Next Article in Journal
Acute Effects of Short-Term Massage Procedures on Neuromechanical Contractile Properties of Rectus Femoris Muscle
Previous Article in Journal
Effect of Remimazolam on Pain Perception and Opioid-Induced Hyperalgesia in Patients Undergoing Laparoscopic Urologic Surgery—A Prospective, Randomized, Controlled Study
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

Adherence to Hydroxyurea and Patients’ Perceptions of Sickle Cell Disease and Hydroxyurea: A Cross-Sectional Study

1
Department of Internal Medicine, Division of Hematology and Oncology, Faculty of Medicine, Jazan University, Jazan 45142, Saudi Arabia
2
Faculty of Medicine, Jazan University, Jazan 45142, Saudi Arabia
3
Department of Medicine, Faculty of Medicine, Jazan University, Jazan 45142, Saudi Arabia
4
Department of Hematology, Prince Mohammed Bin Nasser Hospital, Jazan 82943, Saudi Arabia
*
Author to whom correspondence should be addressed.
Medicina 2024, 60(1), 124; https://doi.org/10.3390/medicina60010124
Submission received: 21 October 2023 / Revised: 18 December 2023 / Accepted: 5 January 2024 / Published: 10 January 2024
(This article belongs to the Section Hematology and Immunology)

Abstract

:
Background and Objectives: Hydroxyurea is a crucial treatment for sickle cell disease (SCD), but some patients’ adherence to it remains suboptimal. Understanding patients’ perspectives on SCD and HU is essential for improving adherence. This study aimed to assess hydroxyurea adherence and patients’ perceptions of SCD and hydroxyurea among SCD patients in the Jazan region of Saudi Arabia. Materials and Methods: This cross-sectional study collected data from 217 SCD patients using self-administered questionnaires from August 2022 to January 2023. The survey covered patient demographics, SCD consequences, and other clinical data. We used the Brief Illness Perception Questionnaire (B-IPQ) to measure patients’ disease perception and the 8-item Morisky Medication Adherence Scale (MMAS-8) to evaluate patients’ adherence to HU. Data were analysed using descriptive, t-test, and chi-square tests, and the p-value was set at <0.05 for significance. Results: More than half of the patients were male, with a mean age of 28.09 ± 8.40 years. About 57.6% of the patients were currently using HU. About 81.6% of HU users reported low adherence. The adherence was lower among individuals with infections/recurrent infections and in patients who received repeated blood transfusions. ICU admission, blood transfusion, and certain SCD complications were associated with HU use. Male patients had a higher perception of SCD consequences, concern, and understanding. ICU-admitted and recurrent hospitalized patients had a higher perception of the SCD-related consequences, symptoms, concerns, and emotional responses. Conclusions: HU seems a well-established and efficacious disease-modifying agent, but its underutilization for SCD patients remains challenging. To overcome the adherence challenges, healthcare providers must educate SCD patients about the role of hydroxyurea in lowering disease severity and addressing side effects to obtain maximum benefits. Healthcare providers may consider tailored educational interventions to improve adherence, particularly for patients with infections, recurrent hospitalizations, or repeated blood transfusions. Further research is needed to identify strategies for improving hydroxyurea adherence and patient education among SCD patients.

1. Introduction

Sickle cell disease (SCD) belongs to a group of inherited disorders known as haemoglobinopathies, which are considered the most common inherited disorder affecting humans. SCD affects the developmental cycle of red blood cells (RBC), resulting in an abnormal form of haemoglobin (Hb) known as HbS [1,2]. The estimated prevalence of SCD is not well known as documented by the Centre for Disease Control and Prevention (CDC), but it affects millions of people worldwide, more commonly in Sub-Saharan Africa, Saudi Arabia, India, Mediterranean countries, and Central and South America [3]. In Saudi Arabia, the prevalence of SCD is estimated to be 24 per 10,000 people [4]. The eastern region has the highest prevalence of sickle cell disease and traits, which is 2.6% for SCD and 2% to 27% for the sickle cell trait (SCT), followed by the Jazan region [5,6].
Individuals with SCD are more likely to have intense painful episodes known as vaso-occlusive crises (VOC), which are the hallmark of the disease and occur when aberrant RBCs occlude small blood vessels [7]. Chronic haemolytic anaemia, pulmonary hypertension, acute chest syndrome (ACS), cerebrovascular accident (CVA), infections, hypoxia, and developmental impairment are all common consequences in those patients [7]. Due to the impact of disease-related consequences and frequent hospitalization, individuals with SCD suffer from a considerable reduction in all domains of the health-related quality of life (HRQoL) across their lifespan [8,9,10].
Throughout the last two decades, the treatment options for patients with SCD have been hydroxyurea (HU), blood transfusion, and stem cell transplantation [11,12]. Multiple pieces of evidence have shown that HU utilization in paediatric and adult patients significantly reduces morbidity and mortality and improves all domains of the HRQOL. Furthermore, it has been shown to be safe, cost-effective, and efficient for such patients [13,14].
Several barriers have been identified by The National Institutes of Health Consensus Development Statement on Hydroxyurea Treatment for SCD to ensure that patients are treated and benefit from HU, and one of the most important barriers is adherence to HU [15]. Patient-level limitations are thought to include a lack of understanding about HU, misconceptions about its detrimental consequences, and low health literacy [16]. Despite being approved as an SCD-modifying medication for decades, research has shown that HU is underutilized among adult SCD patients due to varying perceptions and beliefs [17]. Regarding parents’ perceptions, as reported, the majority of parents thought HU was a beneficial drug that encouraged their children to engage in greater physical activity, have fewer episodes of pain, and miss fewer days of school [18]. However, parental and patient views of treatment advantages versus disadvantages may depend on the severity of the disease and the benefits of HU [19].
The prevalence of SCD in the Jazan region is high, and there is a lack of data considering this topic in Jazan province. Therefore, the present study aimed to assess the adherence of patients with SCD to HU and to evaluate the factors that influence adherence in the Jazan region of Saudi Arabia, as well as how patients’ perceptions of SCD and HU affect their adherence; understanding patients’ and/or parents’ perceptions of SCD and HU is essential to creating behavioural interventions to enhance adherence.

2. Materials and Methods

We conducted this study using a cross-sectional observational design in Jazan Province, located in the southwest corner of Saudi Arabia [20]. We included patients of male and female sexes in Jazan Province who had already been diagnosed with SCD, who were 18 years of age or more, and who were presented to the reference hospital for haemoglobinopathies in the region, between August 2022 and January 2023. After obtaining ethical approval, a list of patients with SCD was provided, and the survey was sent to them. Those who were younger than 18 years of age, living outside Jazan province, and diagnosed with haemoglobin disorders other than SCD, and those who refused to participate, were excluded from the study. Data were gathered using an anonymous self-administrated questionnaire obtained from previously published studies [19,20,21]. The data were collected based on the networks of the trained data collectors and investigators of the study. The questionnaire was composed of three sections. The first section contained sociodemographic questions about matters such as age, sex, current education level of the patients, family income, history of various SCD complications, hospital or ICU admission, history of blood transfusion and surgical procedures, and associated comorbidities. The second section contained questions to assess patients’ awareness about HU and whether they were currently using it or not, followed by a brief illness perception questionnaire (B-IPQ) [22]. The B-IPQ is a tool used to assess a patient’s perception of their illness. It consists of eight items that measure the patient’s beliefs about their illness, including its consequences, personal control, treatment control, identity (symptoms), concern, understanding, and emotional representation. Each item is rated on a scale of 0–10, with higher scores indicating greater concern or negative perceptions about the illness.
The last section involved the ©Modified Morisky Adherence Scale, 8-item (©MMAS-8) [23]. The ©MMAS-8 is a tool used to assess a patient’s HU adherence. It consists of eight items that measure the patient’s behaviour related to taking their HU over the past day and 2 weeks, including forgetfulness, carelessness, stopping medication when feeling better, and stopping medication when feeling worse. Each item is rated on a dichotomous scale (yes or no), with higher scores indicating better adherence. The patients were classified into three categories based on their scores: low adherence (0 to <6), medium adherence (6 to <8), and high adherence (8), respectively.
A pilot study was conducted before the distribution of the questionnaire, and it involved 20 patients to assess the clarity and wording of the questionnaire items and to correct any errors if present. Data obtained from this pilot study were excluded from the final analysis.
We estimated that there were around 30,000 adult individuals with SCD in Jazan Province, and we used the Raosoft sample size calculator to determine the sample size for the study. We aimed to achieve a 95% confidence interval and 10% margin of error, with 50% prevalence of HU use among adults with SCD according to a previous study [24], which resulted in a sample size of 96 SCD patients. For the study, the convenience sampling technique was used. For the data that were gathered, descriptive statistics were presented. For statistical analysis, the one-way ANOVA test and independent t-test were also used. The 0.05 p-value cut-off was used in the statistical analysis of the data using SPSS v.25 (IBM Corp., Armonk, NY, USA). The study was authorized under the reference number No. 2278 on 11 August 2022 by Jazan Health Ethics Committee (REC) at the Ministry of Health. Before beginning the anonymous survey, each participant’s informed consent was requested and obtained. At any point during the research procedure, respondents had the option to abandon the survey. The participants’ anonymity and secrecy were preserved; no one was asked any questions that could have revealed their identity.

3. Results

3.1. Sociodemographic and Clinical Characteristics of the Study Participants

Table 1 summarizes the participants’ sociodemographic and clinical characteristics. A total of 217 patients with SCD met our inclusion criteria, and more than half of the patients were male, representing 54.4% of the study’ participants with a mean age of 28.09 ± 8.40 years (Table 1). About 87.1% of patients were hospitalized due to SCD consequences. Further, 88.9% of patients experienced at least one SCA painful crisis in the last three years. Furthermore, 27.6% of them had been admitted to the Intensive Care Unit (ICU).

3.2. Hydroxyurea Use among the Participants and Its Association with the Sociodemographic and Clinical Characteristics of the Participants

Among all patients, more than half of them (125 patients) were currently using HU. A high monthly income was statistically associated with the increasing use of HU (p-value = 0.008). Additionally, those who had been previously admitted to the ICU, previously needed blood transfusion, or experienced complications like gallstone and joint necrosis were currently using HU more than those who had not been admitted to the ICU (p-value = 0.01, p-value = 0.001 and 0.038, respectively).

3.3. Hydroxyurea Adherence among the Participants and Its Associated Factors

Regarding adherence to HU (Table 2), the patients were divided into two groups as low and moderate/high adherence. Of all the patients, 81.6% of them had low adherence to HU. The adherence rate was lower among those who had infections/recurrent infections and recurrent blood transfusions (p-value = 0.03 and 0.01, respectively).

3.4. Perception of SCD/HU and Participants’ Characteristics, Healthcare Utilization, and Self-Reported Adherence

In our study, we examined the patient’s perception of SCD and HU in relation to the B-IPQ domains. The perception of SCD’s consequences, symptoms, and concern and its impact on the patient’ life was higher among the male sex (mean ± SD = 6.86 ± 2.98), with a statistically significant correlation (p-value = 0.003, 0.01, and 0.002, respectively). Patients with a lower adherence to HU had a higher perception of HU’s benefits in controlling the disease (mean ± SD = 5.77 ± 2.99), as shown in Table 3a.
Patients who had a history of ICU admissions had a higher perception of SCD’s consequences and symptoms (p-value = 0.016 and 0.001). Patients with more frequent hospitalizations perceived more about the SCD-related consequences (mean ± SD = 7.75 ± 2.92, p-value < 0.001), symptoms (mean ± SD = 7.62 ± 2.66, p-value < 0.001), concerns (mean ± SD = 7.44 ± 3.08, p-value = 0.001), and worse emotional responses to SCD (mean ± SD = 7.04 ± 3.13, p-value = 0.04), as described in Table 3c.

4. Discussion

SCD is one of the haemoglobinopathy disorders that has drawn major attention from public health due to its effects on increasing mortality and morbidity [25]. HU is a medication that has been found to lower the incidence and severity of painful crises and other SCD consequences [26]. Despite the high prevalence of SCD in Jazan province, there is a shortage of studies that assess the perceptions of HU and SCD and HU adherence. In this study, we found that the majority of participants were male, and more than half of the patients were on HU, but less than one-fifth of those patients were adherent to HU (Table 1 and Table 2). Using HU was associated with a high income, ICU admission, blood transfusion, and certain SCD complications (Table 1). Most HU users reported low adherence, particularly those with recurrent infections or frequent blood transfusions (Table 2). Male patients perceived more of SCD’s consequences and symptoms than females, while patients with more hospital admissions perceived more of SCD’s consequences, symptoms, concern, and emotional response (Table 3).
Regarding the utilization of hydroxyurea in our study, we found that 125 (57.6%) of the SCD patients were currently using HU (Table 1). This finding was higher than what was reported in older studies published in Europe in 2008, 2016, and 2017, which reported that the proportion of patients on HU was 25%, 39%, and 40%, respectively [26,27,28]. In our region, in a study conducted in Oman in 2018, Jose et al. found that just 43% of the SCD patients were on HU [29]. Another study conducted in the Eastern region of Saudi Arabia in 2022 reported that 38% of the SCD patients were currently on HU [30]. Another study conducted in Riyadh, Saudi Arabia, from May 2017 to January 2018, revealed that approximately 78% of the patients were using HU [31]. However, in Jeddah, approximately 61% (in 2021) of the SCD patients were on HU [32]. These findings suggest that the utilization of HU among SCD patients varies widely between different regions and countries.
Our findings suggest that the adherence to HU among SCD patients in Jazan Province, Saudi Arabia, is relatively low. In this study, 81.6% of the patients were found to have low adherence to HU, while only 18.4% had moderate or high adherence (Table 2). The adherence rates reported in this study are consistent with other studies conducted in the USA and Texas, specifically, which found that approximately 74% and 80% of the participants, respectively, had low adherence to HU [19,33]. However, a study conducted in England among paediatric patients reported higher adherence rates ranging from 77% to 85%. [18]. When it comes to the Middle East, a higher adherence rate to HU among SCD patients was reported in Oman, where 82% of the patients were found to have good adherence to HU [31]. According to a recent meta-analysis study, adherence rates were lower in older patients and those with more recognized barriers [34]; thus, the lower adherence in this study is noticeable as this study was conducted on participants with SCD who were 18 years of age or older. Moreover, it should be considered that low adherence rates in SCD patients may not be exclusive to HU, as the individuals’ beliefs influence the adherence-related behaviour regardless of the number of drugs prescribed, as found by Patel et al. in patients with SCD, wherein adherence to one medication was strongly associated with adherence to additional medications [35].
Our study found a significant association between the use of HU and various SCD complications, including ICU admission, blood transfusion, gallstones, and joint necrosis (Table 2). This finding contradicts a study conducted by Albohassan et al. in the Eastern Saudi Arabian province, which reported a decrease in painful crisis and the need for hospitalization with HU use [30]. This discrepancy in findings may be explained by the fact that most patients in our study were nonadherent to HU, and those with more severe SCD consequences were more likely to use HU compared to those with fewer consequences. Despite this, it is established that HU is effective in reducing severe painful episodes, hospitalizations, the number of blood transfusions, and acute chest syndrome and in improving survival [24,36]. Our study additionally found that adherence to HU was associated with a reduced risk of frequent blood transfusions and recurrent infections (Table 2). However, Namazzi et al. (2021) found that HU use reduced the incidence of clinically diagnosed infections, SCD consequences, and blood transfusions [37]. Thus, it may be considered that patients with a history of recurrent infections may be more likely to skip doses of HU due to disruptions in their daily routine or increased healthcare needs.
The present study did not find a significant association between HU utilization and renal dysfunction, spleen removal, or pulmonary hypertension (Table 1). This lack of association was also observed when comparing these variables between patients who were adherent to HU and those who were not (Supplementary Materials Table S1). These findings are consistent with the BABY HUG randomized controlled trial, which reported no significant difference between HU and a placebo for the preservation of renal or splenic function as primary outcomes [29]. Similarly, in a cross-sectional study conducted by Gordeuk et al. in 2009 among patients with SCD, no significant change in the tricuspid regurgitant jet velocity, a widely used predictor of pulmonary hypertension, was observed between patients who were on HU and those who were not [38]. These studies provide further evidence that HU use is not significantly associated with renal dysfunction, spleen removal, or pulmonary hypertension in patients with SCD.
A study conducted in Chicago in 2017 by Badawy et al. found that participants with moderate or high adherence to HU reported experiencing more benefits of HU, fewer SCD symptoms, and a more positive emotional response compared to those with low adherence [19]. However, our study, which measured adherence to HU using the ©MMAS-8, did not find a significant association between adherence to HU and the perception of SCD according to the B-IPQ domains (Table 3a). Interestingly, low-adherence patients tended to perceive more control over their SCD treatment. Furthermore, several studies in other contexts have demonstrated a significant correlation between patients’ perceptions of the severity of their illness and adherence to their medications [39,40,41,42]. A noteworthy aspect of our study is that male patients perceived more of SCD’s consequences, symptoms, and concerns compared to female patients (Table 3(a)). This finding contradicts Badawy et al.’s previous study, which found that female patients perceived more SCD symptoms [19].
In our study, we found that SCD patients with more frequent hospitalization perceived more of SCD’s consequences, concerns, and symptoms, as well as a negative emotional response to SCD (Table 3c). Also, patients who had a history of ICU admissions perceived more consequences and symptoms of SCD (Table 3b). This result is consistent with the results from two studies conducted by Logan et al. and Mitchell et al. in 2002 and 2007, respectively, and they found that increased healthcare utilization was associated with parental perceptions of the severity of SCD and illness-related stress [43,44]. Similarly, an earlier study showed that patients’ perceptions of more SCD-related symptoms, consequences, worse emotional response to SCD, and a lower perceived benefit of HU were associated with increased hospitalizations and frequent emergency department visits [19]. However, patients and caregivers have different views on disease severity. Connelly et al. found that patients with SCD reported fewer symptoms and lower illness severity than their parents and physicians [45], but we did not investigate the SCD perceptions among various informants in our study, as we just enrolled adult patients with SCD in our study.
This study is one of the few to assess adherence to HU and patients’ perceptions of SCD and HU among adults in Jazan Province in Saudi Arabia, a country that bears a large burden of haemoglobinopathies. Thus, we believe this may evoke the need for enhanced programs to assure the better adherence of SCD patients to HU. This was a cross-sectional study using the convenience sampling method; so, it is to be anticipated that it has the limitations inherent to this method. The cross-sectional design limited our capacity to investigate changes in patients’ perceptions of SCD and adherence to HU over time. The effect of recall and selection bias cannot be disregarded because this study was conducted using an online survey. Those who did not participate because they lacked internet access or were unfamiliar with the platform may, therefore, have had an impact on the overall results. Future studies should consider the relationship between the duration of HU and the occurrence of VOC and other complications related to SCD.

5. Conclusions

In SCD patients: perceptions of the disease and treatment were correlated with subjective and objective measures of adherence. Our findings showed that approximately 81% of patients using HU had low adherence to HU, and the adherence was lower among individuals with infections/recurrent infections and who had more blood transfusions. Regarding the perception of SCD/HU and participants’ characteristics, male patients perceived more of SCD’s consequences, concerns, and symptoms. ICU-admitted patients perceived more of SCD’s consequences and symptoms. Recurrently hospitalized patients perceived more SCD-related consequences, symptoms, concerns, and emotional responses. Adherence to HU is a multifactorial process, and alterations in patients’ perceptions of hydroxyurea help them to maintain a better disease control. For all these reasons, healthcare providers should consider patients’ beliefs about hydroxyurea when counselling about adherence at the time of the initial prescription and during follow-up visits with ongoing engagement in treatment decisions. In addition, initiatives to educate patients about the use, benefits, and potential side effects of hydroxyurea could help alleviate patients’ concerns about the drug and aid in overcoming adherence barriers.

Supplementary Materials

The following are available online at https://www.mdpi.com/article/10.3390/medicina60010124/s1, Table S1: Self-reported adherence to hydroxyurea and its association with sociodemographic and clinical characteristics of the participants.

Author Contributions

Formal analysis, F.H. and B.Z.; Supervision, M.A.M. and A.H.A.; Writing—original draft, M.A.M., F.A., K.M.H., S.A., E.A., S.Z., S.T. and A.H.A.; Writing—review and editing, M.A.M., F.A., F.H., B.Z., K.M.H., S.A., M.M. and H.M. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Institutional Review Board Statement

The study was approved by the Jazan Health Ethics Committee (REC) at the Ministry of Health. The study was authorized under the reference number of No. 2278, date: 11 August 2022.

Informed Consent Statement

Informed consent was obtained from all subjects involved in the study.

Data Availability Statement

The data presented in this study are available on request from the corresponding author.

Acknowledgments

The authors are immensely thankful to the data collectors and the participants of this study.

Conflicts of Interest

The authors declare no conflicts of interest.

References

  1. What is Sickle Cell Disease?|CDC. Available online: https://www.cdc.gov/ncbddd/sicklecell/facts.html (accessed on 26 April 2023).
  2. Epping, A.S.; Myrvik, M.P.; Newby, R.F.; Panepinto, J.A.; Brandow, A.M.; Scott, J.P. Academic attainment findings in children with sickle cell disease. J. Sch. Health 2013, 83, 548–553. [Google Scholar] [CrossRef] [PubMed]
  3. Data & Statistics on Sickle Cell Disease|CDC. Available online: https://www.cdc.gov/ncbddd/sicklecell/data.html (accessed on 26 April 2023).
  4. Al-Qurashi, M.M.; El-Mouzan, M.I.; Al-Herbish, A.S.; Al-Salloum, A.A.; Al-Omar, A.A. The prevalence of sickle cell disease in Saudi children and adolescents. A community-based survey. Saudi Med. J. 2008, 29, 1480–1483. [Google Scholar]
  5. Jastaniah, W. Epidemiology of sickle cell disease in Saudi Arabia. Ann. Saudi Med. 2011, 31, 289–293. [Google Scholar] [CrossRef] [PubMed]
  6. Hazzazi, A.A.; Ageeli, M.H.; Alfaqih, A.M.; Jaafari, A.A.; Malhan, H.M.; Bakkar, M.M. Epidemiology and characteristics of sickle cell patients admitted to hospitals in Jazan region, Saudi Arabia. J. Appl. Hematol. 2020, 11, 10. [Google Scholar] [CrossRef]
  7. Rees, D.C.; Williams, T.N.; Gladwin, M.T. Sickle-cell disease. Lancet 2010, 376, 2018–2031. [Google Scholar] [CrossRef]
  8. Panepinto, J.A.; Bonner, M. Health-related quality of life in sickle cell disease: Past, present, and future. Pediatr. Blood Cancer 2012, 59, 377–385. [Google Scholar] [CrossRef] [PubMed]
  9. Alhazmi, S.A.; Maashi, A.Q.; Shabaan, S.K.; Majrashi, A.A.; Thakir, M.A.; Almetahr, S.M.; Qadri, A.M.; Hakami, A.A.; Abdelwahab, S.I.; Alhazmi, A.H. The Health Belief Model Modifying Factors Associated with Missed Clinic Appointments among Individuals with Sickle Cell Disease in the Jazan Province, Saudi Arabia. Healthcare 2022, 10, 2376. [Google Scholar] [CrossRef]
  10. Piccin, A.; Fleming, P.; Eakins, E.; McGovern, E.; Smith, O.P.; McMahon, C. Sickle cell disease and dental treatment. J. Ir. Dent. Assoc. 2008, 54, 75–79. [Google Scholar]
  11. Yawn, B.P.; Buchanan, G.R.; Afenyi-Annan, A.N.; Ballas, S.K.; Hassell, K.L.; James, A.H.; Jordan, L.; Lanzkron, S.; Lottenberg, R.; Savage, W.J.; et al. Management of sickle cell disease: Summary of the 2014 evidence-based report by expert panel members. JAMA 2014, 312, 1033–1048. [Google Scholar] [CrossRef]
  12. Hurissi, E.; Hakami, A.; Homadi, J.; Kariri, F.; Abu-Jabir, E.; Alamer, R.; Mobarki, R.; Jaly, A.A.; َAlamer, E.; Alhazmi, A.H. Awareness and Acceptance of Hematopoietic Stem Cell Transplantation for Sickle Cell Disease in Jazan Province, Saudi Arabia. Cureus 2022, 14, e21013. [Google Scholar] [CrossRef]
  13. Wang, W.C.; Ware, R.E.; Miller, S.T.; Iyer, R.V.; Casella, J.F.; Minniti, C.P.; Rana, S.; Thornburg, C.D.; Rogers, Z.R.; Kalpatthi, R.V.; et al. Hydroxycarbamide in very young children with sickle-cell anaemia: A multicentre, randomised, controlled trial (BABY HUG). Lancet 2011, 377, 1663–1672. [Google Scholar] [CrossRef] [PubMed]
  14. Strouse, J.J.; Lanzkron, S.; Beach, M.C.; Haywood, C.; Park, H.; Witkop, C.; Wilson, R.F.; Bass, E.B.; Segal, J.B. Hydroxyurea for sickle cell disease: A systematic review for efficacy and toxicity in children. Pediatrics 2008, 122, 1332–1342. [Google Scholar] [CrossRef] [PubMed]
  15. Brawley, O.W.; Cornelius, L.J.; Edwards, L.R.; Gamble, V.N.; Green, B.L.; Inturrisi, C.; James, A.H.; Laraque, D.; Mendez, M.; Montoya, C.J.; et al. National Institutes of Health Consensus Development Conference statement: Hydroxyurea treatment for sickle cell disease. Ann. Intern. Med. 2008, 148, 932–938. [Google Scholar] [CrossRef] [PubMed]
  16. LaVista, J.M.; Treise, D.M.; Dunbar, L.N.; Ritho, J.; Hartzema, A.G.; Lottenberg, R. Development and evaluation of a patient empowerment video to promote hydroxyurea adoption in sickle cell disease. J. Natl. Med. Assoc. 2009, 101, 251–257. [Google Scholar] [CrossRef] [PubMed]
  17. Adewoyin, A.S.; Oghuvwu, O.S.; Awodu, O.A. Hydroxyurea therapy in adult Nigerian sickle cell disease: A monocentric survey on pattern of use, clinical effects and patient’s compliance. Afr. Health Sci. 2017, 17, 255–261. [Google Scholar] [CrossRef] [PubMed]
  18. Thornburg, C.D.; Calatroni, A.; Telen, M.; Kemper, A.R. Adherence to hydroxyurea therapy in children with sickle cell anemia. J. Pediatr. 2010, 156, 415–419. [Google Scholar] [CrossRef]
  19. Badawy, S.M.; Thompson, A.A.; Lai, J.-S.; Penedo, F.J.; Rychlik, K.; Liem, R.I. Adherence to hydroxyurea, health-related quality of life domains, and patients’ perceptions of sickle cell disease and hydroxyurea: A cross-sectional study in adolescents and young adults. Health Qual. Life Outcomes 2017, 15, 136. [Google Scholar] [CrossRef]
  20. Population in Jazan Region by Gender, Age Group, and Nationality (Saudi/Non-Saudi)|General Authority for Statistics. Available online: https://www.stats.gov.sa/en/6140 (accessed on 26 April 2023).
  21. Alhazmi, A.; Hakami, K.; Abusageah, F.; Jaawna, E.; Khawaji, M.; Alhazmi, E.; Zogel, B.; Qahl, S.; Qumayri, G. The impact of sickle cell disease on academic performance among affected students. Children 2022, 9, 15. [Google Scholar] [CrossRef]
  22. Broadbent, E.; Petrie, K.J.; Main, J.; Weinman, J. The brief illness perception questionnaire. J. Psychosom. Res. 2006, 60, 631–637. [Google Scholar] [CrossRef]
  23. Ashur, S.T.; Shamsuddin, K.; Shah, S.A.; Bosseri, S. Reliability and known-group validity of the Arabic version of the 8-item Morisky Medication Adherence Scale among type 2 diabetes mellitus patients. EMHJ 1995, 21, 22–728. [Google Scholar] [CrossRef]
  24. Alsalman, M.; Alkhalifa, H.; Alkhalifah, A.; Alsubie, M.; AlMurayhil, N.; Althafar, A.; Albarqi, M.; Alnaim, A.; Khan, A.S. Hydroxyurea usage awareness among patients with sickle-cell disease in Saudi Arabia. Health Sci. Rep. 2021, 4, e437. [Google Scholar] [CrossRef] [PubMed]
  25. Memish, Z.A.; Owaidah, T.M.; Saeedi, M.Y. Marked regional variations in the prevalence of sickle cell disease and β-thalassemia in Saudi Arabia: Findings from the premarital screening and genetic counseling program. J. Epidemiol. Glob. Health 2011, 1, 61–68. [Google Scholar] [CrossRef] [PubMed]
  26. Nevitt, S.J.; Jones, A.P.; Howard, J. Hydroxyurea (hydroxycarbamide) for sickle cell disease. Cochrane Database Syst. Rev. 2017, 4, CD002202. [Google Scholar] [CrossRef] [PubMed]
  27. Lê, P.Q.; Gulbis, B.; Dedeken, L.; Dupont, S.; Vanderfaeillie, A.; Heijmans, C.; Huybrechts, S.; Devalck, C.; Efira, A.; Dresse, M.; et al. Survival among children and adults with sickle cell disease in Belgium: Benefit from hydroxyurea treatment. Pediatr. Blood Cancer 2015, 62, 1956–1961. [Google Scholar] [CrossRef]
  28. Cela, E.; Bellón, J.M.; de la Cruz, M.; Beléndez, C.; Berrueco, R.; Ruiz, A.; Elorza, I.; de Heredia, C.D.; Cervera, A.; Vallés, G.; et al. National registry of hemoglobinopathies in Spain (REPHem). Pediatr. Blood Cancer 2017, 64, e26322. [Google Scholar] [CrossRef]
  29. Wang, W.C.; Ware, R.E.; Miller, S.T.; Iyer, R.V.; Casella, J.F.; Minniti, C.P.; Rana, S.; Thornburg, C.D.; Rogers, Z.R.; Kalpatthi, R.V.; et al. A multicenter randomised controlled trial of hydroxyurea (hydroxycarbamide) in very young children with sickle cell anaemia. Lancet 2011, 377, 1663. [Google Scholar] [CrossRef] [PubMed]
  30. Albohassan, H.; Ammen, M.; Alomran, A.A.; Shehab, H.B.; Al Sakkak, H.; Al Bohassan, A. Impact of Hydroxyurea Therapy in Reducing Pain Crises, Hospital Admissions, and Length of Stay Among Sickle Cell Patients in the Eastern Region of Saudi Arabia. Cureus 2022, 14, e31527. [Google Scholar] [CrossRef]
  31. Jose, J.; Elsadek, R.A.; Jimmy, B.; George, P. Hydroxyurea: Pattern of use, patient adherence, and safety profile in patients with sickle cell disease in Oman. Oman Med. J. 2019, 34, 327. [Google Scholar] [CrossRef]
  32. Alzahrani, F.; Albaz, G.F.; AlSinan, F.; Alzuhayri, J.; Barnawi, Z.M.; Melebari, N.; Al Twairgi, T.M. Hydroxyurea use among children with sickle cell disease at King Abdulaziz University Hospital in Jeddah City. Cureus 2021, 13, e13453. [Google Scholar] [CrossRef]
  33. Kang, H.A.; Barner, J.C. The association between hydroxyurea adherence and opioid utilization among Texas Medicaid enrollees with sickle cell disease. J. Manag. Care Spec. Pharm. 2020, 26, 1412–1422. [Google Scholar] [CrossRef]
  34. Loiselle, K.; Lee, J.L.; Szulczewski, L.; Drake, S.; Crosby, L.E.; Pai, A.L.H. Systematic and meta-analytic review: Medication adherence among pediatric patients with sickle cell disease. J. Pediatr. Psychol. 2016, 41, 406–418. [Google Scholar] [CrossRef]
  35. Patel, N.G.; Lindsey, T.; Strunk, R.C.; DeBaun, M.R. Prevalence of daily medication adherence among children with sickle cell disease: A 1-year retrospective cohort analysis. Pediatr. Blood Cancer 2010, 55, 554–556. [Google Scholar] [CrossRef] [PubMed]
  36. Strouse, J.J.; Heeney, M.M. Hydroxyurea for the treatment of sickle cell disease: Efficacy, barriers, toxicity, and management in children. Pediatr. Blood Cancer 2012, 59, 365–371. [Google Scholar] [CrossRef]
  37. Namazzi, R.; Conroy, A.L.; Bond, C.; Goings, M.J.; Datta, D.; Ware, R.E.; Jang, J.H.; John, C.C.; Opoka, R.O. Effect of Hydroxyurea Therapy on the Incidence of Infections in Ugandan Children with Sickle Cell Anaemia. Blood 2021, 138, 765. [Google Scholar] [CrossRef]
  38. Gordeuk, V.R.; Campbell, A.; Rana, S.; Nouraie, M.; Niu, X.; Minniti, C.P.; Sable, C.; Darbari, D.; Dham, N.; Onyekwere, O.; et al. Relationship of erythropoietin, fetal hemoglobin, and hydroxyurea treatment to tricuspid regurgitation velocity in children with sickle cell disease. Blood J. Am. Soc. Hematol. 2009, 114, 4639–4644. [Google Scholar] [CrossRef]
  39. Klok, T.; Kaptein, A.A.; Duiverman, E.J.; Brand, P.L. High inhaled corticosteroids adherence in childhood asthma: The role of medication beliefs. Eur. Respir. J. 2012, 40, 1149–1155. [Google Scholar] [CrossRef]
  40. Kung, M.; Koschwanez, H.E.; Painter, L.; Honeyman, V.; Broadbent, E. Immunosuppressant nonadherence in heart, liver, and lung transplant patients: Associations with medication beliefs and illness perceptions. Transplantation 2012, 93, 958–963. [Google Scholar] [CrossRef]
  41. Žugelj, U.; Zupančič, M.; Komidar, L.; Kenda, R.; Varda, N.M.; Gregorič, A. Self-reported adherence behavior in adolescent hypertensive patients: The role of illness representations and personality. J. Pediatr. Psychol. 2010, 35, 1049–1060. [Google Scholar] [CrossRef]
  42. Broadbent, E.; Donkin, L.; Stroh, J.C. Illness and treatment perceptions are associated with adherence to medications, diet, and exercise in diabetic patients. Diabetes Care 2011, 34, 338–340. [Google Scholar] [CrossRef]
  43. Logan, D.E.; Radcliffe, J.; Smith-Whitley, K. Parent factors and adolescent sickle cell disease: Associations with patterns of health service use. J. Pediatr. Psychol. 2002, 27, 475–484. [Google Scholar] [CrossRef]
  44. Mitchell, M.J.; Lemanek, K.; Palermo, T.M.; Crosby, L.E.; Nichols, A.; Powers, S.W. Parent perspectives on pain management, coping, and family functioning in pediatric sickle cell disease. Clin. Pediatr. 2007, 46, 311–319. [Google Scholar] [CrossRef]
  45. Connelly, M.; Wagner, J.L.; Brown, R.T.; Rittle, C.; Cloues, B.; Taylor, L.C. Informant discrepancy in perceptions of sickle cell disease severity. J. Pediatr. Psychol. 2005, 30, 443–448. [Google Scholar] [CrossRef]
Table 1. General sociodemographic, clinical characteristics, and hydroxyurea status among SCA patients in our study.
Table 1. General sociodemographic, clinical characteristics, and hydroxyurea status among SCA patients in our study.
Sociodemographic CharacteristicsFrequency (Percentage)Hydroxyurea Status (Currently Use)p-Value
n = 217Yes
125 (57.6%)
No
92 (42.4%)
Age (mean; SD)28.09; 8.4028.52; 8.1427.50; 8.750.37
Gender
Male118 (54.4%)63 (50.4%)55 (59.8%)0.17
Female99 (45.6%)62 (49.6%)37 (40.2%)
Family Monthly Income (in Riyals)
Less than 5 k 57 (26.3%)33 (26.4%)24 (26.1%)



0.008 *
From 5 to 10 k 77 (35.5%)53 (42.4%)24 (26.1%)
From 10 to 20 k 53 (24.4%)20 (16%)33 (35.9%)
From 20 to 30 k22 (10.1%)15 (12%)7 (7.6%)
More than 30 k 8 (3.7%)4 (3.2%)4 (4.3%)
Educational Level
Uneducated1 (0.5%)1 (0.8%)0 (0%)


0.93
Primary6 (2.8%)4 (3.2%)2 (2.2%)
Medium 6 (2.8%) 4 (3.2%)2 (2.2%)
Secondary 55 (25.3%)31 (24.8%)24 (26.1%)
University143(65.9%)82 (65.6%)61 (66.3%)
Post-Graduate 6 (2.8%)3 (2.4%)3 (3.3%)
How many times a year are you hospitalized for sickle cell anaemia episodes?
0 28 (12.9%)13 (10.4%)15 (16.3%)

0.26
1 33 (15.2%)20 (16%)13 (14.1%)
2 43 (19.8%)23 (18.4%)20 (21.7%)
3 31 (14.3%)20 (16%)11 (12%)
4 27 (12.4%)12 (9.6%)15 (16.3%)
5 55 (25.3%)37 (29.6%)18 (19.6%)
Number of episodes of pain crisis in the last three years
0 24 (11.1%)12 (9.6%)12 (13%)

0.24
1 28 (12.9%)16 (12.8%)12 (13%)
2 23 (10.6%)10 (8%)13 (14.1%)
3 25 (11.5%)11 (8.8%)14 (15.2%)
4 18 (8.3%)12 (9.6%)6 (6.5%)
5 99 (45.6%)64 (51.2%)35 (38%)
Number of episodes of acute chest syndrome in the last three years
0 84 (38.7%)47 (37.6%)37 (40.2%)


0.32
1 35 (16.1%)23 (18.4%)12 (13%)
2 37 (17.1%)21 (16.8%)16 (17%)
3 19 (8.8%)8 (6.4%)11 (12%)
4 17 (7.8%)8 (6.4%)9 (9.8%)
5 25 (11.5%)18 (14.4%)7 (7.6%)
Have you been admitted to the ICU?
Yes60 (27.6%)43 (34.4%)17 (18.5%)0.01 *
No157 (72.4%)82 (65.6%)75 (81.5%)
Did you have an operation for spleen removal?
Yes15 (6.9%)10 (8%)5 (5.4%)0.46
No202 (93.1%)115 (92%)87 (94.6%)
Did you receive blood transfusion due to SCD consequences?
Yes166 (76.5%)104 (83.2%)62 (67.4%)0.007 *
No51 (23.5%)21 (16.8%)30 (32.6%)
Do you have other chronic diseases?
Yes175 (80.6%)104 (83.2%)71 (77.2%)0.26
No42 (19.4%)21 (16.8%)21 (22.8%)
Gallstones
Yes 98 (45.2%)69 (55.2%)29 (31.5%)0.001 *
No119 (54.8%)56 (44.8%)63 (68.5%)
Pulmonary hypertension
Yes12 (5.5%)7 (5.6%)5 (5.4%)0.95
No205 (94.5%)118 (94.4%)87 (94.6%)
Joint necrosis
Yes71 (32.7%)48 (38.4%)23 (25%)0.038 *
No146 (67.3%)77 (61.6%)69 (75%)
Stroke
Yes17 (7.8%)12 (9.6%)5 (5.4%)0.25
No200 (92.2%)113 (90.4%)87 (94.6%)
Kidney dysfunction
Yes14 (6.5%)9 (7.2%)5 (5.4%)0.60
No203 (93.5%)116 (92.8%)87 (94.6%)
Recurrent infections or infections
Yes73 (33.6%)46 (36.8%)27 (29.3%)0.25
No144 (66.4%)79 (63.2%)65 (70.7%)
SD: Standard deviation. ICU: Intensive care unit. * The alpha criterion for the p-value was set to 0.05.
Table 2. Self-reported adherence to hydroxyurea and its association with sociodemographic and clinical characteristics of the participants. (From Supplementary Material Table S1.)
Table 2. Self-reported adherence to hydroxyurea and its association with sociodemographic and clinical characteristics of the participants. (From Supplementary Material Table S1.)
Sociodemographic CharacteristicsHydroxyurea Adherencep-Value
Low Moderate/High
Frequency (n = 125)102 (81.6%)23 (18.4%)
Age (mean; SD)29.15; 8.4325.74; 6.130.89
Did you do the blood transfusion because of the severe shortage of it?
Yes89 (87.3%)15 (56.2%)0.01 *
No13 (12.7%)8 (34.8%)
Recurrent infections or infections
Yes42 (41.2%)4 (17.4%)0.03 *
No60 (58.8%)19 (82.6%)
SD: Standard deviation. * The alpha criterion for the p-value was set to 0.05.
Table 3. a: Scores of B-IPQ according to the level of adherence to HU and gender. b: Scores of B-IPQ according to the history of blood transfusion for ICU admission. c: Scores of B-IPQ according to the number of hospital admission per year.
Table 3. a: Scores of B-IPQ according to the level of adherence to HU and gender. b: Scores of B-IPQ according to the history of blood transfusion for ICU admission. c: Scores of B-IPQ according to the number of hospital admission per year.
(a)
B-IPQ DomainsAll (n = 217)Hydroxyurea AdherenceGender
LowModerate/Highp-ValueMaleFemalep-Value
Consequences 6.30; 3.086.46; 2.967.61; 2.50.086.86; 2.985.62; 3.070.003 *
Personal Control 5.13; 3.055.32; 3.194.57; 2.670.294.82; 3.1645.51; 2.880.10
Treatment Control 5.77; 2.996.38; 2.894.78; 3.50.02 *5.43; 3.046.18; 2.890.06
Identity 6.26; 2.796.39; 2.666.65; 2.420.666.70; 2.795.74; 2.700.01 *
Concerns 6.51; 3.046.42; 2.926.61; 3.050.787.10; 2.795.81; 3.180.002 *
Understanding 7.92; 2.578.13; 2.388.09; 2.620.947.74; 2.668.14; 2.460.25
Emotional Response 6.15; c2.265.99; 3.156.87; 2.980.226.40; 3.155.86; 3.750.25
(b)
B-IPQ DomainsAll (n = 217)Blood TransfusionICU Admission
NoYesp-ValueNoYesp-Value
Consequences 6.30; 3.085.63; 3.176.51; 3.030.0755.99; 2.987.12; 3.220.016 *
Personal Control 5.13; 3.054.82; 3.045.23; 3.0560.405.29; 2.8854.73; 3.440.23
Treatment Control 5.77; 2.995.51; 3.015.86; 2.980.475.85; 2.985.85; 3.010.56
Identity 6.26; 2.795.67; 3.106.45; 2.670.085.86; 2.727.32; 2.710.001 *
Concerns 6.51; 3.046.29; 3.286.58; 2.970.566.29; 2.997.08; 3.130.087
Understanding 7.92; 2.577.43; 3.048.07; 2.400.127.83; 2.548.15; 2.650.42
Emotional Response 6.15; 2.265.43; 3.346.37; 3.210.075.99; 3.316.58; 3.110.22
(c)
B-IPQ DomainsAll (n = 217)Hospital Admission(s) per Year
012345 or Morep-Value
Consequences 6.30; 3.084.54; 3.665.52; 3.045.98; 2.696.19; 2.576.78; 2.757.75; 2.93<0.001 *
Personal Control 5.13; 3.055.79; 3.335.64; 2.215.53; 2.275.39; 2.664.67; 3.484.27; 3.210.14
Treatment Control 5.77; 2.995.68; 3.666.27; 2.305.63; 2.646.16; 3.435.93; 3.195.35; 2.970.74
Identity 6.26; 2.793.68; 3.0195.42; 2.776.00; 2.046.74; 2.237.07; 2.367.62; 2.66<0.001 *
Concerns 6.51; 3.044.54; 3.515.82; 2.686.65; 2.796.65; 2.817.15; 2.597.44; 3.080.001 *
Understanding 7.92; 2.577.36; 3.297.82; 2.407.91; 2.758.52; 2.428.15; 1.757.84; 2.910.65
Emotional Response 6.15; 2.265.11; 3.456.18; 3.085.67; 3.165.42; 3.487.00; 3.007.04; 3.130.04 *
* The alpha criterion for the p-value was set to 0.05
Disclaimer/Publisher’s Note: The statements, opinions and data contained in all publications are solely those of the individual author(s) and contributor(s) and not of MDPI and/or the editor(s). MDPI and/or the editor(s) disclaim responsibility for any injury to people or property resulting from any ideas, methods, instructions or products referred to in the content.

Share and Cite

MDPI and ACS Style

Madkhali, M.A.; Abusageah, F.; Hakami, F.; Zogel, B.; Hakami, K.M.; Alfaifi, S.; Alhazmi, E.; Zaalah, S.; Trabi, S.; Alhazmi, A.H.; et al. Adherence to Hydroxyurea and Patients’ Perceptions of Sickle Cell Disease and Hydroxyurea: A Cross-Sectional Study. Medicina 2024, 60, 124. https://doi.org/10.3390/medicina60010124

AMA Style

Madkhali MA, Abusageah F, Hakami F, Zogel B, Hakami KM, Alfaifi S, Alhazmi E, Zaalah S, Trabi S, Alhazmi AH, et al. Adherence to Hydroxyurea and Patients’ Perceptions of Sickle Cell Disease and Hydroxyurea: A Cross-Sectional Study. Medicina. 2024; 60(1):124. https://doi.org/10.3390/medicina60010124

Chicago/Turabian Style

Madkhali, Mohammed Ali, Faisal Abusageah, Faisal Hakami, Basem Zogel, Khalid M. Hakami, Samar Alfaifi, Essam Alhazmi, Shaden Zaalah, Shadi Trabi, Abdulaziz H. Alhazmi, and et al. 2024. "Adherence to Hydroxyurea and Patients’ Perceptions of Sickle Cell Disease and Hydroxyurea: A Cross-Sectional Study" Medicina 60, no. 1: 124. https://doi.org/10.3390/medicina60010124

Article Metrics

Back to TopTop