Volume 15 Supplement 1
Reducing risks of fetal injury and stillbirths caused by infection/inflammation using healthy behaviors
© McGregor et al; licensee BioMed Central Ltd. 2015
Published: 15 April 2015
Potentially preventable morbid or lethal vertical infections are more common in pregnancy than is recognized . Research suggests about 11% of stillbirths (SBs) in developed countries are caused by infection versus WHO-sponsored estimates of 38% worldwide [2, 3]. Advances in diagnostic technologies, pregnancy immunology, and systematic surveys (“Human Microbiome Project”) have enabled new understanding of primary prevention of pregnancy/lactation-associated infection [3, 4]. What is lacking is a systematic vigorously designed and adequately funded research agenda to provably reduce risks of individual or population-based risks of pregnancy infection. Lacking such “evidence-based” recommendations, some researchers suggest that, except for syphilis and vaccine-preventable infections, there are no satisfactory proven approaches to prevent infection-caused stillbirth . Therefore, we used accumulated knowledge to formulate behavioral “no/low cost” and practicable/actionable pathobiologically and behaviorally informed recommendations to allow families and policy makers to reasonably reduce risks of maternal and pregnancy infection that cause SB. Evidence-based recommendations await controlled trials in suitable populations.
Changes in personal (“lifestyle”) behaviors are now demonstrated to be cost-effective means to enhance individual and population measures of complex chronic diseases. The Institute of Medicine strongly recommends behavioral approaches for preventing common complex diseases such as coronary artery disease (CAD) and stroke .
Primary behaviors for prevention of infection-caused fetal injury or death (stillbirth)
1. “Safe food” (selection, preparation, handwashing)
Enteropathogens (E. coli, Salmonella ssp.)
Ebola (per the CDC, Ebola is not spread in general by food; however, in Africa, Ebola may be spread as a result of handling bushmeat)
2. “Safe sex” (no new partners)
HSV (herpes) 1 and 2
3. “No (bug) bites” (zoonosis, mosquitoes, ticks, flies) and “avoid exposure to infectious animals”
West Nile Virus
Tickborne infections (Rocky Mountain spotted fever, etc.)
Lymphocytic choriomeningitis virus (LCMV)
4. “Hygiene and oral health” (reduce body fluid exposure and bad mouth bacteria/inflammation)
Hepatitis A, B, C
5. “Pregnancy” (follow CDC-recommended protocols)
Group B Streptococcus (GBS)
6. “Optimize pregnancy and birth management to reduce/eliminate ascending infections”
“H” prompts the personal imperatives of handwashing to reduce risks of multiple infections (listeriosis, toxigenic E. coli, and many enteropathogens as well as hand-to-hand spread of influenza viruses) acquired by fecal handling. Handwashing is strongly suggested (without formal evidence) for prevention of cytomegalovirus (CMV) infection during pregnancy, especially among medical personnel and caretakers of toddlers .
“Y” prompts the slogan’s “yes” to walking and exercise, but “no” to insect bites including both 1) mosquitoes which can cause malaria, malaria-like parasitemias, dengue fever agents, West Nile virus and other viral encephalopathies, and 2) multiple tick vectors for Rocky Mountain spotted fever and Lyme disease (Borrelia burgdorferi). The CDC widely recommends means to avoid tick bites (such as avoiding tick-infested areas), routine examination for ticks, and prompt, safe removal if found . Means to prevent mosquito bites include elimination of possible breeding areas and mosquito bed netting in malarial areas. .
“G” prompts prevention of gastrointestinal illness, including reducing risks of listeriosis (Listeria monocytogenes) and toxoplasmosis (Toxoplasma gondii) [9, 10] as well as enteropathogens, not only by handwashing, but also by safe food selection, preparation, and handling .
“I” prompts performance of CDC-recommended immunizations, including rubella, tetanus, influenza, pertussis, viral hepatitis, and yellow fever, in travellers to endemic areas. Newer vaccines such as the tetrapotent vaccine for dengue fever are proven effective, but not yet recommended in pregnancy. Vaccines against multiple other stillbirth-causing infections, including herpes viruses (HSV 1 and 2), cytomegalovirus, other microorganisms including group B Streptococcus, Leptospira, the agents of Q fever and malaria, and common sexually transmitted infections as well as Ebola and human parvovirus (HPV-B19), may hold considerable promise if they become available [12, 13].
“E” mandates consideration of avoiding exposure to infectious stillbirth agents including CMV and human parvovirus (HPV-B19) among susceptible women (daycare providers, teachers, medical personnel, and others who care for children with potentially infectious secretions and coughs). Other infections potentially preventable by eliminating exposure include malaria, malaria-like infections, Lyme disease, and multiple other mosquito and tickborne vector-transmitted infections. Importantly, meth mothers and their sexual partners can prevent infections including syphilis and other sexually transmitted infections/diseases (STIs/STDs) and HIV by avoiding unsafe sexual practices .
“N” stands for “natal” (“pregnancy”) and prompts recognition of pregnancy providers’ “standard of practice” responsibilities to complete recommended screening and indicated treatment of stillbirth-implicated infections including syphilis, rubella, urinary tract infections and bacteriuria, and abnormal vaginal microflora including bacterial vaginosis (BV) and group B Streptococcal infection or colonization .
New expert clinical suggestions for early pregnancy GBS screening by routine antenatal urine culture are increasingly voiced. Some experienced clinicians recommend routine GBS bacteriuria testing for every pregnant woman and, if positive, treatment with oral penicillin. Treatment for any infection in pregnancy is to be followed by a confirmatory “test of cure”. Other obstetrical checklist items are listed in Table 1. New clinical recommendations to prevent “ascending” intrauterine infection include optimizing labor care to prevent “dystocia” and vigorous screening and treatment of all abnormal vaginal bacteria “dysbiosis”. Intrusive “stripping of membranes” to induce labor is both clinically ineffective and may transmit potential cervico-vaginal pathogenic microorganisms into the uterus. Avoidance of this practice is recommended by some experts.
Finally “E” reminds families and practitioners of the increasing role of microbes’ ability to induce damaging placental and fetal inflammation. Work by Nuova and others have shown that multiple types of microorganisms that cause placental inflammation, including enteroviruses (especially Coxsackie viruses), are increasingly implicated in both abortion and stillbirth .
Except for syphilis and both influenza and viral hepatitis which are vaccine-preventable, neither enteroviruses or the more common clinically recognizable infection causes of fetal death have reliably proven primary prevention strategies. In the absence of proven vaccination practices, “HYGIENE”-prompted “healthy pregnancy behaviors“ by both families and pregnancy providers offer potentially powerful protection against stillbirth-associated infections until more specific prevention strategies including vaccination are demonstrated in well-controlled trials and authoritatively recommended.
- Hogue CJ, Parker CB, Silver RM, et al: A population-based case-control study of stillbirth: the relationship of significant life events to the racial disparity for African Americans. American Journal of Epidemiology. 2013, 177 (8): 755-67. 10.1093/aje/kws381.View ArticlePubMedPubMed CentralGoogle Scholar
- Stillbirth Collaborative Research Network Group: Causes of death among stillbirths. JAMA. 2011, 306 (22): 2459-2468.View ArticleGoogle Scholar
- Bhutta ZA, Das JK, Bahl R, et al: Can available interventions end preventable deaths in mothers, newborn babies, and stillbirths, and at what cost?. The Lancet. 2014, 384 (9940): 347-370. 10.1016/S0140-6736(14)60792-3.View ArticleGoogle Scholar
- McClure EM, Goldenberg RL: Infection and stillbirth. Seminars in Fetal and Neonatal Medicine. 2009, 14 (4): 182-9. 10.1016/j.siny.2009.02.003.View ArticlePubMedPubMed CentralGoogle Scholar
- Institute of Medicine (US) Committee on Health and Behavior: Research, Practice, and Policy. Health and Behavior: The Interplay of Biological, Behavioral, and Societal Influences. 2001, Washington (DC): National Academies Press (US), [http://www.ncbi.nlm.nih.gov/books/NBK43743/]Google Scholar
- Centers for Disease Control and Prevention: Cytomegalovirus (CMV) and Congenital CMV Infection. [http://www.cdc.gov/cmv/prevention.html]
- Centers for Disease Control and Prevention: Avoiding Ticks. [http://www.cdc.gov/ticks/]
- World Health Organization: Malaria in pregnant women. [http://www.who.int/malaria/areas/high_risk_groups/pregnancy/en/]
- United States Department of Agriculture: Protect Your Baby and Yourself From Listeriosis. [http://www.fsis.usda.gov/wps/portal/fsis/topics/food-safety-education/get-answers/food-safety-fact-sheets/foodborne-illness-and-disease/protect-your-baby-and-yourself-from-listeriosis/CT_Index]
- Centers for Disease Control and Prevention: Parasites – Toxoplasmosis (Toxoplasma infection). [http://www.cdc.gov/parasites/toxoplasmosis/]
- Centers for Disease Control and Prevention: Recipe for Food Safety. 2013, [http://www.cdc.gov/vitalsigns/listeria/]Google Scholar
- Centers for Disease Control and Prevention: Leptospirosis. [http://www.cdc.gov/leptospirosis/prevention/index.html]
- Centers for Disease Control and Prevention: Q Fever. [http://www.cdc.gov/qfever/info/index.html]
- Centers for Disease Control and Prevention: Sexually Transmitted Diseases (STDs). [http://www.cdc.gov/std/pregnancy/]
- Centers for Disease Control and Prevention: Overview of 2010 Guidelines. [http://www.cdc.gov/groupbstrep/guidelines/new-differences.html]
- Nuova GJ, Cooper LS, Bartholomew D: Histologic, infectious, and molecular correlates of idiopathic spontaneous abortion and perinatal mortality. Diagn Mol Pathol. 2005, 14 (3): 152-8. 10.1097/01.pas.0000176769.18423.37.View ArticleGoogle Scholar
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