The Heel-Prick Test Your Newborn Already Had, and Why You Never Heard the Results
The Neugeborenenscreening, a small blood sample taken from your newborn's heel between the 36th and 72nd hour of life, gets confused with the U-Untersuchungen constantly, but it's actually a genuinely separate official process, and for Berlin and Brandenburg specifically, the samples are sent to one dedicated laboratory: the Neugeborenen-Screeninglabor at Charité, based at Augustenburger Platz 1, rather than being processed by your Kinderarzt's own practice. It screens for a specific set of rare but serious metabolic, hormonal, blood, immune, and neuromuscular conditions where early detection genuinely changes outcomes, and the same lab also runs newborn hearing screening. The detail that confuses a lot of parents, newcomers especially: a normal result generally isn't proactively communicated to you at all, national guidance on this screening is explicit that unremarkable findings are typically only shared if you specifically ask or if your birth clinic or hebamme follows up. Silence is the expected, designed outcome for a normal result, not a sign that something was lost or overlooked.
The Official Rule
Somewhere in the blur of your baby’s first few days, a nurse or midwife pricked their heel for a small blood sample, and unless something specific was flagged, you likely never heard about it again. That silence is genuinely by design, not a gap in the system, but it’s worth understanding what actually happened and why.
The Neugeborenenscreening is taken between the 36th and 72nd hour of your baby’s life, and for Berlin and Brandenburg specifically, it runs through one dedicated laboratory. Charité’s own Neugeborenen-Screeninglabor Berlin, based at Augustenburger Platz 1, processes samples for the region as its own distinct official service, separate from your Kinderarzt’s practice or the U1-U9 checkup sequence documented in the U-Heft. This is a genuinely important distinction: it’s a dedicated screening for a specific set of rare but serious conditions, where catching the condition early genuinely changes the outcome for the child.
| Neugeborenenscreening | U-Untersuchungen (U1-U9) | |
|---|---|---|
| Run by | Charité's Neugeborenen-Screeninglabor (Berlin-Brandenburg) | Your Kinderarzt's practice |
| When | Once, 36-72 hours after birth | Ongoing sequence through age 5 |
| Normal result communication | Only shared if you ask | Documented directly with you at each visit |
What the screening actually covers is broader than many parents expect. The laboratory’s own services page describes extended newborn screening for congenital disorders of metabolism, hormone regulation, blood, the immune system, and the neuromuscular system, plus cystic fibrosis screening, all aimed at enabling early therapy or dietary intervention so affected children can develop normally. The lab’s own overview page confirms it also runs newborn hearing screening for the Berlin-Brandenburg region, under the direction of Dr. Oliver Blankenstein.
The detail that confuses a lot of parents, and newcomers in particular: a normal result generally isn’t proactively communicated to you at all. This is a nationally consistent feature of how the Neugeborenenscreening works, not a Berlin-specific quirk, unremarkable findings are typically only shared if you specifically ask, or if your birth clinic or hebamme follows up on your behalf. Silence is the expected, intentional outcome of a normal screening, not a sign that something was lost or overlooked. This runs counter to how most other medical results work, where you’d typically expect to be told either way, which is exactly why it catches people off guard.
If you want explicit confirmation, the information is genuinely available on request, it just isn’t pushed to you by default. Your birth clinic, your hebamme, or the Charité screening laboratory directly can confirm a result for you, this isn’t a hidden or restricted process, it’s simply not an automatic notification the way other test results often are.

What Real People Say
The recurring pattern in how parents describe this is genuine, if brief, confusion: a heel-prick happened at some point in the newborn blur, and then nothing, no call, no letter, no mention at the next Kinderarzt visit. Once parents learn that silence is the actual designed outcome for a normal result, rather than an oversight, the confusion tends to resolve quickly, though it’s a detail that would be genuinely useful to know upfront rather than discovering after searching for an answer.
Parents who specifically wanted confirmation of a normal result describe simply asking their birth clinic, hebamme, or the Charité screening laboratory directly and getting a straightforward answer, the information isn’t hidden, it’s just not pushed to you automatically the way other results are.
Step by Step
- Know that the heel-prick test your newborn had is a separate, laboratory-run process, not part of your Kinderarzt’s regular U-checkups.
- Don’t interpret silence about the result as something going wrong, a normal result generally isn’t proactively communicated at all.
- If you want explicit confirmation of the result, ask your birth clinic, hebamme, or Charité’s screening laboratory directly, this information is available on request.
- If your baby was transferred to a different hospital shortly after birth, trust that sample processing doesn’t depend on staying in one facility, rather than assuming it may have been lost in the transfer.
- Keep this process mentally separate from the U-Heft and U1-U9 schedule, they’re related in spirit but run through entirely different institutions.
Compliance Note
This page explains the general framework for newborn screening (Neugeborenenscreening) in Berlin and Brandenburg, current as of mid-2026. It is not medical advice. For questions about your specific child’s screening or results, contact your birth clinic, hebamme, Kinderarzt, or the Charité screening laboratory directly.
FAQ & Common Pitfalls
We never heard anything back about our baby's heel-prick test. Does that mean it didn't happen, or got lost?
Almost certainly neither. National guidance on the Neugeborenenscreening is explicit that unremarkable (normal) results generally aren't proactively communicated to parents at all, you're typically only told if you specifically ask or if your birth clinic or hebamme follows up. Silence is the expected, designed outcome for a normal result, not a sign that something went wrong or got lost in the process.
Is this the same thing as the U-Untersuchungen or the U-Heft?
No, and this is exactly the confusion worth clearing up. The Neugeborenenscreening is run through a dedicated screening laboratory, for Berlin and Brandenburg that's Charité's own screening lab, as its own distinct process, separate from your Kinderarzt's practice and the U1-U9 checkup sequence documented in the U-Heft. It happens once, very early, using a heel-prick blood sample, rather than being part of the ongoing U-checkup schedule.
What if our baby gets transferred to a children's hospital shortly after birth? Does the screening still happen?
Yes, this is a routine part of how the screening system is designed to work, sample collection and lab processing don't depend on the baby staying in one specific facility. If you're ever unsure whether the sample was actually taken or processed, your birth clinic, hebamme, or the Charité screening laboratory directly can confirm this for you.
Can we actually get the specific result if we want to see it, even if it's normal?
Yes, the process allows for this, unremarkable results can be shared on request, you're not blocked from finding out, the system is simply designed not to proactively push that information to you by default. If you want confirmation, asking your birth clinic, hebamme, or the Charité screening laboratory directly is the way to get it rather than assuming you have to wait for something to be flagged.