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INTRODUCTION
Postherpetic neuralgia (PHN) is zoster-related neuralgia that is still present one month after the development of skin lesions [1]. The prevalence of PHN increases with age, between 25 to 50 percent of patients with herpes zoster (HZ) older than 50 years of age develop PHN, and up to 75 percent of patients with HZ older than 70 years of age develop PHN [2-4]. The pain can last for weeks or longer, and can last for many years, severely affecting patients’ sleep and other daily activities [5].
Antiviral therapy can reduce the severity and duration of HZ, but cannot prevent PHN [6]. Pharmacological therapy is the basis of PHN treatment [7]. The U.S. Food and Drug Administration has approved some drugs for PHN, including pregabalin, gabapentin, capsaicin patches, and lidocaine patches [1]. But there are still some patients whose pain is not well controlled. Although various procedures aimed at pain relief for PHN have been devised and tested, no established treatment for PHN has yet been identified [8].
Hydromorphone is a semi-synthetic derivative of morphine, which plays an analgesic role in the central nervous system through the excitation of μ-opioid receptors [9]. Hydromorphone is about five to seven times more effective at relieving pain than morphine [10]. Although hydromorphone has been used since 1975 to treat severe pain [11], and opioids have been reported in PHN [12], the use of hydromorphone in PHN has not been reported. Opioids are often administered according to a schedule rather than on-demand, which can lead to inadequate analgesia for patients with PHN. In this study, intravenous patient-controlled analgesia (IV PCA) was used to treat PHN. The purpose of this randomized controlled clinical trial was to evaluate the efficacy of pregabalin combined with IV PCA hydromorphone in patients with PHN and its impact on their quality of life, as well as to evaluate adverse drug reactions and complications.
MATERIALS AND METHODS
This study is a prospective, multicenter, randomized controlled clinical trial. The protocol of this study was approved by the Human Ethics Committee of Nanjing Drum Tower Hospital and implemented in accordance with the Declaration of Helsinki (approval number: 2018-136-02). Informed consent was obtained from all patients prior to the study. The clinical trial was registered with www.chictr.org.cn on December 5, 2018 (No. ChiCTR1800019880). All participants were treated from December 6, 2018 to October 30, 2019 and provided informed written consent.
1. Patients
As no data were available regarding the effect of hydromorphone on PHN patients, sample size was estimated that, to achieve 90% power at the 0.05 significance level with a standard deviation of 20%, a total of 200 patients were required to detect a difference of 15% in change from baseline in numerical rating scale (NRS) scores between the hydromorphone and control groups. From December 6, 2018, to October 30, 2019, 201 patients in 7 hospitals, including Nanjing Drum Tower Hospital, Nanjing First Hospital, Kunshan Hospital of Integrated Traditional Chinese and Western Medicine, Affiliated Hospital of Nantong University, Shanghai Public Health Clinical Center, China-Japan Friendship Hospital, and Bayingolin Mongolian Autonomous Prefecture People’s Hospital were included in this clinical trial (Fig. 1). We defined PHN as HZ-associated neuralgia lasting for more than one month. The inclusion criteria were: being at least 18 years old with a diagnosis of PHN, an average NRS score above 4, and willingness to comply with assigned treatment and follow-up measurements. Exclusion criteria were: significant pain from causes other than PHN, abnormal coagulation, mental illness, substance abuse, previous hypersensitivity to hydromorphone, pregnancy during the study or plans to become pregnant, lack of cooperation, and severe systemic, metabolic, or neurological disease.
2. Procedures
Two hundred and one patients were randomly assigned to one of the following treatment groups: The control group received PHN conventional treatment oral pregabalin (75 mg Lyrica; Pfizer, New York, NY) 75-150 mg bid with IV normal saline (NS) (2 mL/h). During the study period, the use of narcotic analgesics was prohibited. The hydromorphone group, in addition to oral pregabalin, was treated with an IV PCA hydromorphone (2 mg:2 mL, Ruining; Yichang Humanwell Pharmaceutical, Yichang, China)-based dose of 2 mg/d. Patients can add a 0.1 mg bolus with a lockout time of 15 minutes according to their level of pain. The bolus dose was recorded every 24 hours and then increased to the base dose. The treatment course lasted two weeks.
3. Efficacy measures
A computer program was used to randomize patients. Patients were evaluated before randomization, as well as 1 week, 4 weeks, and 12 weeks after treatment. We collected all the demographic and clinical data, including age, sex, duration of pain, location of pain, severity of pain, breakthrough pain, and quality of life. Breakthrough pain is a transient, short-term burst of pain. Patients were asked to quantify their average pain with a NRS. A score of 0 means no pain, and a score of 10 means the most severe pain imaginable [13]. Quality of life was assessed using the Short-Form McGill Pain Questionnaire (SFMPQ) and Pittsburgh sleep quality index (PSQI). The SFMPQ contains 15 descriptors (4 affective descriptors and 11 sensory descriptors), including 4 intensity scales (0 for none and 3 for severe) [14]. A total score was derived from the sum of responses to all 15 descriptors. The PSQI scores range from 0 to 21, with higher scores indicating worse sleep quality [15]. If the patient is not able to return to the pain clinic for a follow-up visit, the follow-up was conducted by telephone. All adverse events and complications associated with hydromorphone, including nausea, vomiting, pruritus, dizziness, drowsiness, constipation, difficulty passing urine, sweating, and respiratory depression, were documented throughout the study.
4. Statistical analysis
All statistical analyses were performed using SPSS statistics ver. 20 (IBM Corp., Armonk, NY). Two-tailed Z tests were used to verify that the 2 groups were balanced in terms of demographic and clinical variables (sex, age, severity of pain, localization of pain, and duration of pain). Changes in pain intensity over time were analyzed with a repeated measures analysis of variance (ANOVA). NRS pain scores were also compared between the 2 groups using repeated-measures ANOVA. Significance was assessed at P < 0.05.
RESULTS
Of the 201 enrolled patients, 100 (49.8%) were assigned to the control group and 101 (50.2%) were assigned to the hydromorphone group. Three in the control group and 5 in the hydromorphone group failed to complete follow-up. Demographics and baseline characteristics are shown in Table 1. The average age of patients in the control group was 66.6 ± 14.9, including 51 males and 46 females. There were 11 cases with PHN pain in the head and face, 15 cases in the neck and shoulders, 45 cases in the chest and back, and 26 cases in the waist and lower limbs. The mean age of patients in the hydromorphone group was 67.2 ± 9.6, including 46 males and 50 females. There were 13 cases with PHN pain in the head and face, 17 cases in the neck and shoulders, 39 cases in the chest and back, and 27 cases in the waist and lower limbs.
The baseline NRS score of the control group was 6.5 ± 1.6, while the baseline NRS score of the hydromorphone group was 6.9 ± 1.5, and there was no statistical difference between the two groups (P = 0.114). The average duration of PHN pain in the control group was 6.4 ± 14.8 months, while that of hydromorphone group was 5.0 ± 19.6 months. There was no statistical difference between the two groups (P = 0.093). Two weeks after treatment, the mean daily dosage of pregabalin in the hydromorphone group was 225.75 ± 74.72 mg, while that of the control group was 234.84 ± 75.34 mg. There was no statistical difference between the two groups (P = 0.054). Two weeks after treatment, the mean daily dosage of hydromorphone in the hydromorphone group was 6.25 ± 1.98 mg.
After treatment, the pain score in both groups was alleviated to varying degrees (Fig. 2). One week, 4 weeks, and 12 weeks after treatment in the control group, the NRS scores were 4.5 ± 1.4, 3.5 ± 1.3, and 3.0 ± 1.0, while the NRS scores for the hydromorphone group were 3.3 ± 1.1, 2.8 ± 0.6, and 2.1 ± 0.5, respectively. The difference between the two groups was statistically significant (P < 0.001, P < 0.001, and P < 0.001, respectively). Moreover, the frequency of breakthrough pain in the hydromorphone group was significantly lower than that in the control group 1 week and 4 weeks after treatment, and the difference was statistically significant (P < 0.001, Fig. 3). Patients in the hydromorphone group had better pain control.
Pain quality was measured using the total score derived from the validated SFMPQ. After treatment, the SFMPQ score in both groups was alleviated to varying degrees (Fig. 4). Before treatment, 1 week, 4 weeks, and 12 weeks after treatment in the control group, the SFMPQ scores were 24.45 ± 4.83, 15.41 ± 3.43, 11.69 ± 2.95, and 10.70 ± 2.46, respectively, while the SFMPQ scores for the hydromorphone group were 25.01 ± 6.72, 12.73 ± 3.97, 8.66 ± 3.11, and 6.56 ± 3.34, respectively. The baseline SFMPQ scores were no statistical difference between the two groups (P = 0.105), while the difference between the two groups after treatment was statistically significant (P < 0.001, P < 0.001, and P < 0.001, respectively). Patients in the hydromorphone group had better pain control.
Sleep quality was measured using the total score derived from the PSQI. After treatment, the PSQI score in both groups was decreased to varying degrees (Fig. 5). Before treatment, 4 weeks, and 12 weeks after treatment in the control group, the PSQI scores were 16.66 ± 1.88, 11.18 ± 1.93, and 9.02 ± 2.10, respectively, while the PSQI scores for the hydromorphone group were 16.68 ± 1.63, 7.55 ± 3.80, and 5.77 ± 2.74, respectively. The baseline PSQI scores showed no statistical difference between the two groups (P = 0.087), while the difference between the two groups after treatment was statistically significant (P < 0.001 and P < 0.001, respectively). Patients in the hydromorphone group had greater sleep improvement.
We evaluated all side effects related to hydromorphone (Table 2). The control group had 3 cases of drowsiness and 5 cases of dizziness one week after treatment, while the hydromorphone group had 5 cases of nausea, 1 case of vomiting, 2 cases of constipation, 2 cases of urinary retention, 2 cases of drowsiness, 5 cases of dizziness, and 3 cases sweating. The control group had 2 cases of drowsiness and 4 cases of dizziness four weeks after treatment, while the hydromorphone group had 1 case of drowsiness and 2 cases of dizziness four weeks after treatment. The control group had 3 cases of drowsiness and 3 cases of dizziness 12 weeks after treatment, while the hydromorphone group had 1 case of drowsiness 12 weeks after treatment. No patient experienced respiratory depression in either group. Adverse reactions were transient and improved after symptomatic treatment. There were no significant differences in side effects after treatment between the two groups (P = 0.144).
DISCUSSION
This was a multicenter, randomized controlled study. The results showed that IV PCA hydromorphone combined with oral pregabalin is more effective in controlling pain in patients with PHN than oral pregabalin alone. The difference between treatments was observed at 1 week after treatment and lasted for 12 weeks.
Hydromorphone, a semisynthetic derivative of morphine, is five to seven times more effective in relieving pain than morphine. Although hydromorphone has been used to treat severe pain since 1975, its use in PHN has not been reported. Opioids are often administered according to a schedule rather than on demand, which can lead to poor pain relief in patients with PHN.
In this study, we treated PHN with IV PCA in order to better control breakthrough pain. Breakthrough pain has a significant negative impact on the overall pain degree of PHN patients, and effective management of breakthrough pain is essential. In this study, patients in the hydromorphone group had better pain control after IV PCA hydromorphone, which may be related to timely and self-administration when the patient was in pain. Hydromorphone usually works 15 minutes after intravenous administration [16], and our research shows that patients use a daily hydromorphone dosage of 2-8 mg. After one week of IV PCA hydromorphone combined with oral pregabalin (150-300 mg/d), the pain was significantly reduced. Four weeks and 12 weeks after treatment, the pain in the hydromorphone group was also significantly improved compared with the control group. Although hydromorphone was only used for two weeks, it rapidly reduced the degree of pain, and the pain did not rebound significantly after withdrawal.
In addition to assessing the pain of patients with PHN through NRS and SFMPQ scores, we also evaluated the quality of sleep through the PSQI. Our study showed that the sleep quality of the patients in the hydromorphone group had a significant improvement at one week after treatment, and the sleep quality in the 4 weeks and 12 weeks after treatment was better than that in the control group. Our study showed that IV PCA hydromorphone can not only improve the pain of patients with PHN, but also improve the daily life of patients, especially the quality of sleep.
Our study found that the control group had adverse reactions such as drowsiness and dizziness, while the hydromorphone group had nausea, vomiting, constipation, urinary retention, drowsiness, dizziness, and sweating. No respiratory depression occurred in either group of patients. Adverse reactions may be related to the use of opioids, but the adverse reactions are transient and improved after symptomatic treatment. The difference in adverse reactions between the two groups after treatment was not statistically significant, indicating that the use of hydromorphone did not significantly increase the probability of adverse reactions.
The strength of this study is the design of a multicenter, randomized control to reduce possible bias, while using multiple methods to assess pain and quality of life in patients with PHN. However, the limitation of the analysis is that it was only followed up for 12 weeks, and no longer follow-up was performed to evaluate hydromorphone’s longer-term safety and effectiveness.
In summary, this study shows that IV PCA hydromorphone combined with oral pregabalin is more effective for patients with PHN than oral pregabalin alone. IV PCA hydromorphone provides rapid onset of pain relief and is worthy of clinical promotion and application.
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