Scolaris Content Display Scolaris Content Display

Butóxido de piperonilo (BOP) combinado con piretroides en los mosquiteros tratados con insecticida para prevenir el paludismo en África

Contraer todo Desplegar todo

Referencias

Awolola 2014 {published data only}

Awolola ST, Adeogun AO, Olojede JB, Oduola AO, Oyewole IO, Amajoh CN. Impact of PermaNet 3.0 on entomological indices in an area of pyrethroid resistant Anopheles gambiae in south-western Nigeria. Parasites & Vectors 2014;7:236. CENTRAL [DOI: 10.1186/1756-3305-7-236]

Bayili 2017 {published data only (unpublished sought but not used)}

Bayili K. Phase II field evaluation of long-lasting nets DawaPlus 3.0 (deltamethrin and PBO in roof panel; deltamethrin alone in the side panels) and DawaPlus 4.0 (deltamethrin and PBO) of Tana Netting against natural populations of Anopheles gambiae s.l in Burkina Faso. Report of the twentieth WHOPES working group meeting, WHO/HQ, Geneva, 20–24 March 2017. http://apps.who.int/iris/bitstream/handle/10665/258921/WHO-HTM-NTD-WHOPES-2017.04-eng.pdf;jsessionid=87560DBD471E349CBB7A99796C513DBC?sequence=1 (accessed 13 September 2017). CENTRAL [WHO/HTM/NTD/WHOPES/2017.04]

Cisse 2017 {published and unpublished data}

Cisse MB, Sangare D, Oxborough RM, Dicko A, Dengela D, Sadou A, et al. A village level cluster-randomized entomological evaluation of combination long-lasting insecticidal nets containing pyrethroid plus PBO synergist in Southern Mali. Malaria Journal 2017;16:477. CENTRAL [DOI: 10.1186/s12936-017-2124-1]

Corbel 2010 {published data only}

Corbel V, Chabi J, Dabiré RK, Etang J, Nwane P, Pigeon O, et al. Field efficacy of a new mosaic long-lasting mosquito net (PermaNet 3.0) against pyrethroid-resistant malaria vectors: a multi centre study in Western and Central Africa. Malaria Journal 2010;9:113. CENTRAL [DOI: 10.1186/1475-2875-9-113]

Koudou 2011 {published data only}

Koudou BG, Koffi AA, Malone D, Hemingway J. Efficacy of PermaNet® 2.0 and PermaNet® 3.0 against insecticide-resistant Anopheles gambiae in experimental huts in Côte d’Ivoire. Malaria Journal 2011;10(1):172. CENTRAL [DOI: 10.1186/1475-2875-10-172]

Menze 2020 {published and unpublished data}

Menze B, Kouamo MF, Wondji MJ, Tchapga W, Tchoupo M, Kusimo MO, et al. An experimental hut evaluation of PBO-based and pyrethroid-only nets against the malaria vector Anopheles funestus reveals a loss of bed nets efficacy associated with GSTe2 metabolic resistance. Genes 2020;11(2):143. CENTRAL [DOI: 10.3390/genes11020143]

Moore 2016 {published and unpublished data}

Moore S. Field evaluation of an alpha-cypermethrin+PBO long-lasting insecticidal net (Veeralin LN) against natural populations of Anopheles arabiensis in experimental huts, Tanzania [Unpublished report to the WHO Pesticide Evaluation Scheme (WHOPES)]. Report of the nineteenth WHOPES working group meeting: WHO/HQ, Geneva, 8–11 February 2016. http://apps.who.int/iris/bitstream/handle/10665/205588/9789241510400_eng.pdf?sequence=1 (accessed 24 August 2017). CENTRAL [WHO/HTM/NTD/WHOPES/2016.2]

Mzilahowa 2014 {unpublished data only}

Mzilahowa T, Luka M, Chiumia M, Gimnig J. Efficacy of the PermaNet 3.0 and the Olyset Plus against pyrethroid resistant An funestus and An arabiensis (as supplied 14 March 2015). Data on file (received 14 March 2015). CENTRAL

N'Guessan 2010 {published data only}

N’Guessan R, Asidi A, Boko P, Odjo A, Akogbeto M, Pigeon O, et al. An experimental hut evaluation of PermaNet(®) 3.0, a deltamethrin-piperonyl butoxide combination net, against pyrethroid-resistant Anopheles gambiae and Culex quinquefasciatus mosquitoes in southern Benin. Transactions of the Royal Society of Tropical Medicine and Hygiene 2010;104(12):758-65. CENTRAL [DOI: 10.1016/j.trstmh.2010.08.008]

Oumbouke 2019 {published data only}

Oumbouke WA, Rowland M, Koffi AA, Alou LPA, Camara S, N’Guessan R. Evaluation of an alpha-cypermethrin + PBO mixture long-lasting insecticidal net VEERALIN® LN against pyrethroid resistant Anopheles gambiae s.s.: an experimental hut trial in M’bé, central Côte d’Ivoire. Parasites & Vectors 2019;12(1):544. CENTRAL [DOI: 10.1186/s13071-019-3796-x]

Pennetier 2013 {published data only}

Pennetier C, Bouraima A, Chandre F, Piameu M, Etang J, Rossignol M, et al. Efficacy of Olyset(R) Plus, a new long-lasting insecticidal net incorporating permethrin and piperonyl-butoxide against multi-resistant malaria vectors [corrected]. PLoS One 2013;8(10):e75134. CENTRAL [DOI: 10.1371/journal.pone.0075134]

Protopopoff 2018 {published data only}

Protopopoff N, Charlwood D, Mosha J, Wright A, Kisinza W, Mosha F, et al. Evaluation of a novel long lasting insecticidal net to indoor residual spray product, separately to together, against malaria transmitted by pyrethroid resistant mosquitoes in northwest Tanzania: a cluster randomized controlled trial. Lancet 2018;391(10130):1577-88. CENTRAL [DOI: 10.1016/S0140-6736(18)30427-6]

Staedke 2020 {published and unpublished data}

ISRCTN17516395. Impact of long-lasting insecticide treated bednets with and without piperonyl butoxide (PBO) on malaria indicators in Uganda. www.isrctn.com/ISRCTN17516395 (accessed 24 August 2018). CENTRAL
Staedke SG, Gonahasa S, Dorsey G, Kamya MR, Maiteki-Sebuguzi C, Lynd A,  et al. Effect of long-lasting insecticidal nets with and without piperonyl butoxide on malaria indicators in Uganda (LLINEUP): a pragmatic, cluster-randomised trial embedded in a national LLIN distribution campaign. Lancet 2020;395(10232):1292-303. CENTRAL [DOI: 10.1016/S0140-6736(20)30214-2]

Stiles‐Ocran 2013 {unpublished data only}

Stiles-Ocran J. Field evaluation of PermaNet® 3.0 in controlling pyrethroid resistant Anopheles gambiae in the Chirano Area, Western Region, Ghana (as supplied 12 March 2015). Data on file2013. CENTRAL

Toé 2018 {published and unpublished data}

Toé KH, Müller P, Badolo A, Traore A, Sagnon N, Dabiré RK, et al. Do bednets including piperonyl butoxide offer additional protection against populations of Anopheles gambiae s.l. that are highly resistant to pyrethroids? An experimental hut evaluation in Burkina Faso. Medical and Veterinary Entomology 2018;32(4):407-16. CENTRAL [DOI: 10.1111/mve.12316]

Tungu 2010 {published data only}10.1186/1475-2875-9-21

Tungu P, Magesa S, Maxwell C, Malima R, Masue D, Sudi W, et al. Evaluation of PermaNet 3.0 a deltamethrin-PBO combination net against Anopheles gambiae and pyrethroid resistant Culex quinquefasciatus mosquitoes: an experimental hut trial in Tanzania. Malaria Journal 2010;9:21. CENTRAL [DOI: 10.1186/1475-2875-9-21]

Darriet 2011 {published data only}

Darriet F, Chandre F. Combining piperonyl butoxide and dinotefuran restores the efficacy of deltamethrin mosquito nets against resistant Anopheles gambiae (Diptera: Culicidae). Journal of Medical Entomology 2011;48(4):952-5. CENTRAL [DOI: 10.1603/ME11022]

Darriet 2013 {published data only}

Darriet F, Chandre F. Efficacy of six neonicotinoid insecticides alone and in combination with deltamethrin and piperonyl butoxide against pyrethroid-resistant Aedes aegypti and Anopheles gambiae (Diptera: Culicidae). Pest Management Science 2013;69(8):905-10. CENTRAL [DOI: 10.1002/ps.3446]

Referencias de los estudios en espera de evaluación

Koudou 2012 {unpublished data only}

Koudou B, Malone D. Does PermaNet® 3.0 protect against pyrethroid resistant mosquitoes?Manuscript in preparation for Acta Tropica (received 14 December 2012). CENTRAL

Shono 2017 {published data only}

Shono Y, Ohashi K, Lucas JR. Biological performance of Olyset® Plus, a long-lasting mosquito net incorporating a mixture of a pyrethroid and synergist. Acta Horticulturae 2017;1169:77-81. CENTRAL

Tungu 2017 {published data only (unpublished sought but not used)}

Tungu P. Phase II study to evaluate the efficacy and wash resistance of DawaPlus 3.0 and DawaPlus 4.0 against natural populations of Anopheles funestus s.s. in experimental huts in Muheza, Tanzania. Report of the twentieth WHOPES working group meeting, WHO/HQ, Geneva, 20–24 March 2017. http://apps.who.int/iris/bitstream/handle/10665/258921/WHO-HTM-NTD-WHOPES-2017.04-eng.pdf;jsessionid=87560DBD471E349CBB7A99796C513DBC?sequence=1 (accessed 13 September 2017). CENTRAL [WHO/HTM/NTD/WHOPES/2017.04]

ISRCTN99611164 {unpublished data only}

ISRCTN99611164. Comparative evaluation of standard and dual-treated insecticide bednets in Sud Ubangi, Democratic Republic of Congo. https://doi.org/10.1186/ISRCTN99611164 (accessed prior to 1 May 2021). CENTRAL

NCT03289663 {unpublished data only}NCT03289663

NCT03289663. Effectiveness study of bednets treated with synergistic combination of insecticides in an area with pyrethroid-resistant vectors in the Democratic Republic of the Congo [Effectiveness study of new generation bednets in the context of conventional insecticide resistance in the Democratic Republic of Congo]. clinicaltrials.gov/show/NCT03289663 (first received 24 August 2018). CENTRAL

NCT04182126 {unpublished data only}

NCT04182126. Environmental modifications in sub-Saharan Africa: changing epidemiology, transmission and pathogenesis of Plasmodium falciparum and P. vivax malaria [HS#2017-3512, adaptive interventions for optimizing malaria control: a cluster-randomized SMART trial]. clinicaltrials.gov/ct2/show/NCT04182126 (first received 2 December 2019). CENTRAL

UMIN000019971 {unpublished data only}

Minakawa N, Kongere JO, Sonye GO, Lutiali PA, Awuor B, Kawada H, et al. A preliminary study on designing a cluster randomized control trial of two new mosquito nets to prevent malaria parasite infection. Tropical Medicine and Health 2020;48(1):98. CENTRAL [DOI: 10.1186/s41182-020-00276-x]
UMIN000019971. Effects of long lasting insecticidal nets incorporating piperonyl butoxidae on malaria transmission among children: a cluster randomized controlled field trial. https://upload.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000023020 (first posted 25 December 2015). CENTRAL

Abílio 2015

Abílio AP, Marrune P, de Deus N, Mbofana F, Muianga P, Kampango A. Bio-efficacy of new long-lasting insecticide-treated bed nets against Anopheles funestus and Anopheles gambiae from central and northern Mozambique. Malaria Journal 2015;14:352. [DOI: 10.1186/s12936-015-0885-y]

Adeogun 2012

Adeogun AO, Olojede JB, Oduola AO, Awolola TS. Efficacy of a combination long lasting insecticidal net (PermaNet® 3.0) against pyrethroid resistant Anopheles gambiae s.s. and Culex quinquefasciatus: an experimental hut trial in Nigeria. Nigerian Journal of Clinical & Biomedical Research 2012;6:37-50.

Aïzoun 2013

Aïzoun N, Ossè R, Azondekon R, Alia R, Oussou O, Gnanguenon V, et al. Comparison of the standard WHO susceptibility tests and the CDC bottle bioassay for the determination of insecticide susceptibility in malaria vectors and their correlation with biochemical and molecular biology assays in Benin, West Africa. Parasites & Vectors 2013;6:147.

Bhatt 2015

Bhatt S, Weiss DJ, Cameron E, Bisanzio D, Mappin B, Dalrymple U, et al. The effect of malaria control on Plasmodium falciparum in Africa between 2000 and 2015. Nature 2015;526(7572):207-11.

Bobanga 2013

Bobanga T, Ayieko W, Zanga M, Umesumbu S, Landela A, Fataki O, et al. Field efficacy and acceptability of PermaNet® 3.0 and OlysetNet® in Kinshasa, Democratic Republic of the Congo. Journal of Vector Borne Diseases 2013;50(3):206-14.

Churcher 2016

Churcher TS, Lissenden N, Griffin JT, Worrall E, Ranson H. The impact of pyrethroid resistance on the efficacy and effectiveness of bednets for malaria control in Africa. eLife 2016;5:e16090. [DOI: http://dx.doi.org/10.7554/eLife.16090]

Deeks 2017

Deeks JJ, Higgins JP, Altman DG (editors), on behalf of the Cochrane Statistical Methods Group. Chapter 9. Analysing data and undertaking meta-analyses. In: Higgins JP, Churchill R, Chandler J, Cumpston MS (editors). Cochrane Handbook for Systematic Reviews of Interventions version 5.2.0 (updated June 2017), Cochrane, 2017. Available from www.training.cochrane.org/handbook.

Djègbè 2011

Djègbè I, Boussari O, Sidick A, Martin T, Ranson H, Chandre F, et al. Dynamics of insecticide resistance in malaria vectors in Benin: first evidence of the presence of L1014S kdr mutation in Anopheles gambiae from West Africa. Malaria Journal 2011;10:261.

GRADEpro GDT 2015 [Computer program]

McMaster University (developed by Evidence Prime)GRADEpro GDT. Version accessed 5 May 2017. Hamilton (ON): McMaster University (developed by Evidence Prime), 2015. Available at gradepro.org.

Hawley 2003

Hawley WA, Phillips-Howard PA, ter Kuile FO, Terlouw DJ, Vulule JM, Ombok M, et al. Community-wide effects of permethrin-treated bed nets on child mortality and malaria morbidity in western Kenya. American Journal of Tropical Medicine & Hygiene 2003;68(4 Suppl):121-7. [DOI: 10.4269/ajtmh.2003.68.121]

Higgins 2003

Higgins JP, Thompson SG, Deeks JJ, Altman DG. Measuring inconsistency in meta-analyses. BMJ 2003;327:557-60.

Higgins 2011

Higgins JP, Deeks JJ, Altman DG, Cochrane Statistical Methods Group. Chapter 16. Special topics in statistics. In: Higgins JP, Green S, editor(s). Cochrane Handbook for Systematic Reviews of Interventions version 5.1.0 (updated March 2011), The Cochrane Collaboration, 2011. Available from handbook.cochrane.org.

Higgins 2017

Higgins JP, Altman DG, Sterne JA (editors). Chapter 8. Assessing risk of bias in included studies. In: Higgins JP, Churchill R, Chandler J, Cumpston MS (editors). Cochrane Handbook for Systematic Reviews of Interventions version 5.2.0 (updated June 2017), Cochrane, 2017. Available from www.training.cochrane.org/handbook.

Killeen 2018

Killeen G, Ranson H. Insecticide-resistant malaria vectors must be tackled. Lancet 2018;391(10130):1551-2.

Kleinschmidt 2018

Kleinschmidt I, Bradley J, Knox TB, Mnzava AP, Kafy HT, Mbogo C, et al. Implications of insecticide resistance for malaria vector control with long-lasting insecticidal nets: a WHO-coordinated, prospective, international, observational cohort study. Lancet 2018;18:20172-5. [DOI: 10.1016/S1473-3099(18)30172-5]

Lengeler 2004

Lengeler C. Insecticide-treated bed nets and curtains for preventing malaria. Cochrane Database of Systematic Reviews 2004, Issue 2. Art. No: CD000363. [DOI: 10.1002/14651858.CD000363.pub2]

Maxwell 2002

Maxwell CA, Msuya E, Sudi M, Njunwa KJ, Carneiro IA, Curtis CF. Effect of community-wide use of insecticide-treated nets for 3-4 years on malarial morbidity in Tanzania. Tropical Medicine & International Health 2002;7(12):1003-8. [DOI: 10.1046/j.1365-3156.2002.00966]

Mitchell 2012

Mitchell SN, Stevenson BJ, Müller P, Wilding CS, Egyir-Yawson A, Field SG, et al. Identification and validation of a gene causing cross-resistance between insecticide classes in Anopheles gambiae from Ghana. Proceedings of the Nationall Academy of Sciences of the United States of America 2012;109(16):6147-52. [DOI: 10.1073/pnas.1203452109]

MPAC 2016

Malaria Policy Advisory Committee. WHO Malaria Policy Advisory Committee (MPAC) meeting report (September 2016). www.who.int/malaria/publications/atoz/mpac-september2016-report.pdf?ua=1 (accessed 1 May 2017).

N'Guessan 2007

N'Guessan R, Corbel V, Akogbéto M, Rowland M. Reduced efficacy of insecticide-treated nets and indoor residual spraying for malaria control in pyrethroid resistance area, Benin. Emerging Infectious Diseases 2007;13(2):199-206. [DOI: 10.3201/eid1302.060631]

Parker 2015

Parker J, Angarita-Jaimes N, Abe M, Towers CE, Towers D, McCall P. Infrared video tracking of Anopheles gambiae at insecticide-treated bed nets reveals rapid decisive impact after brief localised net contact. Scientific Reports 2015;5:e13392.

PMI 2018

PMI. U.S. President’s Malaria Initiative technical guidance, 2018. www.pmi.gov/docs/default-source/default-document-library/tools-curricula/pmi-technical-guidance-(february-2017).pdf?sfvrsn=16.

Ranson 2011

Ranson H, N'Guessan R, Lines J, Moiroux N, Nkuni Z, Corbel V. Pyrethroid resistance in African Anopheline mosquitoes: what are the implications for malaria control? Trends in Parasitology 2011;27(2):91-8. [DOI: 10.1016/j.pt.2010.08.004]

Ranson 2016

Ranson H, Lissenden N. Insecticide resistance in African Anopheles mosquitoes: a worsening situation that needs urgent action to maintain malaria control. Trends in Parasitology 2016;32(3):187-96. [DOI: 10.1016/j.pt.2015.11.010]

Review Manager 2014 [Computer program]

Nordic Cochrane Centre, The Cochrane CollaborationReview Manager 5 (RevMan 5). Version 5.3. Copenhagen: Nordic Cochrane Centre, The Cochrane Collaboration, 2014.

Ridl 2008

Ridl FC, Bass C, Torrez M, Govender D, Ramdeen V, Yellot L, et al. A pre-intervention study of malaria vector abundance in Rio Muni, Equatorial Guinea: their role in malaria transmission and the incidence of insecticide resistance alleles. Malaria Journal 2008;7:194. [DOI: 10.1186/1475-2875-7-194]

Riveron 2015

Riveron JM, Chiumia M, Menze BD, Barnes KG, Irving H, Ibrahim SS, et al. Rise of multiple insecticide resistance in Anopheles funestus in Malawi: a major concern for malaria vector control. Malaria Journal 2015;14:344. [DOI: 10.1186/s12936-015-0877-y]

Schünemann 2013

Schünemann H, Brożek J, Guyatt G, Oxman A, editor(s). Handbook for grading the quality of evidence and the strength of recommendations using the GRADE approach (updated October 2013). GRADE Working Group, 2013. Available from gdt.guidelinedevelopment.org/app/handbook/handbook.html.

Stevenson 2011

Stevenson BJ, Bibby J, Pignatelli P, Muangnoicharoen S, O'Neill PM, Lian LY, et al. Cytochrome P450 6M2 from the malaria vector Anopheles gambiae metabolizes pyrethroids: sequential metabolism of deltamethrin revealed. Insect Biochemistry and Molecular Biology 2011;41(7):492-502. [DOI: 10.1016/j.ibmb.2011.02.003]

Strode 2014

Strode C, Donegan S, Garner P, Enayati AA, Hemingway J. The impact of pyrethroid resistance on the efficacy of insecticide-treated bed nets against African Anopheline mosquitoes: systematic review and meta-analysis. PLoS Medicine 2014;11(3):e1001619. [DOI: 10.1371/journal.pmed.1001619]

Sumitomo 2013

Sumitomo Chemical Co Ltd. Olyset Plus Technical Brochure 2013. sumivector.com/sites/default/files/site-content/pdf/Olyset_Plus_Technical_Brochure_Jan_2013_ENG.pdf (accessed 1 May 2017).

Vestergaard 2015

Vestergaard. Technical basis for deployment of PermaNet® 3.0 in areas with pyrethroid-resistant malaria vectors. PermaNet® 3.0 Technical Brochure. January 2015. www.vestergaard.com/images/pdf/PN3_Tech_Eng_2015.pdf (accessed 1 May 2017).

WHO 2013

World Health Organization Pesticide Evaluation Scheme. Guidelines for laboratory and field testing of long-lasting insecticidal nets. apps.who.int/iris/bitstream/10665/80270/1/9789241505277_eng.pdf (accessed 24 August 2018).

WHO 2016

World Health Organization. Test Procedures for Insecticide Resistance Monitoring in Malaria Vector Mosquitoes. Second edition. Geneva: WHO, 2016.

WHO 2017

World Health Organization/Department of Control of Neglected Tropical Diseases. Design of epidemiological trials for vector control products, Report of a WHO Expert Advisory Group; Château de Penthes, Geneva, 24–25 April 2017. www.who.int/neglected_diseases/vector_ecology/resources/WHO_HTM_NTD_VEM_2017.04/en/ (accessed 11 July 2017).

WHO 2019a

World Health Organization. World malaria report 2019. www.who.int/malaria/publications/world_malaria_report/en/.

WHO 2019b

World Health Organization. Guidelines for malaria vector control. https://apps.who.int/iris/bitstream/handle/10665/310862/9789241550499-eng.pdf?ua=1 (accessed prior to 13 May 2021).

WHO‐GMP 2015

World Health Organization Global Malaria Programme. Conditions for use of long-lasting insecticidal nets treated with a pyrethroid and piperonyl butoxide. www.who.int/malaria/areas/vector_control/use-of-pbo-treated-llins-report-nov2015.pdf (accessed 24 August 2018).

WHO‐GMP 2017a

World Health Organization. Conditions for deployment of mosquito nets treated with a pyrethroid and piperonyl butoxide. apps.who.int/iris/bitstream/handle/10665/258939/WHO-HTM-GMP-2017.17-eng.pdf?sequence=1 (accessed 24 August 2018).

WHO‐GMP 2017b

World Health Organization. The evaluation process for vector control products. www.who.int/malaria/publications/atoz/evaluation-process-vector-control-products/en/ (accessed 24 August 2018).

WHO‐GMP 2017c

World Health Organization Global Malaria Programme. Malaria vector control policy recommendations and their applicability to product evaluation. www.who.int/malaria/publications/atoz/vector-control-recommendations/en/ (accessed 24 August 2018).

WHOPES 2016

WHO/Department of Control of Neglected Tropical Diseases. Report of the nineteenth WHOPES working group meeting: WHO/HQ, Geneva, 8–11 February 2016. Review of Veeralin LN, VectoMax GR, Bactivec SC. apps.who.int/iris/bitstream/10665/205588/1/9789241510400_eng.pdf (accessed 1 May 2017).

Yewhalaw 2012

Yewhalaw D, Asale A, Tushune K, Getachew Y, Duchateau L, Speybroeck N. Bio-efficacy of selected long-lasting insecticidal nets against pyrethroid resistant Anopheles arabiensis from South-Western Ethiopia. Parasites & Vectors 2012;5:159. [DOI: 10.1186/1756-3305-5-159]

Zaim 2000

Zaim M, Aitio A, Nakashima N. Safety of pyrethroid-treated mosquito nets. Medical and Veterinary Entomology 2000;14(1):1-5.

Referencias de otras versiones publicadas de esta revisión

Gleave 2017

Gleave K, Lissenden N, Richardson M, Ranson H. Piperonyl butoxide (PBO) combined with pyrethroids in long-lasting insecticidal nets (LLINs) to prevent malaria in Africa. Cochrane Database of Systematic Reviews 2017, Issue 8. Art. No: CD012776. [DOI: 10.1002/14651858.CD012776]

Gleave 2018

Gleave K, Lissenden N, Richardson M, Choi L, Ranson H. Piperonyl butoxide (PBO) combined with pyrethroids in insecticide-treated nets to prevent malaria in Africa. Cochrane Database of Systematic Reviews 2018, Issue 11. Art. No: CD012776. [DOI: 10.1002/14651858.CD012776.pub2]

Characteristics of studies

Characteristics of included studies [author‐defined order]

Staedke 2020

Study characteristics

Methods

Cluster‐randomized controlled village trial

Participants

Households with at least 1 adult resident and 1 child aged 2 to 10 years, Anopheles species

Interventions

Control: LLIN, PermaNet 2.0

Intervention: LLIN, PermaNet 3.0

Control: LLIN, Olyset Net

Intervention: LLIN, Olyset Plus

Outcomes

Primary outcomes; parasite prevalence (proportion of thick blood smears that are positive for asexual parasites) in children ages 2 to 10 years, assessed before net distribution and 3 times after nets are distributed

Secondary outcomes: prevalence of anaemia; mean haemoglobin in children ages 2 to 10 years; vector density; measures of LLIN ownership; coverage, use, and integrity

Mosquito resistance status

Resistance ‐ high

Net treatment

Nets unholed and unwashed

Location(s)

Uganda ‐ East and West, 104 sub‐districts

Notes

Risk of bias

Bias

Authors' judgement

Support for judgement

Recruitment bias

Low risk

No participants were recruited after clusters had been randomized

Were the mosquitoes in LLIN and LLIN + PBO groups comparable

Unclear risk

Resistance monitoring was not conducted at all study sites due to the size of the RCT

Collectors blinded

High risk

LLIN allocation was not masked; therefore risk of detection bias was high for entomological outcomes

Household blinded

Low risk

LLIN allocation was not masked, but this is unlikely to affect the primary outcome (parasite prevalence)

Treatment allocation (sequence randomly/adequately generated)

Low risk

Randomization was used to allocate clusters to study groups

Allocation concealment (selection bias)

Low risk

Randomization was carried out to allocate treatments to clusters

Were incomplete outcome data adequately addressed

Low risk

No outcome data were incomplete; intention‐to‐treat analysis was conducted

Were the raw data reported for LLIN and LLIN + PBO groups

Low risk

No outcome data were missing

Clusters lost to follow‐up

Unclear risk

14 clusters were lost to follow‐up in the final time point (25 months) due to the COVID‐19 pandemic

Selective reporting (reporting bias)

Low risk

All intended outcomes stated in the pre‐published protocol were reported in the final publication

Correct statistical methods; adjusted for clustering

Low risk

Clustering was not taken into account and adjusted for during statistical analysis. Trial authors did however provide us with an ICC, so we could adjust for clustering

Trial authors' conflicting interest

Low risk

Trial authors declared no conflicting interests

Awolola 2014

Study characteristics

Methods

Village trial

Participants

Ilara ‐ An gambiae (100% S‐form)
Irolu ‐ 95% An gambiae (100% S‐form), 4.5% An arabiensis
Ijesa ‐ 98.1% An gambiae (80% S‐form, 19% M‐form), 1.6% An arabiensis

Interventions

Control: LLIN, PermaNet 2.0

Intervention: LLIN, PermaNet 3.0

Outcomes

Mosquito mortality, blood feeding, sporozoite rate, mosquito density, parity rate

Mosquito resistance status

Ilara ‐ resistant ‐ low (deltamethrin, 72.5% mortality, N = 120)
Irolu ‐ resistant ‐ low (deltamethrin, 62.5% mortality, N = 120)
Ijesa ‐ resistant ‐ low (deltamethrin, 66.7% mortality, N = 120)

Net treatment

Nets unholed and unwashed

Location(s)

Ilara, Nigeria ‐ untreated net
Irolu, Nigeria ‐ PermaNet 2.0
Ijesa, Nigera ‐ PermaNet 3.0

Notes

Trial conducted: March 2012 to March 2013

Risk of bias

Bias

Authors' judgement

Support for judgement

Recruitment bias

Low risk

Recruiment bias is related to human participants and so is not applicable to this study

Were the mosquitoes in LLIN and LLIN + PBO groups comparable

Unclear risk

Mosquito species composition varied slightly pre‐trial and post‐trial between treatment villages. However, resistance level was the same

Collectors blinded

High risk

Not stated whether collectors where blinded; therefore judged as high risk, as this is likely to impact searching efforts

Household blinded

Low risk

Unclear whether households were blinded – not stated in the publication. We judged this as low risk, as it is unlikely to affect the outcome

Treatment allocation (sequence randomly/adequately generated)

Low risk

Villages were randomly assigned to treatment arms

Allocation concealment (selection bias)

Low risk

Allocation concealment procedures were not adhered to; however this is unlikely to affect the results

Were incomplete outcome data adequately addressed

Low risk

There were no incomplete data

Were the raw data reported for LLIN and LLIN + PBO groups

Low risk

All necessary data were reported

Clusters lost to follow‐up

Low risk

No clusters were lost to follow‐up

Selective reporting (reporting bias)

Low risk

It appears that all measured outcomes were reported

Correct statistical methods; adjusted for clustering

High risk

Study did not take clustering into account for statistical methods

Trial authors' conflicting interest

Low risk

Trial authors declared no conflicting interests; however the study was funded by Vestergaard (net manufacturers). Views and findings in the publication are stated to be those of the trial authors

Bayili 2017

Study characteristics

Methods

Experimental hut trial

Participants

An coluzzii

Interventions

Control: LLIN, DawaPlus 2.0

Intervention: LLIN, DawaPlus 3.0, DawaPlus 4.0

Outcomes

Mosquito mortality, blood feeding, deterrence, exophily

Mosquito resistance status

Resistant ‐ high (6% mortality, N = 98)

Net treatment

Nets holed, nets unwashed and washed (x 20)

Location(s)

Vallée du Kou, Burkina Faso

Notes

Trial conducted: August 2016 to October 2016

Risk of bias

Bias

Authors' judgement

Support for judgement

Were the mosquitoes in LLIN and LLIN + PBO groups comparable

Low risk

The hut trial was conducted in the same area; therefore characteristics are similar

Collectors blinded

Unclear risk

Paper does not state whether collectors were blinded

Sleepers blinded

Unclear risk

Paper does not state whether sleepers were blinded

Sleeper bias

Low risk

Sleepers were rotated between huts according to a Latin square design

Treatment allocation (sequence randomly/adequately generated)

Low risk

Treatments were not randomly allocated to huts; however the trial completed a full rotation through the huts

Treatment rotation

Low risk

Treatments were rotated between huts according to a Latin square design + 2 weeks

Standardized hut design

Low risk

Huts were built previously according to standard West African design

Hut cleaning between treatments

Unclear risk

Trial authors do not state whether huts were cleaned between treatments

Were incomplete outcome data adequately addressed

Low risk

No data were incomplete

Were the raw data reported for LLIN and LLIN + PBO groups

Low risk

All necessary data were reported

Trial authors' conflicting interest

Low risk

Trial authors declare no conflicting interest in the WHOPES report

Cisse 2017

Study characteristics

Methods

Village trial

Participants

An gambiae s.s.

Interventions

Control: LLIN, Olyset Net, PermaNet 2.0

Intervention: LLIN, Olyset Plus, PermaNet 3.0

Outcomes

Sporozoite rate, mosquito density, parity rate

Mosquito resistance status

Olyset Net villages ‐ resistance ‐ high (1% mortality, N = 305)
Olyset Plus villages ‐ resistance ‐ high (2% mortality, N = 411)
PermaNet 2.0 villages ‐ resistance ‐ high (29% mortality, N = 410)
PermaNet 3.0 villages ‐ resistance ‐ moderate (38% mortality, N = 408)

Net treatment

Nets unholed and unwashed

Location(s)

Sikasso region, Mali

PermaNet 2.0 villages ‐ Beko East, Dalabani, Berila, Dierila
PermaNet 3.0 villages ‐ Beko West, Farabacoura East, Kola Djokada, Tieblembougou
Olyset Net villages ‐ Karako, Geleba 2, Toula East, Toula West
Olyset Plus villages ‐ Dialake, Farabacoura West, Deneklin, Faradjele

Notes

Trial conducted: January 2014 to January 2015

Risk of bias

Bias

Authors' judgement

Support for judgement

Recruitment bias

Low risk

Recruiment bias is related to human participants and so is not applicable to this study

Were the mosquitoes in LLIN and LLIN + PBO groups comparable

Unclear risk

Mosquito species composition is constant between villages; however resistance level varies slightly

Collectors blinded

High risk

Not stated whether collectors where blinded; therefore judged as high risk, as this is likely to affect searching efforts

Household blinded

Low risk

Unclear whether households were blinded – not stated in the publication. We judged this as low risk, as this is unlikely to affect the outcome

Treatment allocation (sequence randomly/adequately generated)

Low risk

Villages were randomly assigned to treatment arms

Allocation concealment (selection bias)

Low risk

Allocation concealment procedures were not adhered to; however this is unlikely to affect study results

Were incomplete outcome data adequately addressed

Low risk

No data were incomplete

Were the raw data reported for LLIN and LLIN + PBO groups

Low risk

All necessary data were reported

Clusters lost to follow‐up

Low risk

No clusters were lost to follow‐up

Selective reporting (reporting bias)

Low risk

It appears that all measured outcomes were reported

Correct statistical methods; adjusted for clustering

High risk

Study did not take clustering into account for statistical methods

Trial authors' conflicting interest

Low risk

Trial authors have no competing interests

Corbel 2010

Study characteristics

Methods

Experimental hut trial

Participants

Vallée du Kou, Burkina Faso ‐ 100% An gambiae: M‐form (15%), S‐form (85%)

Malanville, Benin ‐ 95% An gambiae: M‐form (100%), 5% An arabiensis

Pitoa, Cameroon ‐ 5% An gambiae: S‐form (100%), 95% An arabiensis

Interventions

Control: LLIN, PermaNet 2.0

Intervention: LLIN, PermaNet 3.0

Outcomes

Mosquito mortality, blood feeding, deterrence, exophily

Mosquito resistance status

Vallée du Kou, Burkina Faso ‐ resistant – high (deltamethrin, 23% mortality, N = 100)

Malanville, Benin ‐ resistant – low (deltamethrin, 85% mortality, N = 100)

Pitoa, Cameroon ‐ resistant – low (deltamethrin, 70% mortality, N = 100)

Net treatment

Nets holed, nets unwashed and washed (x 20)

Location(s)

Vallée du Kou, Burkina Faso

Malanville, Benin

Pitoa, Cameroon

Notes

Trial conducted:

Vallée du Kou, Burkina Faso ‐ September 2007 to November 2007

Malanville, Benin ‐ July 2008 to September 2008

Pitoa, Cameroon ‐ July 2008 to September 2008

Risk of bias

Bias

Authors' judgement

Support for judgement

Were the mosquitoes in LLIN and LLIN + PBO groups comparable

Low risk

Huts situated in the same area: mosquito characteristics will be the same

Collectors blinded

Unclear risk

Unclear whether collectors were blinded – not stated in the publication

Sleepers blinded

Unclear risk

Unclear whether sleeper was blinded – not stated in the publication

Sleeper bias

Low risk

Sleepers were rotated between huts according to a Latin square design

Treatment allocation (sequence randomly/adequately generated)

Low risk

Treatments were randomly allocated to huts

Treatment rotation

Low risk

Treatments were rotated between huts according to a Latin square design

Standardized hut design

Low risk

Huts were built according to a standard West African design

Hut cleaning between treatments

Unclear risk

Unclear whether huts were cleaned between treatments – not stated in the publication

Were incomplete outcome data adequately addressed

Low risk

No outcome data were incomplete

Were the raw data reported for LLIN and LLIN + PBO groups

Low risk

All necessary data were reported

Trial authors' conflicting interest

Low risk

Trial authors have no competing interests

Koudou 2011

Study characteristics

Methods

Experimental hut trial

Participants

An gambiae s.s.

Interventions

Control: LLIN, PermaNet 2.0

Intervention: LLIN, PermaNet 3.0

Outcomes

Mosquito mortality, deterrence, exophily

Mosquito resistance status

Resistant ‐ high (deltamethrin, 10.6% mortality, N = 80 min)

Net treatment

Nets not holed, nets unwashed and washed (x 20)

Location(s)

Yaokoffikro, Côte d'Ivoire

Notes

Trial conducted: April 2009 to July 2009

Risk of bias

Bias

Authors' judgement

Support for judgement

Were the mosquitoes in LLIN and LLIN + PBO groups comparable

Low risk

Huts situated in the same area – mosquito characteristics will be the same

Collectors blinded

Unclear risk

Unclear whether collectors were blinded – not stated in the publication

Sleepers blinded

Unclear risk

Unclear whether sleeper was blinded – not stated in the publication

Sleeper bias

Low risk

Sleepers were rotated between huts according to a Latin square design

Treatment allocation (sequence randomly/adequately generated)

Low risk

Treatments were not randomly allocated to the huts

However, results from trials performed before this trial show no significant differences in attractiveness of the different huts

Treatment rotation

Low risk

Treatments were rotated between huts according to a Latin square design

Standardized hut design

Low risk

Huts were built according to a standard West African design

Hut cleaning between treatments

Low risk

All huts were cleaned between treatments

Were incomplete outcome data adequately addressed

Low risk

No outcome data were incomplete

Were the raw data reported for LLIN and LLIN + PBO groups

Low risk

All necessary data were reported

Trial authors' conflicting interest

Low risk

Trial authors declared they had no conflicting interests

Moore 2016

Study characteristics

Methods

Experimental hut trial

Participants

An arabiensis (100%), An funestus group (95% s.s.)

Interventions

Control: LLIN, MAGNet LN

Intervention: LLIN, Veeralin LN

Outcomes

Mosquito mortality, blood feeding, deterrence, exophily

Mosquito resistance status

An arabiensis ‐ susceptible (alpha‐cypermethrin, 100% mortality, N = 97)

An funestus ‐ unclassified

Net treatment

Nets holed, nets unwashed and washed (x 20)

Location(s)

Ifakara, Tanzania

Notes

Although additional data provided, they show resistance to deltamethrin and permethrin in An gambiae s.l.

Risk of bias

Bias

Authors' judgement

Support for judgement

Were the mosquitoes in LLIN and LLIN + PBO groups comparable

Low risk

The hut trial was conducted in the same area; therefore characteristics are similar

Collectors blinded

Unclear risk

Paper does not state whether collectors were blinded

Sleepers blinded

Unclear risk

Paper does not state whether sleepers were blinded

Sleeper bias

Low risk

Sleepers were rotated between huts according to a Latin square design

Treatment allocation (sequence randomly/adequately generated)

Low risk

Treatments were not randomly allocated to huts; however the trial completed a full rotation through the huts

Treatment rotation

Low risk

Treatments were rotated between huts according to a Latin square design

Standardized hut design

Low risk

Study used the standard design of the Ifakara experimental huts

Hut cleaning between treatments

Unclear risk

The paper does not state whether huts were cleared between treatments

Were incomplete outcome data adequately addressed

Low risk

No outcome data were incomplete

Were the raw data reported for LLIN and LLIN + PBO groups

Low risk

No outcome data were missing

Trial authors' conflicting interest

Low risk

Trial authors declared they received prescribed standard fees from Vestergaard Frandsen for evaluating its pesticide products; however this is standard practice

Mzilahowa 2014

Study characteristics

Methods

Village trial

Participants

An gambiae s. l., An funestus group

Interventions

Control: LLIN, Olyset Net, PermaNet 2.0

Intervention: LLIN, Olyset Plus, PermaNet 3.0

Outcomes

Mosquito density, parity rate

Mosquito resistance status

An funestus (Balaka district)

Permethrin ‐ resistant ‐ moderate (55.5% mortality, N = unknown)

Deltamethrin ‐ resistant ‐ high (14.9% mortality, N = unknown)

An gambiae (Balaka district)

Permethrin ‐ resistant ‐ low (84.4% mortality, N = unknown)

(Machinga district)

Deltamethrin ‐ resistant ‐ moderate (54.5% mortality, N = unknown)

Net treatment

Nets unholed and unwashed

Location(s)

Balaka district, Malawi (12 villages)

Notes

Trial conducted: December 2012 to June 2014

Risk of bias

Bias

Authors' judgement

Support for judgement

Recruitment bias

Low risk

Recruiment bias is related to human participants and so is not applicable to this study

Were the mosquitoes in LLIN and LLIN + PBO groups comparable

Unclear risk

Mosquito species composition and resistance status are not recorded per village. Village names are not provided in the study; instead villages are grouped by treatment type

Collectors blinded

High risk

Not stated whether collectors were blinded; therefore judged as high risk, as this is likely to affect searching effort

Household blinded

Low risk

Unclear whether households were blinded – not stated in the publication. We judged this as low risk, as this is unlikely to affect the outcome

Treatment allocation (sequence randomly/adequately generated)

Low risk

Villages were randomly assigned to treatment arms

Allocation concealment (selection bias)

Low risk

Allocation concealment procedures were not adhered to; however this is unlikely to affect the results

Were incomplete outcome data adequately addressed

Low risk

No outcome data were incomplete

Were the raw data reported for LLIN and LLIN + PBO groups

Low risk

All necessary data were reported

Clusters lost to follow‐up

Low risk

No clusters were lost to follow‐up

Selective reporting (reporting bias)

Low risk

It appears that all measured outcomes were reported

Correct statistical methods; adjusted for clustering

High risk

Study did not take clustering into account when statistical methods were performed

Trial authors' conflicting interest

Unclear risk

No information on trial authors' possible conflicting interests is provided

N'Guessan 2010

Study characteristics

Methods

Experimental hut trial

Participants

An gambiae

Interventions

Control: LLIN, PermaNet 2.0

Intervention: LLIN, PermaNet 3.0

Outcomes

Mosquito mortality, blood feeding, deterrence, exophily

Mosquito resistance status

Proxy data. Adjara, Benin: resistant ‐ moderate (deltamethrin, 50% mortality, N = 56) (Aïzoun 2013)

Net treatment

Nets holed, nets unwashed and washed (x 20)

Location(s)

Akron, Benin

Notes

Trial conducted: October 2008 to January 2009

Risk of bias

Bias

Authors' judgement

Support for judgement

Were the mosquitoes in LLIN and LLIN + PBO groups comparable

Low risk

Huts were situated in the same area – mosquito characteristics will be the same

Collectors blinded

Unclear risk

Unclear whether collectors were blinded – not stated in the publication

Sleepers blinded

Unclear risk

Unclear whether sleeper was blinded – not stated in the publication

Sleeper bias

Low risk

Sleepers were rotated between huts according to a Latin square design

Treatment allocation (sequence randomly/adequately generated)

Low risk

Treatments were randomly allocated to huts

Treatment rotation

Low risk

Treatments were rotated between huts according to a Latin square design

Standardized hut design

Low risk

Huts were built according to a standard West African design

Hut cleaning between treatments

Low risk

All huts were cleaned between treatments

Were incomplete outcome data adequately addressed

Low risk

No outcome data were incomplete

Were the raw data reported for LLIN and LLIN + PBO groups

Low risk

All necessary data were reported

Trial authors' conflicting interest

Unclear risk

The trial was sponsored by Vestergaard (net manufacturers), which also commented on the manuscript

Pennetier 2013

Study characteristics

Methods

Experimental hut trial

Participants

95% An gambiae: M‐form (100%), 5% An arabiensis (Corbel 2010)

Interventions

Control: LLIN, Olyset Net

Intervention: LLIN, Olyset Plus

Outcomes

Mosquito mortality, blood feeding, deterrence, exophily

Mosquito resistance status

Proxy data. Resistant ‐ high (permethrin, 22% mortality, N = 100) (Djègbè 2011)

Net treatment

Nets holed, nets unwashed and washed (x 20)

Location(s)

Malanville, Benin

Notes

Trial conducted: September 2011 to December 2011

Risk of bias

Bias

Authors' judgement

Support for judgement

Were the mosquitoes in LLIN and LLIN + PBO groups comparable

Low risk

Huts situated in the same area – mosquito characteristics will be the same

Collectors blinded

Unclear risk

Unclear whether collectors were blinded – not stated in the publication

Sleepers blinded

Unclear risk

Unclear whether sleeper was blinded – not stated in the publication

Sleeper bias

Low risk

Sleepers were rotated between huts according to a Latin square design

Treatment allocation (sequence randomly/adequately generated)

Low risk

Treatments were not randomized to huts but instead were rotated fully between all huts according to a Latin square design

Treatment rotation

Low risk

Treatments were rotated between huts according to a Latin square design

Standardized hut design

Low risk

Huts were built according to a standard West African design

Hut cleaning between treatments

Low risk

All huts were cleaned between treatments

Were incomplete outcome data adequately addressed

Low risk

No outcome data were incomplete

Were the raw data reported for LLIN and LLIN + PBO groups

Low risk

All necessary data were reported

Trial authors' conflicting interest

Low risk

Funders of the trial stated that they had no part in data collection, data analysis, or manuscript preparation

Protopopoff 2018

Study characteristics

Methods

Cluster‐randomized controlled village trial

Participants

3966 children analysed (21 months after intervention) aged 6 months to 14 years (excluding the severely ill), Anopheles species (pooled). Total core cluster population ranged from 14,845 to 16,358

Interventions

Control: LLIN, Olyset Net

Intervention: LLIN, Olyset Plus

Outcomes

Malaria parasite prevalence, sporozoite rate, mosquito density

Mosquito resistance status

Resistance ‐ high (17.8% mortality, N = 107)

Net treatment

Nets unholed and unwashed

Location(s)

Muleba District, Tanzania

Notes

Trial conducted: March 2014 to December 2016

Risk of bias

Bias

Authors' judgement

Support for judgement

Recruitment bias

Low risk

No participants were recruited after clusters had been randomized

Were the mosquitoes in LLIN and LLIN + PBO groups comparable

Unclear risk

Resistance level was available only for the whole district ‐ not at the village level

Collectors blinded

Low risk

Field workers were masked to net treatment

Household blinded

Low risk

Inhabitants were masked to net treatment

Treatment allocation (sequence randomly/adequately generated)

Low risk

Restricted randomization was used to allocate clusters to study groups

Allocation concealment (selection bias)

Low risk

Restricted randomization was used to allocate treatments to clusters

Were incomplete outcome data adequately addressed

Low risk

No outcome data were incomplete

Were the raw data reported for LLIN and LLIN + PBO groups

Low risk

No outcome data were missing

Clusters lost to follow‐up

Low risk

No clusters were lost to follow‐up

Selective reporting (reporting bias)

Low risk

It appears that all measured outcomes were reported

Correct statistical methods; adjusted for clustering

Low risk

Clustering was taken into account and was adjusted for during statistical analysis

Trial authors' conflicting interest

Low risk

Trial authors declared no conflicting interests

Stiles‐Ocran 2013

Study characteristics

Methods

Village trial

Participants

An gambiae

Interventions

Control: LLIN, PermaNet 2.0

Intervention: LLIN, PermaNet 3.0

Outcomes

Sporozoite rate, mosquito density, parity rate

Mosquito resistance status

Futa ‐ resistant ‐ moderate (33.3% mortality, N = 96)
Abrabra‐ resistant ‐ moderate (43.7% mortality, N = 126)
Kunkumso ‐ resistant ‐ high (28.4% mortality, N = 109)
Anyinabrim ‐ resistant ‐ moderate (53.2% mortality, N = 109)
Wenchi ‐ resistant ‐ low (61.9% mortality, N =126)

Net treatment

Nets unholed and unwashed

Location(s)

Futa, Ghana ‐ no net control
Abrabra, Ghana ‐ PermaNet 2.0
Kunkumso, Ghana ‐ PermaNet 2.0
Anyinabrim, Ghana ‐ PermaNet 3.0
Wench, Ghana ‐ PermaNet 3.0

Notes

Trial conducted: November 2010 to August 2011

Risk of bias

Bias

Authors' judgement

Support for judgement

Recruitment bias

Low risk

Recruiment bias is related to human participants and so is not applicable to this study

Were the mosquitoes in LLIN and LLIN + PBO groups comparable

Unclear risk

Mosquito species composition varied slightly. Resistance level varies between villages. However, pre‐trial and post‐trial data are provided

Collectors blinded

High risk

Not stated whether collectors were blinded; therefore judged as high risk, as this is likely to affect searching efforts

Household blinded

Low risk

Unclear whether households were blinded – not stated in the publication. We judged this as low risk, as this is unlikely to impact the outcome

Treatment allocation (sequence randomly/adequately generated)

Low risk

Villages were randomly assigned to treatment arms

Allocation concealment (selection bias)

Low risk

Allocation concealment procedures were not adhered to; however this is unlikely to affect the results

Were incomplete outcome data adequately addressed

Low risk

No outcome data were incomplete

Were the raw data reported for LLIN and LLIN + PBO groups

Low risk

All necessary data were reported

Clusters lost to follow‐up

Low risk

No clusters were lost to follow‐up

Selective reporting (reporting bias)

Low risk

It appears that all measured outcomes were reported

Correct statistical methods; adjusted for clustering

High risk

Study did not take clustering into account for statistical methods

Trial authors' conflicting interest

Unclear risk

Study data were collected for use in Vestergaard PermaNet 3.0 product dossier

Toé 2018

Study characteristics

Methods

Experimental hut trial

Participants

An coluzzii

Interventions

Control: LLIN, PermaNet 2.0, Olyset Net

Intervention: LLIN, PermaNet 3.0, Olyset Plus

Outcomes

Mosquito mortality, blood feeding, deterrence, exophily

Mosquito resistance status

Vallée du Kou 5 ‐ resistant – high (deltamethrin, 2.5% mortality, N = 163; permethrin, 5% mortality, N = 153)

Tengrela ‐ resistant – high (deltamethrin, 34% mortality, N = 85; permethrin, 14% mortality, N = 101)

Net treatment

Nets holed, nets unwashed

Location(s)

Vallée du Kou 5, Burkina Faso

Tengrela, Burkina Faso

Notes

Trial conducted: September 2014 to October 2014

Risk of bias

Bias

Authors' judgement

Support for judgement

Were the mosquitoes in LLIN and LLIN + PBO groups comparable

Low risk

Huts situated in the same area – mosquito characteristics will be the same

Collectors blinded

Unclear risk

Unclear whether collectors were blinded – not stated in the publication

Sleepers blinded

Unclear risk

Unclear whether sleeper was blinded – not stated in the publication

Sleeper bias

Low risk

Sleepers were rotated between huts according to a Latin square design

Treatment allocation (sequence randomly/adequately generated)

Low risk

Treatments were not randomized to huts but instead were rotated fully between all huts according to a Latin square design

Treatment rotation

Low risk

Treatments were rotated between huts according to a Latin square design

Standardized hut design

Low risk

Huts were built according to a standard West African design

Hut cleaning between treatments

Unclear risk

Unclear whether huts were cleaned between treatments – not stated in the publication

Were incomplete outcome data adequately addressed

Low risk

No outcome data were incomplete

Were the raw data reported for LLIN and LLIN + PBO groups

Low risk

All necessary data were reported

Trial authors' conflicting interest

Low risk

Trial authors had no competing interests

Tungu 2010

Study characteristics

Methods

Experimental hut trial

Participants

An gambiae

Interventions

Control: LLIN, PermaNet 2.0

Intervention: LLIN, PermaNet 3.0

Outcomes

Mosquito mortality, blood feeding, deterrence, exophily

Mosquito resistance status

Susceptible (deltamethrin, 100% mortality, N = not stated)

Net treatment

Nets holed, nets unwashed and washed (x 20)

Location(s)

Zeneti, Muheza, Tanzania

Notes

Trial conducted: July 2008 to October 2008

Risk of bias

Bias

Authors' judgement

Support for judgement

Were the mosquitoes in LLIN and LLIN + PBO groups comparable

Low risk

Huts situated in the same area – mosquito characteristics will be the same

Collectors blinded

Unclear risk

Unclear whether collectors were blinded – not stated in the publication

Sleepers blinded

Unclear risk

Unclear whether sleeper was blinded – not stated in the publication

Sleeper bias

Low risk

Sleepers were rotated between huts according to a Latin square design

Treatment allocation (sequence randomly/adequately generated)

Low risk

Treatments were randomly allocated to huts

Treatment rotation

Low risk

Treatments were rotated between huts according to a Latin square design

Standardized hut design

Low risk

Huts were built according to a standard West African design

Hut cleaning between treatments

Low risk

All huts were cleaned between treatments

Were incomplete outcome data adequately addressed

Low risk

No outcome data were incomplete

Were the raw data reported for LLIN and LLIN + PBO groups

Low risk

All necessary data were reported

Trial authors' conflicting interest

Low risk

Trial authors had no competing interests

Menze 2020

Study characteristics

Methods

Experimental hut trial

Participants

An funestus

Interventions

Control: LLIN, PermaNet 2.0, Olyset Net

Intervention: LLIN, PermaNet 3.0, Olyset Plus

Outcomes

Mosquito mortality, blood feeding, exophily

Mosquito resistance status

Moderate

Net treatment

Nets unwashed and holed

Location(s)

Mibellon, Cameroon

Notes

Risk of bias

Bias

Authors' judgement

Support for judgement

Were the mosquitoes in LLIN and LLIN + PBO groups comparable

Low risk

Huts situated in the same area – mosquito characteristics will be the same

Collectors blinded

Unclear risk

Unclear whether collectors were blinded – not stated in the publication

Sleepers blinded

Unclear risk

Unclear whether collectors were blinded – not stated in the publication

Sleeper bias

Low risk

Sleepers were rotated between huts according to a Latin square design

Treatment allocation (sequence randomly/adequately generated)

Low risk

Treatments were not randomized to huts but instead were rotated fully between all huts according to a Latin square design

Treatment rotation

Low risk

Treatments were rotated between huts according to a Latin square design

Standardized hut design

Low risk

Huts were built according to a standard West African design

Hut cleaning between treatments

Low risk

All huts were cleaned between treatments

Were incomplete outcome data adequately addressed

Low risk

No outcome data were incomplete

Were the raw data reported for LLIN and LLIN + PBO groups

Low risk

No outcome data were missing

Correct statistical methods; adjusted for clustering

Low risk

Clustering was not taken into account and adjusted for during statistical analysis. We adjusted for clustering by using an ICC value of 0.1

Trial authors' conflicting interest

Low risk

Trial authors state that they have no competing interests

Oumbouke 2019

Study characteristics

Methods

Experimental hut trial

Participants

An gambiae

Interventions

Control: LLIN, MAGNet LN

Intervention: LLIN, Veeralin LN

Outcomes

Mosquito mortality, blood feeding, deterrence, exophily

Mosquito resistance status

Low resistance

Net treatment

Nets holed, nets unwashed and washed (x 20)

Location(s)

M'be Côte d'Ivoire

Notes

Risk of bias

Bias

Authors' judgement

Support for judgement

Were the mosquitoes in LLIN and LLIN + PBO groups comparable

Low risk

Huts situated in the same area – mosquito characteristics will be the same

Collectors blinded

Unclear risk

Unclear whether collectors were blinded – not stated in the publication

Sleepers blinded

Unclear risk

Unclear whether collectors were blinded – not stated in the publication

Sleeper bias

Low risk

Sleepers rotated between huts according to a Latin square design

Treatment allocation (sequence randomly/adequately generated)

Low risk

Treatments were randomly allocated to huts

Treatment rotation

Low risk

Treatment were rotated between huts according to a Latin Square design

Standardized hut design

Low risk

Huts were built previously according to standard West African hut design

Hut cleaning between treatments

Low risk

Huts were thoroughly cleaned and aired for a day at the end of each rotation

Were incomplete outcome data adequately addressed

Low risk

No outcome data were incomplete

Were the raw data reported for LLIN and LLIN + PBO groups

Low risk

No outcome data were missing

Correct statistical methods; adjusted for clustering

Low risk

Clustering was not taken into account and adjusted for during statistical analysis. We adjusted for clustering using an ICC value of 0.1

Trial authors' conflicting interest

Low risk

Trial authors state that they have no conflicting interests

An arabiensis: Anopheles arabiensis; An coluzzii: Anopheles coluzzii; An funestus: Anopheles funestus; An gambiae: Anopheles gambiae; ITN: insecticide‐treated net; LLIN: long‐lasting insecticidal net; PBO: piperonyl butoxide.

Characteristics of excluded studies [ordered by study ID]

Study

Reason for exclusion

Darriet 2011

Study included laboratory data only

Darriet 2013

Study included laboratory data only

Characteristics of studies awaiting classification [ordered by study ID]

Koudou 2012

Methods

Village trial

Participants

Bouaké ‐ 100% An gambiae: (70% S‐form, 30% M‐form)
Tiassalé ‐ 100% An gambiae: (70% S‐form, 30% M‐form)

Interventions

Control: LLIN, PermaNet 2.0 Extra

Intervention: LLIN, PermaNet 3.0

Outcomes

Blood feeding, mosquito density

Mosquito Resistance Status

Bouaké ‐ resistant ‐ moderate (43.9% mortality, N = 114)
Tiassalé ‐ resistant ‐ moderate (7.5% mortality, N = 106)

Net Treatment

Nets unholed and unwashed

Location(s)

Bouaké, Côte d’Ivoire
Tiassalé, Côte d’Ivoire

Notes

Trial conducted: November 2009 to January 2012

Shono 2017

Methods

Not available

Participants

An funestus: Anopheles funestus; An gambiae: Anopheles gambiae

Interventions

Outcomes

Not available

Mosquito Resistance Status

Not available

Net Treatment

Control: LLIN, Olyset Net

Intervention: LLIN, Olyset Plus

Location(s)

Not available

Notes

Tungu 2017

Methods

Experimental hut trial

Participants

An funestus

Interventions

Control: LLIN, DawaPlus 2.0

Intervention: LLIN, DawaPlus 3.0, DawaPlus 4.0

Outcomes

Mosquito mortality, blood feeding, deterrence, exophily

Mosquito Resistance Status

Net Treatment

Nets holed, nets unwashed and washed (x 20)

Location(s)

Muheza, Tanzania

Notes

Characteristics of ongoing studies [ordered by study ID]

ISRCTN99611164

Study name

Comparative evaluation of standard insecticide‐treated bed nets and co‐treated bed nets on malaria prevalence in Sud Ubangi, Democratic Republic of Congo: a cluster‐randomised trial

Methods

Cluster‐randomized trial

Participants

Women (> 15 years) attending first ANC appointment at a clinic that is taking part in the study, who consent to be enrolled in the study

20 visitors per month at each of 7 antenatal clinics (held monthly) in each of 17 study clusters, which gives a total of approximately 2400 participants per month, 28,500 per year, and 86,000 in total

Interventions

Control: bed net treated with pyrethroid only

Intervention: bed net treated with both pyrethroid and PBO

Outcomes

1. Determination of parasite prevalence in women visiting monthly antenatal clinics

2. Entomological collections for surveillance of insecticide resistance and mosquito abundance and parasite infection

3. Assessment of bed net durability (physical and chemical analysis) and bio‐efficacy (against mosquitoes) over time

Starting date

November 2019 (recruitment start date 01/06/2020)

Contact information

Dr David Weetman

Notes

NCT03289663

Study name

Effectiveness study of new‐generation bed nets in the context of conventional insecticide resistance in the Democratic Republic of the Congo (Net‐PBO)

Methods

Cluster‐randomized trial

Participants

1680 participants; 0 to 10‐year‐old subjects in 30 villages

Interventions

Control: bed net treated with pyrethroid only

Intervention: bed net treated with both pyrethroid and PBO

(IRS and LSM included in trial)

Outcomes

Incidence rate of laboratory‐confirmed clinical cases of malaria (time frame: participants will be actively followed up for 12 months, and any suspected case of clinical malaria will immediately lead to microscopy and RDT for confirmation). Microscopy to confirm the diagnosis of malaria sporozoite rate (time frame: Anopheles mosquitoes will be captured every 3 months during 1 year), sporozoite detection by ELISA to determine infectivity of Anopheles

Starting date

2 October 2017

Contact information

Notes

NCT04182126

Study name

HS#2017‐3512. Adaptive interventions for optimizing malaria control: a cluster‐randomized SMART trial

Methods

Cluster‐randomized trial

Participants

122,872 participants (6 months and older, all sexes)

Interventions

Other: regular long‐lasting insecticidal nets (Olyset)

Other: LLIN plus piperonyl butoxide‐treated LLIN (Olyset Plus)

Outcomes

Annual clinical malaria incidence rate

Malaria parasite prevalence

Malaria vector density

Malaria transmission intensity

Starting date

01/12/2019

Contact information

Dr Guiyun Yan

Notes

UMIN000019971

Study name

A preliminary study on designing a cluster randomized control trial of two mosquito nets to prevent malaria parasite infection

Methods

Cluster‐randomized trial

Participants

1360 target participants

Children targeted for malaria transmission survey are aged between 7 and 131 months

Children between 60 and 131 months old are schoolchildren; 170 children are randomly selected from each cluster for survey

Interventions

Control: bed net treated with pyrethroid only

Intervention: bed net treated with both pyrethroid and PBO

Outcomes

Plasmodium falciparum parasite infection after distribution of bed nets with PBO:

PCR‐based infection

Slide‐based infection

Haemoglobin amount

Starting date

Contact information

Dr Noboru Minakawa

Notes

ELISA: enzyme‐linked immunosorbent assay; PBO: piperonyl butoxide.

Data and analyses

Open in table viewer
Comparison 1. Commercial pyrethroid‐PBO nets versus commercial LLINs: village trials

Outcome or subgroup title

No. of studies

No. of participants

Statistical method

Effect size

1.1 Parasite prevalence (pyrethroid‐PBO nets vs non‐PBO LLINs, latest end points in RCT) Show forest plot

2

Odds Ratio (IV, Fixed, 95% CI)

0.79 [0.67, 0.95]

Analysis 1.1

Comparison 1: Commercial pyrethroid‐PBO nets versus commercial LLINs: village trials, Outcome 1: Parasite prevalence (pyrethroid‐PBO nets vs non‐PBO LLINs, latest end points in RCT)

Comparison 1: Commercial pyrethroid‐PBO nets versus commercial LLINs: village trials, Outcome 1: Parasite prevalence (pyrethroid‐PBO nets vs non‐PBO LLINs, latest end points in RCT)

1.2 Parasite prevalence (pyrethroid‐PBO nets vs non‐PBO LLINs, shown at 4 different time points) Show forest plot

2

Odds Ratio (IV, Fixed, 95% CI)

Subtotals only

Analysis 1.2

Comparison 1: Commercial pyrethroid‐PBO nets versus commercial LLINs: village trials, Outcome 2: Parasite prevalence (pyrethroid‐PBO nets vs non‐PBO LLINs, shown at 4 different time points)

Comparison 1: Commercial pyrethroid‐PBO nets versus commercial LLINs: village trials, Outcome 2: Parasite prevalence (pyrethroid‐PBO nets vs non‐PBO LLINs, shown at 4 different time points)

1.2.1 4 to 6 months

2

Odds Ratio (IV, Fixed, 95% CI)

0.74 [0.62, 0.89]

1.2.2 9 to 12 months

2

Odds Ratio (IV, Fixed, 95% CI)

0.72 [0.61, 0.86]

1.2.3 16 to 18 months

2

Odds Ratio (IV, Fixed, 95% CI)

0.88 [0.74, 1.04]

1.2.4 21 to 25 months

2

Odds Ratio (IV, Fixed, 95% CI)

0.79 [0.67, 0.95]

1.3 Mosquito sporozoite‐positive (adjusted ICC 0.1) Show forest plot

4

424

Risk Ratio (M‐H, Random, 95% CI)

0.82 [0.24, 2.75]

Analysis 1.3

Comparison 1: Commercial pyrethroid‐PBO nets versus commercial LLINs: village trials, Outcome 3: Mosquito sporozoite‐positive (adjusted ICC 0.1)

Comparison 1: Commercial pyrethroid‐PBO nets versus commercial LLINs: village trials, Outcome 3: Mosquito sporozoite‐positive (adjusted ICC 0.1)

1.4 Mosquito parous (adjusted ICC 0.1) Show forest plot

3

220

Risk Ratio (M‐H, Random, 95% CI)

0.97 [0.82, 1.13]

Analysis 1.4

Comparison 1: Commercial pyrethroid‐PBO nets versus commercial LLINs: village trials, Outcome 4: Mosquito parous (adjusted ICC 0.1)

Comparison 1: Commercial pyrethroid‐PBO nets versus commercial LLINs: village trials, Outcome 4: Mosquito parous (adjusted ICC 0.1)

Open in table viewer
Comparison 2. Commercial pyrethroid‐PBO nets versus commercial LLINs: hut trials

Outcome or subgroup title

No. of studies

No. of participants

Statistical method

Effect size

2.1 Mosquito mortality (pooled) hut/night (adjusted ICC 0.1) Show forest plot

10

15614

Risk Ratio (M‐H, Random, 95% CI)

1.43 [1.26, 1.62]

Analysis 2.1

Comparison 2: Commercial pyrethroid‐PBO nets versus commercial LLINs: hut trials, Outcome 1: Mosquito mortality (pooled) hut/night (adjusted ICC 0.1)

Comparison 2: Commercial pyrethroid‐PBO nets versus commercial LLINs: hut trials, Outcome 1: Mosquito mortality (pooled) hut/night (adjusted ICC 0.1)

2.1.1 Unwashed

10

8647

Risk Ratio (M‐H, Random, 95% CI)

1.63 [1.29, 2.05]

2.1.2 Washed

8

6967

Risk Ratio (M‐H, Random, 95% CI)

1.19 [1.04, 1.38]

2.2 Mosquito blood‐feeding success (pooled) hut/night (adjusted ICC 0.1) Show forest plot

9

12351

Risk Ratio (M‐H, Random, 95% CI)

0.75 [0.66, 0.85]

Analysis 2.2

Comparison 2: Commercial pyrethroid‐PBO nets versus commercial LLINs: hut trials, Outcome 2: Mosquito blood‐feeding success (pooled) hut/night (adjusted ICC 0.1)

Comparison 2: Commercial pyrethroid‐PBO nets versus commercial LLINs: hut trials, Outcome 2: Mosquito blood‐feeding success (pooled) hut/night (adjusted ICC 0.1)

2.2.1 Unwashed

9

7261

Risk Ratio (M‐H, Random, 95% CI)

0.68 [0.57, 0.80]

2.2.2 Washed

7

5090

Risk Ratio (M‐H, Random, 95% CI)

0.87 [0.74, 1.02]

2.3 Mosquito exophily (pooled) hut/night (adjusted ICC 0.1) Show forest plot

10

13214

Risk Ratio (M‐H, Random, 95% CI)

1.00 [0.94, 1.06]

Analysis 2.3

Comparison 2: Commercial pyrethroid‐PBO nets versus commercial LLINs: hut trials, Outcome 3: Mosquito exophily (pooled) hut/night (adjusted ICC 0.1)

Comparison 2: Commercial pyrethroid‐PBO nets versus commercial LLINs: hut trials, Outcome 3: Mosquito exophily (pooled) hut/night (adjusted ICC 0.1)

2.3.1 Unwashed

10

7699

Risk Ratio (M‐H, Random, 95% CI)

1.00 [0.91, 1.10]

2.3.2 Washed

8

5515

Risk Ratio (M‐H, Random, 95% CI)

1.00 [0.93, 1.07]

2.4 Mosquito mortality (high resistance) hut/night (adjusted ICC 0.1) Show forest plot

5

7997

Risk Ratio (M‐H, Random, 95% CI)

1.58 [1.34, 1.86]

Analysis 2.4

Comparison 2: Commercial pyrethroid‐PBO nets versus commercial LLINs: hut trials, Outcome 4: Mosquito mortality (high resistance) hut/night (adjusted ICC 0.1)

Comparison 2: Commercial pyrethroid‐PBO nets versus commercial LLINs: hut trials, Outcome 4: Mosquito mortality (high resistance) hut/night (adjusted ICC 0.1)

2.4.1 Unwashed

5

4896

Risk Ratio (M‐H, Random, 95% CI)

1.84 [1.60, 2.11]

2.4.2 Washed

4

3101

Risk Ratio (M‐H, Random, 95% CI)

1.20 [0.88, 1.63]

2.5 Mosquito blood‐feeding success (high resistance) hut/night (adjusted ICC 0.1) Show forest plot

4

7134

Risk Ratio (M‐H, Random, 95% CI)

0.66 [0.57, 0.76]

Analysis 2.5

Comparison 2: Commercial pyrethroid‐PBO nets versus commercial LLINs: hut trials, Outcome 5: Mosquito blood‐feeding success (high resistance) hut/night (adjusted ICC 0.1)

Comparison 2: Commercial pyrethroid‐PBO nets versus commercial LLINs: hut trials, Outcome 5: Mosquito blood‐feeding success (high resistance) hut/night (adjusted ICC 0.1)

2.5.1 Unwashed

4

4458

Risk Ratio (M‐H, Random, 95% CI)

0.60 [0.50, 0.71]

2.5.2 Washed

3

2676

Risk Ratio (M‐H, Random, 95% CI)

0.81 [0.72, 0.92]

2.6 Mosquito mortality (moderate resistance) hut/night (adjusted ICC 0.1) Show forest plot

2

1027

Risk Ratio (M‐H, Fixed, 95% CI)

1.47 [1.21, 1.78]

Analysis 2.6

Comparison 2: Commercial pyrethroid‐PBO nets versus commercial LLINs: hut trials, Outcome 6: Mosquito mortality (moderate resistance) hut/night (adjusted ICC 0.1)

Comparison 2: Commercial pyrethroid‐PBO nets versus commercial LLINs: hut trials, Outcome 6: Mosquito mortality (moderate resistance) hut/night (adjusted ICC 0.1)

2.6.1 Unwashed

2

751

Risk Ratio (M‐H, Fixed, 95% CI)

1.68 [1.33, 2.11]

2.6.2 Washed

1

276

Risk Ratio (M‐H, Fixed, 95% CI)

1.07 [0.74, 1.54]

2.7 Mosquito blood‐feeding success (moderate resistance) hut/night (adjusted ICC 0.1) Show forest plot

2

1034

Risk Ratio (M‐H, Random, 95% CI)

0.91 [0.78, 1.05]

Analysis 2.7

Comparison 2: Commercial pyrethroid‐PBO nets versus commercial LLINs: hut trials, Outcome 7: Mosquito blood‐feeding success (moderate resistance) hut/night (adjusted ICC 0.1)

Comparison 2: Commercial pyrethroid‐PBO nets versus commercial LLINs: hut trials, Outcome 7: Mosquito blood‐feeding success (moderate resistance) hut/night (adjusted ICC 0.1)

2.7.1 Unwashed

2

752

Risk Ratio (M‐H, Random, 95% CI)

0.90 [0.72, 1.11]

2.7.2 Washed

1

282

Risk Ratio (M‐H, Random, 95% CI)

0.91 [0.74, 1.13]

2.8 Mosquito mortality (low resistance) hut/night (adjusted ICC 0.1) Show forest plot

2

1970

Risk Ratio (M‐H, Random, 95% CI)

1.30 [1.09, 1.56]

Analysis 2.8

Comparison 2: Commercial pyrethroid‐PBO nets versus commercial LLINs: hut trials, Outcome 8: Mosquito mortality (low resistance) hut/night (adjusted ICC 0.1)

Comparison 2: Commercial pyrethroid‐PBO nets versus commercial LLINs: hut trials, Outcome 8: Mosquito mortality (low resistance) hut/night (adjusted ICC 0.1)

2.8.1 Unwashed

2

948

Risk Ratio (M‐H, Random, 95% CI)

1.25 [0.99, 1.57]

2.8.2 Washed

2

1022

Risk Ratio (M‐H, Random, 95% CI)

1.39 [0.95, 2.04]

2.9 Mosquito blood‐feeding success (low resistance) hut/night (adjusted ICC 0.1) Show forest plot

2

1970

Risk Ratio (M‐H, Random, 95% CI)

0.94 [0.56, 1.57]

Analysis 2.9

Comparison 2: Commercial pyrethroid‐PBO nets versus commercial LLINs: hut trials, Outcome 9: Mosquito blood‐feeding success (low resistance) hut/night (adjusted ICC 0.1)

Comparison 2: Commercial pyrethroid‐PBO nets versus commercial LLINs: hut trials, Outcome 9: Mosquito blood‐feeding success (low resistance) hut/night (adjusted ICC 0.1)

2.9.1 Unwashed

2

948

Risk Ratio (M‐H, Random, 95% CI)

0.75 [0.27, 2.11]

2.9.2 Washed

2

1022

Risk Ratio (M‐H, Random, 95% CI)

1.07 [0.49, 2.33]

2.10 Mosquito mortality (susceptible) hut/night (adjusted ICC 0.1) Show forest plot

2

1916

Risk Ratio (M‐H, Random, 95% CI)

1.05 [0.96, 1.15]

Analysis 2.10

Comparison 2: Commercial pyrethroid‐PBO nets versus commercial LLINs: hut trials, Outcome 10: Mosquito mortality (susceptible) hut/night (adjusted ICC 0.1)

Comparison 2: Commercial pyrethroid‐PBO nets versus commercial LLINs: hut trials, Outcome 10: Mosquito mortality (susceptible) hut/night (adjusted ICC 0.1)

2.10.1 Unwashed

2

948

Risk Ratio (M‐H, Random, 95% CI)

1.20 [0.64, 2.26]

2.10.2 Washed

2

968

Risk Ratio (M‐H, Random, 95% CI)

1.07 [0.92, 1.25]

2.11 Mosquito blood‐feeding success (susceptible) hut/night (adjusted ICC 0.1) Show forest plot

2

1916

Risk Ratio (M‐H, Random, 95% CI)

0.87 [0.40, 1.89]

Analysis 2.11

Comparison 2: Commercial pyrethroid‐PBO nets versus commercial LLINs: hut trials, Outcome 11: Mosquito blood‐feeding success (susceptible) hut/night (adjusted ICC 0.1)

Comparison 2: Commercial pyrethroid‐PBO nets versus commercial LLINs: hut trials, Outcome 11: Mosquito blood‐feeding success (susceptible) hut/night (adjusted ICC 0.1)

2.11.1 Unwashed

2

948

Risk Ratio (M‐H, Random, 95% CI)

0.52 [0.12, 2.22]

2.11.2 Washed

2

968

Risk Ratio (M‐H, Random, 95% CI)

1.25 [0.82, 1.91]

2.12 Mosquito mortality (high resistance/Permanet) hut/night (adjusted ICC 0.1) Show forest plot

3

2806

Risk Ratio (M‐H, Random, 95% CI)

1.59 [1.26, 2.01]

Analysis 2.12

Comparison 2: Commercial pyrethroid‐PBO nets versus commercial LLINs: hut trials, Outcome 12: Mosquito mortality (high resistance/Permanet) hut/night (adjusted ICC 0.1)

Comparison 2: Commercial pyrethroid‐PBO nets versus commercial LLINs: hut trials, Outcome 12: Mosquito mortality (high resistance/Permanet) hut/night (adjusted ICC 0.1)

2.12.1 Not Washed

3

1877

Risk Ratio (M‐H, Random, 95% CI)

1.81 [1.56, 2.10]

2.12.2 Washed

2

929

Risk Ratio (M‐H, Random, 95% CI)

1.18 [0.61, 2.28]

2.13 Mosquito blood‐feeding success (high resistance/Permanet) hut/night (adjusted ICC 0.1) Show forest plot

2

1943

Risk Ratio (M‐H, Random, 95% CI)

0.58 [0.45, 0.76]

Analysis 2.13

Comparison 2: Commercial pyrethroid‐PBO nets versus commercial LLINs: hut trials, Outcome 13: Mosquito blood‐feeding success (high resistance/Permanet) hut/night (adjusted ICC 0.1)

Comparison 2: Commercial pyrethroid‐PBO nets versus commercial LLINs: hut trials, Outcome 13: Mosquito blood‐feeding success (high resistance/Permanet) hut/night (adjusted ICC 0.1)

2.13.1 Unwashed

2

1439

Risk Ratio (M‐H, Random, 95% CI)

0.53 [0.40, 0.69]

2.13.2 Washed

1

504

Risk Ratio (M‐H, Random, 95% CI)

0.76 [0.61, 0.93]

2.14 Mosquito mortality (high resistance/Olyset) hut/night (adjusted ICC 0.1) Show forest plot

2

1410

Risk Ratio (M‐H, Random, 95% CI)

1.73 [1.51, 1.97]

Analysis 2.14

Comparison 2: Commercial pyrethroid‐PBO nets versus commercial LLINs: hut trials, Outcome 14: Mosquito mortality (high resistance/Olyset) hut/night (adjusted ICC 0.1)

Comparison 2: Commercial pyrethroid‐PBO nets versus commercial LLINs: hut trials, Outcome 14: Mosquito mortality (high resistance/Olyset) hut/night (adjusted ICC 0.1)

2.14.1 Unwashed

2

1257

Risk Ratio (M‐H, Random, 95% CI)

1.72 [1.48, 1.99]

2.14.2 Washed

1

153

Risk Ratio (M‐H, Random, 95% CI)

1.81 [1.25, 2.61]

2.15 Mosquito blood‐feeding success (high resistance/Olyset) hut/night (adjusted ICC 0.1) Show forest plot

2

1470

Risk Ratio (M‐H, Random, 95% CI)

0.63 [0.40, 0.98]

Analysis 2.15

Comparison 2: Commercial pyrethroid‐PBO nets versus commercial LLINs: hut trials, Outcome 15: Mosquito blood‐feeding success (high resistance/Olyset) hut/night (adjusted ICC 0.1)

Comparison 2: Commercial pyrethroid‐PBO nets versus commercial LLINs: hut trials, Outcome 15: Mosquito blood‐feeding success (high resistance/Olyset) hut/night (adjusted ICC 0.1)

2.15.1 Unwashed

2

1257

Risk Ratio (M‐H, Random, 95% CI)

0.67 [0.38, 1.18]

2.15.2 Washed

1

213

Risk Ratio (M‐H, Random, 95% CI)

0.50 [0.27, 0.93]

Study flow diagram.

Figuras y tablas -
Figure 1

Study flow diagram.

‘Risk of bias' summary: review authors' judgements about each risk of bias item for each included study.

Figuras y tablas -
Figure 2

‘Risk of bias' summary: review authors' judgements about each risk of bias item for each included study.

Comparison 1: Commercial pyrethroid‐PBO nets versus commercial LLINs: village trials, Outcome 1: Parasite prevalence (pyrethroid‐PBO nets vs non‐PBO LLINs, latest end points in RCT)

Figuras y tablas -
Analysis 1.1

Comparison 1: Commercial pyrethroid‐PBO nets versus commercial LLINs: village trials, Outcome 1: Parasite prevalence (pyrethroid‐PBO nets vs non‐PBO LLINs, latest end points in RCT)

Comparison 1: Commercial pyrethroid‐PBO nets versus commercial LLINs: village trials, Outcome 2: Parasite prevalence (pyrethroid‐PBO nets vs non‐PBO LLINs, shown at 4 different time points)

Figuras y tablas -
Analysis 1.2

Comparison 1: Commercial pyrethroid‐PBO nets versus commercial LLINs: village trials, Outcome 2: Parasite prevalence (pyrethroid‐PBO nets vs non‐PBO LLINs, shown at 4 different time points)

Comparison 1: Commercial pyrethroid‐PBO nets versus commercial LLINs: village trials, Outcome 3: Mosquito sporozoite‐positive (adjusted ICC 0.1)

Figuras y tablas -
Analysis 1.3

Comparison 1: Commercial pyrethroid‐PBO nets versus commercial LLINs: village trials, Outcome 3: Mosquito sporozoite‐positive (adjusted ICC 0.1)

Comparison 1: Commercial pyrethroid‐PBO nets versus commercial LLINs: village trials, Outcome 4: Mosquito parous (adjusted ICC 0.1)

Figuras y tablas -
Analysis 1.4

Comparison 1: Commercial pyrethroid‐PBO nets versus commercial LLINs: village trials, Outcome 4: Mosquito parous (adjusted ICC 0.1)

Comparison 2: Commercial pyrethroid‐PBO nets versus commercial LLINs: hut trials, Outcome 1: Mosquito mortality (pooled) hut/night (adjusted ICC 0.1)

Figuras y tablas -
Analysis 2.1

Comparison 2: Commercial pyrethroid‐PBO nets versus commercial LLINs: hut trials, Outcome 1: Mosquito mortality (pooled) hut/night (adjusted ICC 0.1)

Comparison 2: Commercial pyrethroid‐PBO nets versus commercial LLINs: hut trials, Outcome 2: Mosquito blood‐feeding success (pooled) hut/night (adjusted ICC 0.1)

Figuras y tablas -
Analysis 2.2

Comparison 2: Commercial pyrethroid‐PBO nets versus commercial LLINs: hut trials, Outcome 2: Mosquito blood‐feeding success (pooled) hut/night (adjusted ICC 0.1)

Comparison 2: Commercial pyrethroid‐PBO nets versus commercial LLINs: hut trials, Outcome 3: Mosquito exophily (pooled) hut/night (adjusted ICC 0.1)

Figuras y tablas -
Analysis 2.3

Comparison 2: Commercial pyrethroid‐PBO nets versus commercial LLINs: hut trials, Outcome 3: Mosquito exophily (pooled) hut/night (adjusted ICC 0.1)

Comparison 2: Commercial pyrethroid‐PBO nets versus commercial LLINs: hut trials, Outcome 4: Mosquito mortality (high resistance) hut/night (adjusted ICC 0.1)

Figuras y tablas -
Analysis 2.4

Comparison 2: Commercial pyrethroid‐PBO nets versus commercial LLINs: hut trials, Outcome 4: Mosquito mortality (high resistance) hut/night (adjusted ICC 0.1)

Comparison 2: Commercial pyrethroid‐PBO nets versus commercial LLINs: hut trials, Outcome 5: Mosquito blood‐feeding success (high resistance) hut/night (adjusted ICC 0.1)

Figuras y tablas -
Analysis 2.5

Comparison 2: Commercial pyrethroid‐PBO nets versus commercial LLINs: hut trials, Outcome 5: Mosquito blood‐feeding success (high resistance) hut/night (adjusted ICC 0.1)

Comparison 2: Commercial pyrethroid‐PBO nets versus commercial LLINs: hut trials, Outcome 6: Mosquito mortality (moderate resistance) hut/night (adjusted ICC 0.1)

Figuras y tablas -
Analysis 2.6

Comparison 2: Commercial pyrethroid‐PBO nets versus commercial LLINs: hut trials, Outcome 6: Mosquito mortality (moderate resistance) hut/night (adjusted ICC 0.1)

Comparison 2: Commercial pyrethroid‐PBO nets versus commercial LLINs: hut trials, Outcome 7: Mosquito blood‐feeding success (moderate resistance) hut/night (adjusted ICC 0.1)

Figuras y tablas -
Analysis 2.7

Comparison 2: Commercial pyrethroid‐PBO nets versus commercial LLINs: hut trials, Outcome 7: Mosquito blood‐feeding success (moderate resistance) hut/night (adjusted ICC 0.1)

Comparison 2: Commercial pyrethroid‐PBO nets versus commercial LLINs: hut trials, Outcome 8: Mosquito mortality (low resistance) hut/night (adjusted ICC 0.1)

Figuras y tablas -
Analysis 2.8

Comparison 2: Commercial pyrethroid‐PBO nets versus commercial LLINs: hut trials, Outcome 8: Mosquito mortality (low resistance) hut/night (adjusted ICC 0.1)

Comparison 2: Commercial pyrethroid‐PBO nets versus commercial LLINs: hut trials, Outcome 9: Mosquito blood‐feeding success (low resistance) hut/night (adjusted ICC 0.1)

Figuras y tablas -
Analysis 2.9

Comparison 2: Commercial pyrethroid‐PBO nets versus commercial LLINs: hut trials, Outcome 9: Mosquito blood‐feeding success (low resistance) hut/night (adjusted ICC 0.1)

Comparison 2: Commercial pyrethroid‐PBO nets versus commercial LLINs: hut trials, Outcome 10: Mosquito mortality (susceptible) hut/night (adjusted ICC 0.1)

Figuras y tablas -
Analysis 2.10

Comparison 2: Commercial pyrethroid‐PBO nets versus commercial LLINs: hut trials, Outcome 10: Mosquito mortality (susceptible) hut/night (adjusted ICC 0.1)

Comparison 2: Commercial pyrethroid‐PBO nets versus commercial LLINs: hut trials, Outcome 11: Mosquito blood‐feeding success (susceptible) hut/night (adjusted ICC 0.1)

Figuras y tablas -
Analysis 2.11

Comparison 2: Commercial pyrethroid‐PBO nets versus commercial LLINs: hut trials, Outcome 11: Mosquito blood‐feeding success (susceptible) hut/night (adjusted ICC 0.1)

Comparison 2: Commercial pyrethroid‐PBO nets versus commercial LLINs: hut trials, Outcome 12: Mosquito mortality (high resistance/Permanet) hut/night (adjusted ICC 0.1)

Figuras y tablas -
Analysis 2.12

Comparison 2: Commercial pyrethroid‐PBO nets versus commercial LLINs: hut trials, Outcome 12: Mosquito mortality (high resistance/Permanet) hut/night (adjusted ICC 0.1)

Comparison 2: Commercial pyrethroid‐PBO nets versus commercial LLINs: hut trials, Outcome 13: Mosquito blood‐feeding success (high resistance/Permanet) hut/night (adjusted ICC 0.1)

Figuras y tablas -
Analysis 2.13

Comparison 2: Commercial pyrethroid‐PBO nets versus commercial LLINs: hut trials, Outcome 13: Mosquito blood‐feeding success (high resistance/Permanet) hut/night (adjusted ICC 0.1)

Comparison 2: Commercial pyrethroid‐PBO nets versus commercial LLINs: hut trials, Outcome 14: Mosquito mortality (high resistance/Olyset) hut/night (adjusted ICC 0.1)

Figuras y tablas -
Analysis 2.14

Comparison 2: Commercial pyrethroid‐PBO nets versus commercial LLINs: hut trials, Outcome 14: Mosquito mortality (high resistance/Olyset) hut/night (adjusted ICC 0.1)

Comparison 2: Commercial pyrethroid‐PBO nets versus commercial LLINs: hut trials, Outcome 15: Mosquito blood‐feeding success (high resistance/Olyset) hut/night (adjusted ICC 0.1)

Figuras y tablas -
Analysis 2.15

Comparison 2: Commercial pyrethroid‐PBO nets versus commercial LLINs: hut trials, Outcome 15: Mosquito blood‐feeding success (high resistance/Olyset) hut/night (adjusted ICC 0.1)

Summary of findings 1. Summary of findings table 1

Pyrethroid‐piperonyl butoxide (PBO) nets compared to long‐lasting insecticidal nets (LLINs) for malaria control when insecticide resistance is high

Patient or population: adults and childen living in malaria‐endemic areas, Anopheles gambiae complex or Anopheles funestus group
Setting: areas of high insecticide resistance
Intervention: pyrethroid‐PBO nets
Comparison: LLIN

Outcomes

Anticipated absolute effects* (95% CI)

Relative effect
(95% CI)

Number of participants, 
(trials)

Certainty of the evidence
(GRADE)

Comments

Risk with LLIN

Risk with pyrethroid‐PBO nets

Parasite prevalence

(4‐ to 6‐month follow‐up)

254 per 1000a

201 per 1000 (174 to 233)a

OR 0.74 (0.62 to 0.89)

11,582 people (2 trials, 2 comparisons, 61 PBO clusters, 64 non‐PBO clusters)

⊕⊕⊕⊕
HIGH

Pyrethroid‐PBO nets at 4‐ to 6‐month follow‐up reduce parasite prevalence in areas of high insecticide resistance

Parasite prevalence

(9‐ to 12‐month follow‐up)

224 per 1000a

172 per 1000 (150 to 199)a

OR 0.72 (0.61 to 0.86)

11,370 people (2 trials, 2 comparisons, 61 PBO clusters, 64 non‐PBO clusters)

⊕⊕⊕⊝
MODERATEb

due to inconsistency

Pyrethroid‐PBO nets at 9‐ to 12‐month follow‐up reduce parasite prevalence in areas of high insecticide resistance

Parasite prevalence

(16‐ to 18‐month follow‐up)

248 per 1000a

225 per 1000 (196 to 255)a

OR 0.88 (0.74 to 1.04)

11,822 people (2 trials, 2 comparisons, 61 PBO clusters, 64 non‐PBO clusters)

⊕⊕⊕⊝
MODERATEb

due to inconsistency

Pyrethroid‐PBO nets at 16‐ to 18‐month follow‐up reduce parasite prevalence in areas of high insecticide resistance

Parasite prevalence

(21‐ to 25‐month follow‐up)

350 per 1000a

298 per 1000 (265 to 338)a

OR 0.79 (0.67 to 0.95)

10,603 people (2 trials, 2 comparisons, 54 PBO clusters, 60 non‐PBO clusters)

⊕⊕⊕⊝
MODERATEb

due to inconsistency

Pyrethroid‐PBO nets at 21‐ to 25‐month follow‐up reduce parasite prevalence in areas of high insecticide resistance

Mosquito mortality (unwashed nets)

238 per 1000a

438 per 1000
(381 to 503)a

RR 1.84
(1.60 to 2.11)

14,620 mosquitoes
(5 trials, 9 comparisons)

⊕⊕⊕⊕
HIGHc

Mosquito mortality is higher with unwashed pyrethroid‐PBO nets compared to standard unwashed LLINs in areas of high insecticide resistance

Mosquito mortality (washed nets)

201 per 1000a

242 per 1000
(177 to 328)a

RR 1.20
(0.88 to 1.63)

10,268 mosquitoes
(4 trials, 5 comparisons)

⊕⊝⊝⊝
VERY LOWd,e

due to imprecision and inconsistency

We do not know whether pyrethroid‐PBO nets have an effect on mosquito mortality in areas of high insecticide resistance when the nets have been washed

Blood‐feeding success (unwashed nets)

438 per 1000a

263 per 1000
(241 to 311)a

RR 0.60

(0.50 to 0.71)

 

14,000 mosquitoes
(4 trials, 8 comparisons)

⊕⊕⊕⊕
HIGHc

Mosquito blood‐feeding success is decreased with unwashed pyrethroid‐PBO nets compared to standard unwashed LLINs in areas of high insecticide resistance

Blood‐feeding success (washed nets)

494 per 1000a

400 per 1000
(356 to 454)a

RR 0.81
(0.72 to 0.92)

9674 mosquitoes
(3 trials, 4 comparisons)

⊕⊕⊕⊕
HIGHc

Mosquito blood‐feeding success is decreased with washed pyrethroid‐PBO nets compared to standard washed LLINs in areas of high insecticide resistance

*The risk in the intervention group (and its 95% CI) is based on the assumed risk in the comparison group and the relative effect of the intervention (and its 95% CI).
CI: confidence interval; LLINs: long‐lasting insecticidal nets; OR: odds ratio; PBO: pyrethroid‐piperonyl butoxide; RR: risk ratio.

GRADE Working Group grades of evidence.
High certainty: we are very confident that the true effect lies close to that of the estimate of the effect.
Moderate certainty: we are moderately confident in the effect estimate: the true effect is likely to be close to the estimate of the effect, but there is a possibility that it is substantially different.
Low certainty: our confidence in the effect estimate is limited: the true effect may be substantially different from the estimate of the effect.
Very low certainty: we have very little confidence in the effect estimate: the true effect is likely to be substantially different from the estimate of effect.

aOriginal numbers were used in this table; however in pooled analysis, events and total numbers were generated from cluster‐adjusted results, which use the effective sample size. Note that cluster adjustments do not change the point estimate of the effect size ‐ just the standard error.
bDowngraded by one for inconsistency.
cNot downgraded for imprecision: both best‐ and worst‐case scenarios in this situation are important effects.
dDowngraded by one for imprecision due to wide CIs.
eDowngraded by two for inconsistency due to unexplained qualitative heterogeneity.

Figuras y tablas -
Summary of findings 1. Summary of findings table 1
Summary of findings 2. Summary of findings table 2

Pyrethroid‐piperonyl butoxide (PBO) nets compared to long‐lasting insecticidal nets (LLINs) for malaria control when insecticide resistance is moderate

Patient or population:Anopheles gambiae complex or Anopheles funestus group
Setting: areas of moderate insecticide resistance
Intervention: pyrethroid‐PBO nets
Comparison: LLIN

Outcomes

Anticipated absolute effects* (95% CI)

Relative effect
(95% CI)

Number of mosquitoes
(experimental hut trials)

Certainty of the evidence
(GRADE)

Comments

Risk with LLIN

Risk with pyrethroid‐PBO nets

Mosquito mortality (unwashed nets)

180 per 1000a

303 per 1000
(259 to 411)a

RR 1.68
(1.33 to 2.11)

1007
(2 trials, 3 comparisons)

⊕⊕⊕⊝
MODERATEb

due to imprecision

Mosquito mortality is probably higher with unwashed pyrethroid‐PBO nets compared to standard unwashed LLINs in areas of moderate insecticide resistance

Mosquito mortality (washed nets)

287 per 1000a

307 per 1000
(213 to 443)a

RR 1.07
(0.74 to 1.54)

329
(1 trial, 1 comparison)

⊕⊕⊝⊝
LOWb,c,d

due to imprecision and indirectness

There may be little to no difference in the effect of washed pyrethroid‐PBO nets on mosquito mortality compared to standard washed LLINs (washed) in areas of moderate insecticide resistance

Blood‐feeding success (unwashed nets)

258 per 1000a

232 per 1000
(197 to 304)a

RR 0.90
(0.72 to 1.11)

1006
(2 trials, 3 comparisons)

⊕⊕⊕⊝
MODERATEb

due to imprecision

There is probably little to no difference in the effect of pyrethroid‐PBO nets (unwashed) on mosquito blood‐feeding success compared to standard LLINs in areas of moderate insecticide resistance

Blood‐feeding success (washed nets)

586 per 1000a

533 per 1000
(434 to 662)a

RR 0.91
(0.74 to 1.13)

329
(1 trial, 1 comparison)

⊕⊕⊝⊝
LOWb,c,d

due to imprecision and indirectness

There may be little to no difference in the effect of washed pyrethroid‐PBO nets on mosquito blood‐feeding success compared to standard washed LLINs in areas of moderate insecticide resistance

*The risk in the intervention group (and its 95% CI) is based on the assumed risk in the comparison group and the relative effect of the intervention (and its 95% CI).
CI: confidence interval; LLIN: long‐lasting insecticidal net; PBO: pyrethroid‐piperonyl butoxide; RR: risk ratio.

GRADE Working Group grades of evidence.
High certainty: we are very confident that the true effect lies close to that of the estimate of the effect.
Moderate certainty: we are moderately confident in the effect estimate: the true effect is likely to be close to the estimate of the effect, but there is a possibility that it is substantially different.
Low certainty: our confidence in the effect estimate is limited: the true effect may be substantially different from the estimate of the effect.
Very low certainty: we have very little confidence in the effect estimate: the true effect is likely to be substantially different from the estimate of effect.

aOriginal numbers are used in this table; however for the pooled analysis, we generated events and total numbers from cluster‐adjusted results, which used the effective sample size. Note that cluster adjustments do not change the point estimate of the effect size, just the standard error.
bDowngraded by one for imprecision due to wide CIs.
cNot downgraded for inconsistency, as only one trial measured this outcome in this setting.
dDowngraded by one for indirectness: the outcome is highly context‐specific, and only one trial is included.

Figuras y tablas -
Summary of findings 2. Summary of findings table 2
Summary of findings 3. Summary of findings table 3

Pyrethroid‐piperonyl butoxide (PBO) nets compared to long‐lasting insecticidal nets (LLINs) for malaria control when insecticide resistance is low

Patient or population:Anopheles gambiae complex or Anopheles funestus group
Setting: areas of low insecticide resistance
Intervention: pyrethroid‐PBO nets
Comparison: LLINs

Outcomes

Anticipated absolute effects* (95% CI)

Relative effect
(95% CI)

Number of mosquitoes
(experimental hut trials)

Certainty of the evidence
(GRADE)

Comments

Risk with LLINs

Risk with pyrethroid‐PBO nets

Mosquito mortality (unwashed nets)

527 per 1000a

659 per 1000
(613 to 972)a

RR 1.25
(0.99 to 1.57)

1580
(2 trials, 3 comparisons)

⊕⊕⊕⊝
MODERATEb

due to imprecision

There is probably little to no difference in the effect of unwashed pyrethroid‐PBO nets on mosquito mortality compared to standard unwashed LLINs in areas of low insecticide resistance

Mosquito mortality (washed nets)

394 per 1000a

547 per 1000
(437 to 938)a

RR 1.39
(0.95 to 2.04)

1774
(2 trials, 3 comparisons)

⊕⊝⊝⊝
VERY LOWc,d

due to imprecision and inconsistency

We do not know if pyrethroid‐PBO nets have an effect on mosquito mortality in areas of low insecticide resistance when the nets have been washed

Blood‐feeding success (unwashed nets)

201 per 1000a

151 per 1000
(58 to 456)a

RR 0.75
(0.27 to 2.11)

1580
(2 trials, 3 comparisons)

⊕⊝⊝⊝
VERY LOWc,d

due to imprecision and inconsistency

We do not know if unwashed pyrethroid‐PBO nets have an effect on mosquito blood‐feeding success in areas of low insecticide resistance

Blood‐feeding success (washed nets)

161 per 1000a

172 per 1000
(122 to 578)a

RR 1.07
(0.49 to 2.33)

1774
(2 trials, 3 comparisons)

⊕⊕⊝⊝
LOWd

due to inconsistency

Mosquito blood‐feeding success may decrease with washed pyrethroid‐PBO nets compared to standard washed LLINs in areas of low insecticide resistance

*The risk in the intervention group (and its 95% CI) is based on the assumed risk in the comparison group and the relative effect of the intervention (and its 95% CI).
CI: confidence interval; LLIN: long‐lasting insecticidal net; PBO: pyrethroid‐piperonyl butoxide; RR: risk ratio.

GRADE Working Group grades of evidence.
High certainty: we are very confident that the true effect lies close to that of the estimate of the effect.
Moderate certainty: we are moderately confident in the effect estimate: the true effect is likely to be close to the estimate of the effect, but there is a possibility that it is substantially different.
Low certainty: our confidence in the effect estimate is limited: the true effect may be substantially different from the estimate of the effect.
Very low certainty: we have very little confidence in the effect estimate: the true effect is likely to be substantially different from the estimate of effect.

aOriginal numbers are used in this table; however for the pooled analysis, events and total numbers were generated from cluster‐adjusted results, which use the effective sample size. Note that cluster adjustments do not change the point estimate of the effect size, just the standard error.
bDowngraded by one for imprecision due to wide CIs.
cDowngraded by one for inconsistency due to unexplained heterogeneity.
dDowngraded by two for imprecision due to extremely wide CIs.

Figuras y tablas -
Summary of findings 3. Summary of findings table 3
Summary of findings 4. Summary of findings table 4

Pyrethroid‐piperonyl butoxide (PBO) nets compared to long‐lasting insecticidal nets (LLINs) for malaria control when mosquitoes are susceptible

Patient or population:Anopheles gambiae complex or Anopheles funestus group
Setting: areas of insecticide‐susceptible mosquitoes

Intervention: pyrethroid‐PBO nets
Comparison: LLINs

Outcomes

Anticipated absolute effects* (95% CI)

Relative effect
(95% CI)

Number of mosquitoes
(experimental hut trials)

Certainty of the evidence
(GRADE)

Comments

Risk with LLINs

Risk with pyrethroid‐PBO nets

Mosquito mortality (unwashed nets)

392 per 1000a

471 per 1000
(251 to 887)a

RR 1.20
(0.64 to 2.26)

2791
(2 trials, 2 comparisons)

⊕⊕⊝⊝
LOWb

due to imprecision

There may be little to no difference in the effect of unwashed pyrethroid‐PBO nets on mosquito mortality compared to standard unwashed LLINs in areas of no insecticide resistance

Mosquito mortality (washed nets)

457 per 1000a

489 per 1000
(420 to 571)a

RR 1.07
(0.92 to 1.25)

2644
(2 trials, 2 comparisons)

⊕⊕⊝⊝
LOWb

due to imprecision

There may be little to no difference in the effect of washed pyrethroid‐PBO nets on mosquito mortality compared to standard washed LLINs in areas of no insecticide resistance

Blood‐feeding success (unwashed nets)

57 per 1000a

29 per 1000
(6 to 132)a

RR 0.52
(0.12 to 2.22)

2791
(2 trials, 2 comparisons)

⊕⊝⊝⊝
VERY LOWb,c

due to imprecision and inconsistency

We do not know if unwashed pyrethroid‐PBO nets have an effect on mosquito blood‐feeding success in areas of no insecticide resistance

Blood‐feeding success (washed nets)

64 per 1000a

82 per 1000
(52 to 131)a

RR 1.25
(0.82 to 1.91)

2644
(2 trials, 2 comparisons)

⊕⊝⊝⊝
VERY LOWb,c

due to imprecision and inconsistency

We do not know if washed pyrethroid‐PBO nets have an effect on mosquito blood‐feeding success in areas of no insecticide resistance

*The risk in the intervention group (and its 95% CI) is based on the assumed risk in the comparison group and the relative effect of the intervention (and its 95% CI).
CI: confidence interval; LLINs: long‐lasting insecticidal nets; PBO: pyrethroid‐piperonyl butoxide; RR: risk ratio.

GRADE Working Group grades of evidence.
High certainty: we are very confident that the true effect lies close to that of the estimate of the effect.
Moderate certainty: we are moderately confident in the effect estimate: the true effect is likely to be close to the estimate of the effect, but there is a possibility that it is substantially different.
Low certainty: our confidence in the effect estimate is limited: the true effect may be substantially different from the estimate of the effect.
Very low certainty: we have very little confidence in the effect estimate: the true effect is likely to be substantially different from the estimate of effect.

aOriginal numbers are used in this table; however for the pooled analysis, events and total numbers were generated from cluster‐adjusted results, which use the effective sample size. Note that cluster adjustments do not change the point estimate of the effect size, just the standard error.
bDowngraded by two for imprecision due to extremely wide CIs.
cDowngraded by one for inconsistency due to unexplained heterogeneity.

Figuras y tablas -
Summary of findings 4. Summary of findings table 4
Table 1. World Health Organization Pesticide Evaluation Scheme (WHOPES) classification

WHOPES Phase

Definition

WHOPES Phase I. Laboratory bioassays

Cone bioassays: these studies are conducted in the laboratory setting and use standard WHO protocols (WHO 2013, Section 2.2.1), when mosquitoes are exposed to a suitable LLIN (treated intervention or untreated control) for three minutes using a standard plastic WHO cone. Following net exposure, mosquitoes are transferred to a holding container and are maintained on a sugar solution diet while entomological outcomes (mosquitoes knocked down 1 hour post exposure, and mosquito mortality 24 hours post exposure) are measured.

Tunnel tests: these studies are conducted in the laboratory setting and use standard WHO protocols (WHO 2013, Section 2.2.2). Mosquitoes are released into a glass tunnel covered at each end with untreated netting. The intervention or control LLIN net sample is placed one‐third down the length of the tunnel, and the net contains 9 holes that enable mosquitoes to pass through. A suitable bait is immobilized in the shorter section of the tunnel, where it is available for mosquito biting. Mosquitoes are released into the opposite end of the tunnel and must make contact with the net and locate holes before they are able to feed on the bait. After 12 to 15 hours, mosquitoes are removed from both sections of the tunnel, and entomological outcomes (the number of mosquitoes in each section, mortality, and blood‐feeding inhibition at the end of the assay and 24 hours post exposure) are recorded.

Wire‐ball bioassays: these studies are conducted in the laboratory setting, where mosquitoes are introduced into a wire‐ball frame that has been covered with the intervention or control LLIN. Mosquitoes are exposed for 3 minutes, after which they are transferred to a holding container, and entomological outcomes (mosquitoes knocked down 1 hour post exposure, and mosquito mortality 24 hours post exposure) are measured.

WHOPES Phase II. Experimental hut trials

WHOPES Phase II experimental hut trials are field trials conducted in Africa where wild mosquito populations or local colonized populations are evaluated. Volunteers or livestock sleep in experimental huts under a purposefully holed LLIN, with 1 person or animal per hut. Huts are designed to resemble local housing based on a West or East African design (WHO 2013; Section 3.3.1‐2). However these trials have identical design features, such as eave gaps or entry slits to allow mosquitoes to enter, and exit traps to capture exiting mosquitoes. LLINs and volunteers are randomly allocated to huts and are rotated in a Latin square to avoid bias, with huts cleaned between rotations to avoid contamination. Several nets, including an untreated control net, can be tested at the same time. Dead and live mosquitoes are collected each morning from inside the net, inside the hut, and inside the exit traps. They are then scored as blood‐fed or non‐blood‐fed, and as alive or dead, and live mosquitoes are maintained for a further 24 hours to assess delayed mosquito mortality.

WHOPES Phase III. Village trials

WHOPES Phase III village trials are conducted in Africa where wild mosquito populations are evaluated. Villages chosen to be included in the study are similar in terms of size, housing structure, location, and data available on insecticide resistance status of local malaria vectors. Households are assigned as conventional LLINs or PBO‐LLINs. Randomization can be done at the household or village level. Adult mosquitoes are collected from study houses, and mosquito density is measured. An indication of malaria transmission is measured at the study sites by recording infections in mosquitoes, parasite prevalence, or malaria incidence.

LLIN: long‐lasting insecticidal nets; PBO: piperonyl butoxide; WHOPES: World Health Organization Pesticide Evaluation Scheme.

Figuras y tablas -
Table 1. World Health Organization Pesticide Evaluation Scheme (WHOPES) classification
Table 2. World Health Organization (WHO)‐recommended long‐lasting insecticidal nets (LLINs)

Product name

Product type

Status of WHO recommendation

DawaPlus 2.0

Deltamethrin coated on polyester

Interim

DawaPlus 3.0

Combination of deltamethrin coated onto polyester (side panels) and deltamethrin and PBO incorporated into polyester (roof)

Interim

DawaPlus 4.0

Deltamethrin and PBO incorporated into polyester

Interim

Duranet

Alpha‐cypermethrin incorporated into polyethylene

Full

Interceptor

Alpha‐cypermethrin coated on polyester

Full

Interceptor G2

Alpha‐cypermethrin and chlorfenapyr incorporated into polyester

Interim

LifeNet

Deltamethrin incorporated into polypropylene

Interim

MAGNet

Alpha‐cypermethrin incorporated into polyethylene

Full

MiraNet

Alpha‐cypermethrin incorporated into polyethylene

Interim

Olyset Net

Permethrin incorporated into polyethylene

Full

Olyset Plus

Permethrin (20 g/kg) and PBO (10 g/kg) incorporated into polyethylene

Interim

Panda Net 2.0

Deltamethrin incorporated into polyethylene

Interim

PermaNet 2.0

Deltamethrin coated on polyester

Full

PermaNet 3.0

Combination of deltamethrin coated on polyester with strengthened border (side panels) and deltamethrin and PBO incorporated into polyethylene (roof)

Interim

Royal Sentry

Alpha‐cypermethrin incorporated into polyethylene

Full

SafeNet

Alpha‐cypermethrin coated on polyester

Full

Veeralin

Alpha‐cypermethrin and PBO incorporated into polyethylene

Interim

Yahe

Deltamethrin coated on polyester

Interim

Yorkool

Deltamethrin coated on polyester

Full

LLIN: long‐lasting insecticidal net; PBO: piperonyl butoxide; WHO: World Health Organization.

Figuras y tablas -
Table 2. World Health Organization (WHO)‐recommended long‐lasting insecticidal nets (LLINs)
Table 3. World Health Organization (WHO)‐recommended insecticide products for treatment of mosquito nets for malaria vector control

Insecticide

Formulation

Dosagea

Alpha‐cypermethrin

SC 10%

20 to 40

Cyfluthrin

EW 5%

50

Deltamethrin

SC 1%
WT 25%
WT 25% + binderb

15 to 25

Etofenprox

EW 10%

200

Lambda‐cyhalothrin

CS 2.5%

10 to 15

Permethrin

EC 10%

200 to 500

EC: emulsifiable concentrate; EW: emulsion, oil in water; CS: capsule suspension; SC: suspension concentrate; WT: water dispersible tablet.
aActive ingredient/netting (mg/m²).
bK‐O TAB 1‐2‐3.

Figuras y tablas -
Table 3. World Health Organization (WHO)‐recommended insecticide products for treatment of mosquito nets for malaria vector control
Table 4. Definition of resistance level

Outcome

Confirmed resistance

Suspected resistance

Susceptible

Unclassified

WHO mosquito mortalitya

< 90%

90% to 97%

98% to 100%

Unknown

CDC knock‐downb

< 90%

80% to 97%

98% to 100%

Unknown

CDC: Centers for Disease Control and Prevention; WHO: World Health Organization.
aDefinition of resistance level based on mosquito mortality (%) after exposure to insecticide in a WHO diagnostic dose assay.
bDefinition of resistance level based on mosquito mortality (%) after exposure to insecticide in a CDC bottle bioassay using the methods, diagnostic doses, and diagnostic times recommended by each test respectively.

Figuras y tablas -
Table 4. Definition of resistance level
Table 5. Stratification of resistance level

Outcome

Low

Moderate

High

Unclassified

Mosquito mortalitya

61% to 90%

31% to 60%

< 30%

Unknown

a24‐hour post‐exposure mortality (%).

Figuras y tablas -
Table 5. Stratification of resistance level
Table 6. Study inclusion screening form

Criteria

Assessment

Comments

Yes

No

Unclear

Mosquito population

Did the study test Anopheles gambiae complex or Anopheles funestus group mosquitoes?

State mosquito species

Were a minimum of 50 mosquitoes tested per study arm?

Intervention

Did the study include a long‐lasting insecticidal net (LLIN) or insecticide‐treated net (ITN)?

State net LLIN or ITN

Was the intervention net either of the following?

  1. A piperonyl butoxide (PBO) LLIN that received a minimum of interim World Health Organization (WHO) approval.

State net type

Was the control net either of the following?

  1. A pyrethroid LLIN of the same fabric impregnated with the same insecticide and dose as the intervention net.

  2. A pyrethroid LLIN impregnated with the same insecticide at any dose.

State which objective study meets

Study design

Was the study one of the following?

  1. Experimental hut study

  2. Village trial

State study type

For experimental hut study and village trial. Was the study conducted in Africa?

State country

Outcome

Did the study include at least 1 of the following outcome measures?

  1. Mortality

  2. Blood feeding

  3. Sporozoite rate

  4. Not passed through the net

  5. Deterrence

  6. Exophily

  7. Mosquito density

  8. Parity rate

Decision

Is the study eligible for inclusion?

State reason(s) for exclusion

Discuss with authors

ITN: insecticide‐treated net; LLIN: long‐lasting insecticidal net; PBO: piperonyl butoxide; WHO: World Health Organization.

Figuras y tablas -
Table 6. Study inclusion screening form
Table 7. Experimental hut trials: deterrence data

Study ID

Locality

Net type

Net washed

Total number in ITN hut

Total number in UTN hut

Deterrence (%) reported

Deterrence (%) calculated

Bayili 2017

Vallée du Kou

DawaPlus 2.0

No

1548

1848

16.23

16.23

Bayili 2017

Vallée du Kou

DawaPlus 2.0

Yes

2155

1848

0

‐16.61

Bayili 2017

Vallée du Kou

DawaPlus 3.0

No

1365

1848

26.13

26.14

Bayili 2017

Vallée du Kou

DawaPlus 3.0

Yes

1981

1848

0

‐7.20

Bayili 2017

Vallée du Kou

DawaPlus 4.0

No

846

1848

54.22

54.22

Bayili 2017

Vallée du Kou

DawaPlus 4.0

Yes

1646

1848

10.93

10.93

Corbel 2010

Malanville

Permanet 2.0

Yes

195

285

31.58

31.58

Corbel 2010

Malanville

Permanet 3.0

Yes

210

285

26.32

26.32

Corbel 2010

Malanville

Permanet 2.0

No

243

285

14.74

14.74

Corbel 2010

Malanville

Permanet 3.0

No

214

285

24.91

24.91

Corbel 2010

Pitoa

Permanet 2.0

Yes

310

401

22.69

22.69

Corbel 2010

Pitoa

Permanet 3.0

Yes

163

401

59.35

59.35

Corbel 2010

Pitoa

Permanet 2.0

No

105

401

73.82

73.82

Corbel 2010

Pitoa

Permanet 3.0

No

146

401

63.59

63.59

Corbel 2010

Vallée du Kou

Permanet 2.0

Yes

788

908

13.22

13.22

Corbel 2010

Vallée du Kou

Permanet 3.0

Yes

724

908

20.26

20.26

Corbel 2010

Vallée du Kou

Permanet 2.0

No

329

908

63.77

63.77

Corbel 2010

Vallée du Kou

Permanet 3.0

No

463

908

49.01

49.01

Koudou 2011

Yaokoffikro

Permanet 3.0

No

303

796

62.1

61.93

Koudou 2011

Yaokoffikro

Permanet 2.0

No

317

796

60.4

60.18

Koudou 2011

Yaokoffikro

Permanet 3.0

Yes

313

796

60.1

60.68

Koudou 2011

Yaokoffikro

Permanet 2.0

Yes

281

796

64.4

64.70

Menze 2020

Mibellon

PermaNet 2.0

No

237

390

39.2

39.2

Menze 2020

Mibellon

PermaNet 3.0

No

153

390

60.8

60.8

Menze 2020

Mibellon

Olyset Net

No

176

390

54.9

54.9

Menze 2020

Mibellon

Olyset Plus

No

199

390

49

49

Moore 2016

Ifakara

Veeralin LN

No

722

810

11

10.86

Moore 2016

Ifakara

Veeralin LN

Yes

727

810

10

10.25

Moore 2016

Ifakara

MAGNet LN

No

1070

810

0

‐32.10

Moore 2016

Ifakara

MAGNet LN

Yes

773

810

5

4.57

Moore 2016

Ifakara

Veeralin LN

No

89

170

48

47.65

Moore 2016

Ifakara

Veeralin LN

Yes

85

170

50

50.00

Moore 2016

Ifakara

MAGNet LN

No

114

170

33

32.94

Moore 2016

Ifakara

MAGNet LN

Yes

103

170

39

39.41

N'Guessan 2010

Akron

Permanet 3.0

No

128

185

31

30.81

N'Guessan 2010

Akron

Permanet 3.0

Yes

155

185

NR

16.22

N'Guessan 2010

Akron

Permanet 2.0

No

114

185

38

38.38

N'Guessan 2010

Akron

Permanet 2.0

Yes

174

185

NR

5.95

Pennetier 2013

Malanville

Olyset Plus

No

67

69

NR

2.90

Pennetier 2013

Malanville

Olyset Plus

Yes

101

69

NR

‐46.38

Pennetier 2013

Malanville

Olyset Net

No

96

69

NR

‐39.13

Pennetier 2013

Malanville

Olyset Net

Yes

124

69

NR

‐79.71

Toé 2018

Tengrela

Olyset Net

No

923

480

‐92.29

‐92.29

Toé 2018

Tengrela

Olyset Plus

No

695

480

‐44.79

‐44.79

Toé 2018

Tengrela

Permanet 2.0

No

858

480

‐78.75

‐78.75

Toé 2018

Tengrela

Permanet 3.0

No

794

480

‐65.42

‐65.42

Toé 2018

VK5

Olyset Net

No

1458

1095

‐33.15

‐33.15

Toé 2018

VK5

Olyset Plus

No

1278

1095

‐16.71

‐16.71

Toé 2018

VK5

Permanet 2.0

No

1075

1095

1.83

1.83

Toé 2018

VK5

Permanet 3.0

No

657

1095

40

40.00

Tungu 2010

Zeneti

PermaNet 3.0

No

425

723

41

41.22

Tungu 2010

Zeneti

PermaNet 2.0

No

574

723

21

20.61

Tungu 2010

Zeneti

PermaNet 3.0

Yes

558

723

23

22.82

Tungu 2010

Zeneti

PermaNet 2.0

Yes

586

723

19

18.95

ITN: insecticide‐treated net; LLIN: long‐lasting insecticidal net; NR: not reported; PBO: piperonyl butoxide; UTN: untreated net; WHO: World Health Organization.

Figuras y tablas -
Table 7. Experimental hut trials: deterrence data
Table 8. Village trials: mosquito density data

Study ID

Net type

Species

Density measurement

Collection method

Baseline density

Post‐intervention density

Reduction (%)

Awolola 2014

Untreated

An gambiae s.l.

Mean number caught per house

WT, IRC

16.2

17.1

‐5.56

Awolola 2014

PermaNet 2.0

An gambiae s.l.

Mean number caught per house

WT, IRC

21.3

7.2

66.20

Awolola 2014

PermaNet 3.0

An gambiae s.l.

Mean number caught per house

WT, IRC

20.1

1.4

93.03

Cisse 2017

PermaNet 2.0

An gambiae s.l.

Resting density per room per day

IRC

1.92

Cisse 2017

PermaNet 3.0

An gambiae s.l.

Resting density per room per day

IRC

3.05

Cisse 2017

Olyset

An gambiae s.l.

Resting density per room per day

IRC

3.21

Cisse 2017

Olyset Plus

An gambiae s.l.

Resting density per room per day

IRC

3.7

Mzilahowa 2014

Olyset

An gambiae

Mean number caught per catch

PSC

0.10

Mzilahowa 2014

Olset Plus

An gambiae

Mean number caught per catch

PSC

0.12

Mzilahowa 2014

PermaNet 2.0

An gambiae

Mean number caught per catch

PSC

0.13

Mzilahowa 2014

PermaNet 3.0

An gambiae

Mean number caught per catch

PSC

0.09

Mzilahowa 2014

Olyset

An funestus

Mean number caught per catch

PSC

0.08

Mzilahowa 2014

Olyset Plus

An funestus

Mean number caught per catch

PSC

0.16

Mzilahowa 2014

PermaNet 2.0

An funestus

Mean number caught per catch

PSC

0.27

Mzilahowa 2014

PermaNet 3.0

An funestus

Mean number caught per catch

PSC

0.13

Mzilahowa 2014

Olyset

An gambiae

Mean number caught per catch

LT

1.23

Mzilahowa 2014

Olset Plus

An gambiae

Mean number caught per catch

LT

0.27

Mzilahowa 2014

PermaNet 2.0

An gambiae

Mean number caught per catch

LT

0.96

Mzilahowa 2014

PermaNet 3.0

An gambiae

Mean number caught per catch

LT

1.44

Mzilahowa 2014

Olyset

An funestus

Mean number caught per catch

LT

2.02

Mzilahowa 2014

Olset Plus

An funestus

Mean number caught per catch

LT

2.1

Mzilahowa 2014

PermaNet 2.0

An funestus

Mean number caught per catch

LT

5.76

Mzilahowa 2014

PermaNet 3.0

An funestus

Mean number caught per catch

LT

3.76

Protopopoff 2018

Olyset (2015)

Anopheles species

Mean number caught per house per night

LT

2.61

Protopopoff 2018

Olyset Plus (2015)

Anopheles species

Mean number caught per house per night

LT

1.85

Protopopoff 2018

Olyset (2016)

Anopheles species

Mean number caught per house per night

LT

3.60

Protopopoff 2018

Olyset Plus (2016)

Anopheles species

Mean number caught per house per night

LT

2.68

Staedke 2020

Permanet 2.0 (6 months)

An gambiae s.l.

Mean density per house

IRC

0.3

0.67

Staedke 2020

Permanet 3.0 (6 months)

An gambiae s.l.

Mean density per house

IRC

0.8

0.17

78.75

Staedke 2020

Olyset (6 months)

An gambiae s.l.

Mean density per house

IRC

0.3

0.81

Staedke 2020

Olyset Plus (6 months)

An gambiae s.l.

Mean density per house

IRC

0.1

0.16

Staedke 2020

Permanet 2.0 (12 months)

An gambiae s.l.

Mean density per house

IRC

0.3

1.35

Staedke 2020

Permanet 3.0 (12 months)

An gambiae s.l.

Mean density per house

IRC

0.8

0.52

35

Staedke 2020

Olyset (12 months)

An gambiae s.l.

Mean density per house

IRC

0.3

1.1

Staedke 2020

Olyset Plus (12 months)

An gambiae s.l.

Mean density per house

IRC

0.1

0.23

Staedke 2020

Permanet 2.0 (18 months)

An gambiae s.l.

Mean density per house

IRC

0.3

1.65

Staedke 2020

Permanet 3.0 (18 months)

An gambiae s.l.

Mean density per house

IRC

0.8

1.57

Staedke 2020

Olyset (18 months)

An gambiae s.l.

Mean density per house

IRC

0.3

0.66

Staedke 2020

Olyset Plus (18 months)

An gambiae s.l.

Mean density per house

IRC

0.1

0.19

Stiles‐Ocran 2013

No intervention

An gambiae s.s.

Mean number caught per village

IRC

230

79

65.65

Stiles‐Ocran 2013

Permanet 2.0

An gambiae s.s.

Mean number caught per village

IRC

39

36

7.69

Stiles‐Ocran 2013

Permanet 2.0

An gambiae s.s.

Mean number caught per village

IRC

82

45

45.12

Stiles‐Ocran 2013

Permanet 3.0

An gambiae s.s.

Mean number caught per village

IRC

77

12

84.42

Stiles‐Ocran 2013

Permanet 3.0

An gambiae s.s.

Mean number caught per village

IRC

178

15

91.57

Stiles‐Ocran 2013

No intervention

An gambiae s.s.

Mean number caught per person per night per village

Indoor & outdoor HLC

415

72

82.65

Stiles‐Ocran 2013

Permanet 2.0

An gambiae s.s.

Mean number caught per person per night per village

Indoor & outdoor HLC

33

31

6.06

Stiles‐Ocran 2013

Permanet 2.0

An gambiae s.s.

Mean number caught per person per night per village

Indoor & outdoor HLC

79

64

18.99

Stiles‐Ocran 2013

Permanet 3.0

An gambiae s.s.

Mean number caught per person per night per village

Indoor & outdoor HLC

98

19

80.61

Stiles‐Ocran 2013

Permanet 3.0

An gambiae s.s.

Mean number caught per person per night per village

Indoor & outdoor HLC

156

36

76.92

An funestus: Anopheles funestus; An gambiae: Anopheles gambiae; HLC: human landing catch; IRC: indoor resting catch; LT: light trap; PSC: pyrethrum spray catch; WT: window trap.

Figuras y tablas -
Table 8. Village trials: mosquito density data
Comparison 1. Commercial pyrethroid‐PBO nets versus commercial LLINs: village trials

Outcome or subgroup title

No. of studies

No. of participants

Statistical method

Effect size

1.1 Parasite prevalence (pyrethroid‐PBO nets vs non‐PBO LLINs, latest end points in RCT) Show forest plot

2

Odds Ratio (IV, Fixed, 95% CI)

0.79 [0.67, 0.95]

1.2 Parasite prevalence (pyrethroid‐PBO nets vs non‐PBO LLINs, shown at 4 different time points) Show forest plot

2

Odds Ratio (IV, Fixed, 95% CI)

Subtotals only

1.2.1 4 to 6 months

2

Odds Ratio (IV, Fixed, 95% CI)

0.74 [0.62, 0.89]

1.2.2 9 to 12 months

2

Odds Ratio (IV, Fixed, 95% CI)

0.72 [0.61, 0.86]

1.2.3 16 to 18 months

2

Odds Ratio (IV, Fixed, 95% CI)

0.88 [0.74, 1.04]

1.2.4 21 to 25 months

2

Odds Ratio (IV, Fixed, 95% CI)

0.79 [0.67, 0.95]

1.3 Mosquito sporozoite‐positive (adjusted ICC 0.1) Show forest plot

4

424

Risk Ratio (M‐H, Random, 95% CI)

0.82 [0.24, 2.75]

1.4 Mosquito parous (adjusted ICC 0.1) Show forest plot

3

220

Risk Ratio (M‐H, Random, 95% CI)

0.97 [0.82, 1.13]

Figuras y tablas -
Comparison 1. Commercial pyrethroid‐PBO nets versus commercial LLINs: village trials
Comparison 2. Commercial pyrethroid‐PBO nets versus commercial LLINs: hut trials

Outcome or subgroup title

No. of studies

No. of participants

Statistical method

Effect size

2.1 Mosquito mortality (pooled) hut/night (adjusted ICC 0.1) Show forest plot

10

15614

Risk Ratio (M‐H, Random, 95% CI)

1.43 [1.26, 1.62]

2.1.1 Unwashed

10

8647

Risk Ratio (M‐H, Random, 95% CI)

1.63 [1.29, 2.05]

2.1.2 Washed

8

6967

Risk Ratio (M‐H, Random, 95% CI)

1.19 [1.04, 1.38]

2.2 Mosquito blood‐feeding success (pooled) hut/night (adjusted ICC 0.1) Show forest plot

9

12351

Risk Ratio (M‐H, Random, 95% CI)

0.75 [0.66, 0.85]

2.2.1 Unwashed

9

7261

Risk Ratio (M‐H, Random, 95% CI)

0.68 [0.57, 0.80]

2.2.2 Washed

7

5090

Risk Ratio (M‐H, Random, 95% CI)

0.87 [0.74, 1.02]

2.3 Mosquito exophily (pooled) hut/night (adjusted ICC 0.1) Show forest plot

10

13214

Risk Ratio (M‐H, Random, 95% CI)

1.00 [0.94, 1.06]

2.3.1 Unwashed

10

7699

Risk Ratio (M‐H, Random, 95% CI)

1.00 [0.91, 1.10]

2.3.2 Washed

8

5515

Risk Ratio (M‐H, Random, 95% CI)

1.00 [0.93, 1.07]

2.4 Mosquito mortality (high resistance) hut/night (adjusted ICC 0.1) Show forest plot

5

7997

Risk Ratio (M‐H, Random, 95% CI)

1.58 [1.34, 1.86]

2.4.1 Unwashed

5

4896

Risk Ratio (M‐H, Random, 95% CI)

1.84 [1.60, 2.11]

2.4.2 Washed

4

3101

Risk Ratio (M‐H, Random, 95% CI)

1.20 [0.88, 1.63]

2.5 Mosquito blood‐feeding success (high resistance) hut/night (adjusted ICC 0.1) Show forest plot

4

7134

Risk Ratio (M‐H, Random, 95% CI)

0.66 [0.57, 0.76]

2.5.1 Unwashed

4

4458

Risk Ratio (M‐H, Random, 95% CI)

0.60 [0.50, 0.71]

2.5.2 Washed

3

2676

Risk Ratio (M‐H, Random, 95% CI)

0.81 [0.72, 0.92]

2.6 Mosquito mortality (moderate resistance) hut/night (adjusted ICC 0.1) Show forest plot

2

1027

Risk Ratio (M‐H, Fixed, 95% CI)

1.47 [1.21, 1.78]

2.6.1 Unwashed

2

751

Risk Ratio (M‐H, Fixed, 95% CI)

1.68 [1.33, 2.11]

2.6.2 Washed

1

276

Risk Ratio (M‐H, Fixed, 95% CI)

1.07 [0.74, 1.54]

2.7 Mosquito blood‐feeding success (moderate resistance) hut/night (adjusted ICC 0.1) Show forest plot

2

1034

Risk Ratio (M‐H, Random, 95% CI)

0.91 [0.78, 1.05]

2.7.1 Unwashed

2

752

Risk Ratio (M‐H, Random, 95% CI)

0.90 [0.72, 1.11]

2.7.2 Washed

1

282

Risk Ratio (M‐H, Random, 95% CI)

0.91 [0.74, 1.13]

2.8 Mosquito mortality (low resistance) hut/night (adjusted ICC 0.1) Show forest plot

2

1970

Risk Ratio (M‐H, Random, 95% CI)

1.30 [1.09, 1.56]

2.8.1 Unwashed

2

948

Risk Ratio (M‐H, Random, 95% CI)

1.25 [0.99, 1.57]

2.8.2 Washed

2

1022

Risk Ratio (M‐H, Random, 95% CI)

1.39 [0.95, 2.04]

2.9 Mosquito blood‐feeding success (low resistance) hut/night (adjusted ICC 0.1) Show forest plot

2

1970

Risk Ratio (M‐H, Random, 95% CI)

0.94 [0.56, 1.57]

2.9.1 Unwashed

2

948

Risk Ratio (M‐H, Random, 95% CI)

0.75 [0.27, 2.11]

2.9.2 Washed

2

1022

Risk Ratio (M‐H, Random, 95% CI)

1.07 [0.49, 2.33]

2.10 Mosquito mortality (susceptible) hut/night (adjusted ICC 0.1) Show forest plot

2

1916

Risk Ratio (M‐H, Random, 95% CI)

1.05 [0.96, 1.15]

2.10.1 Unwashed

2

948

Risk Ratio (M‐H, Random, 95% CI)

1.20 [0.64, 2.26]

2.10.2 Washed

2

968

Risk Ratio (M‐H, Random, 95% CI)

1.07 [0.92, 1.25]

2.11 Mosquito blood‐feeding success (susceptible) hut/night (adjusted ICC 0.1) Show forest plot

2

1916

Risk Ratio (M‐H, Random, 95% CI)

0.87 [0.40, 1.89]

2.11.1 Unwashed

2

948

Risk Ratio (M‐H, Random, 95% CI)

0.52 [0.12, 2.22]

2.11.2 Washed

2

968

Risk Ratio (M‐H, Random, 95% CI)

1.25 [0.82, 1.91]

2.12 Mosquito mortality (high resistance/Permanet) hut/night (adjusted ICC 0.1) Show forest plot

3

2806

Risk Ratio (M‐H, Random, 95% CI)

1.59 [1.26, 2.01]

2.12.1 Not Washed

3

1877

Risk Ratio (M‐H, Random, 95% CI)

1.81 [1.56, 2.10]

2.12.2 Washed

2

929

Risk Ratio (M‐H, Random, 95% CI)

1.18 [0.61, 2.28]

2.13 Mosquito blood‐feeding success (high resistance/Permanet) hut/night (adjusted ICC 0.1) Show forest plot

2

1943

Risk Ratio (M‐H, Random, 95% CI)

0.58 [0.45, 0.76]

2.13.1 Unwashed

2

1439

Risk Ratio (M‐H, Random, 95% CI)

0.53 [0.40, 0.69]

2.13.2 Washed

1

504

Risk Ratio (M‐H, Random, 95% CI)

0.76 [0.61, 0.93]

2.14 Mosquito mortality (high resistance/Olyset) hut/night (adjusted ICC 0.1) Show forest plot

2

1410

Risk Ratio (M‐H, Random, 95% CI)

1.73 [1.51, 1.97]

2.14.1 Unwashed

2

1257

Risk Ratio (M‐H, Random, 95% CI)

1.72 [1.48, 1.99]

2.14.2 Washed

1

153

Risk Ratio (M‐H, Random, 95% CI)

1.81 [1.25, 2.61]

2.15 Mosquito blood‐feeding success (high resistance/Olyset) hut/night (adjusted ICC 0.1) Show forest plot

2

1470

Risk Ratio (M‐H, Random, 95% CI)

0.63 [0.40, 0.98]

2.15.1 Unwashed

2

1257

Risk Ratio (M‐H, Random, 95% CI)

0.67 [0.38, 1.18]

2.15.2 Washed

1

213

Risk Ratio (M‐H, Random, 95% CI)

0.50 [0.27, 0.93]

Figuras y tablas -
Comparison 2. Commercial pyrethroid‐PBO nets versus commercial LLINs: hut trials