3.2.1 Definitions of the latent and active first stages of labour | Guidance and protocols for health care facilities without availability of caesarean section will need to be developed that are context- and situation-specific. Introduction of these new definitions and concepts should involve pre-service training institutions and professional bodies, so that training curricula for intrapartum care can be updated as quickly and smoothly as possible. Labour monitoring tools will need to be updated and/or developed to facilitate the new approach. Practice manuals and labour ward protocols will need to be updated and disseminated.
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3.2.2 Duration of the first stage of labour |
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3.2.3 Progress of the first stage of labour |
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3.2.4 Labour ward admission policy | This recommendation requires a well functioning health system with a sufficient number of trained health care professionals. It is important that health care professionals clearly communicate the reason for delaying admission to women in latent labour, and provide them with encouragement, support and advice on how to manage uncomfortable contractions, how to recognize active labour and, if a woman chooses to go home, when to return to the hospital.
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3.2.5 Clinical pelvimetry on admission | |
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3.2.6 Routine assessment of fetal well-being on labour admission | In settings where cardiotocography (CTG) is performed routinely on admission for labouring women with no risk factors for adverse outcomes, it is important to inform health care professionals and other stakeholders that this practice is not evidencebased and increases the risk of unnecessary medical interventions. Policy-makers and relevant stakeholders need to consider how records from auscultation can be validated for use in the defence against potential litigation claims, instead of reliance on admission CTG for this purpose.
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3.2.10 Continuous cardiotocography during labour | The GDG panel is aware that in some countries and settings, continuous CTG is used to protect against litigation. In such settings, health care professionals and women should be advised that this practice is not evidence-based and does not lead to better outcomes. Clinicians might be better protected against litigation by keeping good medical notes and records, which clearly indicate findings of intermittent auscultation (IA), than by relying on continuous CTG tracings.
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3.2.11 Intermittent fetal heart rate auscultation during labour | Policy-makers should consider what method(s) is/are most feasible in their settings. In low-resource settings, Pinard fetal stethoscope would be the most feasible method for intermittent auscultation (IA) as it is not associated with ongoing costs related to supplies and equipment maintenance, and has no infrastructural requirements (e.g. power supply). A practical approach in low-resource settings might be to firstly ensure widespread availability and competence of health care providers to conduct IA with the Pinard fetal stethoscope. Then, as resources become available, the Doppler ultrasound device could be introduced with appropriate pre-service and in-service training. In settings with a high prevalence of litigation, policy-makers and relevant stakeholders need to consider whether records from non-electronic fetal monitoring (and IA in general) would be valid in the defence against potential litigation claims.
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3.2.12 Epidural analgesia for pain relief | Policy-makers need to determine which pain relief measures are most feasible and acceptable in their settings. Facilities offering epidural analgesia need to have staff with the appropriate specialist skills (anaesthetists, obstetricians) as well as equipment and systems in place to monitor, detect and manage any undesirable effects of the procedure during and after labour to ensure the safety of mother and baby. Epidural analgesia should not be introduced in settings where these resources are not consistently available. Systems should be in place to ensure adherence to standardized protocols for epidural analgesia, including correct drugs, doses, techniques, staffing levels and other resource requirements. Oxygen, resuscitation equipment and appropriate drugs for resuscitation should be readily available in labour and postnatal wards where women who have undergone epidural analgesia are cared for. Health care providers and women should be aware that epidural analgesia is a significant procedure that can lead to serious complications. The benefits and risks associated with epidural analgesia should be clearly explained to women considering this method of pain relief. Signed informed consent is necessary for all women undergoing epidural analgesia. Setting-specific protocols for assessing a woman's need for pain relief and for providing a range of pharmacological and non-pharmacological options should be developed to guide clinical management, to support women's decision-making, and to ensure safe and equitable provision of pain relief. Health care professionals should communicate to women the pain relief options available for labour and birth at their facility, and should discuss the advantages and disadvantages of these options, as part of antenatal care education and counselling. A woman's choice of pain relief during labour, if pain relief is required, should be confirmed on admission in labour. In addition, she should be free to change her mind about the type of pain relief she would like if she feels the need to do so. Health care facilities providing pharmacological options for pain relief, including epidural analgesia, should ensure that they have adequately trained staff, clear protocols and the necessary equipment to manage complications, should they arise. Mechanisms should be in place at facilities offering pharmacological pain relief options to ensure that the necessary drugs are kept in stock and can be dispensed when needed. Health care facilities offering epidural analgesia during labour should conduct regular audit and feedback procedures to ensure adherence to clinical protocols and to monitor complications.
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3.2.13 Opioid analgesia for pain relief | Policy-makers need to determine which pain relief measures are most appropriate (feasible and acceptable) in their settings, in consultation with health care professionals and the women using their facilities. Opioid analgesia is not suitable in settings where women and babies cannot be adequately monitored due to staff shortages, or where resuscitation skills, equipment and supplies (oxygen, appropriate drugs) are lacking. Setting-specific protocols for assessing a woman's need for pain relief and for providing a range of pharmacological and non-pharmacological options should be developed to guide clinical management, to support women's decision-making, and to ensure safe and equitable provision of pain relief. Health care facilities providing opioid analgesia should ensure that personnel skilled in performing resuscitation are among the staff on duty at all times. Health care facilities should monitor adherence to clinical protocols and complications related to opioid use (particularly maternal and neonatal respiratory depression) to reduce iatrogenic outcomes. Health care professionals should communicate to women the pain relief options for labour and birth available at their facility, and should discuss the advantages and disadvantages of these options, as part of antenatal care education and counselling. Health care facilities providing pharmacological options for pain relief, including opioid analgesia, should ensure that they have adequately trained staff, clear protocols and the necessary equipment to manage complications, should they arise. Mechanisms should be in place at facilities offering pharmacological pain relief options to ensure that the drugs are kept in stock and can be dispensed when needed. Opioid medication needs to be securely stored and a register kept of its dispensing, to reduce the risk of abuse.
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3.2.14
Relaxation techniques for pain management
3.2.15
Manual techniques for pain management | Health care professionals should communicate to women the pain relief options for labour and birth available at their facility, and should discuss the advantages and disadvantages of these options as early as possible in labour, and ideally as part of antenatal care education and counselling. Training institutions could cover these techniques in health care professionals’ pre-service and in-service training. For lay companions, basic training in these techniques could be facilitated during the antenatal period.
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