Temporal changes in haematocrit following artemisinin-based combination treatments of uncomplicated falciparum malaria in children

Background

Artemisinin-based combination treatments (ACTs) or intravenous artesunate are used in over 100 countries for uncomplicated or severe falciparum malaria. Although intravenous artesunate may cause delayed haemolytic anaemia, there is little evaluation of the temporal changes in haematocrit following ACTs.

Methods

Clinical and parasitological parameters were measured before and following treatment of uncomplicated falciparum malaria in children with artesunate-amodiaquine (AA) or artemether-lumefantrine (AL) over 6-weeks. Changes in haematocrit were characterized in individual patients based on a haematocrit <30 % or ≥30 % before and following treatment. Kinetics of the deficit in haematocrit from <30 % until attainment of ≥30 % were estimated by a non-compartment model.

Results

In 248 of 1180 children eligible for evaluation, common temporal patterns were: no change or increase in haematocrit from ≥ 30 % [50 % of patients], haematocrit >30 % at presentation declining to <30 % within 2 weeks (early monophasic fall) [19 % of patients], and haematocrit <30 % at presentation increasing to ≥ 30 % [23 % of patients]. Haematocrit >30 % at presentation declining to <30 %, 3–5 weeks later (late monophasic fall) occurred in 7 children (3 %). Fall in haematocrit ≥5 units following treatment occurred in 57 children [23 %] between 14 and 28 days after treatment began. Baseline parasitaemia and proportion with > 100,000μL^-1asexual forms were significantly higher in children with ≥5 units compared to <5 units fall in haematocrit 21 or 28 days after treatment began. Irrespective of pattern, declines in haematocrit deficit from <30 % were mono-exponential, with similar half-times for AA- and AL-treated children (1.32 d versus 1.14 d). Anaemia half-time correlated significantly positively with anaemia recovery time in the same patients (r = 0.55, P < 0.0001). Bland-Altman analysis of 9 or 10 multiples of anaemia half-time and anaemia recovery times showed narrow limit of agreement with insignificant biases (P = 0.19 or 0.63, respectively).

Conclusions

In uncomplicated falciparum malaria, increases or falls in haematocrit are common following ACTs. Falls in haematocrit ≥ 5 units are common and may or may not result in early or late anaemia. In children who recovered from acute falciparum malaria-associated anaemia following ACTs, decline in haematocrit deficit is mono-exponential.

Trials registration

Pan African Clinical Trial Registry PACTR201508001188143, 3 July 2015; PACTR201508001191898, 7 July 2015 http://www.pactr.org.

Artemisinin-based combination treatments (ACTs) are the first line treatments of uncomplicated falciparum malaria in over 100 countries [1–4] and intravenous artesunate, considered superior to quinine [5, 6], is now the recommended treatment for severe falciparum malaria [7]. Recent case reports indicate intravenous artesunate may cause delayed haemolytic anaemia in immunologically naïve patients with severe falciparum malaria [8–11] and orally administered ACTs to a lesser extent may cause similar effect even in uncomplicated infections in children from endemic areas [11].

Plasmodium falciparum malaria-associated anaemia, is common in children [12, 13], occurs in 20 – 50 % of African children with falciparum infections [13–15], and is thought to be due to destruction of parasitized and non-parasitized red blood cells and bone marrow dyserythropoiesis of variable intensity and duration [16–18]. Two of the hallmarks of sensitive Plasmodium falciparum infections to ACTs, namely rapid clearance of asexual parasitaemia and recovery from the symptoms and signs of the infections [3, 7], are often followed by increases in haematocrit or haemoglobin in majority of children following recovery from acute infections [12, 13, 19, 20]. A recent study in Nigerian children with uncomplicated falciparum malaria-associated anaemia at presentation showed that time elapsing from commencement of ACTs until resolution of the associated anaemia (anaemia recovery time) was approximately 10 days and was unrelated to age [21].

Despite adoption of ACTs as first line treatments in many endemic countries, there is little information on the patterns of change in haematocrit in individual African children following ACTs of uncomplicated infections. Such information may not only assist with the community management of malaria-associated falls in haematocrit to <30 %, but also with understanding the extent of falls in haematocrit in the different endemic settings, the relationship between falls and time-course of treatment, and the characteristics of the children with different pattern of change in haematocrit following ACTs.

In the present study, the temporal patterns of haematocrit after artemisinin-based combination treatments of uncomplicated falciparum malaria were evaluated in a group of children resident in an endemic area of southwestern Nigeria. The main aims were to: (i) characterize the changes in haematocrit with time in the individual patients, (ii) evaluate the factors contributing to moderate fall (≥5 unit fall from baseline) in haematocrit following treatment, and (iii) characterize, kinetically, recovery from the fall in haematocrit below 30 % associated with the different patterns.

Study location

The study was a prospective study conducted between April 2008 and December 2011 in Ibadan, southwestern Nigeria- an endemic area. It was nested in a larger study of Plasmodium falciparum malaria-associated anaemia in children before, during and after artemisinin-based combination treatments (Pan African Clinical Trial Registry PACTR201508001188143 & PACTR201508001191898). The details of the larger study have been reported elsewhere [20, 22, 23]. The study protocols were approved by the Ministry of Health, Ibadan and the National Health Research Ethics Committee, Abuja, Nigeria.

Patients

Briefly, patients were enrolled in the study if they were aged 6 months–15 years, had symptoms compatible with acute uncomplicated malaria with Plasmodium falciparum mono-infection ≥2000 μL⁻¹ of blood, no history of antimalarial drug ingestion in the two weeks prior to enrolment, absence of severe malaria [24] and written informed consent given by parents or guardians.

Enrolled patients were randomized to receive artemether-lumefantrine or artesunate-amodiaquine (co-formulated). Artemether-lumefantrine (Coartem®, Novatis, Basel, Switzerland) was given according to body weight: patients weighing 5–14 kg received one tablet, those weighing 15–24 kg received two tablets, those weighing 25–34 kg received three tablets, and those weighing >34 kg received four tablets at presentation (0 hour), 8 hours later and at 24, 36, 48 and 60 hours after the first dose. Each tablet of artemether-lumefantrine contains 20 mg of artemether and 120 mg of lumefantrine. Artesunate-amodiaquine (Coarsucam®, Sanofi Aventis, France) was also given according to body weight: patients weighing ≥4.5 to <9 kg received one tablet, those weighing ≥9 to <18 kg received one tablet and those weighing ≥18 to <24 kg received one tablet of the following formulations: 25 mg/67.5 mg, 50 mg/135 mg, 100 mg/270 mg of fixed dose combination of artesunate/amodiaquine, respectively daily for 3 days. Children weighing 24–36 kg and >36 kg received 1.5 and 2 tablets, respectively of 100/270 mg of fixed dose combination of artesunate/amodiaquine daily for 3 days.

All drugs were given orally. All doses of artesunate-amodiaquine were given under direct observed therapy as were the doses of artemether-lumefantrine given at 0, 8, 24 and 48 hours. Doses of artemether-lumefantrine at 36 and 60 hours were given by parents/guardians of the children at home and enquiries were made by telephone calls at the expected times of administration to confirm that the doses were actually given. Artemether-lumefantrine was not given with fatty meals.

Thick and thin blood films prepared from finger prick were stained with Giemsa and examined by light microscopy under oil immersion objective lens 1000 x magnification by two assessors who did not know the drug regimen of the patients. A senior member of the study team reviewed the slides if there was any disagreement by the two microscopists. In addition, the slide of every fourth child enrolled in the study was reviewed by the senior member. Thick and thin blood films obtained from each child as soon as they came to the clinic on to blood slides were carefully labeled with the patients’ codes and air-dried before being stained. Follow-up with clinical and parasitological evaluation was done daily on days 1–3 and on days 7, 14, 21, 28, 35 and 42.

Parasitaemia, asexual or sexual, in thick films were estimated by counting asexual and sexual parasites relative to 500 leukocytes, or 500 asexual or sexual forms whichever occurred first. From this figure, the parasite density was calculated assuming a leukocyte count of 6000 μL⁻¹ of blood. A slide was considered parasite negative if no asexual or sexual parasite was detected after examination of 200 microscope fields. The cure rates on days 21 and 28 were adjusted on the basis of the PCR (polymerase chain reaction) genotyping results of paired samples of patients with recurrent parasitaemia after day 7 of starting treatment as previously described [20].

Capillary blood collected before treatment and during follow-up was used to measure hematocrit using a microhaematocrit tube and microcentrifuge (Hawksley, Lancing, UK). Anaemia was defined as a haematocrit <30 % [12, 13]. Anaemia recovery time (in anaemic patients at presentation) was defined as time elapsing from drug administration to attainment of a hematocrit value ≥30 % [21, 25] in patients with anaemia at presentation. In patients who had early or late monophasic decline in haematocrit which resulted in anaemia, anaemia recovery time was defined as time from appearance of, to recovery from, anaemia. Children were also considered to have late fall in haematocrit attributable to treatment if they had no concomitant illness during the period of the fall and were parasite negative by both microscopy and PCR.

Evaluation of temporal changes in haematocrit following treatment

Haematocrit <30 % and ≥30 % were the reference points in all classified patterns. Temporal changes in haematocrit were classified into the following patterns (Fig. 1).

Classification of temporal patterns of haematocrit after artemisinin-based combination treatments. HCT, haematocrit

Full size image

1. 1.

   Haematocrit ≥30 % before and following treatment.

2. 2.

   Haematocrit ≥30 % before treatment, declining to haematocrit <30 % within 2 weeks of treatment, and thereafter increasing to ≥30 % by 6 weeks after treatment (early monophasic fall).

3. 3.

   Haematocrit ≥30 % before treatment followed by a decline to haematocrit <30 %, 3–5 weeks following treatment and then increasing to ≥30 % by 6 weeks after treatment (late monophasic fall).

4. 4.

   Haematocrit ≥30 % before treatment, 2 consecutive haematocrit <30 % within 14 days of treatment, followed by a rise to haematocrit ≥30 % between 14 and 21 days and a fall to <30 % between day 28–35 (biphasic fall in haematocrit).

5. 5.

   Haematocrit <30 % before and following treatment (persistent anaemia).

6. 6.

   Haematocrit <30 % before treatment followed by an increase to ≥30 % after treatment (malaria-associated anaemia at presentation and recovery from anaemia).

7. 7.

   Haematocrit < 30 % at presentation and till day 14, followed by a rise to ≥30 % on days 21–28 and a fall to <30 % on days 35–42.

8. 8.

   Haematocrit <30 % before treatment, followed by further falls to ≤25 %, 3–5 weeks following treatment.

9. 9.

   Unclassifiable.

Kinetics of the disposition of deficit in haematocrit from 30 %

The kinetics of the disposition of deficit in haematocrit from 30 %, that is, of anaemia, was as previously described [20, 26]. Briefly, in all anaemic patients at enrolment, or when anaemia occurs following treatment, haematocrit values below 30 % (the lower threshold of normal) and at follow-up were subtracted from 30 % at each time of measurement until haematocrit rose to ≥30 %, and the resulting values plotted against time. The final haematocrit when anaemia resolved was therefore zero in all patients. However, the final haematocrit at the time of resolution was assumed to be 0.01 %. The areas under the curve (AUC) of deficit in haematocrit (from 30 %) versus time were obtained, by the trapezoidal rule using the computer program Turbo Ken (designed by Clinical Pharmacology Group, University of Southampton, United Kingdom) as previously described (20, 26). AUC was also obtained manually by calculating the average haematocrit values between two consecutive time measurements and multiplying it by the time interval between the measurements, and summing up all the values, in a manner similar to that for the numerical estimation of area under a drug concentration-time curve [27]. Both measurements by digital computer and manual methods gave the same values. The unit of quantification would be %.d, if hematocrit values were used or g/L.d if hemoglobin values were used. Hematocrit values may be converted to hemoglobin values by dividing by 3 [28]. The apparent terminal elimination rate constant (λ) was obtained by least-square regression analysis of the post-peak log-linear part of the plot of deficit in hematocrit (from 30 %) versus time, and the apparent terminal half-time of anaemia (t_1/2(anaemia)) was calculated from ln/(λ).

Statistical analysis

Data were analyzed using version 6 of Epi-Info software [29] and the statistical program SPSS for Windows version 20.0. [30]. Variables considered in the analysis were related to the densities of P. falciparum asexual and sexual forms. Proportions were compared by calculating χ² using Yates’ correction, Fisher’s exact or Mantel Haenszel tests. Normally distributed, continuous data were compared by Student’s t test and analysis of variance (ANOVA). Data not conforming to a normal distribution were compared by the Mann-Whitney U tests and the Kruskal Wallis tests. The relationship between two continuous variables was assessed by Spearman’s rank correlation coefficient. Agreement between pharmacodynamic and pharmacokinetic methods of evaluating recovery from anaemia was assessed by Bland-Altman analysis [31]. P-values of <0.05 were taken to indicate significant differences. Data were double entered serially using patients’ codes and were only analyzed at the end of the study.

Patients’ characteristics and therapeutic responses

Between April 2008 and December 2011, 1180 patients were enrolled in prospective studies of the efficacy of artemisinin-based combination treatments. All patients, at enrolment and during follow-up, had haematocrit measured. However, two hundred and forty eight patients who had haematocrit measured during the entire period of follow-up were analysed. Of these, 177 and 71 were treated with artesunate-amodiaquine and artemether-lumefantrine, respectively. The clinical characteristics of the patients at enrolment are summarized in Table 1. Forty four per cent of the patients were aged less than 5 years; hyperparasitaemia (>250,000 μL⁻¹) was found in 8.9 % of the patients. In general, PCR-corrected cure rates were similar for both artesunate-amodiaquine and artemether-lumefantrine (98.3 % [95 % CI 96.1-99.3 %] versus 96.9 % [95 % CI 93.9-98.2 %] for artesunate-amodiaquine and artemether-lumefantrine, respectively).

Temporal changes in haematocrit following start of treatment

Tables 2 and 3 show the distribution of patients and their characteristics in the different temporal patterns. Children who were anaemic at presentation (Pattern 6), were younger, weighed significantly less, had significantly longer duration of illness and a significantly higher proportion of children who were hyperpyrexia compared to children without anaemia (Patterns 1 and 2) (Table 2). However, bodyweight was similar in children in patterns 2 and 6 (by post-hoc comparison). Parasitaemia was similar in all three temporal patterns. The features of the other temporal patterns (Patterns 3, 5 and 7) are summarized in Table 3. The features appear similar due to the small number of patients in each pattern. No patient could be classified as pattern 4 or 8. Nine patients could not be classified into any of the patterns described above (unclassifiable).

In all temporal patterns described (Fig. 2), a prominent feature is a fall in haematocrit within the first three days of drug administration–the drug-attributable fall in haematocrit (DAFH [25]). A late fall in haematocrit which began after day 14 and persisted beyond 28 days after treatment began was seen in Patterns 1, 3 & 7 (Fig. 2). The detailed clinical and parasitological characteristics and outcome of treatment of patients with a late fall in haematocrit resulting in anaemia between days 21 and 35 are shown in Table 4. At enrolment, 4 of the 7 patients had parasitaemia >100,000 μL⁻¹, parasitemia cleared within 1 day in 6 of 7 children, 3 of 5 children treated with artesunate-amodiaquine had total dose of artesunate >11 mg/kg, and none of the children required blood transfusion. Also, none of the patients was older than 9 years. On the whole, virtually all of these children were anaemic for a period of approximately 14 days (Additional file 1: Figure S1). The mean duration of anaemia was 16.0 days (95 % CI 12.8–19.2; range 14–21 days).

Temporal patterns of haematocrit after artemisinin-based combination treatments. Single arrow indicates drug attributable fall, and double arrows indicate late fall in haematocrit even in patients with normal haematocrit during entire period of follow up (see Pattern 1)

Full size image

Comparison of children with fall in haematocrit ≥5 units and <5 units following treatment

Because of very few patients with late fall in haematocrit (n = 7), the features of children with ≥5 units and <5 units fall in haematocrit from baseline following artemisinin-based combination treatments were evaluated. Based on the number of patients evaluated per visit day, on day 7, 16 of 23 children and 62 of 87 children had ≥5 and <5 units fall in haematocrit, respectively, following treatment. The difference between these proportions was not significant (χ² = 0.02; P = 0.92). After day 7, overall, 57 of 122 children and 55 of 213 children with ≥5 and <5 units fall in haematocrit, respectively between days 14 and 28 were anaemic (Table 5). The difference between these proportions was significant (χ² = 14.3, P = 0.0001). However, the proportion of children who were anaemic on day 14 in the 2 groups, respectively were similar (29 of 52 v 32 of 65, χ² = 0.3, P = 0.60). On day 21, 20 of 48 children and 18 of 75 children in the 2 groups, respectively were anaemic (χ² = 4.2, P = 0.04 by Mantel Haenszel test). On day 28, 8 of 22 and 5 of 73 children (Table 5) in the 2 groups, respectively were anaemic (χ² = 10.1, P = 0.0001).

Table 6 shows the clinical and parasitological parameters of the 89 children who had a fall of ≥5 or <5 unit in haematocrit from baseline on days 21 or 28, or on both days. Children with ≥5 units fall in haematocrit had significantly higher baseline haematocrit, parasitemia and proportion of children with asexual forms >100,000 μL⁻¹. However, median doses of artesunate were similar in the two groups. Similarly, the median doses of artemether, lumefantrine or amodiaquine were similar in the two groups. In a univariate analysis (see Additional file 2: Table T1), a parasitaemia >100,000 μL⁻¹ at enrollment was significantly associated with ≥5 units fall in haematocrit from baseline on days 21 or 28 or on both days.

Kinetics of the disposition of the deficit in haematocrit from 30 %

(a). Comparison of the kinetics of the disposition of deficit in haematocrit in children with early (Pattern 2) and late (Pattern 3) monophasic falls in haematocrit

Forty-eight (31 treated with artesunate-amodiaquine and 17 treated with artemether-lumefantrine) and 7 (5 treated with artesunate-amodiaquine and 2 treated with artemether-lumefantrine) children, respectively, had early and late monophasic falls in haematocrit. The children from the two groups, respectively had similar clinical and parasitological parameters at presentation (Age 5.6 ± 2.7 years [range 2–14] versus 5.6 ± 2.0 years [range 2–8], P = 0.95; duration of illness 2.8 ± 1.0 d [1–5] versus 2.5 ± 0.8 d [1–3], P = 0.45; body temperature 38.6 ± 1.0 °C [range 35.0–40.1] versus 38.9 ± 1.3 °C [range 36.7–40.6], P = 0.38; haematocrit 32.4 ± 2.8 % [range 30–40] versus 34.1 ± 3.6 % [range 30–40], P = 0.13, and geometric mean asexual parasite density 59,361 μL⁻¹ blood [range 8,000–1,080,200] versus 67,895 μL⁻¹ blood [range 14,792–197,308], P = 0.74). The median doses of the drugs were also similar in the two groups (data not shown). Time to recover from anaemia was significantly shorter in children with early than in those with late monophasic falls in haematocrit (median 11 d [range 2–27; n = 48] versus 14 d [range 14–21; n = 7], P = 0.003). The mean AUC of deficit in haematocrit versus time was significantly lower in children with early monophasic fall than in those with late monophasic fall (mean 14.7 %.d [range 3.7–41.5] versus 54.1 %.d [range 20.2–116.4], P = 0.002). Declines of deficit in haematocrit were monoexponential in both patterns (see Additional file 3: Figure S2). The half-time of decline was significantly shorter in children with early monophasic fall than in those with late monophasic fall in haematocrit (mean 0.9 ± 0.7 d [range 0.2–2.1] versus 1.6 ± 0.4 d [range 1.1–2.1], P = 0.003).

(b). Anaemia at presentation followed by recovery (Pattern 6)

The demographic and other characteristics of the 57 children (n = 39 for artesunate-amodiaquine and n = 18 for artemether-lumefantrine) have been summarized in Table 2. Overall, in all children, mean AUC of deficit in haematocrit versus time was 74.2 %.day (95 % CI 59.3–89.1, range 0.7–286.2) and it was similar in anaemic children treated with artesunate-amodiaquine and artemether-lumefantrine (mean 72.7 %.day [95 % CI 54.1–91.2, range 0.7–286.2] versus mean 77.3 %.day [95 % CI 50.1–104.6, range 0.7–224.6], P = 0.77) (Fig. 3). Overall, in all children, there was mono-exponential decline of the deficit in haematocrit (see Additional file 4: Figure S3) with an estimated half-time (t_½) of 1.3 d (95 % CI 1.2 – 1.5, range 0.2–2.5). Estimated mean t_½ were similar in children treated with artesunate-amodiaquine and artemether-lumefantrine (mean 1.3 d [95 % CI 1.1–1.5, range 0.2–2.5] versus mean 1.3 d [95 % CI 1.1–1.6, range 0.2–2.1], P = 0.93).

Distribution of individual area under curve (AUC) of deficit in haematocrit from 30 % in children with anaemia at presentation (Pattern 6), after treatment of falciparum infections with artemether-lumefantrine (AL) or artesunate-amodiaquine (AA). ALL; all children. Horizontal bars indicate mean AUC

Full size image

(c) Relationship between half time of decline in haematocrit deficit and anaemia recovery time

The relationship between the half-time of decline in haematocrit deficit from 30 % and anaemia recovery time in the same patients with anaemia at presentation was evaluated in 57 children. The mean half-time of decline in haematocrit deficit from 30 % was 1.3 days (95 % CI 1.2–1.5, range 0.2–2.5). The median anaemia recovery time was 14 days (range 1–21). There was a significantly positive correlation between half-time of decline in haematocrit deficit from 30 % and anaemia recovery time (r = 0.55, P < 0.0001, see Additional file 5: Figure S4). The ratio of anaemia recovery time to half time of decline in haematocrit in individual patient was 10.0 (95 % CI 9.0–11.1). Bland-Altman plots of the anaemia recovery times and multiples of anaemia half-times are shown in Fig. 4. The limits of agreement between anaemia recovery times and 9 or 10 multiples of anaemia half-times were narrow. At 9 and 10 anaemia half-time, the limits of agreement were −9.8–12 days and −11–11 days, respectively. The bias at multiples of 9 or 10 anaemia half-times was statistically insignificant (P = 0.19 and 0.63, respectively). However, there was a statistically significant bias at multiples of 7 or 8 anaemia half-times (P < 0.0001 and P = 0.002, respectively).

Bland-Altman plots of anaemia recovery times and multiples [7 a 8 (b), 9 (c) and 10 (d)] of anaemia half-times. Biases were 3.62, 2.29, 0.96 and −0.36 for plots A, B, C and D; P < 0.0001, P = 0.002, 0.19 and 0.63, respectively. The mean values ± 1.96 standard deviation (SD) of the differences are shown

Full size image

In this study, in keeping with previous reports, the commonest changes in haematocrit after successful artemisinin-based combination treatments of uncomplicated falciparum infections in children are increases in haematocrit in non-anaemic (Pattern 1) and anaemic (Pattern 6) children at presentation [12, 13, 19, 20, 23, 25, 32]. When combined with children who had no anaemia – early anaemia – no anaemia pattern (Pattern 2, early monophasic fall in haematocrit), over 90 % of the children could be classed into one of these three patterns. Compared to children with normal haematocrit at presentation and following treatment (Pattern 1) and those with early monophasic fall in haematocrit (Pattern 2), children with anaemia – no anaemia pattern (Pattern 6, acute falciparum malaria-associated anaemia at presentation and recovery from anaemia) were significantly younger and had significantly longer duration of illness in keeping with previous findings [12, 13, 15]. However, baseline parasitaemia was similar in all the three patterns, − a finding in anaemia – no anaemia pattern that is at variance with some reports showing high parasitaemia is a risk factor for anaemia at presentation in children with acute falciparum malaria [12, 13, 15].

Of theoretical interest, for which no child was classified is: no anaemia at presentation, followed by anaemia, recovery from anaemia, and a late fall in haematocrit to anaemia level (Pattern 4). This pattern appears to have combined features of Pattern 2 and Pattern 3 and may be considered a variant of both Patterns 2 and 3. It would appear that the 3 patients included under pattern 7 appeared to have ‘undulating pattern’. We do not have an explanation for this pattern.

It is noteworthy that a late fall in haematocrit to a level below normal occurred in 3 % of the children (Pattern 3, Table 4). Over half of the children with late fall in haematocrit had high parasitaemia (>100,000/μL), virtually all their parasitaemias cleared by 1 day after treatment started and 3 of 5 children treated with artesunate-amodiaquine had >11 mg/kg of artesunate. With the exception of overt clinical and other laboratory manifestations of haemolysis, the features of these children superficially resemble those of immunologically naïve patients with delayed haemolytic anaemia following intravenous artesunate treatment of severe falciparum malaria [8–11]. In some of the children with late fall in haematocrit who were treated with artemether-lumefantrine, the dose of artemether was not particularly high. It is likely that the children who received higher dose of artesunate were on the lower segment of the dose range since co-formulated preparations were used. Thus, in uncomplicated falciparum malaria when compared with severe malaria, the late fall in haematocrit to anaemia level may be associated with subtle clinical or laboratory features of haemolysis.

All of the factors associated with late monophasic fall in haematocrit after artemisinin-based combination treatments of uncomplicated falciparum malaria are not known. In order to understand some of these factors, a comparison of falls in haematocrit from baseline ≥5 units or <5 units after treatment was assessed by comparing the features of patients in the 2 groups. Approximately half of the patients with falls in haematocrit ≥5 units had their falls 21–28 days after treatment began (see Table 5). In these patients, the ≥5 units fall was associated with significantly higher baseline parasitaemia, a significantly higher proportion of patients with a parasitemia in excess of 100,000 asexual forms/μL, but not significantly higher doses of all the combination drugs compared with children who had <5 units fall in haematocrit (from baseline) following treatment. These findings superficially resemble those of the reported cases of late haemolytic anaemia following intravenous artesunate treatment of severe falciparum malaria [9, 10]. Since 40 % of the children with falls in haematocrit ≥5 units between 21 and 28 days after treatment began developed late monophasic anaemia as compared to 16 % of those with <5 units fall in haematocrit during the same period, it follows that late fall in haematocrit from baseline ≥5 units may or may not result in anaemia. This may explain the relatively low prevalence of late monophasic anaemia following artemisinin-based combination treatments in general. In this context, studies on the risk factors for late monophasic anaemia after artemisinin-based combination treatments of uncomplicated falciparum malaria in children are urgently needed in this endemic area.

In the area of study, the relatively common occurrence of the haemoglobinopathies, glucose-6-phosphate dehydrogenase deficiency, and intestinal helminth infections [33–36] may contribute to the background low haematocrit or even to the early monophasic decline in haematocrit following treatment but the extent may be difficult to quantify. However, they are less likely to contribute much to the late monophasic fall in haematocrit. The anaemia associated with falciparum malaria is multifactorial and is thought to be due to greater destruction of unparasitized red blood cells compared to parasitized red blood cells, and bone marrow dyserythropoiesis of variable intensity and duration [16–18, 37–39]. It is likely that the late monophasic fall in haematocrit (Pattern 3) following artemisinin-based combination treatments, is due to the late destruction of red blood cells from which parasites have been removed in the spleen by pitting-the parasite-negative-red cell surface antigen positive red cells [40]. These red blood cells are found in the circulation in large numbers within 24 hours of initiating treatment with artesunate, but they have shortened survival time in severe malaria compared with unparasitized red blood cells [41] and are therefore expected to be destroyed 3–5 weeks after treatment began [10, 11]. Thus, in patients with high parasitaemia, the fall in haematocrit in the first few days following artemisinin-based combination treatments is less than expected were all the parasitized red blood cells to be destroyed [42, 43]. It is also remotely possible that, in addition to these once infected red blood cells, apparently non-infected red blood cells may also be destroyed.

Recent case definition of post-artesunate delayed haemolytic (PADH) syndrome [44, 45] consists of 10 % fall in haemoglobin associated with haptoglobin <0.1 g/L and either an increase in LDH to >390 IL/L or a 10 % rise >7 days after start of treatment with artesunate in naïve patients with severe malaria. This syndrome has been reported in 7 % of African children with severe malaria treated with parenteral artesunate [46]. Although the seven children with delayed fall in haematocrit in our series did not meet this strict case definition, it is likely that the syndrome of delayed fall in haematocrit, not associated with severe malaria may occur in children with uncomplicated falciparum malaria following artemisinin-based combination treatments. In this context, the recent introduction and use of dihydroartemisinin-piperaquine (DHP) for the treatment of uncomplicated falciparum malaria in endemic areas of Africa would require close monitoring for the syndrome of delayed fall in haematocrit or heamoglobin as reported in 3 % of children following artemisinin-based combination treatments in this endemic area. This would be necessary since artesunate and artemether are metabolized to dihydroartemisinin. In addition, monitoring may help define the risk factors for artemisinin-related late falls in haematocrit following treatment of uncomplicated falciparum malaria in children.

Declines in haematocrit deficit from 30 % (that is, recovery from anaemia) were mono-exponential irrespective of whether the deficit was early or late, suggesting that using a non-compartment model, recovery from apparently uncomplicated falciparum malaria-associated anaemia is a first order process. In this and other contexts, early fall in haematocrit to <30 % differs from late fall to <30 % by its shorter half-time of anaemia. These two patterns also differ in their anaemia recovery times and AUC of deficit in haematocrit versus time. These differences suggest that, on the whole, the late monophasic anaemia may be more ‘intense’ than the early monophasic anaemia. A further application of pharmacokinetic principles should permit treatment of the increases in haematocrit associated with artemisinin-based combination treatments of uncomplicated falciparum malaria.

In this study, a pharmacodynamic-pharmacokinetic approach was used to quantify the time to resolve uncomplicated malaria-associated anaemia following artemisinin-based combination treatments. The approach showed the following: (i). Anaemia half-time correlated significantly with anaemia recovery time in the same patient. (ii). Greater than 8 multiples of anaemia half-times showed an insignificant bias when a Bland-Altman analysis was used. Thus, confirming that >8 multiples of anaemia half-times can be used interchangeably with anaemia recovery time for the evaluation of recovery from uncomplicated malaria-associated anaemia following artemisinin-based combination treatments. Therefore, the agreement between 9 or 10 multiples of anaemia half-times and anaemia recovery time was not unexpected since it takes 9 or 10 half-times for 99.6 or 99.9 % completion of an elimination process in a simple one compartment pharmacokinetic model. The ratio of anaemia recovery time to anaemia half-time of approximately 10 in the patients also indirectly support the model.

There are limitations of the present study. First, although the clinical and parasitolgical features of children with fall in haematocrit to anaemia level on days 21–42 after commencement of treatment were characterised, the nature of the anaemia was not fully characterized (i.e. whether it was haemolytic or not in nature). Second, in the children with late fall in haematocrit to anaemia level, quantification of once-infected and infected red blood cells and the disposition of these red cells during the course of follow-up was not evaluated. Third, The precise contribution of the background causes of anaemia in children from the endemic area (such as the haemoglobinopathies, malnutrition and intestinal helminth infections) to the time-course of haematocrit was not assessed.

Increases in haematocrit are common following artemisinin-based combination treatments of uncomplicated falciparum malaria, but falls in haematocrit from baseline ≥5 units are also relatively common and may or may not result in early or late anaemia. In children who recovered from acute falciparum malaria-associated anaemia following artemisinin-based combination treatments, declines in haematocrit deficit (from 30 %, the lower threshold of normal) are mono-exponential.

%:

Percent

μL:

Microliter

AA:

Artesunate-amodiaquine

ACTs:

Artemisinin-based combination treatments

AL:

Artemether-lumefantrine

AnRT:

Anaemia recovery time

AUC:

Area under curve

D:

day

DAFH:

Drug attributable fall in haematocrit

DHP:

Dihydroartemisinin-piperaquine

FCT:

Fever clearance time

G:

Gram

GMPD:

Geometric mean parasite density

HCT:

Haematocrit

Kg:

Kilogram

L:

Litre

M/F:

Male/female

Mg:

Milligram

°C:

Degree Celsius

PCR:

Polymerase chain reaction

PCT:

Parasite clearance time

sd:

Standard deviation

t_½:

Half-time

We are grateful to the parents/guardians and the children who participated in the study. The efficacy studies from which the data were derived were supported by Swiss Pharma Nigeria PLC Grant to AS and by World Bank Malaria Booster Project, and Global Fund for Malaria to Federal Ministry of Health, Abuja, Nigeria through Drug Therapeutic Efficacy Testing in Ibadan, Nigeria.

Affiliations

1. Department of Pharmacology & Therapeutics, University of Ibadan, Ibadan, Nigeria

   • Akintunde Sowunmi
   •  & Kazeem Akano

2. Institute for Medical Research and Training, University of Ibadan, Ibadan, Nigeria

   • Akintunde Sowunmi

3. Department of Paediatrics, University of Ibadan, Ibadan, Nigeria

   • Adejumoke I. Ayede

4. Federal Ministry of Health, Abuja, Nigeria

   • Godwin Ntadom

5. World Health Organization, Regional Office for the Western Pacific, Khan Daun Penh, Phnom Penh, Cambodia

   • Bayo Fatunmbi

6. Department of Clinical Pharmacology, University College Hospital, Ibadan, Nigeria

   • Temitope Aderoyeje

7. Department of Physiology, University of Ibadan, Ibadan, Nigeria

   • Elsie O. Adewoye

Corresponding author

Correspondence to Akintunde Sowunmi.

Competing interests

The authors declare they have no competing interests.

Authors’ contributions

AS led the design, conduct, data analysis and manuscript preparation. KA, AIA, GN, BF, TA and EOA participated in data collections and analysis. All authors read and approved the final draft of the manuscript.

Reprints and Permissions