Impact of the 13-Valent Pneumococcal Conjugate Vaccine on Clinical and Hypoxemic Childhood Pneumonia over Three Years in Central Malawi: An Observational Study

被引:44
作者
McCollum, Eric D. [1 ,2 ]
Nambiar, Bejoy [1 ]
Deula, Rashid [3 ]
Zadutsa, Beatiwel [3 ]
Bondo, Austin [3 ]
King, Carina [1 ]
Beard, James [1 ]
Liyaya, Harry [3 ]
Mankhambo, Limangeni [3 ]
Lazzerini, Marzia [4 ]
Makwenda, Charles [3 ]
Masache, Gibson [3 ]
Bar-Zeev, Naor [5 ,6 ]
Kazembe, Peter N. [7 ]
Mwansambo, Charles [8 ]
Lufesi, Norman [9 ]
Costello, Anthony [1 ]
Armstrong, Ben [10 ]
Colbourn, Tim [1 ]
机构
[1] UCL, Inst Global Hlth, London, England
[2] Johns Hopkins Sch Med, Div Pulmonol, Dept Pediat, Baltimore, MD USA
[3] Parent & Child Hlth Initiat Trust, Lilongwe, Malawi
[4] IRCCS Burlo Garofolo, Inst Maternal & Child Hlth, Collaborating Ctr Maternal & Child Hlth, WHO, Trieste, Italy
[5] Univ Malawi, Coll Med, Malawi Liverpool Wellcome Trust Clin Res Programm, Blantyre, Malawi
[6] Univ Liverpool, Inst Infect & Global Hlth, Liverpool, Merseyside, England
[7] Med Childrens Fdn, Baylor Coll, Lilongwe, Malawi
[8] Minist Hlth, Lilongwe, Malawi
[9] Minist Hlth, Community Hlth Sci Unit, Lilongwe, Malawi
[10] London Sch Hyg & Trop Med, Dept Social & Environm Hlth Res, London, England
来源
PLOS ONE | 2017年 / 12卷 / 01期
基金
美国国家卫生研究院; 比尔及梅琳达.盖茨基金会;
关键词
STREPTOCOCCUS-PNEUMONIAE; DOUBLE-BLIND; CHILDREN; DISEASE; PLACEBO; HOSPITALIZATIONS; IMMUNIZATION; ADMISSIONS; REGRESSION; EFFICACY;
D O I
10.1371/journal.pone.0168209
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Background The pneumococcal conjugate vaccine's (PCV) impact on childhood pneumonia during programmatic conditions in Africa is poorly understood. Following PCV13 introduction in Malawi in November 2011, we evaluated the case burden and rates of childhood pneumonia. Methods and Findings Between January 1, 2012-June 30, 2014 we conducted active pneumonia surveillance in children <5 years at seven hospitals, 18 health centres, and with 38 community health workers in two districts, central Malawi. Eligible children had clinical pneumonia per Malawi guidelines, defined as fast breathing only, chest indrawing +/- fast breathing, or, >= 1 clinical danger sign. Since pulse oximetry was not in the Malawi guidelines, oxygenation <90% defined hypoxemic pneumonia, a distinct category from clinical pneumonia. We quantified the pneumonia case burden and rates in two ways. We compared the period immediately following vaccine introduction (early) to the period with >75% three-dose PCV13 coverage (post). We also used multivariable time-series regression, adjusting for autocorrelation and exploring seasonal variation and alternative model specifications in sensitivity analyses. The early versus post analysis showed an increase in cases and rates of total, fast breathing, and indrawing pneumonia and a decrease in danger sign and hypoxemic pneumonia, and pneumonia mortality. At 76% three-dose PCV13 coverage, versus 0%, the time-series model showed a non-significant increase in total cases (+47%, 95% CI:-13%, +149%, p = 0.154); fast breathing cases increased 135% (+39%, +297%, p = 0.001), however, hypoxemia fell 47% (-5%,-70%, p = 0.031) and hospital deaths decreased 36% (-1%,-58%, p = 0.047) in children <5 years. We observed a shift towards disease without danger signs, as the proportion of cases with danger signs decreased by 65% (-46%,-77%, p<0.0001). These results were generally robust to plausible alternative model specifications. Conclusions Thirty months after PCV13 introduction in Malawi, the health system burden and rates of the severest forms of childhood pneumonia, including hypoxemia and death, have markedly decreased.
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页数:17
相关论文
共 40 条
[1]  
Anonymous, 2010, Morbidity and Mortality Weekly Report, V59, P258
[2]  
[Anonymous], LANCET
[3]  
[Anonymous], 2013, GUID MAN COMM CHILDH
[4]   Effectiveness of a monovalent rotavirus vaccine in infants in Malawi after programmatic roll-out: an observational and case-control study [J].
Bar-Zen, Naor ;
Kapanda, Lester ;
Tate, Jacqueline E. ;
Jere, Khuzwayo C. ;
Iturriza-Gomara, Miren ;
Nakagomi, Osamu ;
Mwansambo, Charles ;
Costello, Anthony ;
Parashar, Umesh D. ;
Heyderman, Robert S. ;
French, Neil ;
Cunliffe, Nigel A. .
LANCET INFECTIOUS DISEASES, 2015, 15 (04) :422-428
[5]   Time series regression studies in environmental epidemiology [J].
Bhaskaran, Krishnan ;
Gasparrini, Antonio ;
Hajat, Shakoor ;
Smeeth, Liam ;
Armstrong, Ben .
INTERNATIONAL JOURNAL OF EPIDEMIOLOGY, 2013, 42 (04) :1187-1195
[6]  
Blaschke AJ, 2009, PEDIATR INFECT DIS J, V30, P289
[7]   Lot Quality Assurance Sampling to Monitor Supplemental Immunization Activity Quality: An Essential Tool for Improving Performance in Polio Endemic Countries [J].
Brown, Alexandra E. ;
Okayasu, Hiromasa ;
Nzioki, Michael M. ;
Wadood, Mufti Z. ;
Chabot-Couture, Guillaume ;
Quddus, Arshad ;
Walker, George ;
Sutter, Roland W. .
JOURNAL OF INFECTIOUS DISEASES, 2014, 210 :S333-S340
[8]  
Brumback BA, 2000, J AM STAT ASSOC, V95, P16
[9]   Efficacy of nine-valent pneumococcal conjugate vaccine against pneumonia and invasive pneumococcal disease in The Gambia: randomised, double-blind, placebo-controlled trial [J].
Cutts, FT ;
Zaman, SMA ;
Enwere, G ;
Jaffar, S ;
Levine, OS ;
Okoko, JB ;
Oluwalana, C ;
Vaughan, A ;
Obaro, SK ;
Leach, A ;
McAdam, KP ;
Biney, E ;
Saaka, M ;
Onwuchekwa, U ;
Yallop, F ;
Pierce, NF ;
Greenwood, BM ;
Adegbola, RA .
LANCET, 2005, 365 (9465) :1139-1146
[10]   The Worldwide Impact of the Seven-valent Pneumococcal Conjugate Vaccine [J].
Fitzwater, Sean P. ;
Chandran, Aruna ;
Santosham, Mathuram ;
Johnson, Hope L. .
PEDIATRIC INFECTIOUS DISEASE JOURNAL, 2012, 31 (05) :501-508