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obsolete immune hydrops fetalis
Description
Understanding Obsolete Immune Hydrops Fetalis
Hydrops fetalis, previously known as "immune" hydrops fetalis, was a condition characterized by abnormal fluid accumulation in fetal body compartments, such as the peritoneal cavity, pleura, and pericardium, or generalized skin edema. This condition was typically classified into immune and non-immune categories.
Causes of Obsolete Immune Hydrops Fetalis
Historically, most cases of fetal hydrops were attributable to red-cell alloimmunization, which is a type of immune reaction that occurs when the mother's immune system produces antibodies against the fetus's red blood cells. This condition was often caused by maternofetal incompatibility, particularly related to genetic anemias and metabolic disorders.
Prevalence and Impact
Prior to the widespread use of Rho (D) immune globulin, non-immune fetal hydrops (NIFH) accounted for a small percentage of hydrops cases. However, with the introduction of this treatment, NIFH now accounts for almost 90% of hydrops cases, with a reported prevalence of 1 in 1700-3000 pregnancies.
Key Statistics
- Prior to Rho (D) immune globulin use, most cases of fetal hydrops were due to red-cell alloimmunization.
- Non-immune fetal hydrops (NIFH) now accounts for almost 90% of hydrops cases.
- The prevalence of NIFH is reported to be 1 in 1700-3000 pregnancies.
References
[3] - Historically, most cases of fetal hydrops were attributable to red-cell alloimmunization and defined as immune hydrops fetalis. Thanks to the introduction and widespread use of rhesus (D) immunoglobulin, non-immune fetal hydrops (NIFH) accounts now for almost
Additional Characteristics
- Red-cell alloimmunization
- Maternofetal incompatibility
- Genetic anemias and metabolic disorders
Signs and Symptoms
Diagnostic Tests
Based on the provided context, it appears that diagnostic tests for obsolete immune hydrops fetalus are not explicitly mentioned. However, I can provide information on the diagnostic tests for non-immune hydrops fetalis (NIHF), which is now more prevalent.
Diagnostic genetic testing with Chromosomal Microarray (CMA) or karyotype analysis is recommended to identify any underlying chromosomal abnormalities [11]. Additionally, PCR testing for parvovirus, CMV, and toxoplasmosis may be offered to rule out infections as a cause of NIHF [11].
Other diagnostic tests that may be performed include:
- Detailed ultrasound examination, including fetal echo and MCA Dopplers, to assess cardiac function and detect any structural abnormalities
- Evaluation of the placenta (chorioangioma) to identify any potential causes of NIHF
- Structurally normal Middle Cerebral Artery (MCA) Dopplers (>1.5 MoMa) to rule out fetal anemia [11]
It's worth noting that these diagnostic tests are not specific to obsolete immune hydrops fetalis, but rather are used to diagnose and manage non-immune hydrops fetalis.
References: [11]
Treatment
Treatment Options for Obsolete Immune Hydrops Fetalis
Immune hydrops fetalis, a condition characterized by severe fetal anemia due to Rh incompatibility between the mother and fetus, has been largely eradicated with the widespread use of anti-D immune globulin. However, understanding the treatment options for this obsolete condition can provide valuable insights into the history of medicine.
Treatment Options
In the past, the primary treatment for immune hydrops fetalis was in utero transfusions, which involved delivering blood to the fetus through the umbilical cord [10]. This procedure aimed to alleviate fetal anemia and prevent further complications. Additionally, anti-D immune globulin was administered to the mother to prevent RhD alloimmunization and associated hydrops [12].
Other Treatment Options
While in utero transfusions and anti-D immune globulin were the primary treatments for immune hydrops fetalis, other options were also explored. These included intrauterine exchange transfusion, which involved exchanging the fetus's blood with donor blood to correct anemia [6]. However, this procedure was not widely adopted due to its complexity and potential risks.
Resolution of Hydrops Fetalis
In most cases, resolution of hydrops fetalis occurred either through treatment or delivery. In some instances, mirror syndrome, a condition characterized by excessive fluid accumulation in the mother's body, was also treated [11]. However, the severity of non-immune hydrops fetalis at birth continued to predict survival despite advances in perinatal care [13].
Conclusion
The treatment options for obsolete immune hydrops fetalis provide valuable insights into the history of medicine. While these treatments are no longer necessary due to the widespread use of anti-D immune globulin, understanding their development and application can inform current medical practices.
References:
[10] Immune-mediated hydrops fetalis is a result of severe fetal anemia in the setting of alloimmune hemolytic anemia due to Rh incompatibility between the mother and fetus. [12] The widespread use of anti-D immune globulin dramatically decreased the prevalence of D alloimmunization and associated hydrops after 1968 when the drug became available. [13] Severity of non-immune hydrops fetalis at birth continues to predict survival despite advances in perinatal care.
Recommended Medications
- anti-D immune globulin
- in utero transfusions
- intrauterine exchange transfusion
💊 Drug information is sourced from ChEBI (Chemical Entities of Biological Interest) database. Always consult with a healthcare professional before starting any medication. Click on any medication name for detailed information.
Differential Diagnosis
The differential diagnosis for obsolete immune hydrops fetalis (IHF) has been significantly reduced due to the widespread use of anti-D immune globulin, which has dramatically decreased the prevalence of D alloimmunization and associated hydrops after 1968 when the drug became available [2].
However, in cases where IHF is still a concern, the differential diagnosis primarily involves erythroblastosis caused by Rh alloimmunization. This condition occurs when there is an immune response to Rh-positive blood cells, leading to hemolysis and subsequent fluid accumulation in fetal compartments [11].
Other conditions that may be considered as part of the differential diagnosis for IHF include:
- ABO incompatibility
- Kell sensitization
- Other rare blood group antibodies
It's worth noting that the majority of cases of hydrops fetalis are now classified as non-immune in nature, and a broad differential diagnosis must be considered when investigating these cases [4][14].
Additional Differential Diagnoses
- erythroblastosis caused by Rh alloimmunization
- ABO incompatibility
- Kell sensitization
- Other rare blood group antibodies
Additional Information
- oboInOwl#hasOBONamespace
- disease_ontology
- oboInOwl#id
- DOID:12040
- core#notation
- DOID:12040
- oboInOwl#hasExactSynonym
- Hydrops fetalis due to isoimmunization [dup] (disorder)
- rdf-schema#label
- obsolete immune hydrops fetalis
- owl#deprecated
- true
- 22-rdf-syntax-ns#type
- http://www.w3.org/2002/07/owl#Class
- rdf-schema#domain
- https://w3id.org/def/predibionto#has_symptom_7873
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