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- Case Report Hyperbaric Oxygen Therapy for the Treatment of Chronic Prostatitis/Chronic Pelvic Pain Syndrome: Case Report
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Kwang Jin Kim1
, Yoonsuk Lee2, Yong Sung Cha2, Tae Wook Kang1, Hyun Chul Chung1, Hong Chung1, Hyun Kim2, Jae Hung Jung1,3,4, -
Urogenital Tract Infection 2024;19(2):44-47.
DOI: https://doi.org/10.14777/uti.2024.19.2.44
Published online: August 31, 2024
1Department of Urology, Yonsei University Wonju College of Medicine, Wonju, Korea
2Department of Emergency Medicine, Yonsei University Wonju College of Medicine, Wonju, Korea
3Department of Medical Informatics and Biostatistics, Yonsei University Wonju College of Medicine, Wonju, Korea
4Center of Evidence-Based Medicine, Institute of Convergence Science, Yonsei University, Seoul, Korea
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Correspondence to: Jae Hung Jung, , Department of Urology, Yonsei University Wonju College of Medicine, 20 Ilsan-ro, Wonju 26426, Korea, Tel: +82-33-741-0652, Fax: +82-33-741-1930, E-mail: geneuro95@yonsei.ac.kr
• Received: May 20, 2024 • Revised: June 10, 2024 • Accepted: June 10, 2024
Copyright © 2024, Korean Association of Urogenital Tract Infection and Inflammation. All rights reserved.
This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
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Abstract
- Hyperbaric oxygen therapy (HBOT) was conducted on two male patients with chronic prostatitis/chronic pelvic pain syndrome who were resistant to conventional medical therapies. Both patients underwent 20 sessions of 100% oxygen inhalation (2.0 atmosphere absolute for 90 min/day, five days/week for four weeks) in a hyperbaric chamber. The follow-up period was three months. Although the patients reported a slight improvement in the pain domain of the National Institutes of Health-Chronic Prostatitis Symptom Index (NIH-CPSI) after HBOT, no changes were noted in the other domains of NIH-CPSI and International Prostate Symptom Score. No adverse events were encountered during or after HBOT.
Chronic prostatitis (CP) is one of the most common urologic conditions. Up to 10% of the male population may complain of the symptoms of CP at some point throughout their lifetime [1]. The estimated prevalence of prostatitis-like symptoms is 2.2-9.7%, and the mean prevalence is 8.2% based on epidemiological studies [2]. Therefore, CP may adversely impact public health and reduce the quality of life (QOL) because of its two main clinical features: pelvic pain and lower urinary tract symptoms (LUTS).
The National Institutes of Health (NIH) classified CP into four types: type I, acute bacterial prostatitis; type II, chronic bacterial prostatitis; type III, CP/chronic pelvic pain syndrome (CP/CPPS); and type IV, asymptomatic prostatitis [3]. CP/CPPS is the most common form of symptomatic prostatitis and is defined by the presence of pelvic pain for at least three of the preceding six months, with no other identifiable causes detected [4].
Many approaches for managing CP/CPPS are available, including pharmacological and non-pharmacological interventions, but no universal cure for the condition has been identified. Recently, hyperbaric oxygen therapy (HBOT) has been proposed for the treatment of CP/CPPS based on its tissue healing effects, including anti-inflammatory effects, increased fibroblastic activity, reduced interstitial fibrosis, reversal of vascular alterations, and microbicidal effects [5,6]. In addition, few trials have been conducted to elucidate the effects of HBOT on interstitial cystitis/bladder pain syndrome (IC/BPS), which may be considered a subset of CP/CPPS because of the similar pathogenesis and clinical presentation shared between CP/CPPS and IC/BPS.
Therefore, the authors have planned and conducted a pilot study of HBOT in two CP/CPPS patients.
CASE REPORT
This case report forms a part of the early pilot study approved by the local ethics committee (Yonsei Wonju Severance Christian Hospital, CR221021); written consent was obtained from each patient.
Study design: adult males aged 18 to 60 years diagnosed with CP/CPPS type III according to the NIH classification, characterized by the following were included in the study: (1) a history of pain or discomfort perceived in the pelvic region (National Institutes of Health-Chronic Prostatitis Symptom Index [NIH-CPSI] greater than 15), and (2) absence of any other lower urinary tract pathology for at least three of the last six months as confirmed by computed tomography and cystoscopy. The patients received HBOT following the protocol: 90-min daily session of 100% O2 breathing in a monoplace or multiplace hyperbaric chamber (IBEX Medical Systems) pressurized at two atmosphere absolute (ATA). This regimen lasted five days a week for four consecutive weeks (20 sessions) [7]. The NIH-CPSI and International Prostate Symptom Score (IPSS) were measured before HBOT and again three months after starting treatment to analyze the clinical efficacy. NIH-CPSI consisted of nine questions addressing three domains (pain, urinary function, and QOL) with a score of 0-14, 15-29, and 30-43 were considered mild, moderate, and severe pain, respectively [3]. The IPSS was comprised of seven questions related to LUTS. A score of 0-7, 8-19, and 20-35 indicated mild symptoms, moderate symptoms, and severe symptoms, respectively [8]. The adverse event of HBOT was evaluated during the study period. Conservative medication, namely an alpha-blocker, was allowed during the study period.
Case 1: a 45-year-old male without any co-morbidities visited the hospital with a complaint of pelvic pain and LUTS. He had undergone standard medical treatment using an antibiotic (quinolone) and alpha-blockers at the primary urology clinic since he was diagnosed with CP/CPPS in 2021. While the patient reported an improvement in the pain domain of NIH-CPSI from 4 at baseline to 0 after HBOT, no changes were noted in the other domains of NIH-CPSI and IPSS (Table 1). No adverse events occurred during or after HBOT.
Case 2: a 56-year-old male with co-morbidities including asthma, chronic kidney disease, and hepatitis B visited the hospital due to pelvic pain and LUTS. Despite receiving conventional treatment, the symptoms had been recurrent since his diagnosis with CP/CPPS in 2010. The patient reported a slight improvement in the pain domain of NIH-CPSI from 17 at the baseline to 15 after HBOT. On the other hand, no changes were observed in the other domains of NIH-CPSI and IPSS (Table 1). No adverse events were reported during or after HBOT.
DISCUSSION
CP/CPPS encompasses typical clinical symptoms, including pelvic pain (e.g., perineum, scrotum) associated with urinary symptoms. While the primary etiology of CP/CPPS remains unclear, its pathophysiology involves various factors, including prostatic inflammation triggered by bacterial prostatitis, unknown antigens, or possibly an autoimmune process, as well as endocrine, muscular, neuropathic, and psychological mechanisms [3,9,10].
Although tools, such as the NIH-CPSI, have been developed to measure the symptom severity and disease impact, a wide variety of interventions are used to treat CP/CPPS, each addressing different pathophysiological or symptomatic frameworks because no reliable treatments have been identified. Antibiotics and anti-inflammatory medications are the mainstay of CP/CPPS treatment, but their effects on prostatitis symptoms may be clinically unimportant compared to a placebo [11].
In the field of urology, HBOT is a well-known treatment for hemorrhagic cystitis secondary to urological malig-nancies, such as bladder and prostate cancer. In addition, HBOT has been used to treat infectious diseases, including Fournier’s gangrene and emphysematous cystitis [12]. Recently, multiple studies have been conducted to elucidate the effectiveness of HBOT in patients with IC/PBS, which have a similar pathogenesis and clinical presentation to CP/CPPS [7]. Loran et al. [5] reported that HBOT with extremely high-frequency therapy showed a positive trend in the urination parameters in the patients with benign prostatic hyperplasia (BPH) with CP compared to the group of BPH without prostatic inflammation. Zadoev et al. [6] reported that HBOT effectively impacted the spermatic morphological and functional characteristics in male infertility. Therefore, an early pilot study was planned to elucidate the effects of HBOT on CP/CPPS.
Regarding the treatment of CP/CPPS, the proposed mechanisms of HBOT include the anti-inflammatory and bactericidal effects on the prostate. HBOT provides 100% oxygen under increased atmospheric pressure, leading to arterial oxygen tension exceeding 2,000 mmHg in damaged prostatic tissue. This increased arterial oxygen tension directly affects bacteria by producing oxygen radicals. In addition, the indirect effects include enhanced microbicidal activity of leukocytes and anti-inflammatory effects due to increased dissolved oxygen in the infected tissue [12]. This study found that HBOT ameliorates the pain symptoms in men with CP/CPPS.
CP/CPPS is a common condition in urology that adversely affects the QOL of men. On the other hand, there is greater uncertainty regarding the effectiveness of pharmacological and non-pharmacological treatments [11,13]. In addition, CP/CPPS is a chronic, recurrent condition even after treatment. Moreover, these patients can transition to a refractory condition [14]. Therefore, there is a need for alternative treatments for CP/CPPS. Based on those findings and the present results, this study postulated that HBOT could be a feasible option for treating CP/CPPS to relieve recurrent or refractory symptoms.
Although HBOT has been performed for infectious and inflammatory diseases in urology, the evidence for CP/CPPS is scarce. In addition, the HBOT protocol for treating CP/CPPS, regarding the duration, number of treatment sessions, and appropriate ATA, has not been established. Future trials should be conducted to evaluate the clinical effects and protocol of HBOT according to higher methodological standards.
ACKNOWLEDGMENTS
None.
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CONFLICT OF INTEREST
No potential conflict of interest relevant to this article was reported.
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FUNDING
This work was supported by the National Research Foundation of Korea Grant funded by the Korean Government (NRF-2021R1G1A1006374).
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AUTHOR CONTRIBUTIONS
Y.L. and J.H.J. paticipated in data collection and wrote the manuscript. Y.S.C., T.W.K., H.C.C., H.C., H.K. participated in the study design. K.J.K. and J.H.J. participated in the study design and coordination and helped to draft the manuscript. All authors read and approved the final manuscript.
NOTES
Table 1
Baseline characteristics of the participants and the effects of hyperbaric oxygen therapy
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Hyperbaric Oxygen Therapy for the Treatment of Chronic Prostatitis/Chronic Pelvic Pain Syndrome: Case Report
Baseline characteristics of the participants and the effects of hyperbaric oxygen therapy
| Case 1 | Case 2 | |
|---|---|---|
| Age (y) | 45 | 56 |
| BMI | 22 | 22 |
| Date of diagnosis (y) | 2021 | 2010 |
| Co-morbidity | None | Chronic kidney disease, asthma, hepatitis B |
| Smoking | Current smoker | Ex-smoker |
| Alcohol consumption | Current drinker | Current drinker |
| NIH classification | IIIA | IIIB |
| NIH-CPSI | ||
| At the baseline | ||
| Pain domain | 4 | 17 |
| Voiding domain | 10 | 7 |
| Quality of life domain | 11 | 10 |
| Overall | 25 | 34 |
| Three months after the baseline | ||
| Pain domain | 0 | 15 |
| Voiding domain | 7 | 6 |
| Quality of life domain | 11 | 10 |
| Overall | 18 | 31 |
| IPSS | ||
| At the baseline | ||
| Voiding symptom | 11 | 8 |
| Storage symptom | 8 | 7 |
| Overall | 19 | 15 |
| Three months after the baseline | ||
| Voiding symptom | 9 | 11 |
| Storage symptom | 5 | 4 |
| Overall | 14 | 15 |
| Overall adverse event | None | None |
BMI: body mass index, NIH: National Institutes of Health, NIH-CPSI: National Institutes of Health-Chronic Prostatitis Symptom Index, IPSS: International Prostate Symptom Score.
Table 1
Baseline characteristics of the participants and the effects of hyperbaric oxygen therapy
BMI: body mass index, NIH: National Institutes of Health, NIH-CPSI: National Institutes of Health-Chronic Prostatitis Symptom Index, IPSS: International Prostate Symptom Score.
