- Case report
- Open Access
Failure of dihydroartemisinin-piperaquine treatment of uncomplicated Plasmodium falciparum malaria in a traveller coming from Ethiopia
© The Author(s) 2016
- Received: 15 July 2016
- Accepted: 16 October 2016
- Published: 3 November 2016
Artemisinin combination therapy (ACT) is used worldwide as the first-line treatment against uncomplicated Plasmodium falciparum malaria. Despite the success of ACT in reducing the global burden of malaria, the emerging of resistance to artemisinin threatens its use.
This report describes the first case of failure of dihydroartemisinin-piperaquine (DHA-PPQ) for the treatment of P. falciparum malaria diagnosed in Europe. It occurred in an Italian tourist returned from Ethiopia. She completely recovered after the DHA-PPQ treatment but 32 days after the end of therapy she had a recrudescence. The retrospective analysis indicated a correct DHA-PPQ absorption and genotyping demonstrated that the same P. falciparum strain was responsible for the both episodes.
In consideration of the growing number of cases of resistance to ACT, it is important to consider a possible recrudescence, that can manifest also several weeks after treatment.
- Dihydroartemisinin-piperaquine (DHA-PPQ)
- Plasmodium falciparum
Artemisinin combination therapy (ACT) is used worldwide as the first-line treatment against uncomplicated falciparum malaria . Dihydroartemisinin-piperaquine (DHA-PPQ) is characterized by a post-treatment prophylactic effect against re-infections that is longer than artemether-lumefantrine . Despite the success of ACT in reducing the global burden of malaria, the emergence of resistance to artemisinin threatens its use. In Cambodia, failure of ACT is now frequently observed [3, 4]. The increase of treatment failures and parasite clearance times observed soon after the widespread introduction of DHA-PPQ suggests a rapid emergence of resistance to both artemisinin and piperaquine components. In Asia, treatment failures have been reported in Myanmar . In South America, data on (good) efficacy of DHA-PPQ is based on only one trial, conducted in Peru between 2003 and 2005 . In Africa, trials conducted in Burkina Faso , Kenya  and Angola  showed that DHA-PPQ was highly effective, with very rare cases of recrudescence invariably within 28 days.
A 72-year-old Italian woman was admitted on 26 November, 2014 to the Centre for Tropical Diseases (CTD) of Negrar (Verona), for myalgias and arthralgias since 2 days, fever (up to 40 °C) and nausea since one day. She had visited Ethiopia (Omo River Valley) from 6 to 18 November 2014. She was vaccinated against yellow fever, hepatitis A and B, but had not taken any malaria chemoprophylaxis. Her travel history included Ethiopia, Niger, India, and Nambia, not South East Asia. Upon admission, her temperature was 38.3 °C, her weight 67.5 kg. Physical examination was unremarkable. The blood tests showed white blood cells (WBCs) 3.85 × 109/L (normal range 5.2–12.4 × 109/L), haemoglobin (Hb) 12.5 g/dL (normal range 14–18 × g/dL), platelets 46 × 109/L (normal range 130–400 × 109/L), C-reactive protein 135 mg/L (normal range 0–5 mg/L), procalcitonin 14 μg/L (normal range 0–0.5 μg/L). The quantitative buffy coat (QBC) test, antigen malarial test and blood smears resulted positive for Plasmodium falciparum, with a parasitaemia of 0.3% (14,600/μL). The patient was treated with DHA-PPQ 320/40 mg, three tablets/day for 3 days. The first day after treatment the parasitaemia dropped to 0.0023% (96/μL). After two days, the blood films and the QBC test resulted negative. Also, iv ceftriaxone 2 g/day was administrated for a left basal bronchopneumonia. The patient was discharged on 5 December, 2014.
At a follow-up visit on 23 December, the QBC test and blood smears were still negative. The blood tests showed WBC 7.98 × 109/L, Hb 11.8 g/dL, platelets 233 × 109/L.
She was re-admitted on 7 January, 2015 complaining of fever, nausea and vomiting that had started 7 days before (more than 4 weeks after anti-malaria treatment). The QBC test, antigen malarial test and blood smears all resulted positive again for falciparum malaria, with a parasitaemia of 0.4% (12,100/μL). WBCs were 5.5 × 109/L, Hb 9.5 g/dL, platelets 96 × 109/L. The patient was treated this time with atovaquone-proguanil 250/100 mg, four tablets/day for 3 days. The parasitaemia decreased to 0.36% (10,930/μL) 24 h after first dose of treatment, 0.16% (5017/μL) the second day, 0.0016% (46/μL) the third day. After 4 days, blood films resulted negative. The patient was discharged on 12 January, 2015.
At follow-up visits 28 and 56 days after the second malaria episode, QBC and blood smears resulted negative and the main laboratory findings were normal.
Serum concentrations of dihydroartemisinin-piperaquine
Hours since last administration
Day 7 (calculated)
Analysis of the molecular markers of P. falciparum linked to drug resistance
This is the first case of failure of DHA-PPQ reported in Europe. The patient returned from Ethiopia, a country where DHA-PPQ failures have not been reported before. In this case, the rapid response to DHA-PPQ and the lack of mutations in the PfK13 gene suggest the involvement of an artemisinin-sensitive strain. Although it was not possible to analyse a specific molecular marker of resistance to PPQ (a newly identified gene, PFE1085w is presumably associated to resistance to this drug) , the combination of results obtained from molecular and pharmacokinetic analyses and the clinical characteristics support that the strain was resistant to the PPQ component.
In the last 2 years (July 2014 to June 2016) DHA-P was administered to 36 patients attended at the CTD for falciparum malaria, observing no other failure. These data are in agreement with the literature. The efficacy of DHA-PPQ has been found very high, particularly in the African continent. There was a relevant delay between the onset of symptoms and the second diagnosis because the index of suspicion was low due to the negative laboratory tests performed at the 28-day follow-up visit. In consideration of the growing number of cases of resistance to ACT, it is important to consider a possible recrudescence, which can manifest several weeks after treatment.
FG, DB and ZB drafted the manuscript. FG, DB and AA collected clinical and laboratory data. MM and CS performed the molecular tests. GL and SG were responsible for the pharmacokinetic analysis. All authors commented and agreed upon the final manuscript. All authors read and approved the final manuscript.
The authors declare that they have no competing interests.
Consent for publication
Written informed consent for the publication of the present case was obtained from the patient.
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