FAQs

The objective Lens should always be kept clean. Using index-matching oil at high magnifications could leave some remains on the slide and may get on to other objective lenses. Oil, water or particles of any kind will degrade the image quality and must be removed. The lens should be cleaned only with MILD SOLVENTS (Recommended: Methyl, Ethyl, Isopropyl alcohol or distilled water). 

The fan filter should be cleaned every two months; if conditions are extremely dusty clean the fan filter monthly.  

Cleaning & Disinfection: The objective lens may be cleaned as required with a dry lens cloth only. The laser objective top lens should be cleaned only when needed and with extreme care not to damage, scratch, or remove the anti-reflective coating. At no time should any liquid be allowed to penetrate any part of the system. Refer to the user manual for further instructions. 

You may email support@hamiltonthorne.com at any time to obtain help from our team. Our support team is available to call Monday through Friday 9am to 5pm Eastern Standard Time.  

In the event of an error, a detailed set of data may be saved and sent to Hamilton Thorne to help determine the cause of the problem. In addition to mandatory storage of the Event Log and Application Settings, Report, Templates and Database may also be saved. All data is compressed into a single zip file. 

For blastomere biopsy, the laser is used to drill an opening in the zona pellucida to facilitate insertion of the pipet used to remove the blastomere. For trophectoderm biopsy, the laser is first used to create an opening in the zona to promote herniation of the trophectoderm. After the trophectoderm has protruded, the laser is also used to help separate the trophectoderm cells.

Once a year. Every preventive maintenance performed should include a copy of the preventive maintenance checklist, which must be sent back to the Hamilton Thorne office. 

Please refer to the End of Service life document. 

Laser-assisted hatching may require less embryo handling than other assisted hatching methods. Also, laser-assisted hatching may be faster than other methods and therefore the embryo may spend less time outside of the incubator.

Using the laser for embryo biopsy requires less embryo handling, allows for more precision and control, is less traumatic, and reduces technician variation as compared to chemical and mechanical methods. Because laser embryo biopsy is faster than the other methods, the embryo spends less time outside the incubator and is less likely to be harmed.

There are three methods of assisted hatching: mechanical, chemical, and laser-assisted. With mechanical methods, an incision or hole is made in the zona pellucida using a tool such as a microsurgical knife or a special glass needle. The chemical method directs a stream of acidic hatching solution against outer shell to digest a portion of the zona pellucida. Laser-assisted hatching (LAH) uses a highly focused laser beam to remove the zona pellucida in very precise increments.

There are three methods of biopsy procedures: mechanical, chemical, and laser zona drilling. With mechanical methods, an incision or hole is made in the zona pellucida (the outer layer) using a tool such as a microsurgical knife or a special glass needle. The chemical method directs a stream of acidic solution to digest a portion of the zona pellucida. Laser zona drilling uses a highly focused laser beam to remove the zona pellucida in very precise increments.

The most commonly used indications for PGD are:

• Carriers of single gene disorders.
  These patients benefit from PGD by reducing the risk of conceiving an affected baby.
• Recurrent Miscarriage
  Fertile couples with repeated miscarriages should be evaluated for the presence of a chromosomal abnormality. The female or male partner may be a carrier of a balanced translocation or be an aneuploid mosaic.
• Unsuccessful IVF cycles
  Couples with repeated unsuccessful IVF cycles should be evaluated for the presence of a chromosome abnormality. The female or male partner may be a carrier of a balanced translocation or be an aneuploid mosaic.
• Unexplained Infertility
  The most probable cause of unexplained infertility or history of habitual miscarriage is a chromosome abnormality. The male OR female partner may be a carrier of a translocation or be an aneuploid mosaic.
• Aneuploidy and Advanced Maternal Age
  Women of advanced maternal age (> 35) are at a higher risk of producing aneuploid embryos, resulting in implantation failure, a higher risk of miscarriage or the birth of a child with a chromosome abnormality (e.g. Down syndrome).

The risks of assisting hatching using the laser are similar to the risks when using chemical or mechanical methods. These risks include possible damage / destruction to the embryo and a possible increased chance of monozygotic (identical) twinning.

The risks of embryo biopsy using the laser are similar to the risks when using chemical or mechanical methods. These risks include possible damage / destruction to the embryo and a possible increased chance of monozygotic (identical) twinning.

In recent follow-up studies of babies born after laser-assisted hatching, no increase in major or minor congenital abnormalities and no observable changes in the cells’ genetic material were noted.

In order for an embryo to implant in the uterine lining, the inner embryo (blastocyst) must “hatch” from its protective outer shell (the zona pellucida). Assisted hatching is a technique in which the zona pellucida of an embryo is purposely weakened or cut to help the embryo hatch more easily and promote implantation.

Blastomere biopsy is one method used for embryo biopsy. When an embryo reaches the third day of development, it normally has eight cells. One or two of these cells, called “blastomeres,” can be removed from the embryo. The embryo can go on to develop just as though the one cell or two cells were never removed.

Trophectoderm biopsy is another method used for embryo biopsy. Trophectoderm cells are extra-embryonic tissue; this means that it does not become part of the fetus but becomes part of supporting structures, such as the placenta and membranes. Trophectoderm biopsy takes place at the 16-32 cell “blastocyst” stage of development, as the trophectoderm is beginning to herniate through the zona pellucida. Instead of removing individual blastomeres, several trophectoderm cells are removed.

To date, PGD has been most widely used to enable the birth of children free from diseases such as Down's Syndrome, Tay-Sachs disease, Beta-thalassemia, Cystic Fibrosis, and Duchenne Muscular Dystrophy. Any gene disorder in which the DNA base pairs or code is known can be detected by PGD.

The most commonly used indications for use of assisted hatching are:

The cells removed during the biopsy procedure are used to perform pre-implantation genetic diagnosis (PGD), which shows the chromosomal composition of the embryos, and if they carry a specific disease-producing mutation. One or more embryos free of conditions that would cause serious disease may then be implanted in a woman's uterus.