Use this URL to cite or link to this record in EThOS:
Title: Intrathecal drug delivery for chronic non-malignant pain : pharmacological complications, cost effectiveness and long-term outcomes
Author: de Sousa Rego Vieira Duarte, Rui Miguel
ISNI:       0000 0004 2712 6201
Awarding Body: Birmingham City University
Current Institution: Birmingham City University
Date of Award: 2011
Availability of Full Text:
Access from EThOS:
Access from Institution:
Background and aims Intrathecal drug delivery (IDD) is a last resort treatment for the management of severe chronic pain due to its invasive nature, high initial cost, concerns about long-term opioid use and possible complications related to the procedure. Although it has been available since 1981 some of the possible complications of this treatment have only recently been observed and are not fully understood. Additionally the current available literature exploring the longterm effectiveness and cost effectiveness of IDD is limited. The aims of this study were to explore some of the least investigated complications, long-term effectiveness and cost effectiveness of IDD. Methods The methodology used included both retrospective and prospective data collection to investigate intrathecal morphine dose escalation, granuloma formation, hormonal effects, bone mineral density (BMD), long-term effectiveness and cost effectiveness of IDD. Results A model was developed that allows the prediction of the intrathecal opioid dose at year six of therapy based on year two dose and the duration of pain prior to initiation of intrathecal therapy. An association between opioid concentration and formation of intrathecal granulomas was confirmed for the first time in humans and a tool to assist recognition of asymptomatic granulomas was identified. It was observed that hypogonadism is prevalent in this population and free testosterone is a more reliable method to diagnose this condition. An association between low BMD and hypogonadism as a result of IDD was reported for the first time. Effectiveness of IDD was verified following a mean of 13.5 years of therapy. A new concept with implications for cost analyses was identified. Conclusion This study presents a thorough analysis of IDD therapy. Despite potential side effects, this therapy can be effective over periods longer than 10 years in appropriately selected patients. The cost effectiveness of IDD systems was confirmed based on real patients' data. Most side effects can be prevented with attentive follow-ups.
Supervisor: Not available Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID:  DOI: Not available
Keywords: B700 Nursing ; B900 Others in Subjects allied to Medicine