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| ORIGINAL ARTICLE |
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| Year : 2018 | Volume
: 9
| Issue : 1 | Page : 22-28 |
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Clinical features and outcome of sickle cell anemia in a tertiary center: A retrospective cohort study
Abdulrahman Musaad Alhumaid1, Abdulmalek Suliman Aleidi1, Abdullelah Saleh Alfakhri1, Naif Khalil Alosaimi1, Yosra Z Ali2, Mohsen Saadi Alzahrani2
1 King Saud Bin Abdulaziz University for Health Sciences, College of Medicine, Riyadh, Kingdom of Saudi Arabia
2 Department of Hematology, King Saud Bin Abdulaziz University for Health Sciences, National Guard Health Affairs, Riyadh, Kingdom of Saudi Arabia
| Date of Web Publication | 22-Mar-2018 |
Correspondence Address:
Dr. Mohsen Saadi Alzahrani
King Saud Bin Abdulaziz University for Health Sciences, Department of Hematology, National Guard Health Affairs, P.O. Box 22490, Riyadh 11426
Kingdom of Saudi Arabia
 Source of Support: None, Conflict of Interest: None  | Check |
DOI: 10.4103/joah.joah_48_17
Introduction: Sickle cell anemia (SCA) is one of the most common genetic diseases worldwide. Patients with SCA present with varied clinical features and complications that may affect many organs in the human body. There are few treatment options for SCA, and patient responses vary; the only curative therapy is a stem cell transplant or gene therapy. We seek to study the clinical features and treatment options for patients with sickle cell disease treated in King Abdulaziz Medical City, Riyadh.
Methods: This study was a retrospective cohort study of all adult SCA patients who were admitted to our institution during the period from 1983 to 2016. Data were entered into Excel spreadsheets and managed with SPSS. Chi-square test was used to compare responses to therapy and in patients with different presentations.
Results: A total of 106 patients with sickle cell disease were included in this study. The percentages with respect to hospital admissions per year were as follows: 34.9% (37 patients) were never admitted, 26.4% (28 patients) were admitted fewer than 2 times, 24.5% (26 patients) were admitted 3–5 times, and 13.2% (14 patients) were admitted more than 5 times. The number of complications was used to measure the severity of the disease. The disease severity was higher in males than in females (67.3% vs. 32.7%, respectively; P = 0.018). The disease severity was higher in those who were born in the Western and Southwestern areas than in other areas (84.2% vs. 15.8%, respectively; P = 0.007). Hydroxyurea significantly reduced the severity of SCA with a P = 0.002.
Conclusion: Our study showed that vaso-occlusive crisis was the most common complication and indication for hospital admission. Treatment with hydroxyurea led to a significant reduction in the number of hospital admissions. Keywords: Anemia, complication, hemoglobin, hemoglobin SS, hospitalization, sickle cell, sickle cell disease
How to cite this article:
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 |
How to cite this URL:
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 [serial online] 2018 [cited 2023 Oct 2];9:22-8. Available from: https://www.jahjournal.org/text.asp?2018/9/1/22/228331 |
| Introduction | |  |
Sickle cell anemia (SCA) is one of the most common genetic diseases in the world. It is an autosomal recessive condition, in which the normally freely flowing cytosol of red cells is viscous, making them much less deformable and affecting their ability to traverse narrow capillary beds.[1],[2] These irregularly shaped blood cells can get stuck in blood vessels, blocking or slowing blood flow and oxygen to the organs, and causing pain and organs damage.[3],[4],[5],[6] The mutation in the β-globin chain results from a substitution of valine for glutamic acid at the sixth codon.[7],[8],[9] The prevalence is not limited to a certain race; however, the disease mostly affects African populations and those of African descent in many other countries.[10],[11],[12],[13],[14],[15],[16] The prevalence of sickle cell disease differs in different parts of Saudi Arabia, with the highest prevalence in the eastern province followed by the Southwestern provinces and the severity of the disease differs from region to another.[17],[18] Currently, approximately 61,000 individuals have the disease in Saudi Arabia.[19] Sickle cell disease is commonly observed in clinical practice in Saudi Arabia. The purpose of this research is to study the variations in clinical features and treatment options for patients with sickle cell disease treated at King Abdulaziz Medical City, Riyadh.
| Methods | | |
The study was a retrospective cohort study, and we targeted all patients diagnosed with SCA from the year 1983–2016. All patients who admitted with a diagnosis of SCA to King Abdulaziz Medical City in Riyadh were included in this study. A data collection sheet was formulated by the researchers, and it included the following variables: patient demographic data, diagnostic and laboratory data, clinical data, and disease complications. The data were collected from patient files as well as from the electronic medical record system. We used a unique identification number for every patient instead of name or medical record number. The data were kept confidential and stored in a safe place. Data were entered into Excel spreadsheets and then managed with SPSS (Statistical package for the social Sciences) version 22 using descriptive methods: Mean and standard deviation for numerical variables and percentages and frequencies for all categorical variables. Chi-square test was used to compare responses to therapy and in patients with different presentations.
| Results | | |
We included 106 patients with sickle cell disease diagnosed during the period from 1983 to 2015. Male patients were more prevalent in this population (55.7%) compared to female patients (44.3%). The median age was 27 years. Of the enrolled patients, 30.2% (32 patients) were diagnosed with SCA hemoglobin type SS and 1.9% (2 patients) with SCA hemoglobin type SC. The majority of patients in this study were from the Southwestern region (38.7%; 41 patients), followed by 13.2% (14 patients) from the Western region, 14.2% (15 patients) from the Central region, 7.5% (8 patients) from the Eastern region, 0.9% (1 patient) from the Northern region, and 25.5% (27 patients) with no available data of city of origin. The unmarried patients made up 59.4% (63 patients) of the cohort and 32.1% (34 patients) of patients were married. A total of 49.1% (52 patients) had a family history of SCA or sickle cell trait. [Table 1] shows the summary of demographic data.
Disease complications are shown in [Table 2]. A total of 30.2% of patients (32 patients) presented with acute painful crisis as the initial manifestation, 28.3% (30 patients) presented with anemia, and 1.9% (2 patients) presented with dactylitis. The average number of hospital admissions per year for the last 3 years at the time of data collection was as follows: 34.9% (37 patients) of patients were not admitted, 26.4% (28 patients) were admitted fewer than 2 times, 24.5% (26 patients) were admitted 3–5 times, and 13.2% (14 patients) were admitted more than 5 times [Graph 1]. The number of admissions to the hospital was used as an indicator of disease severity. Veno-occlusive disease was seen in 84% (89 patients) of patients and was the most common complication. Of this group, 23.6% of patients manifested with fewer than 3 instances per year, 22.5% with 3–5 instances per year, and 25.8% with more than 5 instances per year. Acute chest syndrome was seen in 43.4% of patients (46 patients). Of this group, 21.8% of patients experienced 1 instance, 26.1% had 2 instances, and 13% had 3 or more instances. Stroke was seen in 1.9% of patients (2 patients) as a single stroke instance; one was ischemic and the other was hemorrhagic at ages 22 and 49 years old, respectively. Seizures were seen in 5.7% of patients (6 patients). Avascular necrosis (AVN) of joints was seen in 21.7% of patients (23 patients). Seventeen patients (73.9%) had 1 joint involvement, and 26.1% (6 patients) had 2 or more joints involvements. Joint replacement as treatment for AVN was performed for 13.2% (14 patients) of the entire patient population. Osteomyelitis was seen in 2.3% of patients (13 patients); 4.7% (5 patients) had an aplastic crisis and 20.8% (22 patients) had a hemolytic crisis. Furthermore, 10.4% of patients (11 patients) were found to have pulmonary hypertension, 6.6% (7 patients) had splenic sequestration, 5.7% (6 patients) had a history of venous thrombosis, and 2.8% (3 patients) had hepatic sickling. Psychiatric complications were found in 4.7% of patients (5 patients) and 80% of these (4 patients) had experienced depression [Graph 2].
Treatment and responses
Different treatment modalities were used in our patient cohorts depending on the severity and complications. Hydroxyurea was used for 53.8% of patients (57 patients). The average number of admissions per year before starting hydroxyurea was 5 admissions per year; after starting hydroxyurea, we have observed a reduction in the admission rate to two admissions per year per patient, which may indicate a therapeutic response to hydroxyurea. Blood transfusions were frequently used in our group, with 10.4% of patients (11 patients) receiving regular monthly blood transfusions. The indications for blood transfusion were as follows: Recurrent uncontrolled painful vaso-occlusive crisis (VOC) crises in 17 patients, acute chest syndrome in 12 patients, stroke in 1 patient, and recurrent priapism in 1 patent. By contrast, approximately 37.7% of patients (40 patients) received occasional blood transfusions and the common indications for blood transfusions in this group were as follows: Painful crises in 40 patients, hemolytic crises in 17 patients, severe anemia in 13 patients, aplastic crises in 4 patients, and sequestration crises in 3 patients. A total of 14.2% (15 patients) were given iron chelation, 46.7% of which were compliant with the iron chelation therapy. Folic acid tablets were given to 80.2% of patients (85 patients) and 44.3% (47 patients) were on prophylactic antibiotics. We did not find accurate data regarding the vaccination rate in our group; however, 10.4% of our group was documented as having received the influenza virus vaccine and 3.8% received regular (annual) vaccinations. In hyposplenic cases, triple vaccination was documented in only 0.9%. Regarding pain-relieving medications, 51.9% of the group was given narcotics and 61.8% of these were chronic users. A total of 10.9% of patients receiving narcotics were reported to be dependent on narcotic medications. Nonsteroidal anti-inflammatory drugs were given to 86.8% of patients. The compliance is defined as complete adherence to the medications rather than erratic use of medications [Table 3].
The number of complications was used to measure the severity of the disease. Several factors that were considered significantly affect both the severity and course of the disease. Male gender correlated with increased severity, 67.3% of males (35 patients) had three or more complications compared to 32.7% of females (17 patients) who had three or more complications (P = 0.018). Another significant factor was area of origin; 84.2% of patients (32 patients) who were born in the Western and Southwestern areas had three or more complications. However, only 15.8% (6 patients) of those born in the Northern, Eastern, and Central areas had three or more complications (P = 0.007). Patients with positive family history have shown increased disease severity, with 90% (27 patients) of those with positive family history having three or more complications and 10% (3 patients) with no family history having three or more complications (P = 0.009) [Table 4]. | Table 4: Univariate analysis: Factors affecting severity outcome of the sickler patients
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| Discussion | | |
Demographic data has been shown to significantly influence the course of the disease. As indicated in the results, male patients were shown to have a higher incidence than female patients in our sample and male gender was associated with a more severe disease course. In addition, a study performed in Eastern Saudi Arabia reported that males have higher disease severity compared to females.[20] Our results are consistent with studies reporting that SCA in males takes a more severe course compared to that in females.[21],[22],[23] Individuals diagnosed with SCA from specific areas in Saudi Arabia, such as the Western and Southwestern provinces, have a higher incidence of complications and disease severity. The genotype of SCA in these areas correlated with the Benin-African genotype, which is known to be associated with a more severe disease phenotype compared with the Indian-Arab genotype, which is typically seen in patients from the Eastern region.[17] Our study has shown that the predominant subtype is the SS type, which is associated with a higher rate of complications. In addition, a previous study reported that certain phenotypes such as the SS type had higher complication rates.[17] In our study, it was not possible to assess or compare the different subtypes of SCA, as the predominant subtype in our patients was SS.
The majority of our patients presented with an acute painful crisis as an initial manifestation. Many studies worldwide have reported findings similar to those in our study; common reported manifestations include mild-to-severe anemia, painful crises, frequent infections, hand and foot syndrome, and stroke.[24],[25],[26],[27],[28] This might be because the sample included patients with an SS type. The rate of other complications in our patient subgroup was similar to what has been reported in other studies, with minor differences. In comparison, stroke was seen in <2% of our group, while it is expected to be found in 10% of SCA patients in general.[29],[30],[31] This could be due to the small sample size, the fact that the majority of patients in our group are adults and our inclusion of only a hospital-based patient cohort rather than a community cohort.
Our study has shown the average number of hospital admissions due to complications; VOC was the most common complication, a finding that was consistent with many studies globally.[32],[33],[34],[35] A study performed in 2012 had findings similar to ours that 95% of their sample experienced a vaso-occlusive complication that required admission and they considered this “a hallmark” of the disease.[36] The study also demonstrated that acute chest syndrome came after the VOC as a common complication. This same study demonstrated that 50% of cases occurred after the hospital admission for acute painful crisis.[36] This might be because patients who are admitted are more susceptible to infections. Another study conducted in 1997 showed that the most common age group affected was children.[37] This might be due to the maturity of the immune system of adults since children have immature immune systems.[38]
We have studied AVN as a complication of Sickle cell anemia, specifically the number of joint involved and whether the patient had undergone joint replacement surgery. The study that was performed in 2012 also discussed AVN as a complication, especially the epiphyseal bones of the hip, shoulder, and spine; however, any joint could be affected. The prevalence was 26% in children and 48.6% in adults.[36] The occurrence of AVN might be due to recurrent episodes of VOC since pain crises could cause infarcts and necrotization of the bones and with time could lead to damage in the bone marrow.[39]
Hydroxyurea can be considered the standard of care and ideal agent for treating SCA as it provides multiple therapeutic benefits.[40],[41],[42],[43],[44] We have also studied the efficacy of hydroxyurea treatment on hospital admissions due to SCD complications, before starting hydroxyurea, the average admission was five admissions in an average for 3 years, after initiating hydroxyurea, the average admission was three admissions in an average of 3 years. A study was published in November 2016 that included a group of pediatric age showed a decrease in hospital admissions, pain incidence, and emergency department visits due to complications.[37] Our study discussed only the adult group, which may show different percentages since age could play a role in the efficacy of the treatment. A study conducted in 2014 showed that women with SCA had a higher rate of complications than those in the general population. The hemoglobin SS type also correlated with much worse complications than those in the hemoglobin SC type.[45]
| Conclusion | | |
Although our study included a small sample and was performed at a single center, it showed that our patient group has clinical features and complications that are similar to those in previously reported studies. We found that the following three factors correlate with disease severity: Patient gender, region of origin, and family history of severe disease. The retrospective nature of the study may limit the accuracy of some of the data and more extensive studies are needed at a larger scale. These data need to be confirmed in a larger prospective or registry-based study.
Acknowledgements
The authors would like to acknowledge the help of Nature Editing Services for reviewing the manuscript and necessary editing for English grammar.
Financial support and sponsorship
Nil.
Conflicts of interest
There are no conflicts of interest.
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[Table 1], [Table 2], [Table 3], [Table 4]
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