WHO recommendations on antenatal care for a positive pregnancy experience
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2. Methods<br />
<str<strong>on</strong>g>WHO</str<strong>on</strong>g> <str<strong>on</strong>g>recommendati<strong>on</strong>s</str<strong>on</strong>g> <strong>on</strong> <strong>antenatal</strong> <strong>care</strong> <strong>for</strong> a <strong>positive</strong> <strong>pregnancy</strong> <strong>experience</strong><br />
The guideline was developed in accordance with<br />
the methods described in the <str<strong>on</strong>g>WHO</str<strong>on</strong>g> handbook <strong>for</strong><br />
guideline development (14). In summary, the process<br />
included: identificati<strong>on</strong> of priority questi<strong>on</strong>s and<br />
outcomes, retrieval of evidence, assessment<br />
and synthesis of the evidence, <strong>for</strong>mulati<strong>on</strong><br />
of <str<strong>on</strong>g>recommendati<strong>on</strong>s</str<strong>on</strong>g>, and planning <strong>for</strong> the<br />
implementati<strong>on</strong>, disseminati<strong>on</strong>, impact evaluati<strong>on</strong><br />
and updating of the guideline.<br />
2.1 <str<strong>on</strong>g>WHO</str<strong>on</strong>g> Steering Group<br />
The <str<strong>on</strong>g>WHO</str<strong>on</strong>g> Steering Group that guided the entire<br />
guideline development process comprised <str<strong>on</strong>g>WHO</str<strong>on</strong>g><br />
staff members from the Department of Reproductive<br />
Health and Research (RHR), the Department of<br />
Maternal, Newborn, Child and Adolescent Health<br />
(MCA), and the Department of Nutriti<strong>on</strong> <strong>for</strong> Health<br />
and Development (NHD) (see Annex 1 <strong>for</strong> the list<br />
of members). Regi<strong>on</strong>al advisors from <str<strong>on</strong>g>WHO</str<strong>on</strong>g> regi<strong>on</strong>s<br />
also participated in the guideline development<br />
process. The Steering Group drafted the initial scope<br />
of the guideline and drafted the key recommendati<strong>on</strong><br />
questi<strong>on</strong>s in PICO <strong>for</strong>mat (populati<strong>on</strong>, interventi<strong>on</strong>,<br />
comparator, outcome), identified individuals to be<br />
invited to participate as guideline methodologists<br />
and as members of the systematic review teams,<br />
the Guideline Development Group (GDG) and<br />
the External Review Group (ERG), supervised the<br />
evidence retrieval and synthesis, organized the<br />
Technical C<strong>on</strong>sultati<strong>on</strong>s (or GDG meetings), drafted<br />
<str<strong>on</strong>g>recommendati<strong>on</strong>s</str<strong>on</strong>g>, and finalized and published the<br />
guideline document. Additi<strong>on</strong>ally, the Steering Group<br />
will oversee disseminati<strong>on</strong> of the guideline.<br />
2.2 Guideline Development Group (GDG)<br />
The Steering Group identified and invited 20 external<br />
experts and stakeholders from the six <str<strong>on</strong>g>WHO</str<strong>on</strong>g> regi<strong>on</strong>s<br />
to <strong>for</strong>m the GDG, ensuring geographic representati<strong>on</strong>,<br />
gender balance, and no important c<strong>on</strong>flicts of<br />
interest. The GDG was a diverse group of individuals<br />
with expertise in research, guideline development<br />
methods, and clinical policy and programmes relating<br />
to interventi<strong>on</strong>s <strong>for</strong> ANC and service delivery, also<br />
including a patient/c<strong>on</strong>sumer representative. The<br />
curriculum vitae of the members were published<br />
<strong>on</strong> the RHR departmental website prior to the GDG<br />
meetings (which occurred between October 2015<br />
and March 2016). Subgroups were invited to each of<br />
the meetings based <strong>on</strong> their expertise.<br />
Selected members of the GDG provided input into<br />
the drafting of the scope of the guideline, the PICO<br />
questi<strong>on</strong>s and the prioritizati<strong>on</strong> of outcomes, which<br />
guided the evidence reviews. The GDG as a whole<br />
appraised the evidence used to in<strong>for</strong>m the guideline,<br />
advised <strong>on</strong> the interpretati<strong>on</strong> of this evidence,<br />
<strong>for</strong>mulated the final <str<strong>on</strong>g>recommendati<strong>on</strong>s</str<strong>on</strong>g> at faceto-face<br />
meetings, and reviewed and approved the<br />
final guideline document be<strong>for</strong>e its submissi<strong>on</strong> to<br />
the <str<strong>on</strong>g>WHO</str<strong>on</strong>g> Guidelines Review Committee (GRC) <strong>for</strong><br />
approval. A list of the members of the GDG can be<br />
found in Annex 1.<br />
2.3 External Review Group (ERG)<br />
The membership of the ERG was geographically<br />
and gender-balanced, and there were no important<br />
c<strong>on</strong>flicts of interest that prohibited any member<br />
from serving (see Annex 1 <strong>for</strong> the list of members).<br />
There were six members of the ERG, including<br />
technical experts and other stakeholders with<br />
sufficient interests in the provisi<strong>on</strong> of evidencebased<br />
ANC. This group peer reviewed the final<br />
guideline document to identify any factual errors and<br />
comment <strong>on</strong> the clarity of the language, c<strong>on</strong>textual<br />
issues, and implicati<strong>on</strong>s <strong>for</strong> implementati<strong>on</strong>. The<br />
group ensured that the guideline decisi<strong>on</strong>-making<br />
processes had c<strong>on</strong>sidered and incorporated the<br />
c<strong>on</strong>textual values and preferences of pers<strong>on</strong>s<br />
affected by the <str<strong>on</strong>g>recommendati<strong>on</strong>s</str<strong>on</strong>g>, including<br />
pregnant women, health-<strong>care</strong> professi<strong>on</strong>als and<br />
policy-makers. It was not within the ERG’s remit to<br />
change <str<strong>on</strong>g>recommendati<strong>on</strong>s</str<strong>on</strong>g> previously <strong>for</strong>mulated by<br />
the GDG.<br />
2.4 Technical Working Group (TWG)<br />
The TWG comprised systematic review teams<br />
and guideline methodologists. In relati<strong>on</strong> to<br />
quantitative evidence <strong>on</strong> the effectiveness of different<br />
interventi<strong>on</strong>s, the Cochrane Pregnancy and Childbirth<br />
Group (PCG) provided input <strong>on</strong> the scoping of the<br />
guideline and supervised the updating of all relevant<br />
systematic reviews following the standard processes<br />
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