Grant C. Fowler MD, in Pfenninger and Fowler's Procedures for Primary Care, 2020 Detection of fetal heart activity by the second and
third trimester of pregnancy should be reliable by transabdominal scanning [seeChapter 142, Obstetric Ultrasound]. Earlier detection may require transvaginal scanning. The absence of fetal cardiac activity and fetal movement after scanning for a 5-minute interval in a pregnancy of more than 20 weeks’ gestation is said to be 100% reliable for diagnosing a fetal demise. For a
first-trimester pregnancy, if uncertainty exists about fetal heart activity, rescanning should be performed in 1 to 2 weeks. Secondary criteria for fetal demise using POCUS include fetal anomalies such as hydrops, ascites, and pleural or pericardial effusions. Echogenic gas in the fetal heart and vessels may be early findings. Late findings include morphologic changes such as skeletal anomalies and unusual fetal positioning. Reaction to external stimulation or uterine manipulation should cause brisk reflexes in viable fetuses, as opposed to the passive motions seen with a fetal demise. Avoid misinterpreting the passive motions from uterine contractions around a dead fetus as fetal activity. Because abruptio placentae cannot always be diagnosed with ultrasound [i.e., it is a clinical diagnosis], ultrasound studies should be used in
conjunction with maternal–fetal monitoring in the pregnant patient with significant abdominal trauma. A 4-hour monitoring period should be sufficient to identify fetal distress.Emergency Department, Hospitalist, and Office Ultrasound [POCUS]
Evaluation of Fetal Viability
Interpretation
PATHOLOGY OF THE PLACENTA: AN INTRODUCTION AND OVERVIEW
Harold Fox MD FRCPath FRCOG, Neil J. Sebire MB BS BClinSci MD DRCOG MRCPath, in Pathology of the Placenta [Third Edition], 2007
Abnormal cardiotocograph [CTG]
Fetal wellbeing before and during labour is usually assessed by recording of the fetal heart rate in relation to uterine contractions in the form of a cardiotocograph tracing [CTG]. There are well-established parameters indicating normality and abnormality according to gestational age [Gauge & Henderson 1999] and an ‘abnormal’ cardiotocographic pattern usually means either persistent fetal tachycardia or bradycardia, or abnormal decelerations following contractions in the form of persistent variable or late decelerations. These abnormal findings indicate abnormalities in the fetal cardiovascular response and may be associated with fetal hypoxia. In the context of pathological examination of the placenta, an ‘abnormal’ cardiotocograph should therefore prompt a search for features of underlying conditions likely to contribute to fetal hypoxia such as uteroplacental vascular disease; cord lesions and cord compression are also potent causes of fetal hypoxia and of abnormal tocographic traces. In many cases however, there is no underlying detectable morphological abnormality, the cardiotocographic features being a consequence of excessive stimulation of contractions in labour.
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Obstetric Factors Associated with Infections of the Fetus and Newborn Infant
Christopher B. Wilson MD, in Remington and Klein's Infectious Diseases of the Fetus and Newborn Infant, 2016
Preterm Premature Rupture of the Membranes Before Fetal Viability
The recommended approaches to PPROM before 23 to 24 weeks of gestation include labor induction or expectant management because the fetus is not yet viable. With expectant management for PROM before fetal viability, the latency period is relatively long [mean, 12-19 days; median, 6-7 days],281-285 although this may not achieve a gestational age consistent with neonatal survival. Neonatal survival depends on the gestational age at membrane rupture and duration of the latent period. In cases with PPROM at less than 23 weeks, the perinatal survival rate was 13% to 47%; with PPROM at 24 to 26 weeks, it was 50%. The incidence of stillbirth is greater [15%] with midtrimester PPROM than with later PPROM [1%]. The incidence of lethal pulmonary hypoplasia is 50% to 60% when membrane rupture occurs before 19 weeks.286 Although maternal clinically evident infections are common [chorioamnionitis: 35%-59% and endometritis: 13%-17%] few of these infections are serious; however, maternal death from sepsis has been reported.283,285 If labor induction is chosen, after appropriate counseling, it can be facilitated by usual obstetric methods such as oxytocin or misoprostol administration.
Anthropology: Forensic Anthropology and Childhood
P. LefèvreF. BeauthierJ.-P. Beauthier, in Encyclopedia of Forensic and Legal Medicine [Second Edition], 2016
Infanticide and Death in the Neonatal Period
Viability of the Fetus
Fetal viability is a major issue that is dependent on the evolution and progress of modern neonatology [Beauthier, 2007]. It is generally accepted that a 28-week-old fetus that doesn't need resuscitation is viable. However, according to WHO, fetal viability is possible after 20 weeks of fetal life [22 weeks of amenorrhea].Anthropometrical characteristics as well as clinical parameters of fetal age estimation are of high importance.
Determination of Fetal Age
A simple way to calculate fetal age [in lunar months] is to divide the fetal length [in cm] by 4 for fetuses less than 5 months' gestation. If it is less than 5 months' gestation the length [in cm] is divided by 5. Anthropometric measurements collected during examination of the fetus are used to estimate its age more accurately [Beauthier, 2011b]. Three types of data can be gathered from radiologic investigations [Scheuer et al., 1980]:
•direct fetal age estimation from measurement of the length of long bones [Scheuer et al., 1980];
•fetal age estimation from measurement of the long bones and calculation of fetal stature [crown–heel or crown–rump length] [O'Rahilly and Müller, 2001; Scheuer and Black, 2004]; and
•a more difficult method involving the degree of deciduous teeth calcification; this method requires the conservation of dental crowns and is not particularly suitable for this type of investigation.
Scheuer reports the following values from her study on full-term fetuses in the UK [Scheuer et al., 1980]:
•crown–rump length: from 28 to 32 cm; and
•crown–heel length: from 48 to 52 cm.
Various authors have highlighted the importance of long bones radiography, in particular the fetal femoral diaphysis [Odita et al., 1982; Piercecchi-Marti et al., 2002]. A study was carried out to investigate the fidelity and reproducibility of the radiographic methods used for measuring the femoral diaphysis [Adalian et al., 2001]. The regression equation obtained was as follows:
Fetalage[inweeks]=6.93+0.434×femurlength[inmm]
The lower limb centers of ossification [distal epiphysis of the femur, proximal epiphysis of the tibia, posterior tarsus] are of great practical interest.
Echographic examination can provide useful information in the living subject.
Many studies have been carried out using ultrasonography, with a focus on the length of fetal long bones [Jeanty et al., 1984], the length of the femur, the relationship between the length of the femur and fetal weight [Honarvar et al., 2001], biparietal diameter, and cephalic and abdominal perimeters [Davis et al., 1993; Nasrat and Bondagji, 2005; Yagel et al., 1986]. Using ultrasonography other authors have examined the relationship between fetal weight, abdominal perimeter, and femur length, and a mathematical model was proposed [Ferrero et al., 1994].
Table 2 shows some useful anthropometric and visceral parameters in the full-term fetus.
Table 2. Anthropometric and visceral parameters of the full-term fetus
Weight | 3250–3500 g |
Stature | 50 [range 48–52] cm |
Crown–rump length | 28–32 cm |
Maximum cranial perimeter [large cranial circumference] | 37 cm |
Minimum cranial perimeter [small cranial circumference] | 33 cm |
Biparietal diameter | 9.5 cm |
Bitemporal diameter | 8 cm |
Occipito-gnathion diameter | 13 cm |
Occipito-frontal diameter | 11.5 cm |
Suboccipito-frontal diameter | 11 cm |
Subgnathion-bregmatic vertical diameter | 9.5 cm |
Suboccipito-bregmatic diameter | 9.5 cm |
Abdominal perimeter [at umbilical] | 30 cm |
Transverse abdominal diameter | 9.5 cm |
Bitrochanteric diameter | 9 cm |
Length of long bones – average values in brackets [Fazekas and Kósa, 1978; Scheuer and Black, 2004] | |
Length of humerus | 61.6–70 mm [64.9 mm] |
Length of radius | 47.5–58.0 mm [51.8 mm] |
Length of ulna | 55.0–65.5 mm [59.3 mm] |
Length of femur | 69.0–78.7 mm [74.3 mm] |
Length of tibia | 60.0–71.5 mm [65.1 mm] |
Length of fibula | 58.0–68.5 mm [62.3 mm] |
Weight of left lung | 25 g |
Weight of right lung | 30 g |
Weight of heart | 18 g |
Weight of liver | 100–125 g |
Weight of spleen | 9 g |
Weight of brain | 350 g |
Centers [points] of ossification | Full-term fetus [40 weeks] |
Calcaneus [appearance: 27th week] [between 24th and 28th weeks] | + |
Talus [appearance: 28th week] | + |
Femur distal epiphysis [knee] [appearance: 37th week] | + |
Tibia proximal epiphysis [knee] [appearance: 40th week] | + |
Source: Beauthier, J-P., 2011a. La problématique du foetus et du nouveau-né en médecine légale. In: Beauthier, J-P. [Ed.], Traité de Médecine Légale. Bruxelles: De Boeck Université, pp. 389–402.
Signs Observed in the Stillborn Baby
Differentiating between the stillborn baby and the child who has not lived is not easy. The phenomena of maceration [aseptic autolysis which occurs when the fetus dies in utero] and putrefaction [postmortem ex utero deterioration] can notably complicate the medicolegal approach.
Descriptions of the criteria of extrauterine life are based on the existence of respiratory events and an effective circulatory system after birth. Cardiovascular function is evident in children who are victims of physical violence in particular [bruising, vital tegumentary lesions, associated fractures, and hemorrhage]. Ventilatory function is assessed by histological study of the lung, and the presence or absence of territorial atelectasis is established. Multiple samples are required to clarify the matter.
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Obstetric Ultrasound : Imaging, Dating, Growth, and Anomaly
Mark B. Landon MD, in Gabbe's Obstetrics: Normal and Problem Pregnancies, 2021
M-Mode
For most obstetric applications, the familiar two-dimensional [2D] grayscale real-time ultrasound is used. This is formally known asB-mode ultrasound. Another ultrasound modality that is available on most machines is referred to asM-mode ultrasound [motion mode]. M-mode ultrasound shows changes along a single ultrasound beam over time. M-mode is useful for documenting the presence and rate of fetal cardiac contractions [Fig. 9.3,eFig. 9.6] and is also used for specialized echocardiography applications, such as defining cardiac arrhythmias [eFig. 9.7].
eFig. 9.6. M-Mode Application in an 8-Week-Old Fetus. The row of dots in theleft panel indicates the location of echoes, in this case cardiac pulsations, being displayed over time in theright panel. M-mode is preferred to Doppler for documenting fetal viability before 10
weeks. Note the prominent brain vesicle in the fetal head, a normal finding. eFig. 9.7. M-Mode Ultrasound Demonstrating Premature Atrial Contractions. The cursor line passes through the left ventricle[LV] then the right atrium[RA]. The movement along the cursor
line over time is shown in the lower display. Thered arrows show ventricular contractions, and thegreen arrows show atrial contractions. Note that when there is a premature atrial contraction[magenta arrow], the ventricle is in a refractory state, resulting in a pause between contractions.
Best Practice for Quantifying the Microscopic Structure of Mouse Placenta
Mariana M. Veras, ... Terry Mayhew, in The Guide to Investigation of Mouse Pregnancy, 2014
Overview
Fetal well-being depends on a satisfactorily functioning placenta. A proper understanding of the placenta requires an integrated approach that embraces all the biomedical disciplines including anatomy/morphology. As for other organs and tissues, information about three-dimensional [3D] structure is needed in order to better understand the processes by which the placenta develops, grows, and serves the needs of the embryo-fetus during normal and compromised pregnancies.1–6
Whether a quantitative or qualitative approach is adopted, methods for correlating structure and function need to be objective, precise [reliable, reproducible], unbiased or minimally biased [no or little systematic error], and efficient [giving a reasonable precision per unit of cost expressed as time, effort, or expense]. The generation of hard [biologically useful] information about structure also raises issues of study design.
Biological structures exist and operate in 3D space, so valid interpretation of their functional relevance must recognize this fact. This is especially critical in the realms of optical and electron microscopy, where fine resolution of microstructure relies on cutting specimens into thin slices. In fact, the process of thin sectioning has several practical consequences. First, it limits the fraction of the specimen that can be examined; therefore, one needs to be confident that the fraction finally examined fairly reflects the whole. This implies that the sampling process itself is critical. Second, sectioning reduces 3D reality to a two-dimensional [2D] or planar representation. Thus, volumes appear on section planes as profile areas, surfaces appear as linear features [known as boundary traces], and linear structures [e.g., blood vessels] and particulate structures [e.g., cells and their nuclei] appear as transections or profiles. Therefore, there is a need for tools that allow researchers to extrapolate 3D quantities from those displayed on 2D images. Failure to recognize these consequences of sectioning will impair or frustrate the ability to draw hard biological interpretations.
Stereology7–10 provides valuable tools for obtaining functionally relevant 3D quantitative information at different levels of structural organization of biological specimens. Validity and efficiency are determined by designing random sampling methods at different stages of the hierarchical procedure for preparing specimens for microscopic examination.5,11 This includes selecting tissue blocks from the organ, cutting histological and other thin sections, and selecting microscopic fields of view [FOVs]. Stereological tools have been applied successfully to placentas of different types, from mouse to human, and to investigate a variety of relevant processes, including placental growth and development, oxygen transport, fetoplacental angiogenesis, trophoblast turnover, immunogold-labeled protein localization, and the effects of maternal diet, environmental pollution, and pregnancy complications.1–6,12–23
In this chapter, we describe how to apply state-of-the-art stereology for basic morphofunctional analysis of the mouse placenta. Broadly speaking, stereological analysis involves a two-step process: [1] randomly sampling the organ/tissue/cell to generate sets of mechanical or optical sections and [2] sizing and/or counting structural features of interest on the sampled sections using appropriate geometric probes [test points, lines, planes or volumes].
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Fetal Heart Failure
Edgar T. Jaeggi, Mary T. Donofrio, in Heart Failure in the Child and Young Adult, 2018
Prenatal Assessment
Introduction
Assessments of the fetal well-being and cardiac function and identification of a likely disease mechanism are important diagnostic steps in the clinical evaluation of the fetus with cardiac compromise. Table 28.1 summarizes the echocardiographic features of the main conditions associated with in-utero HF. The prenatal diagnosis of HF primarily relies on the ultrasound-based documentation of systolic and/or diastolic cardiac dysfunction and the circulatory consequences [31].
Table 28.1. Echocardiographic Features of Conditions Associated With Fetal Heart Failure
Myocarditis• Viral •Anti-Ro/SSA antibodies | – | N or ↑ | ↓ | ↓ | N or ↓ | Pericardial effusion Anemia; ischemia; hypoalbuminemia Myocardial echogenicity; CHB |
Nonhypertrophic CM | – | N or ↑ | ↓ | ↓ | ↓ | EFE; calcifications; NC; other anomalies |
Hypertrophic CM | Global | N | ↓ | N | ↓ | Other anomalies |
Diabetic hypertrophy | IVS > free wall | N | N or ↓ | N | N | Macrosomia |
TTTS [recipient] | RV > LV | ↑ | RV > LV | RV > LV | ↓ RV > LV | Polyhydramnios |
Vascular tumors; TRAP | – | ↑ | N | ↑ | ↑ | Dilated systemic vein[s] |
Agenesis of the DV | – | ↑ | N | ↑ | ↑ | Dilated umbilical vein |
Constriction of the DA | – | ↑ RV | ↓ RV | ↓ RV | ↓ RV | Tricuspid regurgitation |
Fetal anemia | – | ↑ | N | ↑ | ↑ | ↑ peak MCA Doppler flow |
Fetal hypoxemia ± acidosis | – | ↑ | N or ↓ | N or ↓ | N or ↓ | Brain sparing |
CCAM | – | ↓ | ↓ | N or ↓ | ↓ | Chest mass |
Large pericardial effusion | – | ↓ | ↓ | N or ↓ | ↓ | Pericardial teratoma |
CCAM, congenital cystic adenomatoid malformations of the lung; CHB, complete heart block; CM, cardiomyopathy; DA, ductus arteriosus; DV, ductus venosus; EFE, endocardial fibroelastosis; MCA, middle cerebral artery; N, normal; NC, ventricular noncompaction; RV > LV, right ventricle more severely affected than the left ventricle; TRAP, twin reversed arterial perfusion sequence; TTTS, twin–twin transfusion syndrome; ↑, increased; ↓, decreased; –, absent.
Measures of the Cardiovascular Status
In early stages of HF, disease manifestations that are readily detectable by echocardiography may be subtle. At more advanced stages [Fig. 28.1], findings include ascites, pleural effusion, pericardial effusion, or a combination of these findings, in addition to cardiomegaly, valvar regurgitation, poly- or oligohydramnios, preferential shunting of blood flow to the brain and heart, absence or reversal of the end-diastolic umbilical artery [UA] flow, and reduced or absent fetal movements. In end-stage HF, generalized skin edema is seen easily over the scalp and abdominal wall.
Figure 28.1. Cardiac four-chamber view of a fetus diagnosed at 30 gestational weeks with a severe form of nonhypertrophic cardiomyopathy of unknown etiology. Findings included massive cardiomegaly, severe biventricular dilatation and dysfunction, and fetal hydrops.
Measures of Cardiac Function
M-mode is useful to quantify the fetal systolic ventricular function by measurements of the changes in ventricular dimensions at the end of diastole [EDD] and of systole [ESD], respectively. Ventricular shortening fraction is calculated as SF [%] = [EDD-ESD]/EDD × 100. An LV or RV SF