Endovesical instillation of platelet rich fibrin for treatment of interstitial cystitis: case report of two patients
1Department of Urology, Villa Betania Hospital of Rome, Via Pio IV 42, 00165 Rome, Italy.
2Department of Hematology, Campus Biomedico University of Rome, Via Alvaro del Portillo 200, 00128 Rome, Italy.
3Department of General Surgery, University of Turin, Via Giuseppe Verdi 8, 10124 Turin, Italy.
4Hygiene and Public Health, Campus Biomedico University of Rome, Via Alvaro del Portillo 200, 00128 Rome, Italy.
5Department of Urology, Campus Biomedico University of Rome, Via Alvaro del Portillo 200, 00128 Rome, Italy.
Correspondence Address: Dr. Falavolti Cristina, Department of Urology, Villa Betania Hospital of Rome, Via Pio IV 42, 00165 Rome, Italy. E-mail:
Interstitial cystitis, also called painful bladder syndrome, is a chronic condition causing bladder pain and sometimes pelvic pain. The exact cause of interstitial cystitis is not known. Often, signs and symptoms are hard to elucidate and no single treatment works for everyone. We report two cases of patients affected by interstitial cystitis treated with endovesical instillation of platelets rich fibrin (PRF). PRF is an autologous component that promotes angiogenesis, tissue growth and repair. This report presents the safety and the efficacy of PRF instillations in controlling clinical symptoms and restoring quality of life.
Benign diseases of bladder such as interstitial cystitis (IC) and complex hemorrhagic radiation-induced cystitis are highly disabling. IC is not a specific disease but represents a complex set of symptoms also called “bladder pain syndrome”. This differs from common bacterial cystitis as it is a non-infective bladder inflammation. IC is caused by cellular alteration of bladder wall. The etiology causing the mucosal damage is still unclear. The urothelium sustains multiple injuries in contact with the acidic urine and this leads to an increase in local nervous sensibility for pain regulation. Patients are more sensitive to voiding stimuli and suffer chronic pelvic pain, urgency and predisposition to urinary infections. These symptoms dramatically impact quality of life. Females are more affected than males. In 90% of cases, the patients are 20-40 years old. Prevalence is increasing. In 1999, the Nurses’ Health Study has published a paper on over one million women affected by IC in the United States. Pathogenesis is still unclear and could be multifactorial including: urothelium dysfunction, mast cell activation and neurogenic inflammation. Mast cells accumulate into the sub-urothelium, proliferate forming pericapillaries cluster and release numerous inflammatory molecules [histamine; cytokines; prostaglandins; platelet-activating factor and proteolytic enzymes (tryptase and kinase)]. The process may result in ulcerative cystitis. The “up-regulation” of bladder sensitive afferents is the cause of symptoms such as urgency, frequency and/or pain.
There is no standard treatment. The 2011 AUA Treatment Guidelines include a treatment protocol ranging from conservative treatments to more invasive interventions. The aim of that study was to test the efficacy of platelets rich fibrin (PRF) in patients affected by IC in controlling the clinical symptoms and restoring the correct functioning of urothelium coating. PRF[5-9] is a blood component for local use. It can be obtained from fresh frozen plasma or bought in synthetic form. It has hemostatic properties replicating the final phase of the coagulation cascade leading to the fibrin coat. PRF is composed of fibrin glue and threefold the number of platelets than normal human blood. PRF is stable and biocompatible. It is safe and functional. It promotes angiogenesis, tissue growth and repair through multiple growth factors such as transforming growth factor-beta, vascular endothelial growth factor and platelet-derived growth factor. PRF applications do not induce inflammatory processes, adverse reactions and tissue fibrosis. PRF is nowadays widely applied in different clinical scenarios, such as orthopedics, ophthalmology and healing therapies, as a growth factor pool for improving tissue regeneration.
The ethics committee of Campus Bio-Medico University of Rome approved the study (REC number: 27/14 PAR) on March 2014. From March 2014 to September 2014, we enrolled two women affected by IC who presented clinical symptoms such as pain, overactive bladder, dysuria, recurrent urinary infections previously treated by conventional drugs without any responses. The mean age was 60 years (range 57-63 years). The exclusion criteria were: patients with Performance Status Karnofsky index ≤ 50%; patients who needed major surgery; patients affected by cancer disease; patients presenting platelets counts ≤ 100,000 or affected by coagulopathy; pregnancy. Both patients were negative for coagulation pathway alteration or urinary infection.
Patients underwent flexible diagnostic cystoscopy and biopsy 1 to 4 weeks before the application of PRF to exclude bladder cancer. One patient had a histopatological diagnosis of IC due to a previous transurethral resection of the bladder for suspicious carcinoma in situ of the bladder. Each patient filled in the urinary symptoms questionnaire for IC[11-15] and the SF (Short Form)-36 questionnaire[16-18] before the endoscopic procedure and application of PRF. The urinary symptoms questionnaire was composed of 73 questions covering the following domains: urinary symptoms, pain symptoms, sexual function, menstrual variability, and general health status. The SF-36 questionnaire was used to test the quality of life, using a baseline of 50 represented the general health of the unaffected Italian population. The results of SF-36 questionnaire are shown in Table 1. Summary score of IC symptom index was higher than 6 for both patients. This score indicates that patients affected by IC present significant voiding and pain symptoms.
Preoperative SF-36 questionnaire score
|Patient||Preoperative SF-36 score physical health (baseline 50)||Preoperative SF-36 score mental health (baseline 50)|
After the written informed consent was obtained, we took 120 mL of autologous blood sample about 1 h before the procedure from a peripheral vein (30 min is the time for preparing about 6 mL of PRF). PRF was obtained from autologous patient’s blood through the Vivostat system (Vivolution, Birkeroed, Denmark) according to the standards for autologous donation (Ministerial Decrees of March 2005). Vivostat system is composed of 3 parts: an automated processor unit, an automated applicator unit and a sterile unit for dispensing which includes a set of preparation and an endoscopic applicator. PRF was controlled for hepatitis B virus, hepatitis C virus, and human immunodeficiency virus. We obtained about 6 mL of PRF from each patient through the Vivostat system. Thereafter, we performed an operative rigid cystoscopy with Carbon Dioxide Insufflation. One patient was treated under sedation, the other one received subarachnoid anesthesia due to serious asthma condition. We instilled 6 mL of PRF in a spray fashion all over the bladder walls [Figures 1 and 2] through the endoscopic applicator. Then we placed the vesical catheter and monitored the urine output. Both patients maintained the vesical catheter postoperatively and presented good urinary output. We discharged patients after removal of the catheter and spontaneous urination.
The follow-up was performed at 28 days, and 3 months through clinical visits and patients were asked to fill in the SF-36 questionnaire again. During the last follow-up at 3 months, patients filled in also the Patient Global Impression of Improvement (PGI-I) questionnaire. PGI-I is a 1-item questionnaire designed to assess the patient’s impression of changes in urinary symptoms on a 7-point scored scale. Global clinical response was evaluated through clinical examinations and postoperative questionnaires that patients filled in during the follow-up. Patients reported significant improvement of symptoms (pain and dysuria) and quality of life especially regarding the mental health at the SF-36 questionnaire [Figures 3 and 4]. Both patients answered the PGI-I questionnaire to feel “much better” after PRF instillation. Neither patient treated with PRF experienced any short- or long-term side effects.
Figure 3. Physical health improvement after platelets rich fibrin instillation (Short Form-36 questionnaire score)
During the 2003 Kyoto workshop, the IC was defined to be a syndrome characterized by 3 main symptoms: frequency; urgency; pain. The discomfort significantly alters the quality of life of patients. The etiology and pathogenesis of this condition are still unknown and it remains diagnosed by exclusion. According to the European Society for the study of IC/BPS (ESSIC) recommendations, the first line of diagnosis is patient selection based on symptoms and exclusion of other diseases with similar presentation. During the cystoscopy, little pink ulcerations (ulceration of Hunner) described in 1914 and “glomerulation” described by Keene in 1920 as sub-mucosal capillary bleeding can be found. The histologic findings are also neither specific for diagnosis nor correlated with symptoms. The histologic sample of bladder biopsy can show the coating involution, the urothelium thinning, the inflammatory sub-urothelium infiltration and the mast cells presence. While a patient’s history and examination are important, bladder biopsy is not essential. The most common indication for bladder biopsy is a search for urothelial carcinoma/carcinoma in situ of the bladder, which may be confused with IC.
We enrolled patients according to their typical and highly disabling symptoms. Once we excluded the presence of bladder cancer, the aim of this study was to test the safety and the efficacy of endovesical instillation of PRF to stimulate tissue regeneration and control the clinical symptoms. Because standardized treatment for IC does not exist, patients usually try many kinds of procedures such as many drugs (pentosan polysulphate, antidepressants); endovesical instillation of hyaluronic acid or Bacillus Calmette-Guerin; sacral neuromodulation or surgery (laser ablation of ulceration, cystectomy, bladder augmentation). Instillation therapy has a direct action on the urothelium and sub-urotheliium to restore the normal bladder lining. Endovesical fibrin glue has been succesfully used also for refractory hemorrhagic cystitis occurred after unrelated marrow, cord blood, and haploidentical hematopoietic stem cell transplantation. Campus Bio-Medico University (Urology and Hematology Departments) has already conducted, as coordinating center of Rome Transplanta Network in 2009, a study on 35 patients affected by severe hemorrhagic cystitis after allogeneic hematopoietic stem cell transplantation. All 35 patients showed clinical response and pain resolution. In this new study, we treated patients affected by IC and we demonstrated that the typical urothelium coating involution can be successfully helped by PRF that promotes angiogenesis, tissue growth and repair through multiple growth factors as showed for transplanted patients.
A significant number of patients with ulcerative IC show ulceration, severe inflammation, and granulation tissue. The inflammatory infiltrates are usually superficial, and restricted to the lamina propria. The lamina propria is edematous, with stromal hemorrhage and congested venules. In these patients, the rupture of the bladder mucosa subsequently resulted in reparative granulation tissue. Hemorrhage is present in 90% of nonulcerative IC. While generally localized, the hemorrhage may extend into the urothelium and causes the mucosal rupture. Usually inflammation is mild, but edema and vascular congestion are frequently seen. In both cases (ulcerative and non-ulcerative IC) the urothelium is particularly fragile. Baseline symptom assessment and regular symptom level reassessment are essential to document efficacy of single and combined treatments. We used different types of questionnaires to compare the entity of patients’ discomfort before and after the endoscopic application of PRF. Questionnaires score showed a significant improvement of patients’ symptomatology during the follow-up. Our patients presented improvement in quality of life and symptoms especially regarding the mental health. Both the mental and the physical health increased significantly and remained stable after 28 days and 3 months. PGI-I and SF-36 questionnaires can provide an overall appraisal of a patients’ condition and they are practical for clinical use by their simplicity in administration and interpretability. The interstitial cystitis symptom index has been designed to capture the most important voiding and pain symptoms and to assess how problematic patients find them. Almost no IC patients score less than 6 while almost no controls score as high as 6. In our study, the symptom index was higher than 6 for both patients and this value is comparable to the score of O’Leary et al.. No further clinical improvements were seen after the first weeks after PRF instillation. This may justify revaluation during the follow-up for new endovesical treatments even though they presented partial or no response. PRF is an autologous blood component and it is safe and biocompatible. Patients treated with PRF did not present any immediately or long term side effects. The small series represents the major limitation of the study. Further cases are needed to achieve stronger results.
In conclusion, PRF is an autologous component that promotes angiogenesis, tissue growth and repair through multiple growth factors. It is safe and biocompatible; it is widely applied in different clinical scenarios to promote the tissue regeneration. Our preliminary data show that patients affected by IC who underwent endovesical application of PRF over the damaged urothelium, present significant improvement in clinical symptoms and quality of life. Further studies are needed to obtain more data.
Study conception and design: F. Cristina
PRF production: M.C. Tirindelli
Data collection: A. Nicotera
Analysis and interpretation of data: T. Petitti
Drafting of manuscript: M. Buscarini
Critical revision: G. AvvisatiFinancial support and sponsorship
None.Conflicts of interest
There are no conflicts of interest.Patient consent
Obtained from both patients.Ethics approval
The ethics committee of Campus Bio-Medico University of Rome approved the study (REC number: 27/14 PAR) on March 2014.Copyright
© The Author(s) 2017.
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Cite This Article
Cristina F, Tirindelli MC, Nicotera A, Petitti T, Avvisati G, Buscarini M. Endovesical instillation of platelet rich fibrin for treatment of interstitial cystitis: case report of two patients. Mini-invasive Surg 2017;1:186-90. http://dx.doi.org/10.20517/2574-1225.2017.22
Cristina F, Tirindelli MC, Nicotera A, Petitti T, Avvisati G, Buscarini M. Endovesical instillation of platelet rich fibrin for treatment of interstitial cystitis: case report of two patients. Mini-invasive Surgery. 2017; 1: 186-90. http://dx.doi.org/10.20517/2574-1225.2017.22
Cristina, Falavolti, Maria Cristina Tirindelli, Antonella Nicotera, Tommasangelo Petitti, Giuseppe Avvisati, Maurizio Buscarini. 2017. "Endovesical instillation of platelet rich fibrin for treatment of interstitial cystitis: case report of two patients" Mini-invasive Surgery. 1: 186-90. http://dx.doi.org/10.20517/2574-1225.2017.22
Cristina, F.; Tirindelli MC.; Nicotera A.; Petitti T.; Avvisati G.; Buscarini M. Endovesical instillation of platelet rich fibrin for treatment of interstitial cystitis: case report of two patients. Mini-invasive. Surg. 2017, 1, 186-90. http://dx.doi.org/10.20517/2574-1225.2017.22
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