Estimated 7% of world population is carrier of hemoglobin disorders [1] and approximately 1.5% of world population carries gene for beta Thalassemia [2]. Each year, 50,000 to 100,000 children die of thalassemia major in low and middle income countries [1]. Worldwide incidence level is estimated as 1 in every 100,000 [3]. Unfortunately, in Pakistan the number of children affected with transfusion dependent thalassemia is relatively higher than in most countries [4]. This is attributed to factors such as high frequency of gene, consanguineous marriages, high birth rate and rapidly increasing population [5]. Presence of thalassemia has been observed in all parts of the country [4]. Every year, 5000 children are born with thalassemia major in Pakistan, which puts the estimate of affected children in 5 out of 100, with the carrier rate being 5% [6] [7]. Furthermore, it was found in a study that children affected with refractory anemia had 83% chances to be detected with beta thalassemia [8]. A wide phenotypic spectrum of thalassemia has been observed and β-thalassemia major is a severe transfusion-dependent form of the disease, associated with various different complications that are caused by tissue hypoxia and also because of iron overload. Repeated transfusions and increased intestinal iron absorption are the two main sources of iron overload [9].

In developing countries lack of competence in dealing effectively with the disease arises due to a number of factors [10]. Β-thalassemia is renowned as the most commonly occurring disorder in the inherited hematological and single gene disorders family [11] [12]. In this disorder, a reduced production of hemoglobin is observed causing a severe case of anemia among patients [13]. Hemoglobin molecule is primarily composed of two of each alpha and beta chains, characterized by their formation [3] [13]. Due to a defect in messenger RNA, the beta chain acquires an erroneous synthesis causing a deformation of RBCs [14]. The occurrence of severe anemia requires the patients to be transfused with blood at regular intervals along with iron chelation therapy and sometimes bone marrow transplantation [15] [16]. However, the compliance with treatment poses several challenges to the families of the affected individuals [17].

In thalassemia, patient serum ferritin detects total body iron, if the level of ferritin is above 2500 mg/d, in 15 years, this leads to multiple complications such as cardiac disease. Parents of thalassemic children are also concerned about many other problems such as bony deformity, appearance of the child, poor self-image, short stature delayed sexual development, and frequent hospital visits. Hemosiderosis is a major cause of mortality in these patients [1] [18]. Such patients also develop complication like cardiovascular diseases infections, bone defects and diabetes [19]. Thalassemic patients can only be cured by bone marrow transplant but unfortunately is beyond the reach of majority of the families in Pakistan [20].

In high-income countries, to prevent the disease related complications and improve outcomes for thalassemia patients variable measures are implemented such as the provision of safe blood transfusions, oral and parenteral iron chelating agents, noninvasive and regular iron monitoring, plus many other methods of supportive care [21] [22].

These challenges are examined separately in this study with the context of psychological, financial and social aspects.

This cross-sectional study was carried out at PNS Shifa Hospital Karachi, Jinnah Post Graduate Institute Karachi, and Civil Hospital Hyderabad. Data was collected based on a structured questionnaire. Parents of children suffering from transfusion dependent thalassemia major were included in the study. Data collection spanned over a period of 6 months, from June 2018 to December 2018. The sample size was determined to be 237, as calculated by standard formula. The Parents were interviewed using a preset questionnaire by the researcher after acquisition of verbal consent from each participant and explaining the aims and objectives of the study.

Questions concerning the educational status of parents, monthly income, expenses on travelling to hospital, transfusions, chelating medicines, social life of parents and how their child’s terminal illness affects their relationship and mental health were included. Data collected was analyzed through software SPSS version 25. This study has been approved by ethical review committee of Bahria University Medical and Dental College. Reference No: ERC 57/2018.

Sample size was calculated from online software openepi.com version 3. The statistical parameters were 95% confidence 5% margin of error. Population size for finite population correction factor N = 100,000 and prevalence of beta thalassemia was 5% (reference study). The required sample size was 237.

Formula used was,

Samplesizen = [ DEFF ∗ N p ( 1 − p ) ] / [ ( d 2 / Z 2 1 − α / 2 ∗ ( N − 1 ) ) + p ∗ ( 1 − p ) ]

Results obtained from the data are analyzed from the tabulated frequencies attained through utilization of SPSS 25 incorporating frequency analysis, crosstab analysis and chi square tests.

Thalassemia major is a chronic, lifelong illness, requiring scheduled blood transfusion, regular medicines and repeated hospital visits, which place patients and their families under great psychological and financial burden. The primary purpose of this study was to evaluate the impact on families of thalassemia major patients in three distinctive areas. The data generated from the questionnaire and evaluated in the results has equipped us with the ability to form a few inferences. Financially, it was observed that lower income class families, mostly from the PK Rupees 5000 - 15,000 monthly income group, were affected the most in contrast to the higher income groups. 83% admitted to having financial constraints with 74% severely affected by purchasing blood, medicines, traveling to hospital and admissions. A study conducted in Multan produced similar results [23]. A study conducted in Srilanka showed 30% of families had severe economic problems [24]. Irrespective of the income classes, the responses centered majorly on moderate scale (Figure 2). However, through chi square tests, the p value obtained enabled us to deduce the inferences in significance of the income classes. Furthermore, among social implications it was observed that the ratio of illiteracy in mothers of the affected patients was higher in comparison with fathers. 17.3% respondents had confessed to have troubled relationship with their spouse as a consequence of dealing with the child’s illness, while it was 23% in another study [25]. 39% participants revealed lack of support from relatives. 62% participants had difficulty managing routine activities, similar to another research that was conducted [25]. This study revealed that 19.8% feel they give lesser attention to other children because of their child disease. 80% participants reported to feel depressed or sad, 24% take medication for depression. In a study conducted in Multan 29% parents had moderate to severe depression while 3% had severe depression [20]. The study shows that 92% participants felt there is nothing in the future to be hopeful regarding their child’s terminal illness. Through this analysis it can be concluded that psychological implications on the families of thalassemia major patients are significant.

Through the findings of this research it was established that lower income classes had a higher chance of suffering economically due to presence of a child suffering from thalassemia major. Adverse consequences of the disease on mental health of the families of affected children were also deduced.

Conception and design: Nimra Shafi, Shakeel Ahmed;

Collection of data: Nimra Shafi, Abdul Raheem;

Analysis and interpretation of data: Nimra Shafi, Shakeel Ahmed;

Statistical analysis: Faisal Fahim;

Drafting of article: Nimra Shafi;

Critical review of article: Shakeel Ahmed.

We gratefully thank Faisal Fahim for statistical assistance.

The authors declare that there is no conflict of interest.

Shafi, N., Ahmed, S. and Siddique, A.R. (2021) The Psychosocial and Financial Ramifications of Thalassemia on Parents of Thalassemic Children Presented at Tertiary Care Hospitals. Open Journal of Pediatrics, 11, 379-387. https://doi.org/10.4236/ojped.2021.113034