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October 2022, Volume 72, Issue 10

KAP Study

Pain in sickle cell diseases; physicians’ knowledge, attitude, and barriers: A cross sectional study

Ohoud Aljuhani  ( Department of Pharmacy Practice, King Abdulaziz University, Jeddah, Saudi Arabia. )

Abstract

Objective: To assess the status of acute pain management in sickle cell disease patients, and to explore the association between professional experience and therapeutic preferences among the physicians for the management of sickle cell disease-related acute pain management.

 

Method: The cross-sectional study was conducted from June to September 2018 and comprised physicians from 20 hospitals across Saudi Arabia. Data was collected using a 13-item survey form investigating physicians' general information and related barriers regarding acute pain management in sickle cell disease patients. Data was analysed using SPSS 25.

 

Results: Of the 300 individuals approached through emails, 201(67%) responded. There were 122(61%) males and 78(39%) females; 126(63%) had experience <5 years, while 41(20%) had experience >10 years; the largest group of physicians belonged to Internal Medicine 46(23%); 41(20.4%) came across sickle cell disease patients 'very often' and 31(15.4) had never come across such a patient. There was no significant association between professional experience and therapeutic management preferences (p>0.05).

 

Conclusion: Physicians' knowledge, attitude and practice related to acute pain management in sickle cell disease patients was adequate. More awareness is needed for optimal management of pain in such patients.

 

Keywords: SCD, Sickle cell disease, Opioids, Acute pain, Physicians. (JPMA 72: 2043; 2022)

 

DOI:  https://doi.org/10.47391/JPMA.3255

 

Introduction

 

Sickle cell disease (SCD) is an autosomal recessive disorder characterised by the production of abnormal haemoglobin S.1 The disease is associated with high morbidity and mortality.1 SCD is a common genetic disease in Saudi Arabia, with the highest prevalence in the Eastern province, followed by the Southwestern provinces.2 Several SCD-related complications, such as stroke, seizure, iron overload, and acute pain associated with acute vaso-occlusive crisis (AVOC) and acute chest syndrome (ACS) require frequent hospital admissions.1 The ACS and AVOC are the two majors painful SCD complications that require urgent and effective medical management. However, despite being a common disorder, there is limited information on overall mortality from SCD in Saudi Arabia. The available report of hospital-based studies from the Eastern province shows that 73% of patients aged <30 years with SCD died due to complications mostly related to ACS and infections.2 A retrospective study showed that AVOC was a common cause of hospital admission, with 30.2% of such patients presenting with an acute painful crisis, and 52% of the patients were prescribed narcotics, with 11% of them reportedly being narcotic-dependent.3

The American Society of Haematology (ASH) guideline on SCD recommends that the SCD-related painful VOC should be treated primarily with an analgesic agent, typically opioids.4 Evidence has shown that appropriate management of SCD-related painful VOC could prevent comorbid conditions and hospitalisations.5

Although opioids were considered the mainstay in the management of SCD acute pain, several studies also reported the use of nonsteroidal anti-inflammatory drugs (NSAIDs).6 Although conflicting evidence exists in literature regarding the use of NSAIDS in SCD-related pain, ASH guideline suggests NSAIDS' use in the management of mild to moderate pain or as an adjuvant for opioids in severe pain.4 A study has demonstrated that some clinicians prefer prescribing NSAIDS to patients to avoid adverse effects related to tolerance, physical dependence, confusion and addiction to opioid use.6 A study in Saudi Arabia found that the frequent SCD-related emergency department (ED) utilisation, defined as 3 or more SCD-related ED visits within a 6-month period, was highly prevalent in Saudi population (64.3%).7 While some studies in Saudi Arabia focussed on the perspectives of patients and their families about SCD pain management,8,9no such information is available from the physicians who managed these patients. To date, different opinions exist among the physicians in Saudi Arabia regarding pain management in patients with SCD, and the issue is not widely discussed in local medical practice. The current study was planned to assess the status of acute pain management in SCD patients in Saudi Arabia, and to explore the association between professional experiences and therapeutic preferences among the physicians for the management of SCD-related acute pain management.

 

Subjects and Methods

 

 

The cross-sectional study was conducted from June to September 2018 and comprised physicians from 20 hospitals representing all the five geopolitical zones of Saudi Arabia. After approval from the unit of Biomedical Ethics research committee at King Abdulaziz University, the sample size was calculated using an online calculator.10 As there was no relevant literature available, frequency of outcome variable was taken as 50% with 95% confidence interval (CI) and 5% margin of error. The sample was raised from among physicians of either gender who were directly involved in the management of patients with SCD working as consultants, specialists, residents and interns in the departments of Internal Medicine, Surgery, Emergency, Intensive Care, Paediatrics and Pain Management.

The eligible participants were approached through emails. The mail list was obtained from hospitals' directories. The list was stratified based on the province where the hospitals were located. The survey questionnaire in Microsoft format was sent on the relevant email addresses. The questionnaire contained the study information, aims, survey questions, confidentiality, ethical conduct, and a consent form. Consent in this study was implied by completing the survey. Those who did not respond were excluded. Data was collected related to gender, years of experience, area of specialty, and frequency of participation in SCD acute pain management.

The survey questionnaire was developed based on literature review.11-13 The draft questions were presented to subject experts on the subject matter. Five experts were selected based on convenience. They were asked to review and provide feedback. The draft questionnaire was then pretested on 10 physicians from the target population. The questionnaire was modified based on the feedback received from the experts and the pre-test. The final survey questionnaire consisted of13 items (Appendix).

Physicians' general information and therapeutic options selection for SCD-related pain management was assessed using questions related to AVOC as SCD pain, side effects of opioids, use of NSAIDS, and drug-seeking behaviour in the patients. Other items were used to describe use of opioids at home following ED discharge, opioids use restriction, and assessment of SCD pain severity using pain scale. Finally, barriers to SCD pain management were investigated by asking the participants five questions.

Data was analysed using SPSS 25. Data was analysed using descriptive statistics. Categorical variables were presented as frequencies and percentages. Chi-square test was applied to determine the association between years of experience and attitudes toward acute SDC pain management. P<0.05 was considered statistically significant.

 

Results

 

Of the 300 individuals approached, 201(67%) responded. There were 122(61%) males and 78(39%) females; 126(63%) had experience <5 years, while 41(20%) had experience >10 years; the largest group of physicians belonged to Internal Medicine 46(23%); 41(20.4%) came across SCD patients 'very often' and 31(15.4) had never come across such a patient (Table-1).

Knowledge, attitude and barriers related to SCD acute pain management of the sample were noted through responses to the 13-item questionnaire (Table-2).

There was no significant association between professional experience and therapeutic management preferences (p>0.05).

 

Discussion

 

The outcomes revealed that most of the physicians had enough information about AVOC pain in patients with SCD. Most of them believed that VOC pain was common in SCD.

There is no similar study in literature to allow for comparisons. The current study found that more than 50% participants believed that uncontrolled pain is the most common reason for frequent ED visits by SCD patients. Also, most of them admitted that drug-seeking behaviours were one of the major related complaints associated with the frequent ED visits by patients with SCD. The finding is similar to a previous study conducted among 366 patients with SCD, which showed that pain was the most common complication of SCD requiring ED visits and hospitalisation.7

In the current study, physicians with <5 years of experience had higher frequency of participating in SCD pain management. It is possible that this category of physicians was applying fresh knowledge about SCD pain management acquired from medical school. Also, given the complex nature of the SCD pain management, those with more years of practice may decline to be involved in the pain management practice. However, future studies should explore this disparity.

Internal Medicine physicians accounted for the highest number of participants with frequent participation in SCD pain management. The lower proportion among other specialists may be related to being uncomfortable in managing complex SCD pain. This issue has been reported in a previous study that measured the comfort level of family physicians in treating SCD patients,8 and reported that family physicians were generally uncomfortable with managing SCD patients and SCD complications.

The present study indicated that about 30% respondents agreed that non-opioid analgesics were as effective as opioids for SCD acute pain management. While more evidence from large randomised clinical trials (RCTs) is needed to provide information regarding the effectiveness of non-opioid analgesics in SCD pain management, the Saudi guideline expert panel did not discuss SCD pain management using non-opioid analgesics.9 However, the ASH guideline recommends opioids as the mainstay for acute severe SCD pain and suggest utilising NSAIDs for mild to moderate pain. Also, the ASH guideline reported the importance of evaluating the opioids requirement for SCD patients upon ED discharge. The suggested recommendation is to utilise a timely patient-specific opioid dosing to prevent opioids withdrawal and breakthrough pain, especially in opioid-tolerant patients.1 Therefore, there is a need for more evidence from the Saudi population and recommendations on the use of opioid and non-opioid analgesics for the management of SCD acute pain in Saudi Arabia.

Three factors were identified to limit optimal utilisation of opioids for the management of SCD pain crisis: accountability of promoting opioid addiction in patients with SCD; national law regarding narcotic use; and some patients' cultural beliefs. These factors could guide less-experienced physicians to frequently prescribe opioids to SCD patients with drug-seeking behaviours, leading to medication misuse.

The present study has limitations. First, the survey format using email may limit some eligible physicians who do not have an active email account or are not familiar with electronic surveys. Secondly, the sample size was small owing to the low response rate of 67%. The drawbacks may limit the generalisation of the findings.

 

Conclusion

 

Physicians had enough information about SCD pain management. Most of the participants agreed that non-opioid analgesics are more effective in managing SCD acute pains compared to opioids. Including SCD acute pain management guidelines, including the use of opioid and non-opioid analgesics in SCD national protocols, is needed for optimal management of patients with SCD pain. Provision of interventions to improve patient education and awareness among physicians on rational use of opioids could enhance appropriate utilisation of opioids.

 

Acknowledgments: The author, therefore, acknowledge with thanks DSR for technical and financial 200 support. Special thanks are due to Rahaf Mohammed and Lujain Hussain for their help in survey data collection.

 

Disclaimer: None.

 

Conflict of Interest: None.

 

Source of Funding: his project was funded by the Deanship of Scientific Research (DSR) at King Abdulaziz University, 199 Jeddah, under grant no.15-249-1439.

 

References

 

1.      Zúñiga CP, Martínez GC, González RLM, Rendón CDS, Rojas RN, Barriga CF, et al. Enfermedad de células falciformes: Un diagnóstico para tener presente [Sickle cell disease: A diagnosis to keep in mind]. Rev Chil Pediatr. 2018; 89:525-9.

2.      Haseeb YA, Al Qahtani NH. Outcome of Pregnancy in Saudi Women with Sickle Cell Disease Attending the Tertiary Care University Hospital in Eastern Province of Saudi Arabia. Afr J Reprod Health. 2019; 23:42-8.

3.      Alhumaid AM, Aleidi AS, Alfakhri AS, Alosaimi NK, Ali YZ, Alzahrani MS. Clinical features and outcome of sickle cell anemia in a tertiary center: A retrospective cohort study. J Appl Hematol. 2018; 9:22-8.

4.      Brandow AM, Carroll CP, Creary S, Edwards-Elliott R, Glassberg J, Hurley RW, et al. American Society of Hematology 2020 guidelines for sickle cell disease: management of acute and chronic pain. Blood Adv.2020; 4:2656-701.

5.      Tanabe P, Silva S, Bosworth HB, Crawford R, Paice JA, Richardson LD, et al. A randomized controlled trial comparing two vaso-occlusive episode (VOE) protocols in sickle cell disease (SCD). Am J Hematol. 2018; 93:159-68.

6.      Han J, Saraf SL, Lash JP,Gordeuk VR. Use of Anti-inflammatory Analgesics in Sickle Cell Disease. J Clin Pharm Ther.2017; 42:656-60.

7.      Ahmed AE, Alaskar AS, McClish DK, Ali YZ, Aldughither MH, Al-Suliman AM, et al. Saudi SCD patients' symptoms and quality of life relative to the number of ED visits. BMC Emerg Med. 2016; 16:1-6.

8.      Kamal S, Naghib MM, Al Zahrani J, Hassan H, Moawad K, Arrahman O. Influence of Nutrition on Disease Severity and Health-related Quality of Life in Adults with Sickle Cell Disease: A Prospective Study. Mediterr J Hematol Infect Dis 2021;13:1-15

9.      Albagshi Muneer, Tarawah Ahmad, Aljishi Dr, Abu-harbesh Saud, Alsalman Khaled, Bashir Dr. et al. (2015). Management of Sickle Cell Disease Guideline Panel Members. [Online] 2015 [Cited 2021 July 21].Available from: URL: https://www.moh.gov.sa/HealthAwareness/EducationalContent/  Diseases/Hematology/Pages/SickleCell-Anemia.aspx

10.    Sample size calculator. [Online] 2021 [Cited 2021 July 21]. Available from: URL:https://www.calculator.net/sample-size calculator.html?type=1&cl=95&ci=5&pp=50&ps=300&x=66&y=4.

11.    Shapiro BS, Benjamin LJ, Payne R, Heidrich G. Sickle cell-related pain: perceptions of medical practitioners. J Pain Symptom Manage. 1997; 14:168-74.

12.    Martin OY, Thompson SM, Carroll AE, Jacob SA. Emergency Department Provider Survey Regarding Acute Sickle Cell Pain Management. J Pediatr Hematol Oncol. 2020; 42:375-80.

13.    Darbari DS, Brandow AM. Pain-measurement tools in sickle cell disease: where are we now? Hematology Am Soc Hematol Educ Program. 2017; 2017:534-41.

14. Patrick PA, Rosenthal BM, Iezzi CA, Brand DA. Timely pain management in the emergency department. J Emerg Med. 2015; 48 :267-73.

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