public PathologyReportContainer GetReport()
{
var RequestedDate = new DateTimeOffset(2020, 09, 19, 00, 00, 00, TimeSpan.FromHours(10));
var CollectionDateTime = new DateTimeOffset(2020, 09, 20, 08, 20, 00, TimeSpan.FromHours(10));
var SpecimenReceivedDateTime = new DateTimeOffset(2020, 09, 20, 09, 35, 00, TimeSpan.FromHours(10));
var ReportReleaseDateTime = new DateTimeOffset(2020, 09, 22, 11, 15, 00, TimeSpan.FromHours(10));
var ObservationDateTime = ReportReleaseDateTime.Subtract(TimeSpan.FromMinutes(5));
return(new PathologyReportContainer()
{
PathologyReport = new PathologyReport()
{
PerformingLaboratory = LaboratoryFactory.GetPITUSLaboratory(),
Patient = PatientFactory.GetNormanMANNING(),
Request = new Request()
{
RequestedDate = RequestedDate,
OrderNumber = "00000005",
RequestingFacility = new Organisation()
{
Name = "Sunrise Hospital Metabolic Clinic",
Identifier = new Identifier()
{
Value = "75C38DF6-BE0B-4287-8D46-6395CACAAD7A",
Type = IdentifierType.GUID
}
},
RequestingApplication = "Best Practice 1.8.5.743",
RequestingProvider = ProviderFactory.GetTrishFamilyDr(MedicareProviderNumber: "2359622W"),
ClinicalNotes = "? Hereditary haemochromatosis. Arthritis, increased iron stores",
CallBackPhoneNumber = null,
CopyToList = new List <Provider>()
{
ProviderFactory.GetGeneticsClinic(),
ProviderFactory.GetBjornGeneticCounsellor()
}
},
PdfFileName = "Exemplar Report Haemochromatosis gene screening v1.5.pdf",
ReportList = new List <Report>()
{
new Report()
{
ReportId = "1978881777",
CollectionDateTime = CollectionDateTime,
SpecimenReceivedDateTime = SpecimenReceivedDateTime,
ReportReleaseDateTime = ReportReleaseDateTime,
ReportType = new ReportType()
{
Local = new Code()
{
Term = "HFE", Description = "Haemochromatosis gene screening"
},
Snomed = new Code()
{
Term = "401085002", Description = "Haemochromatosis gene screening test"
}
},
ReportStatus = ResultStatusType.Final,
Department = DiagnosticService.Genetics,
ReportingPathologist = ProviderFactory.GetKondoPathologist(),
Panel = new Panel()
{
ResultList = new List <Result>()
{
new Result()
{
Type = new ResultType()
{
Local = new Code()
{
Term = "C28Y",
Description = "C28Y mutation analysis"
},
Lonic = null,
},
DataType = "ST",
Value = "Not Detected",
Units = null,
ReferenceRange = null,
AbnormalFlag = "N",
ObservationDateTime = ObservationDateTime,
Status = ResultStatusType.Final,
ChildResultList = null
},
new Result()
{
Type = new ResultType()
{
Local = new Code()
{
Term = "H63D",
Description = "H63D mutation analysis"
},
Lonic = null,
},
DataType = "ST",
Value = "Homozygous",
Units = null,
ReferenceRange = null,
AbnormalFlag = "N",
ObservationDateTime = ObservationDateTime,
Status = ResultStatusType.Final,
ChildResultList = null
},
new Result()
{
Type = new ResultType()
{
Local = new Code()
{
Term = "RES",
Description = "Results"
},
Lonic = null,
},
DataType = "FT",
Value = "Two copies of the p.His63Asp variant were detected in the patient. The p.Cys282Tyr variant was not detected.\\.br\\" +
"The diagnosis of the most common form of HFE-related hereditary haemochromatosis is excluded.\\.br\\",
Units = null,
ReferenceRange = null,
AbnormalFlag = "N",
ObservationDateTime = ObservationDateTime,
Status = ResultStatusType.Final,
ChildResultList = null
},
new Result()
{
Type = new ResultType()
{
Local = new Code()
{
Term = "INTER",
Description = "Interpretation"
},
Lonic = null,
},
DataType = "FT",
Value = "Hereditary haemochromatosis (HH) is a recessive genetic disorder of iron metabolism. Greater than 90% of HFE\\.br\\" +
"related hereditary haemochromatosis is associated with homozygosity for p.(Cys282Tyr) (c.845G>A; aka p.C282Y).\\.br\\" +
"Compound heterozygosity for p. (Cys282Tyr) and p. (His63Asp) (c.187C>G; aka p.H63D) may be a risk factor\\.br\\" +
"predisposing to mild to moderate forms of iron overload when in association with other risk factors. Both mutations\\.br\\" +
"are detected by real-time PCR amplification and fluorescent detection of alleles.",
Units = null,
ReferenceRange = null,
AbnormalFlag = "N",
ObservationDateTime = ObservationDateTime,
Status = ResultStatusType.Final,
ChildResultList = null
}
}
}
}
}
}
});
}
public PathologyReportContainer GetReport()
{
var RequestedDate = new DateTimeOffset(2019, 09, 23, 00, 00, 00, TimeSpan.FromHours(10));
var CollectionDateTime = new DateTimeOffset(2019, 09, 25, 08, 20, 00, TimeSpan.FromHours(10));
var SpecimenReceivedDateTime = new DateTimeOffset(2019, 09, 25, 11, 15, 00, TimeSpan.FromHours(10));
var ReportReleaseDateTime = new DateTimeOffset(2019, 09, 26, 10, 00, 00, TimeSpan.FromHours(10));
var ObservationDateTime = ReportReleaseDateTime.Subtract(TimeSpan.FromMinutes(5));
return(new PathologyReportContainer()
{
PathologyReport = new PathologyReport()
{
PerformingLaboratory = LaboratoryFactory.GetPITUSLaboratory(),
Patient = PatientFactory.GetLarissaFERNIE(),
Request = new Request()
{
RequestedDate = RequestedDate,
OrderNumber = "00000010",
RequestingFacility = new Organisation()
{
Name = "Sunrise Hospital Fertility Clinic",
Identifier = new Identifier()
{
Value = "501970A0-1E1F-40D8-9656-61899527203F",
Type = IdentifierType.GUID
}
},
RequestingApplication = "Best Practice 1.8.5.743",
RequestingProvider = ProviderFactory.GetTrishFamilyDr(MedicareProviderNumber: "951577QT"),
ClinicalNotes = "Primary infertility",
CallBackPhoneNumber = null,
CopyToList = new List <Provider>()
{
ProviderFactory.GetGeneticCounsellingClinicCoordinator(),
ProviderFactory.GetSarsgaardGeneticCounsellor(),
}
},
PdfFileName = "Exemplar Report Chromosome studies v1.4.pdf",
ReportList = new List <Report>()
{
new Report()
{
ReportId = "1978881874",
CollectionDateTime = CollectionDateTime,
SpecimenReceivedDateTime = SpecimenReceivedDateTime,
ReportReleaseDateTime = ReportReleaseDateTime,
ReportType = new ReportType()
{
Local = new Code()
{
Term = "CHROMOSTUD", Description = "Chromosome studies"
},
Snomed = null
//Snomed = new Code() { Term = "1308381000168103", Description = "Whole blood cytogenetic analysis" }
},
ReportStatus = ResultStatusType.Final,
Department = DiagnosticService.Hematology,
ReportingPathologist = ProviderFactory.GetKondoPathologist(),
Panel = new Panel()
{
ResultList = new List <Result>()
{
new Result()
{
Type = new ResultType()
{
Local = new Code()
{
Term = "KARYO",
Description = "Cytogenetic karyotyping"
},
Lonic = null
},
DataType = "ST",
Value = "46,X,del(X)(q11.2)",
Units = null,
ReferenceRange = null,
AbnormalFlag = "N",
ObservationDateTime = ObservationDateTime,
Status = ResultStatusType.Final,
ChildResultList = null
},
new Result()
{
Type = new ResultType()
{
Local = new Code()
{
Term = "RES",
Description = "Results"
},
Lonic = null
},
DataType = "FT",
Value = "An abnormal female result showing a deletion of the long arm of the X-chromosome at band q11.2.\\.br\\" +
"This aberration was observed in all cells analysed.\\.br\\" +
"GTG banded analysis was performed on 5 cells analysed and 10 cells counted at a resolution of 550 bands.",
Units = null,
ReferenceRange = null,
AbnormalFlag = "N",
ObservationDateTime = ObservationDateTime,
Status = ResultStatusType.Final,
ChildResultList = null
},
new Result()
{
Type = new ResultType()
{
Local = new Code()
{
Term = "INTERP",
Description = "Interpretation"
},
Lonic = null
},
DataType = "FT",
Value = "Deletions of the long arm of the X-chromosome are associated with a variable phenotype in females. Common\\.br\\" +
"findings include short stature, gonadal dysgenesis and premature ovarian failure. It is likely that this aberration is the\\.br\\" +
"cause of the primary infertility observed in this patient. Genetic counselling is recommended.",
Units = null,
ReferenceRange = null,
AbnormalFlag = "N",
ObservationDateTime = ObservationDateTime,
Status = ResultStatusType.Final,
ChildResultList = null
}
}
}
}
}
}
});
}