antiseptic preparations based on chlorhexidine for skin preparation [17]. Their effectiveness is compared to preparations with povidone-iodine. In the case of CS, the most effective method of skin preparation has not yet been determined, and the results of studies are varied. There are also no guidelines regarding the methods and time of antiseptic agents application. Skin should be prepared at the surgical site immediately before the incision. The antiseptic solutions should dry in the air [9, 17, 18]. Caissutti et al. [19] recommend vaginal cleansing before CS (sponge stick preparation of povidone-iodine 10% for at least 30 seconds). This procedure has not been shown to decrease the frequency of postoperative wound infections in elective cases [20]. It mainly counteracts postpartum endometrial infection, especially in patients who had a rupture of the fetal membranes. Due to short time of the procedure and low cost, it can be considered for routine practice [20, 21].

Different types of skin incisions of the abdominal wall can be used for CS. For better cosmetic appearance transverse abdominal incision in accordance with the course of Langer’s lines is recommended. Incision made transversely to Langer’s lines (vertical incision), is associated with postoperative wound dehiscence, postoperative hernia development, and formation of scar contractures. The Pfannenstiel incision (“bikini incision”, “smiley incision”) is an 812 cm curved incision made at a distance of the thickness of two fingers above the pubic symphysis, ending 23 cm medially from the anterior superior iliac spine. It provides good surgical access and satisfactory cosmetic results. The Joel-Cohen incision is a 1517 cm straight incision, about 3 cm below the line connecting the anterior superior iliac spines, made more cranially compared to the Pfannenstiel incision. The Pfannenstiel incision is used in Pfannenstiel-Kerr method and the modified Misgav-Ladach method. The Joel-Cohen incision is used in the Joel-Cohen and Misgav-Ladach method [4, 22–24]. When comparing CS techniques with regard to skin scar appearance, it is assumed that better cosmetic effects are obtained with the Pfannenstiel incision [22]. In the case scar is located lower, often hidden in a natural skin depression, may partly be covered by pubic hair, and its length is shorter. On the other hand, the Joel-Cohen technique brings other benefits such as shorter operation time, fewer occurrences of fever and pain, and reduced blood loss. Preparation of tissues with blunt technique reduces the risk of nerve and blood vessel damage, which affects the healing rate of the wound [25, 26]. Therefore, chronic pain in skin scar area is more commonly reported in patients after the Pfannenstiel incision [27]. Less invasive CS performed using the Joel-Cohen technique and its modifications are associated with shorter procedure time, and better postoperative patient’s condition, but or worse cosmetic appearance. The results of research comparing the type of abdominal incision technique with the healing of the postoperative wound are inconsistent [23–28].

The length of incision is important for scar aesthetics, but it must be sufficient for the quick and safe delivery of the baby. The minimum length of the incision with the Pfannenstiel method is 150 mm, and the Allis forceps of the same length can be used to determine it (the “Allis test”) [29]. Ulubay et al. [29] among the important factors affecting length of the incision, mention operator’s experience (residents: 159.5 ± 13.1 mm; minmax, 132195 mm, specialists 154.5 ± 14.8 mm; minmax, 127195 mm) and the patient’s BMI. Sutton [30] analyzed the relationship between length of the incision and postoperative wound complications. The average and median lengths of incision were similar (15.3 cm and 15 cm). Longer incisions were not associated with an increased risk of postoperative complications. They were more frequent in overweight patients.

Excessing tension on the wound increases the risk for dehiscence, and decreasing perfusion to the healing wound. Mechanical forces (stretching, compression, hydrostatic pressure and osmotic pressure) acting on a healing wound can also disrupt the scar formation process and lead to the formation of keloids or hypertrophic scars. The risk of pathological scarring is reduced by the use of fascia sutures (deep and superficial fascia). Natural, and tension-free wound adhesion is achieved by bringing the edges of deeper structures together [31].

Absorbable and non-absorbable sutures, staples, surgical tapes, and tissue adhesives are used for skin closure after CS. An optimal method is still being sought (fast, technically easy, without any complications, and with good cosmetic results). The choice of type for skin closure potentially influences the risk of wound infection and complications. No guidelines have been developed in this area yet. The selection of skin closure method depends on the operator’s preferences. It is recommended to suture the subcutaneous tissue if its thickness is greater than 2 centimeters. This is associated with a lower rate of wound complications, specifically infection and wound separation. Routine subcutaneous tissue drainage and re-disinfection of the skin before suturing is not recommended [32–35]. Studies evaluating different methods of skin closure analyze the frequency and type of complications (SIS, wound separation), pain and cosmetic effect. Metal staples and absorbable sutures are the two methods most commonly used and compared. Routine staple skin closure is not recommended, although staples significantly reduce time of skin closure [6, 33]. In Aabake et al. [35] research half of the skin incision was closed with subcuticular sutures and the other half was closed with staples. Significantly more women preferred the stapled side in terms of cosmetic effect and reported staples as their preferred technique. Tissue adhesive is a more expensive and less commonly used method. The efficacy of tissue adhesive is comparable to conventional suture. No differences were noted in blood loss, surgical site infection, length of postpartum hospitalization, or wound disruption. Tissue adhesive can be used safely and effectively for skin closure after CS [36, 37]. Although absorbable sutures are recommended in areas that require a good aesthetic effect (plastic surgery, gynecology), from personal observations, a better result is achieved using non-absorbable sutures.

The surgical incision should be covered with an appropriate interactive dressing at the end of the operation [9]. In case of patients with a risk of abnormal wound healing (e.g. obese BMI > 45 kg/m2), prophylactic postoperative use of vacuum dressings might be considered [38].

POSTOPERATIVE CARE

In this stage, standard aseptic and antiseptic principles should be followed to prevent SIS. Because wound infections typically appear after leaving the hospital (postoperative days 47), patient education about wound healing, recognizing signs of infection, hygiene as well as care at home are very important [39, 40]. Additional measures to prevent wound separation and the formation of postoperative hernias include proper ways of changing positions and stabilizing the operated area with hands during activities that involve the abdominal muscles (coughing, sneezing, pushing, changing positions). The dressing is usually removed after 2448 hours after the procedure. The results of studies evaluating the effects of earlier dressing removal are inconsistent. Kilic et al. [41] compared dressing removal 24 hours versus 48 hours after surgery. At the six-week follow-up, the wound score (the ASEPSIS score system) was significantly less in the 48-hour group, indicating better wound healing in this group. On the other hand, Peleg et al. [42] did not observe any differences in the wound healing process in the group with dressing removal 6 hours after CS versus 24 hours. The wound should be kept clean and dry, without any dressing. Frequent hand washing is recommended, particularly before and after using the toilet and before touching the wound. Soaking the wound is not recommended. Showers with pouring water over the wound area are advised. Soap, including chlorhexidine soap, is allowed, but skin should not be scrubbed. Wearing cotton, breathable underwear and loose clothing, is also recommended. Depilation or pubic area shaving is not recommended within 34 weeks after CS [6, 9, 38].

CONCLUSIONS

Caesarean section is one of the most commonly performed major abdominal operations. With the increasing percentage of CS being performed women’s awareness of the adverse health consequences of this procedure is growing. Proper pre- , intra-, and post-operative management combined with patient education are important for wound healing and cosmetic appearance of skin scar.

Article information and declarations
Conflict of interest

All authors declare no conflict of interest.

REFERENCES

  1. Bagłaj M, Bagłaj M. Blizny jako problem kliniczny w praktyce dermatologa estetycznego. Dermatol Estet. 2014; 16(2): 8085.
  2. Stanirowski P, Sawicki W. Nowoczesne metody terapii trudno gojących się położniczo-ginekologicznych ran pooperacyjnych analiza przydatności i skuteczności stosowania. Post Nauk Med. 2013; 26(7): 475487.
  3. Kokanalı D, Kokanalı MK, Topcu HO, et al. Are the cesarean section skin scar characteristics associated with intraabdominal adhesions located at surgical and non-surgical sites. J Gynecol Obstet Hum Reprod. 2019; 48(10): 839843, doi: 10.1016/j.jogoh.2019.03.026, indexed in Pubmed: 30928543.
  4. Elprince M, Taha OT, Ibrahim ZM, et al. Prediction of intraperitoneal adhesions using striae gravidarum and scar characteristics in women undergoing repeated cesarean sections. BMC Pregnancy Childbirth. 2021; 21(1): 286, doi: 10.1186/s12884-021-03763-z, indexed in Pubmed: 33836692.
  5. Knight J, Escobar PF. Strategie zmierzające do zminimalizowania powikłań w trakcie gojenia się rany pooperacyjnej. Ginekol Dypl. 2012; 6: 3338.
  6. Kawakita T, Landy HJ. Surgical site infections after cesarean delivery: epidemiology, prevention and treatment. Matern Health Neonatol Perinatol. 2017; 3: 12, doi: 10.1186/s40748-017-0051-3, indexed in Pubmed: 28690864.
  7. Różańska A, Jarynowski A, Kopeć-Godlewska K, et al. Polish Society of Hospital Infections Team. Does surgical site infection after caesarean section in Polish hospitals reflect high-quality patient care or poor postdischarge surveillance? Results from a 3-year multicenter study. Am J Infect Control. 2018; 46(1): 2025, doi: 10.1016/j.ajic.2017.07.025, indexed in Pubmed: 28967511.
  8. Pomorski M, Woytoń R, Woytoń P, et al. Cięcia cesarskie a porody siłami natury aktualne spojrzenie. Ginekol Pol. 2010; 81: 347351.
  9. Welsh Healthcare Associated Infection Programme (WHAIP). Caesarean Section Surgical Site Wound Care and Management Public Health Wales 2015.
  10. Tanner J, Norrie P, Melen K. Preoperative hair removal to reduce surgical site infection. Cochrane Database Syst Rev. 2011(11): CD004122, doi: 10.1002/14651858.CD004122.pub4, indexed in Pubmed: 22071812.
  11. Webster J, Osborne S. Preoperative bathing or showering with skin antiseptics to prevent surgical site infection. Cochrane Database Syst Rev. 2015, doi: 10.1002/14651858.cd004985.pub5.
  12. Chlebicki MP, Safdar N, O’Horo JC, et al. Preoperative chlorhexidine shower or bath for prevention of surgical site infection: a meta-analysis. Am J Infect Control. 2013; 41(2): 167173, doi: 10.1016/j.ajic.2012.02.014, indexed in Pubmed: 22722008.
  13. Smaill FM, Gyte GMl. Antibiotic prophylaxis versus no prophylaxis for preventing infection after cesarean section. Cochrane Database Syst Rev. 2010(1): CD007482, doi: 10.1002/14651858.CD007482.pub2, indexed in Pubmed: 20091635.
  14. Mackeen AD, Packard RE, Ota E, et al. Timing of intravenous prophylactic antibiotics for preventing postpartum infectious morbidity in women undergoing cesarean delivery. Cochrane Database Syst Rev. 2014(12): CD009516, doi: 10.1002/14651858.CD009516.pub2, indexed in Pubmed: 25479008.
  15. Jyothirmayi CA, Halder A, Yadav B, et al. A randomized controlled double blind trial comparing the effects of the prophylactic antibiotic, Cefazolin, administered at caesarean delivery at two different timings (before skin incision and after cord clamping) on both the mother and newborn. BMC Pregnancy Childbirth. 2017; 17(1): 340, doi: 10.1186/s12884-017-1526-y, indexed in Pubmed: 28974203.
  16. WHO Guidelines Development Group. Global Guidelines for the Prevention of Surgical Site Infection. WHO, Geneva 2016: 1521.
  17. Hadiati DR, Hakimi M, Nurdiati DS, et al. Skin preparation for preventing infection following caesarean section. Cochrane Database Syst Rev. 2012; 10(9): CD007462, doi: 10.1002/14651858.CD007462.pub2, indexed in Pubmed: 22972109.
  18. Huang H, Li G, Wang H, et al. Optimal skin antiseptic agents for prevention of surgical site infection in cesarean section: a meta-analysis with trial sequential analysis. J Matern Fetal Neonatal Med. 2018; 31(24): 32673274, doi: 10.1080/14767058.2017.1368481, indexed in Pubmed: 28817989.
  19. Caissutti C, Saccone G, Zullo F, et al. Vaginal cleansing before cesarean delivery: a systematic review and meta-analysis. Obstet Gynecol. 2017; 130(3): 527538, doi: 10.1097/AOG.0000000000002167, indexed in Pubmed: 28796683.
  20. Aref NK. Vaginal cleansing prior to caesarian section: To do or not to do?: A randomized trial. J Gynecol Obstet Hum Reprod. 2019; 48(1): 6568, doi: 10.1016/j.jogoh.2018.11.002, indexed in Pubmed: 30447348.
  21. Haas DM, Morgan S, Contreras K, et al. Vaginal preparation with antiseptic solution before cesarean section for preventing postoperative infections. Cochrane Database Syst Rev. 2013; 7(1): CD007892, doi: 10.1002/14651858.CD007892.pub3, indexed in Pubmed: 23440819.
  22. Bolla D, Schöning A, Drack G, et al. Technical aspects of the cesarean section. Gynecol Surg. 2010; 7(2): 127132, doi: 10.1007/s10397-010-0560-9.
  23. Vitale SG, Marilli I, Cignini P, et al. Comparison between modified Misgav-Ladach and Pfannenstiel-Kerr techniques for cesarean section: review of literature. J Prenat Med. 2014; 8(3-4): 3641, indexed in Pubmed: 26265999.
  24. Gizzo S, Andrisani A, Noventa M, et al. Caesarean section: could different transverse abdominal incision techniques influence postpartum pain and subsequent quality of life? A systematic review. PLoS One. 2015; 10(2): e0114190, doi: 10.1371/journal.pone.0114190, indexed in Pubmed: 25646621.
  25. Hofmeyr GJ, Mathai M. Techniques for caesarean section. Cochrane Database of Syst Rev. 2004, doi: 10.1002/14651858.cd004662.
  26. Karanth KL, Sathish N. Review of advantages of Joel-Cohen surgical abdominal incision in caesarean section: a basic science perspective. Med J Malaysia. 2010; 65(3): 204208, indexed in Pubmed: 21939169.
  27. Loos MJ, Scheltinga MR, Mulders LG, et al. The Pfannenstiel incision as a source of chronic pain. Obstet Gynecol. 2008; 111(4): 839846, doi: 10.1097/AOG.0b013e31816a4efa, indexed in Pubmed: 18378742.
  28. Şahin N, Genc M, Turan GA, et al. A comparison of 2 cesarean section methods, modified Misgav-Ladach and Pfannenstiel-Kerr: a randomized controlled study. Adv Clin Exp Med. 2018; 27(3): 357361, doi: 10.17219/acem/66215, indexed in Pubmed: 29533540.
  29. Ulubay M, Öztürk M, Fidan U, et al. Skin incision lengths in caesarean section. Cukurova Medical Journal. 2016; 41(1): 82, doi: 10.17826/cutf.147190.
  30. Sutton A. 548: Impact of cesarean skin incision length on post-operative wound complications. Am J Obstet Gynecol. 2018; 218(1): S327S328, doi: 10.1016/j.ajog.2017.11.075.
  31. Ogawa R, Akaishi S, Huang C, et al. Clinical applications of basic research that shows reducing skin tension could prevent and treat abnormal scarring: the importance of fascial/subcutaneous tensile reduction sutures and flap surgery for keloid and hypertrophic scar reconstruction. J Nippon Med Sch. 2011; 78(2): 6876, doi: 10.1272/jnms.78.68, indexed in Pubmed: 21551963.
  32. Poprzeczny AJ, Grivell RM, Louise J, et al. Skin and subcutaneous fascia closure at caesarean section to reduce wound complications: the closure randomised trial. BMC Pregnancy Childbirth. 2020; 20(1): 606, doi: 10.1186/s12884-020-03305-z, indexed in Pubmed: 33032560.
  33. Dahlke JD, Mendez-Figueroa H, Rouse DJ, et al. Evidence-based surgery for cesarean delivery: an updated systematic review. Am J Obstet Gynecol. 2013; 209(4): 294306, doi: 10.1016/j.ajog.2013.02.043, indexed in Pubmed: 23467047.
  34. Dhama V, Chaudhary R, Singh S, et al. Three techniques for skin closure in caesarean section (stapler, absorbable subcuticular, non-absorbable subcuticular suture). Indian J Obstet Gynecol Res. 2016; 3(1): 6872, doi: 10.5958/2394-2754.2016.00014.x.
  35. Aabakke AJM, Krebs L, Pipper CB, et al. Subcuticular suture compared with staples for skin closure after cesarean delivery: a randomized controlled trial. Obstet Gynecol. 2013; 122(4): 878884, doi: 10.1097/AOG.0b013e3182a5f0c3, indexed in Pubmed: 24084548.
  36. Kwon JiY, Yun HG, Park InY. n-Butyl-2-cyanoacrylate tissue adhesive (Histoacryl) vs. subcuticular sutures for skin closure of Pfannenstiel incisions following cesarean delivery. PLoS One. 2018; 13(9): e0202074, doi: 10.1371/journal.pone.0202074, indexed in Pubmed: 30216337.
  37. Daykan Y, Sharon-Weiner M, Pasternak Y, et al. Skin closure at cesarean delivery, glue vs subcuticular sutures: a randomized controlled trial. Am J Obstet Gynecol. 2017; 216(4): 406.e1406.e5, doi: 10.1016/j.ajog.2017.01.009, indexed in Pubmed: 28153666.
  38. Mosoń K. Rana po cięciu cesarskim jak zmniejszyć ryzyko nieprawidłowego gojenia? Post N Med. 2016; 29(7): 448451, doi: 10.5604/08606196.1210324.
  39. Zuarez-Easton S, Zafran N, Garmi G, et al. Postcesarean wound infection: prevalence, impact, prevention, and management challenges. Int J Womens Health. 2017; 9: 8188, doi: 10.2147/IJWH.S98876, indexed in Pubmed: 28255256.
  40. Zarei M, Rostami F, Bozorghnejad M, et al. Effect of self-care training program on surgical incision wound healing in women undergoing cesarean section: a quasi-experimental study. Med Surg Nurs J. 2021; 9(4): e108800, doi: 10.5812/msnj.108800.
  41. Kilic GS, Demirdag E, Findik MF, et al. Impact of timing on wound dressing removal after caesarean delivery: a multicentre, randomised controlled trial. J Obstet Gynaecol. 2021; 41(3): 348352, doi: 10.1080/01443615.2020.1736015, indexed in Pubmed: 32312139.
  42. Peleg D, Eberstark E, Warsof SL, et al. Early wound dressing removal after scheduled cesarean delivery: a randomized controlled trial. Am J Obstet Gynecol. 2016; 215(3): 388.e1388.e5, doi: 10.1016/j.ajog.2016.03.035, indexed in Pubmed: 27018465.

Regulations

Important: This website uses cookies. More >>

The cookies allow us to identify your computer and find out details about your last visit. They remembering whether you've visited the site before, so that you remain logged in - or to help us work out how many new website visitors we get each month. Most internet browsers accept cookies automatically, but you can change the settings of your browser to erase cookies or prevent automatic acceptance if you prefer.

By VM Media Group sp. z o.o., ul. Świętokrzyska 73, 80–180 Gdańsk
tel.:+48 58 320 94 94, faks:+48 58 320 94 60, e-mail:  viamedica@viamedica.pl