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. 2019 Apr 8;20:122. doi: 10.1186/s12882-019-1316-z

Quality of life among patients with moderate to advanced chronic kidney disease in Ghana - a single centre study

Elliot K Tannor 1,, Betty R Norman 2, Kwame K Adusei 3, Fred S Sarfo 2, Mogamat R Davids 4, George Bedu-Addo 2
PMCID: PMC6454740  PMID: 30961570

Abstract

Background

The prevalence of chronic kidney disease (CKD) is increasing worldwide and in Africa. Health related quality of life (QOL) has become an essential outcome measure for patients with CKD and end stage renal disease (ESRD). There is growing interest worldwide in QOL of CKD patients but paucity of data in Ghana. This study sought to assess QOL in patients with moderate to advanced CKD (not on dialysis) and establish its determinants.

Methods

We conducted a cross sectional observational study at the renal outpatient clinic at Komfo Anokye Teaching Hospital (KATH). We collected demographic, clinical and laboratory data. A pretested self-administered Research and Development corporation (RAND®) 36-Item Health Survey questionnaire was administered and QOL scores in physical component summary (PCS) and mental component summary (MCS) were computed. Determinants of QOL were established by simple and multiple linear regression. P value of < 0.05 was considered statistically significant.

Results

The study included 202 patients with CKD not on dialysis. There were 118(58.5%) males. Mean age was 46.7 ± 16.2 years. The majority, 165(81.7%) of patients were on monthly salaries of less than GHS 500 (~USD 125). Chronic glomerulonephritis was the most common cause of CKD in 118 (58.5%) patients followed by diabetes mellitus in 40 (19.8%) patients and hypertension in 19 (9.4%) patients. The median serum creatinine was 634.2 μmol/L (IQR 333–1248) and the median eGFR was 7 ml/min/1.73m2 (IQR 3–16). The most common stage was CKD stage 5 accounting for 143 (71.1%), followed by CKD stage 4 with 45 (22.4%) of cases and 13 (6.5%) of CKD stage 3. The overall mean QOL score was 40.3 ± 15.4. MCS score was significantly lower than PCS score (37.3 ± 10.8 versus 43.3 ± 21.6, P < 0.001). Multiple linear regression showed that low monthly income (p = 0.002) and low haemoglobin levels (p = 0.003) were predictive of overall mean QOL.

Conclusion

Patients with moderate to advanced CKD had low-income status, presented with advanced disease and had poor QOL. Anaemia and low-income status were significantly associated with poor QOL.

Keywords: Quality of life, Chronic kidney disease, Ghana

Background

The prevalence of chronic kidney disease (CKD) is increasing worldwide and in Africa [1, 2]. The global prevalence is estimated to be 10–13% [1, 3]. The prevalence of CKD in sub-Saharan Africa was found to be 13.9% in a meta-analysis [4]. Chronic glomerulonephritis together with non-communicable diseases such as hypertension and diabetes mellitus account for the increasing prevalence of CKD in Sub-Saharan Africa and in Ghana [5]. CKD is associated with increasing morbidity and mortality and also known to impact negatively on quality of life (QOL) [6, 7].

QOL is defined by the World Health Organisation (WHO) as “an individual’s perception of their position in life in the context of the culture and value system where they live, and in relation to their goals, expectations, standards, and concerns” [8]. It is a comparison between patients’ expectations and reality. QOL also reflects treatment quality in patients with CKD and end stage renal disease (ESRD) since adapting to CKD involves physical, psychological and social processes to achieve the best outcomes [9]. QOL also represents a functional impact of a disease or its treatment on the subjective feeling of the affected individual about their physical, mental, spiritual, emotional, social and functional wellbeing [10]. The collection of QOL data helps patients understand their disease and the implications of treatment on their health [11].

Progression to ESRD also serves as an important burden on health care systems [12]. Management of ESRD involves haemodialysis (HD), peritoneal dialysis (PD), renal transplantation and conservative management. Conservative management is now established as a treatment option among geriatric patients in some developed countries [13].

In Ghana, like most countries in Sub-Saharan Africa, most patients with ESRD cannot afford renal replacement therapy (RRT). There is lack of governmental support for chronic dialysis and most patients have to pay out of pocket to survive. Ghana has a national health insurance scheme that covers some medical conditions but not chronic haemodialysis. In most cases, patients and their relatives may need to solicit for funds from their families, community, corporate organizations and religious groups to enable them go through with their haemodialysis sessions and plan renal transplantation outside the country as Ghana currently does not have a renal transplant programme. The social support system for patients with CKD is mainly by their families, community, work place and religious groups.

In majority of cases, conservative management is not the patient’s choice as seen in developed countries. When conservation management is resorted to in Ghana, medications are prescribed to make patients comfortable both on admission and after discharge from hospital. They are extensively counselled about end of life decisions. Palliative care is not free in Ghana. Patients and or their families have to pay for palliative care and treatments if medications or procedures performed are not covered by the national health insurance scheme. This worsened the financial burden on patients and in some situations, they just request to be discharged home against medical advice.

Haemodialysis, which is the most common form of RRT in Ghana, only provides a partial solution to the deteriorating kidney function. Patients still have to deal with some symptoms of the disease, many medications, a strict diet, regular hospital visits, multiple admissions and changes in body image when dialysis catheters are inserted or arteriovenous fistulae are made.

With many patients with ESRD unlikely to gain access to RRT in Ghana mainly because of financial constraints, it is imperative to ensure that CKD patients with advanced disease have the best QOL when being managed. There has been growing interest lately in improving the QOL of patients with kidney disease worldwide and not just on survival [1416] but very few studies have focused on QOL of patients with CKD and ESRD in Ghana.

We therefore set out to establish the QOL of patients with moderate to advanced CKD in Ghana and determine the predictors of QOL. This will aid in the holistic management of patients with CKD and ESRD more especially in the absence of RRT. It will serve as the baseline data for further QOL studies in patients on RRT in Ghana.

Methods

We conducted a cross sectional study at renal out-patient clinic of the Komfo Anokye Teaching Hospital (KATH). KATH is a 1200 bed capacity tertiary level health facility located in Kumasi in the Ashanti region of Ghana. KATH runs a twice-a-week out-patients’ clinic for patients with CKD and ESRD. Due to poor economic status, most patients seen are unable to afford RRT and are managed conservatively even in ESRD with indications for haemodialysis. Haemodialysis is the main RRT modality in Ghana. Ghana does not have a renal transplant program and does not offer peritoneal dialysis as a treatment modality for adult patients with ESRD. The study was conducted from October 2016 to August 2017.

Participants were included in the study if they had confirmed CKD with estimated glomerular filtration rate (eGFR) of less than 60 ml/min/1.73m2 as estimated by the Modification of Diet in Renal Disease (MDRD) equation [17] and gave a written informed consent. They were then staged according to Kidney Disease Outcomes Quality Initiative (KDOQI) [18] and Kidney Disease Improving Global Outcome (KDIGO) criteria [19]. Patients with acute kidney injury, on RRT or with concurrent chronic illness such as malignancy, chronic liver disease or stroke unrelated to the CKD or admitted to hospital within the last 1 month were excluded from the study. The clinical aetiology of CKD as diagnosed by the attending nephrologist was recorded from clinical notes.

A structured questionnaire was administered to each patient to obtain the following data: age, sex, level of education, marital status, occupation and monthly salary in Ghanaian Cedis (GHS). Clinical and laboratory data such as blood pressure, haemoglobin level, mean corpuscular volume (MCV), mean corpuscular haemoglobin (MCH), serum urea and serum creatinine were also recorded.

Anaemia was defined as haemoglobin level of less than 12 g/dl as suggested by the KDIGO guidelines [19]. Participants were then required to complete a pre-tested, validated, structured and a self-administered RAND 36-Item Health Survey (Version 1.0) [20]. The Short Form (SF-36) scoring system has been widely used and validated in most European countries. It was developed in the United States during the medical outcome survey between 1985 and 1992 and has been translated into 55 languages [21]. The questionnaire includes eight concepts: physical functioning, bodily pain, role limitations due to physical health problems, role limitations due to personal or emotional problems, emotional well-being, social functioning, energy/fatigue, and general health perceptions. It also includes a single item that provides an indication of perceived change in health. Scores range from 0 to 100 with 100 representing the best QOL score and zero representing the worst QOL scores.

Data was entered into a Microsoft software Excel® 2016 by a data entry clerk. The data was then cleaned and backed-up onto an external drive. Double entry was done to ensure the quality of the data obtained. Data collected was then exported into the statistical package Stata® version 13 [22]. Descriptive analysis was performed as means ± standard deviations if data is normally distributed and medians and inter-quartile ranges if data was not normally distributed. Percentages and frequencies were used to describe variables where appropriate.

Chi square test was used for comparisons between groups with categorical variables and an unpaired Student t test was used to compare groups with normally distributed continuous variables and Mann Whitney U test when not normally distributed. Simple and multiple linear regression analysis were then performed on the physical component summary (PCS) scores and the mental component summary (MCS) scores for determinants of QOL. Statistically significant variables identified in the simple linear regression were then included in a multiple linear regression model to establish the independent predictors for the QOL among patients with moderate to advanced CKD. Statistical significance was set at a two tailed p-value of less than 0.05.

Ethical approval from the Committee on Human Research, Publications and Ethics (CHRPE), Kwame Nkrumah University of Science and Technology and KATH was obtained before the commencement of the study.

Results

The study included 202 patients with moderate to advanced CKD not on dialysis. There were 118 (58.4%) males. The mean age of participants was 46.7 ± 16.2 years. Ninety-six (47.5%) of patients were fully employed and 83 (41.1%) were unemployed. Majority, 176 (87.1%) did not attain tertiary level of education. The vast majority, 165 (81.7%) of patients were on monthly salaries of less than GHS 500 (~USD 120). Socio-demographic data of participants are shown in Table 1. The most common cause of CKD was chronic glomerulonephritis accounting for 118 (58.4%) of patients followed by diabetes mellitus in 40 (19.8%) patients and hypertension in 19 (9.4%) patients. The most common stage of presentation of CKD was stage 5 with eGFR of less than 15 ml/min/1.73m2 accounting for 143 (71.1%) of the cases. The median eGFR at presentation was 7 ml/min/1.73m2 (IQR 3–16). Most, 187(92.6%) of patients had hypertension. The mean haemoglobin level was 9.2 ± 2.5 g/dl. All as shown in Table 1.

Table 1.

Characteristics of patients with moderate to advanced chronic kidney disease at Komfo Anokye Teaching Hospital n = 202

Characteristic n = 202
Age (yrs) μ SD 46.7 ± 16.2
Male Gender n (%) 118 (58.4%)
Marital status
 Married n (%) 137 (67.8)
 Single n (%) 42 (20.8)
 Divorced/separated n (%) 12 (5.9)
 Widowed n (%) 11(5.5)
Educational level
 No formal education n (%) 22 (10.9)
 Primary education n (%) 21 (10.4)
 Junior high school n (%) 56 (22.7)
 Senior high school n (%) 77 (38.1)
 Tertiary n (%) 26 (12.9)
Employment status
 Full time employment n (%) 96 (47.5)
 Part time employment n (%) 4 (2.0)
 Unemployed n (%) 83 (41.1)
 In training n (%) 4 (2.0)
 Retired n (%) 15 (7.4)
Monthly income status
 Less than GHS 500 n (%) 165 (81.7)
 GHS 500–1499 n (%) 20 (9.9)
 GHS 1500–2499 n (%) 9 (4.5)
 GHS 2500–3499 n (%) 2 (1.0)
 Greater than GHS 3500 n (%) 6 (3.0)
Cause of CKD
 Chronic glomerulonephritis n (%) 118 (58.4)
 Diabetes mellitus n (%) 40 (19.8)
 Hypertension n (%) 19 (9.4)
 Polycystic kidney disease n (%) 14 (6.9)
 HIVAN n (%) 5 (2.5)
 Obstructive uropathy n (%) 2 (1.0)
 Others n (%) 4 (2.0)
Stage of CKD
 Stage 3 n (%) 13 (6.5)
 Stage 4 n (%) 45 (22.4)
 Stage 5 n (%) 143 (71.1)
 Systolic BP mmHg μ SD 152.3 ± 30.0
 Diastolic BP mmHg μ SD 88.6 ± 19.8
 Hypertension n (%) 187 (92.6)
Laboratory characteristics
 Haemoglobin levels (g/dL)) μ SD 9.2 ± 2.5
 Anaemia (Hb < 12 g/dL) n (%) 164 (81.2)
 MCV fL μ SD 81.4 ± 7.6
 MCH pg/cell μ SD 28.0 ± 3.2
 Serum Urea mmol/L M (IQR) 19.2 (12.5–30.5)
 Serum Creatinine umol/L M (IQR)) 634.2 (333–1248)
 GFR ml/min/1.73m2 M (IQR) 7 (3–16)
Medications used
 ACEi/ARBs n (%) 141 (70.2)
 Calcium channel blockers n (%) 161 (80.1)
 Diuretics n (%) 160 (79.6)
 Beta- blockers n (%) 56 (27.9)
 Hydralazine n (%) 56 (27.9)
 Methyldopa n (%) 80 (39.8)
 ESA n (%) 19 (9.4)
 Intravenous iron n (%) 4 (2.0)

Yrs years, SD standard deviation, μ mean, n. number, GHS Ghanaian cedis, USD United States dollars, MCV mean corpuscular volume, MCH mean corpuscular haemoglobin, SD standard deviation, μ mean, IQR interquartile range, M median, BP blood pressure, GFR glomerular filtration rate, fL femtolitres, pg pigogram, CKD chronic kidney disease, HIVAN human immunodeficiency virus associated nephropathy, ACEi angiotension converting enzyme inhibitor, ARBs angiotensin II receptor blocker, ESA erythropoietin stimulating agent, others chronic schistosomiasis and posttraumatic nephrectomy

The most commonly used antihypertensive class was calcium channel blockers used by 161 (80.1%) of patients and diuretics used by 160 (79.6%) of patients. Only 19 (9.4%) of patients with moderate to advanced CKD were on subcutaneous erythropoietin and 4 (2%) were on intravenous iron preparations. All as shown in Table 1.

The overall mean QOL score was 40.3 ± 15.4. Mean mental component summary (MCS) score (37.3 ± 10.8, 95% CI [35.8–38.8]) was significantly lower than the mean physical component summary (PCS) scores (43.3 ± 21.6, 95% CI [40.3–46.3], P < 0.001). The scores for the various sub-domain are shown in Table 2.

Table 2.

Quality of life scores for physical component summary and mental component summary and their subdomains of patients with CKD n = 202

Principal domains Sub-domain Mean (SD) Total mean (SD)
Physical health 44.8 ± 30.0
Role physical 12.4 ± 33.0
Bodily pain 59.2 ± 29.0
General health 56.8 ± 15.8
Mean physical component summary scores 43.3 ± 21.6
Role emotional 12.4 ± 33.0
Social function 46.2 ± 20.7
Emotional wellbeing 40.7 ± 9.8
Energy 50.1 ± 9.1
Mean Mental component summary score 37.3 ± 10.8
Overall mean Quality of life score 40.3 ± 15.4

Patients with low monthly income less than GHS 500 (~USD 125) had a significantly lower overall mean QOL score than those with higher monthly income above GHS 500 (38.5 ± 14.1 versus 48.4 ± 18.3, p < 0.001). Patients with anaemia also had a significantly lower overall mean QOL score as compared to those with haemoglobin levels greater than 12 g/dl (38.3 ± 13.6 versus 49.2 ± 19.3, p < 0.001). Patients with low mean corpuscular volume (MCV) had a significantly lower overall mean QOL score 36.9 ± 10.7 as compared to those with normal or high MCV (42.8 ± 17.7, p = 0.007). Patients with CKD stage 5 also had a significantly lower overall mean QOL score as compared to those presenting with CKD stages 3 and 4 (37.9 ± 13.6 versus 46.4 ± 17.9, p < 0.001). Patients with serum urea greater than 20 mmol/L as compared to those with urea less than 20 mmol/L also had significantly lower overall mean QOL scores (36.1 ± 13.1 versus 44.0 ± 16.7, p = 0.004). All as shown in Table 3.

Table 3.

Independent variables and their association with the overall mean quality of life among patients with moderate to advanced chronic kidney disease n = 202

Variable Mean ± SD Frequency P value
Age (yrs) ≥50 39.8 ± 15.5 93 0.687
Age (yrs) < 50 40.7 ± 15.4 109
Female gender 38.9 ± 14.2 84 0.268
Male gender 41.3 ± 16.2 118
Above JHS 41.1 ± 16.2 103 0.486
JHS and below 39.5 ± 14.5 99
Employed 39.9 ± 15.9 100 0.673
Unemployed 40.8 ± 15.0 102
Monthly income(GHS) < 500 38.5 ± 14.1 165 < 0.001
Monthly income(GHS) ≥ 500 48.4 ± 18.3 37
Married 41.0 ± 15.6 137 0.373
Unmarried 38.9 ± 15.0 65
Haemoglobin < 12 g/dL 38.3 ± 13.6 164 < 0.001
Haemoglobin level ≥ 12 g/dL 49.2 ± 19.3 38
MCV < 80 fL 36.9 ± 10.7 85 0.007
MCV ≥ 80 fL 42.8 ± 17.7 117
MCH < 27 pg/cell 39.9 ± 14.4 62 0.783
MCH ≥ 27 pg/cell 40.5 ± 15.9 140
CKD stage 5 37.9 ± 13.6 143 < 0.001
CKD Stage 3 and 4 46.4 ± 17.9 58
Serum urea≥20 mmol/L 36.1 ± 13.1 90 0.004
Serum urea < 20 mmol/L 44.0 ± 16.7 101
ESA use 41.9 ± 12.9 19 0.651
Not on ESA 40.2 ± 15.7 182
IV iron use 50.4 ± 19.6 4 0.191
No IV iron 40.2 ± 15.3 197

JHS junior high school, MCV mean corpuscular volume, MCH mean corpuscular haemoglobin, GHS Ghana Cedis, CKD chronic kidney disease, ESA erythropoietin stimulating agent, IV intravenous, SD standard deviation

Linear regression analysis

In simple linear regression, PCS scores were associated with low monthly income status (p < 0.001), low haemoglobin (p < 0.001), low MCV (0.019), serum urea > 20 mmol/L (p < 0.001) and CKD stage 5 (p < 0.001). All as shown in Table 4.

Table 4.

Simple linear regression analysis of physical component summary scores in patients with moderate to advanced chronic kidney disease n = 202

Variable Coefficient Standard error t 95% CI P value
Age −0.02 0.09 −0.25 − 0.21–0.16 0.806
Educational level 1.61 3.04 0.53 −4.38–7.60 0.597
Employment status −1.23 3.04 −0.40 −7.22–4.77 0.687
Low income −13.61 3.81 −3.57 −21.13–−6.09 < 0.001
Marital status 3.49 3.24 1.07 −2.91–9.90 0.284
Hypertension −5.35 3.28 −1.63 −11.81–1.11 0.104
Hemoglobin 2.97 0.57 5.23 1.85–4.09 < 0.001
MCV 0.46 0.19 2.36 0.07–0.85 0.019
MCH 0.67 0.48 1.40 − 0.27–1.61 0.163
Uraemia −11.87 3.04 −3.89 −17.89–−5.86 < 0.001
CKD stage 5 −12.63 3.25 −3.88 −19.04–−6.22 < 0.001
ESA use 3.03 5.21 0.58 −7.24–13.30 0.561
IV Iron use 6.25 10.91 0.57 −15.27–27.77 0.567

MCV mean corpuscular volume, MCH mean corpuscular haemoglobin, CKD 5 chronic kidney disease with GFR < 15 ml/min/1.73m2, ESA erythropoietin stimulating agent, IV intravenous, CI confidence interval, uraemia serum urea > 20 mmol/L

Simple linear regression analysis of mental component summary scores were associated with low monthly income status (p = 0.002), CKD stage 5 (p = 0.009), low haemoglobin levels (p < 0.001), low MCV (p = 0.037) serum urea > 20 mmol/L (p = 0.015) and the use of IV iron preparation (p = 0.009) as shown in Table 5.

Table 5.

Simple linear regression analysis of mental component summary scores in patients with moderate and advanced chronic kidney disease n = 202

Variable Coefficient Standard error t 95% confidence interval P value
Age −0.01 0.05 −0.01 − 0.93–0.09 0.995
Educational level 1.42 1.51 0.94 − 1.56–4.41 0.348
Employment status −0.61 1.51 −0.40 −3.60–2.38 0.690
Low income −6.08 1.91 −3.18 −9.84–−2.30 0.002
Marital status 0.66 1.62 0.41 −2.54–3.86 0.685
Hypertension −1.70 1.64 −1.03 −4.93–1.54 0.303
Hemoglobin 1.15 0.29 3.95 0.57–1.72 < 0.001
MCV 0.21 0.10 2.10 0.01–0.40 0.037
MCH 0.32 0.24 1.35 −0.15–0.80 0.178
Uraemia −3.78 1.55 −2.45 −6.83–−0.73 0.015
CKD stage 5 −4.36 1.65 −2.64 −7.62–1.10 0.009
ESA use 0.34 2.60 .0.13 −4.76–5.48 0.895
IV Iron 14.12 5.35 2.64 3.56–24.69 0.009

MCV mean corpuscular volume, MCH mean corpuscular haemoglobin, CKD 5 chronic kidney disease with GFR < 15 ml/min/1.73m2, ESA erythropoietin stimulating agent, IV intravenous, CI confidence interval, uraemia serum urea > 20 mmol/L

Simple linear regression of the overall QOL scores showed low haemoglobin level (P < 0.001), low MCV (0.0179), uraemia (p < 0.001), low monthly income status (p = 0.004) and CKD stage 5 (P = 0.003) as significant determinants as shown in Table 6.

Table 6.

Simple linear regression analysis of independent variables of overall mean quality of life score in patients with chronic kidney disease n = 202

Variable Coefficient Standard error t 95% confidence interval P value
Age − 0.01 0.07 0.86 −0.14–−0.12 0.862
Educational level 1.52 2.17 0.70 −2.76–5.80 0.486
Employment status −0.92 2.17 −0.42 −5.20–3.37 0.673
Low income −0.84 2.72 −3.62 −15.21–4.48 < 0.001
Marital status 2.07 2.32 0.89 −2.50–6.65 0.373
Hypertension −3.52 2.34 −1.50 −8.14–1.10 0.134
Hemoglobin 2.06 0.41 5.06 1.26–2.86 < 0.001
MCV 0.34 0.14 2.39 0.06–0.62 0.018
MCH 0.50 0.34 1.45 −0.18–1.17 0.148
Uraemia −7.83 2.19 −3.58 −12.15–−3.51 < 0.001
CKD stage 5 −8.50 2.33 −3.64 −13.10–−3.90 < 0.001
ESA use 1.69 3.72 0.45 −5.65–9.03 0.650
IV Iron 10.19 7.77 1.31 −5.13–25.51 0.191

MCV mean corpuscular volume, MCH mean corpuscular haemoglobin, CKD 5 chronic kidney disease with GFR < 15 ml/min/1.73 m2, ESA erythropoietin stimulating agent, IV intravenous, uraemia urea> 20 mmol/L

Multiple linear regression analysis

Multiple linear regression analysis showed that low monthly income status (p = 0.002) and haemoglobin levels were significant predictors of mean PCS scores. Multiple linear regression revealed the predictors of mean MCS scores as low monthly income status (p = 0.004), low haemoglobin (p = 0.025) and the use of intravenous iron preparation (p = 0.001). Predictors of overall mean QOL score were low-income status (p = 0.002) and low haemoglobin level (p = 0.003) in multiple linear regression all as shown in Table 7.

Table 7.

Multiple linear regression analysis of independent variables for physical, mental component summary and overall QOL scores in patients with CKD

Variable Beta coeff Standard error t 95% CI P value
Physical component Summary score Adjusted R2 = 0.18
 Low income −0.21 3.52 −3.18 −19.69–−4.62 0.002
 CKD stage 5 −0.07 3.97 −0.93 −11.53–4.13 0.352
 haemoglobin 0.24 0.67 3.13 0.77–3.4 0.002
 MCV 0.77 0.20 1.12 −0.17–0.61 0.264
 uraemia −0.13 3.33 −1.73 −12.31–0.81 0.209
Mental Component summary Score Adjusted R2 = 0.15
 Low income −0.20 1.94 −2.91 −9.47–−1.81 0.004
 CKD stage 5 −0.04 2.02 −0.41 −4.82–3.14 0.689
 haemoglobin 0.18 0.34 2.26 −0.10–1.43 0.025
 MCV 0.13 0.10 1.82 −0.02–0.38 0.070
 uraemia −0.09 1.70 −1.13 −5.27–1.44 0.261
 IV iron use 0.23 5.13 3.30 6.81–27.04 0.001
Overall QOL Score Adjusted R2 = 0.17
 Low income −0.21 2.75 −3.16 −14.11–−3.27 0.002
 CKD stage 5 −0.07 2.86 −0.85 −8.05–3.22 0.398
 haemoglobin 0.24 0.48 3.02 0.50–2.40 0.003
 MCV 0.09 0.14 1.27 −0.10–0.46 0.205
 uraemia −0.11 2.39 −1.49 −8.28–1.16 0.138

MCV mean corpuscular volume, CKD 5 chronic kidney disease with GFR < 15 ml/min/1.73 m2, IV intravenous, SD standard deviation, QOL quality of life, CI confident interval, uraemia serum urea> 20 mmol/L, coeff coefficient

Discussion

To our knowledge, this is the first ever study to assess the quality of life among patients with moderate to advanced CKD not on dialysis using the RAND® 36-Item Health Survey questionnaire in Ghana. Our study showed that the QOL of patients with moderate to advanced CKD was poor. Low-income status, anaemia and CKD stage 5 were identified to be significantly associated with poor QOL.

There was a slight predominance of males over females as shown in other studies [23, 24]. Male gender has been associated with faster progression of renal disease as compared to females [25]. Worse progression of CKD in males have also been validated in a meta-analysis of eight studies involving 2229 patients [24]. The mean age in our cohort was 46 years similar to an earlier study in Ghana [23] but lower than shown in the meta-analysis with a mean age of 48.1 years [24]. The mean age of CKD patients in developed countries has been shown however to be higher than 50 years in most studies [2628].

The overall mean QOL score in patients with moderate to advanced CKD not on dialysis in our cohort was lower as compared to a study by Perlman et al. [29]. This may be due to low median eGFR of 7 ml/min/1.73m2 in our patients as compared to 23 ml/min/1.73m2 in their study. The QOL scores were low for both physical component summary (PCS) and mental component summary (MCS) scores. MCS scores were significantly lower than PCS (37.3 versus 43.3; p < 0.001). This may be due to the greater impact of the disease burden on the mental status of patients that may be overlooked by attending physicians and nephrologists in most cases. Management of patients with CKD by their physicians mainly focus on making patients physically healthy with less emphasis on the mental and psychological impact of the disease on their general wellbeing. Focus on the mental health of patients with CKD may therefore be necessary to improve their QOL. It has been shown that the psychological impact of chronic diseases including CKD is underestimated by health care workers and patients relatives [11].

Low-income status was identified as a predictor of poor QOL as also shown in other studies [30, 31]. Most patients with CKD were of low monthly income status about or just minimally higher the minimum wage currently in Ghana. Over 80% of patients were on a monthly income of less than GHS 500 (USD 125). The minimum wage in Ghana is currently pegged at GHS 8.8 (∼USD 2.2) per day with a monthly income of about USD 66 [32]. Furthermore, majority (87.1%) of patient’s did not get to tertiary level academically. These patients may therefore lack the requisite knowledge in the prevention and early management of CKD. Patients with CKD also have poor health seeking behaviour due to their low-income status and low literacy rate. They therefore present late with very advanced CKD as shown in our study. Patients with CKD are also unable to afford the cost of management of CKD and RRT when they progress to ESRD due to their low socioeconomic status [33]. The cost of haemodialysis in Ghana is currently between GHS190 to 260 (~USD 50–65) per session. The cost of chronic haemodialysis is not covered by the national health insurance scheme (NHIS). Practically, the NHIS only pays for acute haemodialysis in very few situations (if any), up to GHS 850 (∼USD 265) [33] irrespective of the number of sessions required for recovery. Patients are also required to buy their medications such as anti-hypertensives, haematinics, intravenous iron preparations and subcutaneous erythropoietin stimulation agents (ESA) and carry out routine laboratory investigations to assess their response to treatment. Patients’ inability to afford treatment especially for anaemia may negatively affect their QOL as shown in our study.

Prevalence of anaemia among our patients with moderate to advanced CKD was 81.2% as shown in other studies [23, 34]. Anaemia is a common presentation in patients with CKD and progressively worsens with advancing renal disease. Most patients had normocytic normochromic anemia which has been described as the characteristic form of anaemia in renal disease due to decreased production of erythropoietin since 1950 [35]. Lately, increase in hepcidin as a result of chronic inflammation has been described in the pathogenesis of anaemia in patients with CKD [36]. Forty-two percent of patients presented however with low MCV anaemia which may have resulted from anorexia [37], occult gastrointestinal bleeding, iron deficiency or the presence of hepcidin causing anaemia of chronic disease [36]. Anaemia could also be due to low red cell survival which has also been reported in patients with CKD [37]. Iron absorption is poor in patients with CKD making intravenous iron more beneficial in improving iron status in patients with kidney disease but most patients with moderate to advanced CKD cannot afford intravenous iron preparations. Anaemia could also be due to chronic bleeding from uraemia associated platelet dysfunction and frequent phlebotomy [37].

Unfortunately, only 9% of the patients in our cohort were on ESA. This is because most of the patients are of low socioeconomic status and cannot afford the ESA. ESA is therefore less prescribed by attending physicians and nephrologists. ESAs have been used over the years with many benefits in improving symptoms, avoiding frequent haemotransfusions and to prevent complications associated with transfusions like iron overload, infections and transfusion related reactions [3840]. ESA has been shown to be associated with hypertension, increased thrombosis and malignancies [41]. ESA use with haemoglobin target levels beyond 13 g/dL has not been shown to be beneficial and even associated with poorer outcomes in major studies [19, 39]. Anorexia in patients with CKD and vomiting associated with uraemia also leads to decreased intake and absorption of iron from the gut. Intravenous iron is warranted in some cases but the use of intravenous iron was also low due to its high cost and under-prescription by attending physicians. Only 4% patients in our cohort were on intravenous iron preparations.

Patients with haemoglobin levels less than 12 g/dl had poorer QOL as compared to patients without anaemia (38.3 ± 13.6 versus 49.2 ± 19.3; p < 0.001). Anemia has been shown in several studies to be associated with adverse clinical outcome [34] and affects QOL in patients with CKD [42, 43]. Anaemia was found to predict poor PCS scores, MCS scores and the overall mean QOL scores in multiple linear regression analysis as also shown in other studies in both developing and developed countries [4446].

Low MCV was significantly associated with mean MCS scores (p = 0.037), PCS scores (0.019) and overall mean QOL (p = 0.018). This may be related to iron deficiency, which may have resulted from anorexia, occult blood loss from uraemic gastritis or bleeding diathesis from dysfunctional platelets seen in patients with CKD [37]. Low MCV was however insignificant in a multiple linear regression analysis for PCS, MCS scores and overall mean QOL scores and not a predictor of poor QOL.

The use of IV iron preparation was found to be significantly associated with MCS scores but not overall mean QOL or PCS scores. This may be because those who could afford IV iron were mainly of high-income status, which may have positively affected their MCS scores. The number of patients on intravenous iron preparations was however very small.

Majority (71%) of patients had CKD stage 5 as also shown in some studies in Africa [23, 47]. Patients reporting late with CKD stage 5 also had a poorer QOL as compared to those reporting with CKD stages 3 and 4. This may be because patients with CKD stage 5 present with more symptoms, greater disease burden and had significantly lower haemoglobin levels (8.4 versus 11.1, P < 0.001). Symptoms of uraemia such as anorexia, nausea and vomiting may have also contributed to their poor QOL.

QOL was however not associated with age, gender, educational status, employment status, marital status and mean corpuscular haemoglobin (MCH) in our cohort similar to that found by Suet et al. [48] who found no association with age and marital status. This differed from another study that found an association with age, gender and race [49]. Male gender, Asian ethnicity and poor nutritional status were found to be associated with poor QOL in another study [50]. Czyzewski et al. showed that increasing age, increased body mass index and unemployment were associated with lower QOL scores [51]. Patients with higher socioeconomic status, male gender and unmarried were shown by Alveres et al. in a large multi center study of over 3000 participants in Brazil to be associated with improved quality of life scores [31].

Our study had a number of limitations. Iron studies were not assessed due to financial constraints. Iron studies would have helped identify clearly if iron deficiency was the cause of the low MCV. The RAND® 36-Item questionnaire [20] was interpreted to few participants who could not read nor write. This may have introduced interviewer bias because the tool was supposed to be a self-administered questionnaire. It was also a tertiary hospital based study were the worst of cases are referred to very late. This may have led to selection bias in their poorer outcomes.

Conclusions

The overall QOL in patients with moderate to advanced CKD was poor. MCS score was significantly poorer than PCS scores. Determinants of poor QOL were low economic status, patients with CKD stage 5 and anaemia. There is the need for governmental support for patients with CKD to improve their QOL. QOL assessment should be introduced for routine clinical review to identify those with poor QOL for proper management based on the determinants of poor QOL. A psychologist and or psychiatrists should be involved in the management of patients with moderate to advanced CKD to focus on mental components that affects the QOL to improve the overall health of patients with moderate to advanced CKD in Ghana.

Acknowledgements

We like to acknowledge Evans X. Amuzu of the Research and Development unit who helped with the data analysis. We also like to acknowledge Dr. Dennis Laryea and Dr. Anthony Enimil who helped with the proposal writing of the study. We appreciate the effort and contribution of all doctors and nurses who are seeing these patients and participants who agreed to take part in this study to make this manuscript possible.

Funding

None (The research project was self-funded by the authors).

Availability of data and materials

Not applicable.

Authors’ contributions

EKT, MRD and GBA initiated the study and wrote up the first version of the manuscript. KKA managed the data collection and cleaning of the data for analysis. EKT also cleaned the data and performed the data analysis. EKT, BRN, MRD and FSS revised the first edition of the manuscript. All authors were involved in critically revising the manuscript, and read and approved the final manuscript before submission.

Ethics approval and consent to participate

Ethical approval from the Committee on Human Research, Publications and Ethics (CHRPE), Kwame Nkrumah University of Science and Technology and KATH was obtained before the commencement of the study. Written informed consent was provided by all participants.

Consent for publication

Informed consent provided by the participants. All authors read the final manuscript and consented to publication.

Competing interests

The authors declare that they have no competing interests.

Publisher’s Note

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Contributor Information

Elliot K. Tannor, Email: elliotktannor@yahoo.co.uk

Betty R. Norman, Email: branorman@yahoo.com

Kwame K. Adusei, Email: edmondadusei@rocketmail.com

Fred S. Sarfo, Email: stephensarfo78@gmail.com

Mogamat R. Davids, Email: mrd@sun.ac.za

George Bedu-Addo, Email: gbeduaddo@gmail.com.

References

  • 1.Coresh J, Selvin E, Stevens LA, et al. Prevalence of chronic kidney disease in the United States. JAMA. 2007;298:2038–2047. doi: 10.1001/jama.298.17.2038. [DOI] [PubMed] [Google Scholar]
  • 2.Seck SM, Diallo IM, Diagne SIL. Epidemiological patterns of chronic kidney disease in black African elders: a retrospective study in West Africa. Saudi J Kidney Dis Transpl. 2013;24:1068. doi: 10.4103/1319-2442.118104. [DOI] [PubMed] [Google Scholar]
  • 3.Stenvinkel P. Chronic kidney disease: a public health priority and harbinger of premature cardiovascular disease. J Intern Med. 2010;268:456–467. doi: 10.1111/j.1365-2796.2010.02269.x. [DOI] [PubMed] [Google Scholar]
  • 4.Stanifer JW, Jing B, Tolan S, et al. The epidemiology of chronic kidney disease in sub-Saharan Africa: a systematic review and meta-analysis. Lancet Glob Health. 2014;2:e174–ee81. doi: 10.1016/S2214-109X(14)70002-6. [DOI] [PubMed] [Google Scholar]
  • 5.Pakasa NM, Sumaili EK. The nephrotic syndrome in the Democratic Republic of Congo. N Engl J Med. 2006;354:1085–1086. doi: 10.1056/NEJMc052696. [DOI] [PubMed] [Google Scholar]
  • 6.Li W, Liu L, Puente JG, et al. Hypertension and health-related quality of life: an epidemiological study in patients attending hospital clinics in China. J Hypertens. 2005;23:1667–1676. doi: 10.1097/01.hjh.0000174971.64589.39. [DOI] [PubMed] [Google Scholar]
  • 7.Wang R, Zhao Y, He X, et al. Impact of hypertension on health-related quality of life in a population-based study in Shanghai, China. Public Health. 2009;123:534–539. doi: 10.1016/j.puhe.2009.06.009. [DOI] [PubMed] [Google Scholar]
  • 8.The World Health Organization Quality of Life Assessment (WHOQOL): development and general psychometric properties. Soc Sci Med. 1998;46:1569–1585. doi: 10.1016/S0277-9536(98)00009-4. [DOI] [PubMed] [Google Scholar]
  • 9.Fructuoso M, Castro R, Oliveira L, Prata C, Morgado T. Quality of life in chronic kidney disease. Nefrologia. 2011;31:91–96. doi: 10.3265/Nefrologia.pre2010.Jul.10483. [DOI] [PubMed] [Google Scholar]
  • 10.Callahan D. The WHO Definition of Health. Hastings Center Studies. 1973;1(3):77–87. [PubMed]
  • 11.Fayers PM, Machin D. Quality of life: the assessment, analysis and interpretation of patient-reported outcomes. 2. 2007. Scores and measurements: validity, reliability, sensitivity; pp. 77–108. [Google Scholar]
  • 12.Batlle D, Ramadugu P, Soler M. Progress in retarding the progression of advanced chronic kidney disease: grounds for optimism. Kidney Int. 2006;70:S40–SS4. doi: 10.1038/sj.ki.5001976. [DOI] [Google Scholar]
  • 13.Alston H. Conservative care for end-stage kidney disease: joint medical conference with the Renal Association, British Geriatrics Society and Association for Palliative Medicine. Clin Med. 2013;13:383–386. doi: 10.7861/clinmedicine.13-4-383. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 14.Boima V, Ganu V, Adjei D, et al. Changing trends in mental health care and research in Ghana. 2015. Psychological wellbeing and quality of life among chronic kidney disease patients in Ghana. [Google Scholar]
  • 15.Moosa M, Kidd M. The dangers of rationing dialysis treatment: the dilemma facing a developing country. Kidney Int. 2006;70:1107–1114. doi: 10.1038/sj.ki.5001750. [DOI] [PubMed] [Google Scholar]
  • 16.Lee Martin B., Bargman Joanne M. Survival by Dialysis Modality—Who Cares? Clinical Journal of the American Society of Nephrology. 2016;11(6):1083–1087. doi: 10.2215/CJN.13261215. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 17.Levey AS, Bosch JP, Lewis JB, Greene T, Rogers N, Roth D. A more accurate method to estimate glomerular filtration rate from serum creatinine: a new prediction equation. Ann Intern Med. 1999;130:461–470. doi: 10.7326/0003-4819-130-6-199903160-00002. [DOI] [PubMed] [Google Scholar]
  • 18.National KF. K/DOQI clinical practice guidelines for chronic kidney disease: evaluation, classification, and stratification. Am J Kidney Dis. 2002;39:S1. [PubMed] [Google Scholar]
  • 19.Locatelli F, Nissenson AR, Barrett BJ, et al. Clinical practice guidelines for anemia in chronic kidney disease: problems and solutions. A position statement from Kidney Disease: Improving Global Outcomes (KDIGO) Kidney Int. 2008;74:1237–1240. doi: 10.1038/ki.2008.299. [DOI] [PubMed] [Google Scholar]
  • 20.Hays RD, Amin N, Leplege A, et al. Kidney disease quality of life short form (KDQOL-SFtm), version 1.2: a manual for use and scoring (French Questionnaire, France) Santa Monica: RAND; 1997. [Google Scholar]
  • 21.Ware JE, Gandek B, Kosinski M, et al. The equivalence of SF-36 summary health scores estimated using standard and country-specific algorithms in 10 countries: results from the IQOLA project. J Clin Epidemiol. 1998;51:1167–1170. doi: 10.1016/S0895-4356(98)00108-5. [DOI] [PubMed] [Google Scholar]
  • 22.StataCorp . Stata 13 Survival Analysis and Epidemiological Tables Reference Manual. College Station: Stata Press; 2014. [Google Scholar]
  • 23.Amoako YA, Laryea DO, Bedu-Addo G, Andoh H, Awuku YA. Clinical and demographic characteristics of chronic kidney disease patients in a tertiary facility in Ghana. Pan Afr Med J. 2014;18(274). [DOI] [PMC free article] [PubMed]
  • 24.Neugarten J, Acharya A, Silbiger SR. Effect of gender on the progression of nondiabetic renal disease a meta-analysis. J. Am Soc Nephrol. 2000;11(2):319–29. [DOI] [PubMed]
  • 25.Silbiger SR, Neugarten J. The impact of gender on the progression of chronic renal disease. Am J Kidney Dis. 1995;25:515–533. doi: 10.1016/0272-6386(95)90119-1. [DOI] [PubMed] [Google Scholar]
  • 26.Fox CS, Larson MG, Vasan RS, et al. Cross-sectional association of kidney function with valvular and annular calcification: the Framingham heart study. J Am Soc Nephrol. 2006;17:521–527. doi: 10.1681/ASN.2005060627. [DOI] [PubMed] [Google Scholar]
  • 27.Brugts JJ, Knetsch AM, Mattace-Raso FU, Hofman A, Witteman JC. Renal function and risk of myocardial infarction in an elderly population: the Rotterdam study. Arch Intern Med. 2005;165:2659–2665. doi: 10.1001/archinte.165.22.2659. [DOI] [PubMed] [Google Scholar]
  • 28.Zhang Q-L, Rothenbacher D. Prevalence of chronic kidney disease in population-based studies: systematic review. BMC Public Health. 2008;8:117. doi: 10.1186/1471-2458-8-117. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 29.Perlman RL, Finkelstein FO, Liu L, et al. Quality of life in chronic kidney disease (CKD): a cross-sectional analysis in the renal research institute-CKD study. Am J Kidney Dis. 2005;45:658–666. doi: 10.1053/j.ajkd.2004.12.021. [DOI] [PubMed] [Google Scholar]
  • 30.Masina T, Chimera B, Kamponda M, Dreyer G. Health related quality of life in patients with end stage kidney disease treated with haemodialysis in Malawi: a cross sectional study. BMC Nephrol. 2016;17:61. doi: 10.1186/s12882-016-0292-9. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 31.Alvares J, Cesar CC, Acurcio Fde A, Andrade EI, Cherchiglia ML. Quality of life of patients in renal replacement therapy in Brazil: comparison of treatment modalities. Qual Life Res. 2012;21:983–991. doi: 10.1007/s11136-011-0013-6. [DOI] [PubMed] [Google Scholar]
  • 32.Minimum Wages in Ghana with effect from 01-01-2017. Mywage.org/Ghana, 2016 (Accessed 8 June 2017, 2017, at http://www.mywage.org/ghana/home/salary/minimum-wages.)
  • 33.Antwi S. State of renal replacement therapy services in Ghana. Blood Purif. 2015;39:137–140. doi: 10.1159/000368942. [DOI] [PubMed] [Google Scholar]
  • 34.Dowling TC. Prevalence, etiology, and consequences of anemia and clinical and economic benefits of anemia correction in patients with chronic kidney disease: an overview. Am J Health Syst Pharm. 2007;64. [DOI] [PubMed]
  • 35.Erslev A. Humoral regulation of red cell production. Blood. 1953;8:349–357. [PubMed] [Google Scholar]
  • 36.Babitt JL, Lin HY. Molecular mechanisms of hepcidin regulation: implications for the anemia of CKD. Am J Kidney Dis. 2010;55:726–741. doi: 10.1053/j.ajkd.2009.12.030. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 37.Fudin R, Jaichenko J, Shostak A, Bennett M, Gotloib L. Correction of uremic iron deficiency anemia in hemodialyzed patients: a prospective study. Nephron. 1998;79:299–305. doi: 10.1159/000045053. [DOI] [PubMed] [Google Scholar]
  • 38.National KF. KDOQI clinical practice guidelines and clinical practice recommendations for anemia in chronic kidney disease. Am J Kidney Dis. 2006;47:S11. doi: 10.1053/j.ajkd.2006.03.010. [DOI] [PubMed] [Google Scholar]
  • 39.Winearls C, Pippard M, Downing M, Oliver D, Reid C, Cotes PM. Effect of human erythropoietin derived from recombinant DNA on the anaemia of patients maintained by chronic haemodialysis. Lancet. 1986;328:1175–1178. doi: 10.1016/S0140-6736(86)92192-6. [DOI] [PubMed] [Google Scholar]
  • 40.Eschbach JW, Egrie JC, Downing MR, Browne JK, Adamson JW. Correction of the anemia of end-stage renal disease with recombinant human erythropoietin. N Engl J Med. 1987;316:73–78. doi: 10.1056/NEJM198701083160203. [DOI] [PubMed] [Google Scholar]
  • 41.Vaziri ND. Mechanism of erythropoietin-induced hypertension. Am J Kidney Dis. 1999;33:821–828. doi: 10.1016/S0272-6386(99)70413-0. [DOI] [PubMed] [Google Scholar]
  • 42.Kimel M, Leidy NK, Mannix S, Dixon J. Does epoetin alfa improve health-related quality of life in chronically ill patients with anemia? Summary of trials of cancer, HIV/AIDS, and chronic kidney disease. Value Health. 2008;11:57–75. doi: 10.1111/j.1524-4733.2007.00215.x. [DOI] [PubMed] [Google Scholar]
  • 43.Leaf DE, Goldfarb DS. Interpretation and review of health-related quality of life data in CKD patients receiving treatment for anemia. Kidney Int. 2009;75:15–24. doi: 10.1038/ki.2008.414. [DOI] [PubMed] [Google Scholar]
  • 44.Drüeke TB, Locatelli F, Clyne N, et al. Normalization of hemoglobin level in patients with chronic kidney disease and anemia. N Engl J Med. 2006;355:2071–2084. doi: 10.1056/NEJMoa062276. [DOI] [PubMed] [Google Scholar]
  • 45.Kalantar-Zadeh K, McAllister CJ, Lehn RS, Liu E, Kopple JD. A low serum iron level is a predictor of poor outcome in hemodialysis patients. Am J Kidney Dis. 2004;43:671–684. doi: 10.1053/j.ajkd.2003.12.029. [DOI] [PubMed] [Google Scholar]
  • 46.Kamal NN, Kamel EG, Eldessouki KH, Ahmed MG. Health-related quality of life among hemodialysis patients at El-Minia University Hospital, Egypt. J Public Health. 2013;21:193–200. doi: 10.1007/s10389-012-0538-3. [DOI] [Google Scholar]
  • 47.Ashuntantang Gloria, Osafo Charlotte, Olowu Wasiu A, Arogundade Fatiu, Niang Abdou, Porter John, Naicker Saraladevi, Luyckx Valerie A. Outcomes in adults and children with end-stage kidney disease requiring dialysis in sub-Saharan Africa: a systematic review. The Lancet Global Health. 2017;5(4):e408–e417. doi: 10.1016/S2214-109X(17)30057-8. [DOI] [PubMed] [Google Scholar]
  • 48.Suet-Ching WL. The quality of life for Hong Kong dialysis patients. J Adv Nurs. 2001;35:218–227. doi: 10.1046/j.1365-2648.2001.01839.x. [DOI] [PubMed] [Google Scholar]
  • 49.Liem YS, Bosch JL, Hunink MM. Preference-based quality of life of patients on renal replacement therapy: a systematic review and meta-analysis. Value Health. 2008;11:733–741. doi: 10.1111/j.1524-4733.2007.00308.x. [DOI] [PubMed] [Google Scholar]
  • 50.Bakewell AB, Higgins RM, Edmunds ME. Quality of life in peritoneal dialysis patients: decline over time and association with clinical outcomes. Kidney Int. 2002;61:239–248. doi: 10.1046/j.1523-1755.2002.00096.x. [DOI] [PubMed] [Google Scholar]
  • 51.Czyzewski L, Sanko-Resmer J, Wyzgal J, Kurowski A. Assessment of health-related quality of life of patients after kidney transplantation in comparison with hemodialysis and peritoneal dialysis. Ann Transplant. 2014;19:576–585. doi: 10.12659/AOT.891265. [DOI] [PubMed] [Google Scholar]

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