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Page 3 of 10  Original Research


              Services (NHLS). Some data that were more than 1 year old,   Antiretroviral therapy treatment,
              were excluded as these did not represent the patient’s status   clinical and laboratory
              at the time of the study census. These data included laboratory
              values of creatinine, haemoglobin and total cholesterol blood   characteristics
              results.
                                                                    Out of 157 participants for whom the ART regimens and the
              Data analysis                                         latest serum creatinine blood results were available, some
                                                                    12/150 participants (8%) had an eGFR of ≤ 50 mL/min/1.73m³
              A list of study definitions can be found in Appendix 1. Stata/  whilst on first-line ART. Those on second-line ART showed a
              IC 16.0 software (STATA Corporation, LLC, TX, US 2019) was   low eGFR in 1/7 participants (14.3%). Not a single participant
              used to analyse data. For descriptive statistics numbers,   with a serum creatinine of ≤ 100 µmol/L had renal dysfunction
              percentages, medians, minimum and maximum values and   as per the  chronic kidney disease  (CKD)-  Epidemiology
              interquartile ranges (IQR) were used. For evaluating   Collaboration Equation (EPI) equation, whereas 13/36
              associations between demographic, clinical and laboratory   (36.1%) of those with a creatinine of ≥ 100 µmol/L had renal
              characteristics with four treatment outcomes viz.  the  most   dysfunction, according to this equation.
              recent VL and CD4 cell count, LTFU and death, Pearson’s chi-
              square, Fisher’s exact, Mann–Whitney (Wilcoxon rank-sum),   Twenty-nine  out  of 34  participants  (85.3%)  with  an
              Kruskall-Wallis or  Spearman’s correlation  tests  were  used   unsuppressed VL (≥ 400 copies/mL) remained on a non-
              where appropriate. Most values for the continuous variables   nucleoside reverse transcriptase inhibitor (NNRTI)-based
              were shown to be non-normally distributed as per the   ART regimen, whereas 5/34 (14.7%) were on a second-line
              Shapiro–Wilk normality test. Even after logarithmic   regimen with a protease inhibitor (PI) boosted with ritonavir.
              transformation, the data were non-normally distributed. All   The PI was lopinavir in all cases. Of the participants with a
              variables were initially assessed individually against the   VL of 400 copies/mL – 999 copies/mL, 14/16 (87.5%) were
              treatment outcomes. If p values were ≤ 0.05 or there were > 0.5   on a NNRTI first-line regimen, whereas for those with a VL of
              correlations for measures of association, these predictors were   ≥ 1000 copies/mL, 15/18 (83.3%) were on a NNRTI first-line
              entered into a linear or logistic regression model where   regimen.
              appropriate.  A level of  ≤ 0.05 was considered statistically
              significant. During the initial analysis, the VL and latest CD4   The  median  CD4  cell  count  improved  from  a  baseline
              cell count outcomes were assessed as continuous variables as   of  279.5  cells/mm³ (IQR 167–433) to 536 cells/mm³
              well as clinical categories. Whenever there was a statistically   (IQR 337.5–703.5) at the most recent CD4 cell count
              significant relationship between any continuous or categorical   monitoring visit, resulting in a median improvement of
              outcome in the initial analysis, it was used in the binomial   256.5  cells/mm³. Moreover, some 33% of the cohort had a
              logistic regression model provided that the number of   CD4 cell count of ≥ 350 cells/mm³ at baseline compared to
              observations was ≥ 10 per cell. The binomial logistic regression   70.7%  at  the  most recent CD4 cell count monitoring visit.
              model categorised the VL as suppressed (< 400 copies/mL) or   Close  to 10% of the  cohort  still  had a CD4 cell  count  of
              unsuppressed (≥ 400 copies/mL) and the latest CD4 cell as   <  200  cells/mm³ at the latest CD4 cell count monitoring
                              3
              high (≥ 350 cells/mm ) or low (< 350 cells/mm³).      visit.  For  this group, 10/19 (52.3%)  participants had  an
                                                                    unsuppressed VL of  ≥ 400 cells/mL. This group also
              Ethical consideration                                 showed  that  12/19  (63.2%)  suffered  from  a  defined
                                                                    co-morbidity. The majority of this group (n = 16/19, 84.2%)
              Ethical clearance was granted by both the Human Research   were on first-line ART.
              Ethics Committee (Medical) of the University of the
              Witwatersrand, Johannesburg (M180304) and the North West   Recent haemoglobin blood results were available for
              Health Research Committee (NW_2018_006). The Tlokwe   24 participants. Of these, 4/24 (16.7%) had a haemoglobin of
              sub-district Office of the Primary Health Care Manager also   < 8g/dL, whilst 3/24 (12.5%) had a haemoglobin of 8 g/dL –
              granted permission for the research. Owing to the     12 g/dL and 17/24 (70.8%) had a haemoglobin of ≥ 12g/dL.
              retrospective nature of the study, patient’s anonymised data   Total cholesterol blood results were available for 75 participants.
              were evaluated. Consequently, informed consent was waived   Of these, 40/74 (53.3%) had readings of < 5 mmol/L and 35/74
              for this study.                                       (46.7%) had readings of  ≥ 5 mmol/L. For participants who
                                                                    were classified with hypercholesterolaemia, 9/14 (64.3%)
              Results                                               had recent total cholesterol readings of ≥ 5 mmol/L whereas
                                                                    26/61 (42.6%) participants who were not classified to have
              Data from a total of 191 clinic files of OPLWH were   hypercholesterolaemia had recent total cholesterol readings of
              examined.  Clinic A provided  n = 38/191 (19.9%), Clinic B,   ≥ 5 mmol/L.
              n  =  96/191 (50.2%) and Clinic C,  n = 57/191 (29.8%). One
              patient file from Clinic A had to be excluded as this was a   Co-morbidities
              duplicate file. Eleven patient files were missing from Clinic B,
              as were 12 files from Clinic C. An overview of the demographic,   One or more co-morbidity was found in 123/199 (64.4%)
              treatment, clinical and laboratory characteristics is provided   participants. Eighty-four participants (44%) had one chronic
              in Table 1. All participants were pensioners.         condition,  a  number  of  34  participants  (17.8%)  had  two

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