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Microporous Polysaccharide Hemospheres and Seroma Formation After Mastectomy and Axillary Dissection in Rats

Year 2012, Volume: 2012 Issue: 2, 179 - 183, 01.02.2012
https://doi.org/10.5152/balkanmedj.2012.005

Abstract

Objective: Seroma is the most common complication after breast surgery. Several methods have been proposed to prevent seroma, but none of these provided a significant effect. A prolonged wound healing process is the most important cause of seroma. Microporous polysaccharide hemospheres (MPH) are used to achieve hemostasis. They may also accelerate wound healing. In this study, the effects of MPH on seroma formation were investigated. Material and Methods: Female Wistar rats weighing between 200 g and 250 g were used. There were eight rats in each of the control and study groups. Right breast mastectomy and axillary dissection were performed in all rats. While no application was performed after the operation in the control group, MPH was locally applied to the surgical site in the study group. Ten days after the operation, seroma fluid was aspirated and the total volume was recorded. The aspirates were analyzed and tissue samples were obtained from the surgical site. Results: Seroma was significantly lower in the study group (p=0.001). The mean albumin and lactate dehydrogenase levels were significantly lower in the study group (p=0.003). Pathological examination revealed that increase in fibrous tissue was significantly greater in the control group (p=0.032). Conclusion: MPH may reduce seroma after mastectomy. Turkish Başlık: Ratlarda Mastektomi ve Aksiller Diseksiyon Sonrası Mikro Gözenekli Polisakkarit Kürecikler Kullanımının Seroma Oluşumu Üzerine Etkisi Anahtar Kelimeler: Seroma, mastectomy, microporous polysaccharide hemospheres, wound healing Amaç: Seroma meme cerrahisi sonrasi en sık görülen komplikasyondur. Seroma oluşumunu önlemek için bazı yöntemler düşünülmüştür fakat bu yöntemlerin hiçbirinin belirgin bir etkisi olduğu gösterilememiştir. Uzamış yara iyileşme süreci seroma oluşumunun en önemli sebebidir. Hemostazı sağlamak için mikroporlu polisakkarid hemosferler (MPH) kullanılır. Bunlar ayrıca yara iyileşmesini hızlandırabilir. Bu çalışmada seroma oluşumunda MPH nin etkileri araştırılmıştır. Hastalar ve Yöntem: Ağırlığı 200g ile 250 g arasında değişen dişi Wistar sıçanları kullanıldı. Tüm çalışma ve kontrol gruplarında 8 sıçan vardı. Tüm sıçanlarda sağ meme mastektomisi ve aksiller disseksiyon yapıldı. Kontrol grubunda ameliyat sonrası hiçbir uygulama yapılmazken çalışma grubunda cerrahi sonrası lokal olarak MPH uygulandı. Ameliyattan 10 gün sonra seroma sıvısı aspire edildi toplam sıvı miktarı kaydedildi. Aspiratlar analiz edildi ve cerrahi sahadan doku örnekleri alındı. Sonuçlar: Çalışma grubunda seroma belirgin olarak az idi (p=0.001). Çalışma grubunda ortalama albümin ve LDH seviyeleri belirgin olarak düşük idi (p=0.003). Patolojik değerlendirme gösterdi ki kontrol grubunda fibröz dokuda belirgin artış vardı (p=0.32). Çıkarım: MPH mastektomi sonrası seroma gelişimini azaltabilir.

References

  • McCaul JA, Aslaam A, Spooner RJ, Louden I, Cavanagh T, Purushotham AD. Aetiology of seroma formation in patients undergoing surgery for breast cancer. Breast 2000;9:144-8. [CrossRef]
  • Chung TL, Holton LH 3rd, Goldberg NH, Silverman RP. Seroma prevention using Mytilus edulis protein in a rat mastectomy model. Breast J 2006;12:442-5. [CrossRef]
  • Gonzalez EA, Saltzstein EC, Riedner CS, Nelson BK. Seroma formation following breast cancer surgery. Breast J 2003;9:385-8. [CrossRef]
  • Hashemi E, Kaviani A, Najafi M, Ebrahimi M, Hooshmand H, Montazeri A. Seroma formation after surgery for breast cancer. World J Surg Oncol 2004;9;2:44.
  • Kuroi K, Shimozuma K, Taguchi T, Imai H, Yamashiro H, Ohsumi S, et al. Evidence-based risk factors for seroma formation in breast surgery. Jpn J Clin Oncol 2006;36:197-206. [CrossRef]
  • Kuroi K, Shimozuma K, Taguchi T, Imai H, Yamashiro H, Ohsumi S, et al. Pathophysiology of seroma in breast cancer. Breast Cancer 2005;12:288-93. [CrossRef]
  • Tekin E, Kocdor MA, Saydam S, Bora S, Harmancioglu O. Seroma prevention by using Corynebacterium parvum in a rat mastectomy model. Eur Surg Res 2001;33:245-8. [CrossRef]
  • Pogson CJ, Adwani A, Ebbs SR. Seroma following breast cancer surgery. Eur J Surg Oncol 2003;29:711-7. [CrossRef]
  • Gardner A, Pass HA, Prance S. Techniques in the prevention and management of breast seroma: An evaluation of current practice. DWOR 2005;5:135-43. [CrossRef]
  • Stehbens WE. Postmastectomy serous drainage and seroma: probable pathogenesis and prevention. ANZ J Surg 2003;73:877-80. [CrossRef]
  • Murat FJ, Ereth MH, Dong Y, Piedra MP, Getman MT. Evaluation of microporous polysaccharide hemospheres as a novel hemo static agent in open partial nephrectomy: favorable experimental results in the porcine model. J Urol 2004;72:1119-22. [CrossRef]
  • Tan SR, Tope WD. Effectiveness of microporous polysaccharide hemospheres for achieving hemostasis in mohs micrographic surgery. Dermatol Surg 2004;30:908-14. [CrossRef]
  • Schepetkin IA, Quinn MT. Botanical polysaccharides: macrophage immunomodulation and therapeutic potential. Int Immunopharmacol 2006;6:317-33. [CrossRef]
  • Kwon KH, Kim KI, Jun WJ, Shin DH, Cho HY, Hong BS. In vitro and in vivo effects of macrophage-stimulatory polysaccharide from leaves of Perilla frutescens var. crispa. Biol Pharm Bull 2002;25:367-71. [CrossRef]
  • Cheng A, Wan F, Wang J, Jin Z, Xu X. Macrophage immunomodulatory activity of polysaccharides isolated from Glycyrrhiza uralensis fish. Int Immunopharmacol 2008;:43-50. [CrossRef]
  • Artursson P, Edman P, Ericsson JL. Macrophage stimulation with some structurally related polysaccharides. Scand J Immunol 1987;25:245-54. [CrossRef]
  • Siripokasupkul R, Chansiripornchai P, Pramatwinai C, Rangsipipat A, Pongsamart S. The wound healing efficacy of durian polysaccharide gel (PG) dressing film in dog skin. Thai J Pharm Sci 2004;28:29.
  • Trombetta D, Puglia C, Perri D, Licata A, Pergolizzi S, Lauriano ER, et al. Effect of polysaccharides from Opuntia ficus-indica (L.) cladodes on the healing of dermal wounds in the rat. Phytomedicine 2006;13:352-8. [CrossRef]
  • Su CH, Sun CS, Juan SW, Hu CH, Ke WT, Sheu MT. Fungal mycelia as the source of chitin and polysaccharides and their applications as skin substitutes. Biomaterials 1997;8:1169-74. [CrossRef]
  • Chansiripornchai P, Pramatwinai C, Rungsipipat A, Ponsamart S, Nakchat O. The efficiency of polysaccharide gel extracted from fruit-hulls of durian (Durio zibethinus L.) for wound healing in pig skin. Acta Hort 2005;679:37-43.
  • Harada RN, Pressler VM, McNamara JJ. Fibrin glue reduces seroma formation in the rat after mastectomy. Surg Gynecol Obstet 1992;175:450-4.
  • Wei D, Zhang L, Williams DL, Browder IW. Glucan stimulates human dermal fibroblast collagen biosynthesis through a nuclear factor-1 dependent mechanism. Wound Repair Regen 2002;10:161-8. [CrossRef]
  • Wei D, Williams D, Browder W. Activation of AP-1 and SP1 correlates with wound growth factor gene expression in glucan-treated human fibroblasts. Int Immunopharmacol 2002;2:1163-72. [CrossRef]
  • Tang XM, Chegini N, Rossi MJ, Fay MF, Masterson BJ. The effect of surgical glove powder on proliferation of human skin fibroblast and monocyte/macrophage. J Gynecol Surg 1994;10:139-50. [CrossRef]
  • Broughton G 2nd, Janis JE, Attinger CE. The basic science of wound healing. Plast Reconstr Surg 2006;117:12S-34S. [CrossRef]
  • Halsted WS. Developments in skin-grafting operation for cancer of the breast. JAMA 1913;60:416-8. [CrossRef]
  • Aitken DR, Hunsaker R, James AG. Prevention of seromas following mastectomy and axillary dissection. Surg Gynecol Obstet 1984;158:327-30.
  • Coveney EC, O’Dwyer PJ, Geraghty JG, O’Higgins NJ. Effect of closing dead space on seroma formation after mastectomy-a prospective randomized clinical trial. Eur J Surg Oncol 1993;19:143-6.

Microporous Polysaccharide Hemospheres and Seroma Formation After Mastectomy and Axillary Dissection in Rats

Year 2012, Volume: 2012 Issue: 2, 179 - 183, 01.02.2012
https://doi.org/10.5152/balkanmedj.2012.005

Abstract

References

  • McCaul JA, Aslaam A, Spooner RJ, Louden I, Cavanagh T, Purushotham AD. Aetiology of seroma formation in patients undergoing surgery for breast cancer. Breast 2000;9:144-8. [CrossRef]
  • Chung TL, Holton LH 3rd, Goldberg NH, Silverman RP. Seroma prevention using Mytilus edulis protein in a rat mastectomy model. Breast J 2006;12:442-5. [CrossRef]
  • Gonzalez EA, Saltzstein EC, Riedner CS, Nelson BK. Seroma formation following breast cancer surgery. Breast J 2003;9:385-8. [CrossRef]
  • Hashemi E, Kaviani A, Najafi M, Ebrahimi M, Hooshmand H, Montazeri A. Seroma formation after surgery for breast cancer. World J Surg Oncol 2004;9;2:44.
  • Kuroi K, Shimozuma K, Taguchi T, Imai H, Yamashiro H, Ohsumi S, et al. Evidence-based risk factors for seroma formation in breast surgery. Jpn J Clin Oncol 2006;36:197-206. [CrossRef]
  • Kuroi K, Shimozuma K, Taguchi T, Imai H, Yamashiro H, Ohsumi S, et al. Pathophysiology of seroma in breast cancer. Breast Cancer 2005;12:288-93. [CrossRef]
  • Tekin E, Kocdor MA, Saydam S, Bora S, Harmancioglu O. Seroma prevention by using Corynebacterium parvum in a rat mastectomy model. Eur Surg Res 2001;33:245-8. [CrossRef]
  • Pogson CJ, Adwani A, Ebbs SR. Seroma following breast cancer surgery. Eur J Surg Oncol 2003;29:711-7. [CrossRef]
  • Gardner A, Pass HA, Prance S. Techniques in the prevention and management of breast seroma: An evaluation of current practice. DWOR 2005;5:135-43. [CrossRef]
  • Stehbens WE. Postmastectomy serous drainage and seroma: probable pathogenesis and prevention. ANZ J Surg 2003;73:877-80. [CrossRef]
  • Murat FJ, Ereth MH, Dong Y, Piedra MP, Getman MT. Evaluation of microporous polysaccharide hemospheres as a novel hemo static agent in open partial nephrectomy: favorable experimental results in the porcine model. J Urol 2004;72:1119-22. [CrossRef]
  • Tan SR, Tope WD. Effectiveness of microporous polysaccharide hemospheres for achieving hemostasis in mohs micrographic surgery. Dermatol Surg 2004;30:908-14. [CrossRef]
  • Schepetkin IA, Quinn MT. Botanical polysaccharides: macrophage immunomodulation and therapeutic potential. Int Immunopharmacol 2006;6:317-33. [CrossRef]
  • Kwon KH, Kim KI, Jun WJ, Shin DH, Cho HY, Hong BS. In vitro and in vivo effects of macrophage-stimulatory polysaccharide from leaves of Perilla frutescens var. crispa. Biol Pharm Bull 2002;25:367-71. [CrossRef]
  • Cheng A, Wan F, Wang J, Jin Z, Xu X. Macrophage immunomodulatory activity of polysaccharides isolated from Glycyrrhiza uralensis fish. Int Immunopharmacol 2008;:43-50. [CrossRef]
  • Artursson P, Edman P, Ericsson JL. Macrophage stimulation with some structurally related polysaccharides. Scand J Immunol 1987;25:245-54. [CrossRef]
  • Siripokasupkul R, Chansiripornchai P, Pramatwinai C, Rangsipipat A, Pongsamart S. The wound healing efficacy of durian polysaccharide gel (PG) dressing film in dog skin. Thai J Pharm Sci 2004;28:29.
  • Trombetta D, Puglia C, Perri D, Licata A, Pergolizzi S, Lauriano ER, et al. Effect of polysaccharides from Opuntia ficus-indica (L.) cladodes on the healing of dermal wounds in the rat. Phytomedicine 2006;13:352-8. [CrossRef]
  • Su CH, Sun CS, Juan SW, Hu CH, Ke WT, Sheu MT. Fungal mycelia as the source of chitin and polysaccharides and their applications as skin substitutes. Biomaterials 1997;8:1169-74. [CrossRef]
  • Chansiripornchai P, Pramatwinai C, Rungsipipat A, Ponsamart S, Nakchat O. The efficiency of polysaccharide gel extracted from fruit-hulls of durian (Durio zibethinus L.) for wound healing in pig skin. Acta Hort 2005;679:37-43.
  • Harada RN, Pressler VM, McNamara JJ. Fibrin glue reduces seroma formation in the rat after mastectomy. Surg Gynecol Obstet 1992;175:450-4.
  • Wei D, Zhang L, Williams DL, Browder IW. Glucan stimulates human dermal fibroblast collagen biosynthesis through a nuclear factor-1 dependent mechanism. Wound Repair Regen 2002;10:161-8. [CrossRef]
  • Wei D, Williams D, Browder W. Activation of AP-1 and SP1 correlates with wound growth factor gene expression in glucan-treated human fibroblasts. Int Immunopharmacol 2002;2:1163-72. [CrossRef]
  • Tang XM, Chegini N, Rossi MJ, Fay MF, Masterson BJ. The effect of surgical glove powder on proliferation of human skin fibroblast and monocyte/macrophage. J Gynecol Surg 1994;10:139-50. [CrossRef]
  • Broughton G 2nd, Janis JE, Attinger CE. The basic science of wound healing. Plast Reconstr Surg 2006;117:12S-34S. [CrossRef]
  • Halsted WS. Developments in skin-grafting operation for cancer of the breast. JAMA 1913;60:416-8. [CrossRef]
  • Aitken DR, Hunsaker R, James AG. Prevention of seromas following mastectomy and axillary dissection. Surg Gynecol Obstet 1984;158:327-30.
  • Coveney EC, O’Dwyer PJ, Geraghty JG, O’Higgins NJ. Effect of closing dead space on seroma formation after mastectomy-a prospective randomized clinical trial. Eur J Surg Oncol 1993;19:143-6.
There are 28 citations in total.

Details

Primary Language English
Subjects Health Care Administration
Journal Section Articles
Authors

Tufan Egeli This is me

Ali İbrahim Sevinç This is me

Seymen Bora This is me

Mehmet Can Yakut This is me

Tansu Cevizci This is me

Tülay Canda This is me

Ali Rıza Şişman This is me

Publication Date February 1, 2012
Published in Issue Year 2012 Volume: 2012 Issue: 2

Cite

APA Egeli, T., Sevinç, A. İ., Bora, S., Yakut, M. C., et al. (2012). Microporous Polysaccharide Hemospheres and Seroma Formation After Mastectomy and Axillary Dissection in Rats. Balkan Medical Journal, 2012(2), 179-183. https://doi.org/10.5152/balkanmedj.2012.005
AMA Egeli T, Sevinç Aİ, Bora S, Yakut MC, Cevizci T, Canda T, Şişman AR. Microporous Polysaccharide Hemospheres and Seroma Formation After Mastectomy and Axillary Dissection in Rats. Balkan Medical Journal. February 2012;2012(2):179-183. doi:10.5152/balkanmedj.2012.005
Chicago Egeli, Tufan, Ali İbrahim Sevinç, Seymen Bora, Mehmet Can Yakut, Tansu Cevizci, Tülay Canda, and Ali Rıza Şişman. “Microporous Polysaccharide Hemospheres and Seroma Formation After Mastectomy and Axillary Dissection in Rats”. Balkan Medical Journal 2012, no. 2 (February 2012): 179-83. https://doi.org/10.5152/balkanmedj.2012.005.
EndNote Egeli T, Sevinç Aİ, Bora S, Yakut MC, Cevizci T, Canda T, Şişman AR (February 1, 2012) Microporous Polysaccharide Hemospheres and Seroma Formation After Mastectomy and Axillary Dissection in Rats. Balkan Medical Journal 2012 2 179–183.
IEEE T. Egeli, “Microporous Polysaccharide Hemospheres and Seroma Formation After Mastectomy and Axillary Dissection in Rats”, Balkan Medical Journal, vol. 2012, no. 2, pp. 179–183, 2012, doi: 10.5152/balkanmedj.2012.005.
ISNAD Egeli, Tufan et al. “Microporous Polysaccharide Hemospheres and Seroma Formation After Mastectomy and Axillary Dissection in Rats”. Balkan Medical Journal 2012/2 (February 2012), 179-183. https://doi.org/10.5152/balkanmedj.2012.005.
JAMA Egeli T, Sevinç Aİ, Bora S, Yakut MC, Cevizci T, Canda T, Şişman AR. Microporous Polysaccharide Hemospheres and Seroma Formation After Mastectomy and Axillary Dissection in Rats. Balkan Medical Journal. 2012;2012:179–183.
MLA Egeli, Tufan et al. “Microporous Polysaccharide Hemospheres and Seroma Formation After Mastectomy and Axillary Dissection in Rats”. Balkan Medical Journal, vol. 2012, no. 2, 2012, pp. 179-83, doi:10.5152/balkanmedj.2012.005.
Vancouver Egeli T, Sevinç Aİ, Bora S, Yakut MC, Cevizci T, Canda T, Şişman AR. Microporous Polysaccharide Hemospheres and Seroma Formation After Mastectomy and Axillary Dissection in Rats. Balkan Medical Journal. 2012;2012(2):179-83.